H. Lee, S. M. Dellatore, W. M. Miller, and P. Messersmith, Mussel-Inspired Surface Chemistry for Multifunctional Coatings, Science, vol.39, issue.7, pp.426-430, 2007.
DOI : 10.1038/nrc1391
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2601629/pdf

Y. Ding, L. Weng, M. Yang, Z. Yang, X. Lu et al., Insights into the Aggregation/Deposition and Structure of a Polydopamine Film, Langmuir, vol.30, issue.41, pp.12258-12269, 2014.
DOI : 10.1021/la5026608

M. Mÿller and B. Kessler, Deposition from Dopamine Solutions at Ge Substrates: An in Situ ATR-FTIR Study, Langmuir, vol.27, issue.20, pp.12499-12505, 2011.
DOI : 10.1021/la202908b

S. Hong, C. F. Schaber, K. Dening, E. Appel, S. N. Gorb et al., Air/Water Interfacial Formation of Freestanding, Stimuli-Responsive, Self-Healing Catecholamine Janus-Faced Microfilms, Advanced Materials, vol.115, issue., Suppl, pp.7581-7587, 2014.
DOI : 10.1016/j.zool.2011.11.002

L. Xu, X. Liu, and D. Wang, Interfacial Basicity-Guided Formation of Polydopamine Hollow Capsules in Pristine O/W Emulsions ??? Toward Understanding of Emulsion Template Roles, Chemistry of Materials, vol.23, issue.23, pp.5105-5110, 2011.
DOI : 10.1021/cm2028417

H. Lee, J. Rho, and P. B. Messersmith, Facile Conjugation of Biomolecules onto Surfaces via Mussel Adhesive Protein Inspired Coatings, Advanced Materials, vol.8, issue.4, pp.431-434, 2009.
DOI : 10.1002/adma.200801222

H. O. Ham, Z. Q. Liu, K. H. Lau, H. Lee, and P. Messersmith, Facile DNA Immobilization on Surfaces through a Catecholamine Polymer, Angewandte Chemie International Edition, vol.7, issue.3, pp.732-736, 2011.
DOI : 10.1016/j.elecom.2004.11.010
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090509/pdf

F. Bernsmann, B. Frisch, C. Ringwald, and . V. Ball, Protein adsorption on dopamine???melanin films: Role of electrostatic interactions inferred from ??-potential measurements versus chemisorption, Journal of Colloid and Interface Science, vol.344, issue.1, pp.54-60, 2010.
DOI : 10.1016/j.jcis.2009.12.052

Y. Liu, K. Ai, and L. Lu, Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields, Chemical Reviews, vol.114, issue.9, pp.5067-5115, 2014.
DOI : 10.1021/cr400407a

V. Ball, D. Del-frari, M. Michel, M. J. Buehler, V. Toniazzo et al., Deposition Mechanism and Properties of Thin Polydopamine Films for High Added Value Applications in Surface Science at the Nanoscale, BioNanoScience, vol.133, issue.1, pp.16-34, 2012.
DOI : 10.1021/ja1100189

L. E. Lynge, R. Van-der-westen, A. Postma, and B. Stadler, Polydopamine???a nature-inspired polymer coating for biomedical science, Nanoscale, vol.11, issue.12, pp.4916-4928, 2011.
DOI : 10.1038/nm1314

M. Ryou, D. J. Lee, J. Lee, Y. M. Lee, J. K. Park et al., Excellent Cycle Life of Lithium-Metal Anodes in Lithium-Ion Batteries with Mussel-Inspired Polydopamine-Coated Separators, Advanced Energy Materials, vol.48, issue.121, pp.645-650
DOI : 10.1002/anie.200803786

Y. J. Nam, J. Cha, S. H. Lee, W. J. Yoo, and D. Jung, A new mussel-inspired polydopamine phototransistor with high photosensitivity: signal amplification and light-controlled switching properties, Chem. Commun., vol.5, issue.12, pp.1458-1461, 2014.
DOI : 10.1021/am302833j

H. Long, D. Del-frari, A. Martin, J. Didierjean, V. Ball et al., Polydopamine as a promising candidate for the design of high performance and corrosion-tolerant polymer electrolyte fuel cell electrodes, Journal of Power Sources, vol.307, issue.15, pp.569-577, 2016.
DOI : 10.1016/j.jpowsour.2015.12.138

W. Zhang, F. K. Yang, Y. Han, R. Gaikwad, Z. Leonenko et al., Surface and Tribological Behaviors of the Bioinspired Polydopamine Thin Films under Dry and Wet Conditions, Biomacromolecules, vol.14, issue.2, pp.394-405, 2013.
DOI : 10.1021/bm3015768

N. Farnad, K. Farhadi, and N. H. Voelcker, Polydopamine Nanoparticles as a New and Highly Selective Biosorbent for the Removal of Copper (II) Ions from Aqueous Solutions, Water, Air, & Soil Pollution, vol.157, issue.93, pp.3535-3544, 2012.
DOI : 10.1016/j.jhazmat.2008.01.005

M. Lee, J. Rho, D. Lee, S. Hong, S. Choi et al., Water Detoxification by a Substrate-Bound Catecholamine Adsorbent, ChemPlusChem, vol.6, issue.653, pp.987-990, 2012.
DOI : 10.2217/nnm.11.76
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670806/pdf

L. Hong and J. Simon, Current Understanding of the Binding Sites, Capacity, Affinity, and Biological Significance of Metals in Melanin, The Journal of Physical Chemistry B, vol.111, issue.28, pp.7938-7947, 2007.
DOI : 10.1021/jp071439h

V. Ball, D. Del-frari, V. Toniazzo, and D. Ruch, Kinetics of polydopamine film deposition as a function of pH and dopamine concentration: Insights in the polydopamine deposition mechanism, Journal of Colloid and Interface Science, vol.386, issue.1, pp.366-372, 2012.
DOI : 10.1016/j.jcis.2012.07.030

S. Hong, J. Kim, Y. S. Na, J. Park, S. Kim et al., Poly(norepinephrine): Ultrasmooth Material-Independent Surface Chemistry and Nanodepot for Nitric Oxide, norepinephrine): Ultrasmooth Material Independent Surface Chemistry and Nanodepot for Nitric Oxide, pp.9187-9191, 2013.
DOI : 10.1006/niox.2001.0359

Z. Wang, Y. Xu, Y. Liu, and L. Shao, A novel mussel-inspired strategy toward superhydrophobic surfaces for self-driven crude oil spill cleanup, Journal of Materials Chemistry A, vol.1, issue.23
DOI : 10.1021/am800116d

I. You, Y. C. Seo, and H. Lee, Material-independent fabrication of superhydrophobic surfaces by mussel-inspired polydopamine, RSC Advances, vol.24, issue.20, pp.10330-10333, 2014.
DOI : 10.1021/la802160a

P. Si, J. Wang, J. Guo, S. Li, W. Cai et al., Mussel-inspired one-step modification of a porous structured surface with self-cleaning properties for oil sorption, New Journal of Chemistry, vol.140, issue.402
DOI : 10.1080/00986449608936463

B. D. Freeman, Influence of Polydopamine Deposition Conditions on Pure Water Flux and Foulant Adhesion Resistance of Reverse Osmosis, Ultrafiltration, and Microfiltration Membranes, Polymer, vol.51, pp.3472-3485, 2010.

K. A. Amoaka, K. E. Cook, P. Marek, K. Senecal, and S. Jiang, Achieving One-Step Surface Coating of Highly Hydrophilic Poly(Carboxybetaine Methacrylate) Polymers on Hydrophobic and Hydrophilic Surfaces, Adv. Mater. Interfaces, vol.1, p.1400071, 2014.

C. Yang, K. J. Liao, H. Huang, Q. Y. Wu, L. S. Wana et al., Mussel-inspired modification of a polymer membrane for ultra-high water permeability and oil-in-water emulsion separation, J. Mater. Chem. A, vol.7, issue.418, pp.10225-10230, 2014.
DOI : 10.1021/nn400650f

P. Meredith and T. Sarna, The physical and chemical properties of eumelanin, Pigment Cell Research, vol.77, issue.6, pp.572-594, 2006.
DOI : 10.1007/s007020200055

M. P. Grunze and P. A. Levkin, UV-Triggered Dopamine Polymeization: Control of Polymerization, Surface Coating, and Photoppaterning, Adv. Mater, vol.26, pp.8029-8033, 2014.

M. Li, C. Liu, Q. Xiang, S. Xie, and . Yao, Electrochemical quartz crystal microbalance study on growth and property of the polymer deposit at gold electrodes during oxidation of dopamine in aqueous solutions, Thin Solid Films, vol.497, issue.1-2, pp.270-278, 2006.
DOI : 10.1016/j.tsf.2005.10.048

F. Bernsmann, J. Voegel, and V. Ball, Different Synthesis Methods Allow to Tune the Permeability and Permselectivity of Dopamine-Melanin Films to Electrochemical 96

V. Toniazzo and D. Ruch, Dopamine-melanin film deposition depends on the used oxidant and buffer solution, Langmuir, vol.27, pp.2819-2825, 2011.

Q. Wei, F. Zhang, J. Li, B. Li, and C. Zhao, Oxidant-induced dopamine polymerization for multifunctional coatings, Polymer Chemistry, vol.329, issue.9, pp.1430-1433, 2010.
DOI : 10.1039/c0py00215a

W. Zheng, H. Fan, L. Wang, and Z. Jin, Oxidative Self-Polymerization of Dopamine in an Acidic Environment, Langmuir, vol.31, issue.42, pp.31-11671, 2015.
DOI : 10.1021/acs.langmuir.5b02757

K. L?ster, C. Schÿler, C. Heidrich, R. Horstkorte, and W. Reutter, Quantification of Cell???Matrix and Cell???Cell Adhesion Using Horseradish Peroxidase, Analytical Biochemistry, vol.244, issue.1, pp.96-102, 1997.
DOI : 10.1006/abio.1996.9883

E. Herlinger, R. Jameson, and W. Linert, Spontaneous autoxidation of dopamine, Journal of the Chemical Society, Perkin Transactions 2, issue.2
DOI : 10.1039/p29950000259

S. W. Weidman and E. T. Kaiser, The Mechanism of the Periodate Oxidation of Aromatic Systems. III. A Kinetic Study of the Periodate Oxidation of Catechol, Journal of the American Chemical Society, vol.88, issue.24
DOI : 10.1021/ja00976a024

D. Vecchia, N. F. Avolio, R. Alfe, M. Errico, M. E. Napolitano et al., Building-Block Diversity in Polydopamine Underpins a Multifunctional Eumelanin-Type Platform Tunable Through a Quinone Control Point, Advanced Functional Materials, vol.20, issue.10, pp.1331-1340, 2013.
DOI : 10.1111/j.1600-0749.2006.00359.x

C. Lim, J. Huang, S. Kim, H. Lee, H. Zeng et al., Nanomechanics of Poly(catecholamine) Coatings in Aqueous Solutions, Angewandte Chemie International Edition, vol.126, issue.10, pp.3342-3346, 2016.
DOI : 10.1002/ange.201406858

J. Voegel, P. Schaaf, and V. Ball, Characterization of Dopamine-Melanin Growth on Silicon Oxide, J. Phys. Chem. C, vol.113, pp.8234-8242, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00430678

S. H. Hong, S. Hong, M. Ryou, J. W. Choi, and S. M. Kang, Lee; H. Spayable Ultrafast Polydopamine Surface Modifications, Polydopamine and its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields, pp.5067-5115, 2014.

J. Sed?, J. Saiz-poseu, F. Busqu?, and D. Ruiz-molina, Catechol-Based Biomimetic Functional Materials, Advanced Materials, vol.113, issue.5, pp.653-701, 2013.
DOI : 10.1021/jp9019574

H. C. Yang, J. Luo, Y. Lv, P. Shen, and Z. K. Xu, Surface engineering of polymer membranes via mussel-inspired chemistry, Journal of Membrane Science, vol.483, pp.42-59, 2015.
DOI : 10.1016/j.memsci.2015.02.027

H. Lee, S. M. Dellatore, W. M. Miller, and P. B. Messersmith, Mussel-Inspired Surface Chemistry for Multifunctional Coatings, Science, vol.39, issue.7, pp.318-426, 2007.
DOI : 10.1038/nrc1391
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2601629/pdf

S. H. Hong, S. Hong, R. Myung-hyun, J. W. Choi, S. M. Kang et al., Sprayable Ultrafast Polydopamine Surface Modifications, Advanced Materials Interfaces, vol.24, issue.211, pp.10-1002, 2016.
DOI : 10.1021/cm301967f

F. Ponzio, J. Barthes, J. Bour, M. Michel, P. Bertani et al., Oxidant Control of Polydopamine Surface Chemistry in Acids: A Mechanism-Based Entry to Superhydrophilic-Superoleophobic Coatings, Chemistry of Materials, vol.28, issue.13, 2016.
DOI : 10.1021/acs.chemmater.6b01587

M. E. Lynge, R. Van-der-westen, A. Postma, and B. St?dler, Polydopamine???a nature-inspired polymer coating for biomedical science, Nanoscale, vol.11, issue.12, pp.4916-4928, 2011.
DOI : 10.1038/nm1314

M. Lee, J. Rho, D. Lee, S. Hong, S. Choi et al., Water Detoxification by a Substrate-Bound Catecholamine Adsorbent, ChemPlusChem, vol.6, issue.653, pp.987-990
DOI : 10.2217/nnm.11.76
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670806/pdf

R. Mrówczy@bulletski, A. Bunge, and J. Liebscher, Polydopamine?An Organocatalyst Rather than an Innocent Polymer, Chemistry?A European Journal, vol.20, issue.1528, pp.8647-8653, 2014.

K. Ai, Y. Liu, C. Ruan, L. Lu, and G. M. Lu, Sp2 C-Dominant N-Doped Carbon Submicrometer Spheres with a Tunable Size: A Versatile Platform for Highly Efficient Oxygen- Reduction Catalysts, Advanced Materials, issue.7, pp.25-998, 2013.

A. Postma, Y. Yan, Y. Wang, A. N. Zelikin, E. Tjipto et al., Self-Polymerization of Dopamine as a Versatile and Robust Technique to Prepare Polymer Capsules, Chemistry of Materials, vol.21, issue.14, pp.3042-3044, 2009.
DOI : 10.1021/cm901293e

S. Quignard, M. Ischia, Y. Chen, and J. Fattaccioli, Ultraviolet-Induced Fluorescence of Polydopamine-Coated Emulsion Droplets, ChemPlusChem, vol.19, issue.9, pp.1254-1257, 2014.
DOI : 10.1111/j.1600-0749.2006.00345.x

H. C. Yang, W. Xu, Y. Du, J. Wu, and Z. K. Xu, Composite free-standing films of polydopamine/polyethyleneimine grown at the air/water interface, RSC Adv., vol.20, issue.85, pp.45415-45418, 2014.
DOI : 10.1039/c0jm01339k

N. Schweigert, A. J. Zehnder, and R. I. Eggen, Chemical properties of catechols and their molecular modes of toxic action in cells, from microorganisms to mammals. Minireview, Environmental Microbiology, vol.119, issue.2, pp.81-91, 2001.
DOI : 10.1023/A:1007573414306

H. C. Yang, Q. Y. Wu, L. S. Wan, and Z. K. Xu, Polydopamine gradients by oxygen diffusion controlled autoxidation, Chemical Communications, vol.33, issue.89, pp.49-10522, 2013.
DOI : 10.1016/j.biomaterials.2012.08.011

B. P. Lee, J. L. Dalsin, and P. Messersmith, Synthesis and Gelation of DOPA-Modified Poly(ethylene glycol) Hydrogels, Biomacromolecules, vol.3, issue.5, pp.1038-1047, 2002.
DOI : 10.1021/bm025546n

P. Ball, Does nature know best?, Nature Materials, vol.2, issue.8, pp.509-510, 2003.
DOI : 10.1038/nmat952

J. H. Waite, Evidence for a Repeating 3,4-Dihydroxyphenylalanine-and n the Adhesive Protein of the Hydroxyproline-containing Decapeptide in Mussel, Biol. Chem, vol.258, pp.2911-2915, 1983.

G. A. Young and . Allen, Chapter, pp.19-39, 1982.

H. G. Silverman and F. Roberto, Understanding Marine Mussel Adhesion, Marine Biotechnology, vol.13, issue.35, pp.661-681, 2007.
DOI : 10.1016/B978-0-12-751401-7.50018-1
URL : https://link.springer.com/content/pdf/10.1007%2Fs10126-007-9053-x.pdf

J. Comyn, The relationship between joint durability and water diffusion. Developments in adhesives-2 London, pp.279-313, 1981.

D. L. Schmidt, R. F. Brady, K. Lam, D. C. Schmidt, and M. K. Chaudhury, Contact Angle Hysteresis, Adhesion, and Marine Biofouling, Langmuir, vol.20, issue.7, pp.2830-2836, 2004.
DOI : 10.1021/la035385o

E. C. Bell and J. M. Gosline, Strategies for life in flow:tenacity, morphometry, and probability of dislodgment of two Mytilus species, Marine Ecology Progress Series, vol.159, pp.197-208, 1997.
DOI : 10.3354/meps159197

A. J. Kinloch, Adhesion and Adhesives, Science and Technology, Chapman and Hall, 1987.

S. Suresh, Graded Materials for Resistance to Contact Deformation and Damage, Science, vol.292, issue.5526, pp.2447-2451, 2001.
DOI : 10.1126/science.1059716
URL : http://science.sciencemag.org/content/sci/292/5526/2447.full.pdf

J. H. Waite, N. H. Andersen, S. Jewhurst, and C. Sun, Mussel Adhesion: Finding the Tricks Worth Mimicking, The Journal of Adhesion, vol.302, issue.3-4, pp.297-317, 2005.
DOI : 10.1021/bm015650p

J. Waite and M. Tanzer, Polyphenolic Substance of Mytilus edulis: Novel Adhesive Containing L-Dopa and Hydroxyproline, Science, vol.212, issue.4498, pp.1038-1040, 1981.
DOI : 10.1126/science.212.4498.1038

X. Qin and J. Waite, Exotic collagen gradients in the byssus of themussel Mytilus edulis, J Exp Biol, vol.198, pp.633-644, 1995.

J. H. Waite, Adhesion a la Moule, Integrative and Comparative Biology, vol.42, issue.6, pp.1172-1180, 2002.
DOI : 10.1093/icb/42.6.1172
URL : https://academic.oup.com/icb/article-pdf/42/6/1172/2055423/i1540-7063-042-06-1172.pdf

B. P. Lee, P. B. Messersmith, J. N. Israelachvili, and J. H. Waite, Mussel-Inspired Adhesives and Coatings, Mussel-Inspired Adhesives and Coatings, pp.99-132, 2011.
DOI : 10.1146/annurev-matsci-062910-100429
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207216/pdf

D. S. Hwang, H. Zeng, A. Masic, M. J. Harrington, J. N. Israelachvili et al., Protein- and Metal-dependent Interactions of a Prominent Protein in Mussel Adhesive Plaques, Journal of Biological Chemistry, vol.18, issue.33, pp.285-25850, 2010.
DOI : 10.1242/jeb.009753

Q. Lin, D. Gourdon, C. Sun, N. Holten-andersen, T. H. Anderson et al., Adhesion mechanisms of the mussel foot proteins mfp-1 and mfp-3, Proceedings of the National Academy of Sciences, vol.192, issue.2, pp.3782-3786, 2007.
DOI : 10.1016/0003-2697(91)90560-G

T. H. Anderson, J. Yu, A. Estrada, M. U. Hammer, J. H. Waite et al., The Contribution of DOPA to Substrate-Peptide Adhesion and Internal Cohesion of Mussel-Inspired Synthetic Peptide Films, Advanced Functional Materials, vol.74, issue.23, pp.20-4196, 2010.
DOI : 10.1002/adfm.201000932

J. Yu, W. Wei, E. Danner, R. K. Ashley, J. N. Israelachvili et al., Mussel protein adhesion depends on interprotein thiol-mediated redox modulation, Nature Chemical Biology, vol.7, issue.9, pp.588-590, 2011.
DOI : 10.1080/00218460903291353
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158268/pdf

H. Yamamoto, Adhesive studies of synthetic polypeptides: A model for marine adhesive proteins, Journal of Adhesion Science and Technology, vol.65, issue.1, pp.177-183, 1987.
DOI : 10.1017/S0025315400050487

D. R. 25-filpula, S. M. Lee, R. P. Link, S. L. Strausberg, and R. L. Strausberg, Structural and functional repetition in a marine mussel adhesive protein, Biotechnology Progress, vol.6, issue.3, pp.171-177, 1990.
DOI : 10.1021/bp00003a001

B. P. Lee, J. L. Dalsin, and P. Messersmith, Synthesis and Gelation of DOPA-Modified Poly(ethylene glycol) Hydrogels, Biomacromolecules, vol.3, issue.5, pp.1038-1047, 2002.
DOI : 10.1021/bm025546n

C. Lee, J. Shin, J. S. Lee, E. Byun, J. H. Ryu et al., Bioinspired, calciumfree alginate hydrogels with tunable physical and mechanical properties and improved biocompatibility, Biomacromolecules, issue.6, pp.14-2004, 2013.
DOI : 10.1021/bm400352d

R. M. Wightman, L. J. May, and A. C. Michael, Detection of Dopamine Dynamics in the Brain, Analytical Chemistry, vol.60, issue.13, pp.769-793, 1988.
DOI : 10.1021/ac00164a718

N. Ben-jonathan, Dopamine: A Prolactin-Inhibiting Hormone*, Endocrine Reviews, vol.6, issue.4, pp.564-589, 1985.
DOI : 10.1210/edrv-6-4-564

F. Ponzio, J. Barthes, J. Bour, M. Marc, P. Bertani et al., Oxidant Control of Polydopamine Surface Chemistry in Acids: A Mechanism-Based Entry to Superhydrophilic-Superoleophobic Coatings, Chemistry of Materials, vol.28, issue.13, 2016.
DOI : 10.1021/acs.chemmater.6b01587

T. 33-@bulletuczak, Preparation and characterization of the dopamine film electrochemically deposited on a gold template and its applications for dopamine sensing in aqueous solution, Electrochimica Acta, vol.53, issue.19, pp.5725-5731, 2008.

J. D. Simon and D. N. Peles, The Red and the Black, Accounts of Chemical Research, vol.43, issue.11, pp.1452-1460, 2010.
DOI : 10.1021/ar100079y

A. J. Hamilton and B. L. Gomez, Melanins in fungal pathogens, Journal of medical microbiology, vol.51, issue.3, p.189, 2002.

H. Xu, X. Liu, and D. Wang, Interfacial Basicity-Guided Formation of Polydopamine Hollow Capsules in Pristine O/W Emulsions ??? Toward Understanding of Emulsion Template Roles, Chemistry of Materials, vol.23, issue.23, pp.5105-5110, 2011.
DOI : 10.1021/cm2028417

J. Cui, J. Iturri, J. Paez, Z. Shafiq, C. Serrano et al., Dopamine-Based Coatings and Hydrogels: Toward Substitution-Related Structure-Property Relationships, Macromolecular Chemistry and Physics, vol.5, issue.24, pp.215-2403, 2014.
DOI : 10.1021/am302956h

S. Hong, J. Kim, Y. S. Na, J. Park, S. Kim et al., Poly (norepinephrine): Ultrasmooth Material-Independent Surface Chemistry and Nanodepot for Nitric Oxide, Angewandte Chemie International Edition, issue.35, pp.52-9187, 2013.
DOI : 10.1002/anie.201301646

V. Ball, D. Frari, D. Toniazzo, V. Ruch, and D. , Kinetics of polydopamine film deposition as a function of pH and dopamine concentration: Insights in the polydopamine deposition mechanism, Journal of Colloid and Interface Science, vol.386, issue.1, pp.366-372, 2012.
DOI : 10.1016/j.jcis.2012.07.030

D. Vecchia, N. F. Avolio, R. Alf@bullet, M. Errico, M. E. Napolitano et al., Building-Block Diversity in Polydopamine Underpins a Multifunctional Eumelanin-Type Platform Tunable Through a Quinone Control Point, Advanced Functional Materials, issue.10, pp.23-1331, 2013.

M. Lee, S. H. Lee, I. K. Oh, and H. Lee, Microwave-Accelerated Rapid, Chemical Oxidant-Free, Material-Independent Surface Chemistry of Poly(dopamine), Small, vol.371, issue.4, 2016.
DOI : 10.1006/abbi.1999.1420

F. Bernsmann, V. Ball, F. Addiego, A. Ponche, M. Michel et al., Dopamine???Melanin Film Deposition Depends on the Used Oxidant and Buffer Solution, Langmuir, vol.27, issue.6, pp.27-2819, 2011.
DOI : 10.1021/la104981s

K. Y. Ju, Y. Lee, S. Lee, S. B. Park, and J. K. Lee, Bioinspired Polymerization of Dopamine to Generate Melanin-Like Nanoparticles Having an Excellent Free-Radical-Scavenging Property, Biomacromolecules, vol.12, issue.3, pp.625-632, 2011.
DOI : 10.1021/bm101281b

H. W. Kim, B. D. Mccloskey, T. H. Choi, C. Lee, M. J. Kim et al., Oxygen Concentration Control of Dopamine-Induced High Uniformity Surface Coating Chemistry, ACS Applied Materials & Interfaces, vol.5, issue.2, pp.233-238, 2013.
DOI : 10.1021/am302439g

Q. Wei, F. Zhang, J. Li, B. Li, and C. Zhao, Oxidant-induced dopamine polymerization for multifunctional coatings, Polymer Chemistry, vol.329, issue.9, pp.1430-1433, 2010.
DOI : 10.1039/c0py00215a

J. P. Park, I. T. Song, J. Lee, J. H. Ryu, Y. Lee et al., Vanadyl???Catecholamine Hydrogels Inspired by Ascidians and Mussels, Chemistry of Materials, vol.27, issue.1, pp.105-111, 2014.
DOI : 10.1021/cm503425d

X. Du, L. Li, J. Li, C. Yang, N. Frenkel et al., UV-Triggered Dopamine Polymerization: Control of Polymerization, Surface Coating, and Photopatterning. Advanced Materials, issue.47, pp.26-8029, 2014.

D. Ischia, M. Napolitano, A. Ball, V. Chen, C. T. Buehler et al., Polydopamine and eumelanin: from structure?property relationships to a unified tailoring strategy, Accounts of chemical research, issue.12, pp.47-3541, 2014.

F. Bernsmann, A. Ponche, C. Ringwald, J. Hemmerl?, J. Raya et al., Characterization of dopamine? melanin growth on silicon oxide, The Journal of Physical Chemistry C, issue.19, pp.113-8234, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00430678

S. E. Forest and J. D. Simon, Wavelength-dependent Photoacoustic Calorimetry Study of Melanin, Photochemistry and Photobiology, vol.384, issue.3, pp.296-298, 1998.
DOI : 10.1038/384256a0

R. C. Sealy, J. S. Hyde, C. C. Felix, I. A. Menon, and G. Prota, Eumelanins and pheomelanins: characterization by electron spin resonance spectroscopy, Science, vol.217, issue.4559, pp.217-545, 1982.
DOI : 10.1126/science.6283638

B. Zhu and S. Edmondson, Polydopamine-melanin initiators for Surface-initiated ATRP, Polymer, vol.52, issue.10, pp.2141-2149, 2011.
DOI : 10.1016/j.polymer.2011.03.027

W. Wang, Y. Jiang, Y. Liao, M. Tian, H. Zou et al., Fabrication of silver-coated silica microspheres through mussel-inspired surface functionalization, Journal of Colloid and Interface Science, vol.358, issue.2, pp.567-574, 2011.
DOI : 10.1016/j.jcis.2011.03.023

B. Fei, B. Qian, Z. Yang, R. Wang, W. C. Liu et al., Coating carbon nanotubes by spontaneous oxidative polymerization of dopamine, Carbon, vol.46, issue.13, pp.46-1795, 2008.
DOI : 10.1016/j.carbon.2008.06.049

B. Szpoganicz, S. Gidanian, and P. Kong, Metal binding by melanins: studies of colloidal dihydroxyindole-melanin, and its complexation by Cu(II) and Zn(II) ions, Journal of Inorganic Biochemistry, vol.89, issue.1-2, pp.45-53, 2002.
DOI : 10.1016/S0162-0134(01)00406-8

J. E. Mcginness, Mobility Gaps: A Mechanism for Band Gaps in Melanins, Science, vol.177, issue.4052, pp.896-897, 1972.
DOI : 10.1126/science.177.4052.896

M. M. Jastrzebska, H. Isotalo, J. Paloheimo, and H. Stubb, Electrical conductivity of synthetic DOPA-melanin polymer for different hydration states and temperatures, Journal of Biomaterials Science, Polymer Edition, vol.11, issue.7, pp.577-586, 1996.
DOI : 10.1016/1011-1344(91)80042-G

A. B. Mostert, B. J. Powell, F. L. Pratt, G. R. Hanson, T. Sarna et al., Role of semiconductivity and ion transport in the electrical conduction of melanin, Proceedings of the National Academy of Sciences, vol.289, issue.290, pp.8943-8947, 2012.
DOI : 10.1016/S0921-4526(00)00328-8

H. Wei, J. Ren, B. Han, L. Xu, L. Han et al., Stability of polydopamine and poly(DOPA) melanin-like films on the surface of polymer membranes under strongly acidic and alkaline conditions, Colloids and Surfaces B: Biointerfaces, vol.110, pp.22-28, 2013.
DOI : 10.1016/j.colsurfb.2013.04.008

Q. Liu, B. Yu, W. Ye, and F. Zhou, Highly Selective Uptake and Release of Charged Molecules by pH-Responsive Polydopamine Microcapsules, Macromolecular Bioscience, vol.5, issue.9, pp.1227-1234, 2011.
DOI : 10.1002/mabi.200500176

B. Yu, J. Liu, S. Liu, and F. Zhou, Pdop layer exhibiting zwitterionicity: a simple electrochemical interface for governing ion permeability, Chemical Communications, vol.36, issue.12, pp.46-5900, 2010.
DOI : 10.1039/c0cc00596g

S. H. Ku, J. Ryu, S. K. Hong, H. Lee, and C. B. Park, General functionalization route for cell adhesion on non-wetting surfaces, Biomaterials, vol.31, issue.9, pp.31-2535, 2010.
DOI : 10.1016/j.biomaterials.2009.12.020

Y. Liu, K. Ai, J. Liu, M. Deng, Y. He et al., Dopamine-Melanin Colloidal Nanospheres: An Efficient Near-Infrared Photothermal Therapeutic Agent for In Vivo Cancer Therapy, Advanced Materials, vol.8, issue.9, pp.1353-1359, 2013.
DOI : 10.1089/ars.2006.8.691

C. J. Bettinger, J. P. Bruggeman, A. Misra, J. T. Borenstein, and R. Langer, Biocompatibility of biodegradable semiconducting melanin films for nerve tissue engineering, Biomaterials, vol.30, issue.17, pp.30-3050, 2009.
DOI : 10.1016/j.biomaterials.2009.02.018

H. W. Chien, W. H. Kuo, M. J. Wang, S. W. Tsai, and W. B. Tsai, Tunable Micropatterned Substrates Based on Poly(dopamine) Deposition via Microcontact Printing, Langmuir, vol.28, issue.13, pp.28-5775, 2012.
DOI : 10.1021/la300147p

S. H. Yang, S. M. Kang, K. B. Lee, T. D. Chung, H. Lee et al., Mussel-Inspired Encapsulation and Functionalization of Individual Yeast Cells, Journal of the American Chemical Society, vol.133, issue.9, pp.2795-2797, 2011.
DOI : 10.1021/ja1100189

H. Xu, X. Shi, H. Ma, Y. Lv, L. Zhang et al., The preparation and antibacterial effects of dopa-cotton/AgNPs, Applied Surface Science, vol.257, issue.15, pp.6799-6803, 2011.
DOI : 10.1016/j.apsusc.2011.02.129

X. Ding, C. Yang, T. P. Lim, L. Y. Hsu, A. C. Engler et al., Antibacterial and antifouling catheter coatings using surface grafted PEG-b-cationic polycarbonate diblock copolymers, Biomaterials, vol.33, issue.28, pp.33-6593, 2012.
DOI : 10.1016/j.biomaterials.2012.06.001

W. B. Tsai, W. T. Chen, H. W. Chien, W. H. Kuo, and M. J. Wang, Poly(dopamine) coating of scaffolds for articular cartilage tissue engineering, Acta Biomaterialia, vol.7, issue.12, pp.4187-4194, 2011.
DOI : 10.1016/j.actbio.2011.07.024

S. H. Ku and C. B. Park, Human endothelial cell growth on mussel-inspired nanofiber scaffold for vascular tissue engineering, Biomaterials, vol.31, issue.36, pp.31-9431, 2010.
DOI : 10.1016/j.biomaterials.2010.08.071

X. Zhang, S. Wang, L. Xu, L. Feng, Y. Ji et al., Biocompatible polydopamine fluorescent organic nanoparticles: facile preparation and cell imaging, Nanoscale, vol.13, issue.18, pp.5581-5584, 2012.
DOI : 10.1007/s11051-011-0603-9

C. T. Chen, V. Ball, J. J. De-almeida-gracio, M. K. Singh, V. Toniazzo et al., Self-Assembly of Tetramers of 5,6-Dihydroxyindole Explains the Primary Physical Properties of Eumelanin: Experiment, Simulation, and Design, ACS Nano, vol.7, issue.2, pp.1524-1532, 2013.
DOI : 10.1021/nn305305d

R. Li, K. Parvez, F. Hinkel, X. Feng, and K. Mÿllen, Bioinspired Wafer-Scale Production of Highly Stretchable Carbon Films for Transparent Conductive Electrodes, Angewandte Chemie, vol.24, issue.21, pp.5645-5648, 2013.
DOI : 10.1002/adma.201104211

M. Kohri, Y. Shinoda, H. Kohma, Y. Nannichi, M. Yamauchi et al., Facile Synthesis of Free-Standing Polymer Brush Films Based on a Colorless Polydopamine Thin Layer, Macromolecular Rapid Communications, vol.7, issue.15, pp.34-1220, 2013.
DOI : 10.1039/C0SM01105C

X. H. Yang and Y. Xia, The effect of oxygen pressures on the electrochemical profile of lithium/oxygen battery, Journal of Solid State Electrochemistry, vol.46, issue.1, pp.109-114, 2010.
DOI : 10.1007/s10008-009-0791-8

M. Armand and J. M. Tarascon, Building better batteries, Nature, vol.128, issue.7179, pp.451-652, 2008.
DOI : 10.1038/451652a
URL : https://hal.archives-ouvertes.fr/hal-00258391

J. W. 92-fergus, Ceramic and polymeric solid electrolytes for lithium-ion batteries, Journal of Power Sources, vol.195, issue.15, pp.4554-4569, 2010.
DOI : 10.1016/j.jpowsour.2010.01.076

M. H. Ryou, D. J. Lee, J. N. Lee, Y. M. Lee, J. K. Park et al., Excellent Cycle Life of Lithium-Metal Anodes in Lithium-Ion Batteries with Mussel-Inspired Polydopamine-Coated Separators, Advanced Energy Materials, vol.48, issue.121, pp.645-650, 2012.
DOI : 10.1002/anie.200803786

H. J. Nam, B. Kim, M. J. Ko, M. Jin, J. M. Kim et al., A New Mussel-Inspired Polydopamine Sensitizer for Dye-Sensitized Solar Cells: Controlled Synthesis and Charge Transfer, Chemistry - A European Journal, vol.35, issue.44, pp.18-14000, 2012.
DOI : 10.1007/s00249-005-0020-z

H. Jiang, L. Yang, C. Li, C. Yan, P. S. Lee et al., High???rate electrochemical capacitors from highly graphitic carbon???tipped manganese oxide/mesoporous carbon/manganese oxide hybrid nanowires, Energy & Environmental Science, vol.45, issue.5, pp.1813-1819, 2011.
DOI : 10.1016/j.carbon.2007.08.024

Y. M. Yu, J. H. Zhang, C. H. Xiao, J. D. Zhong, X. H. Zhang et al., High Active Hollow Nitrogen-Doped Carbon Microspheres for Oxygen Reduction in Alkaline Media, Fuel Cells, vol.44, issue.3, pp.506-510, 2012.
DOI : 10.1016/j.carbon.2006.08.022

H. Gao, Y. Sun, J. Zhou, R. Xu, and H. Duan, Mussel-Inspired Synthesis of Polydopamine-Functionalized Graphene Hydrogel as Reusable Adsorbents for Water Purification, ACS Applied Materials & Interfaces, vol.5, issue.2, pp.425-432, 2013.
DOI : 10.1021/am302500v

C. Cheng, S. Li, J. Zhao, X. Li, Z. Liu et al., Biomimetic assembly of polydopamine-layer on graphene: Mechanisms, versatile 2D and 3D architectures 101, situ synthesis of polydopamine?Ag hollow microspheres for hydrogen peroxide sensing, pp.31-35, 2012.

Y. Wang, L. Liu, M. Li, S. Xu, and F. Gao, Multifunctional carbon nanotubes for direct electrochemistry of glucose oxidase and glucose bioassay, Biosensors and Bioelectronics, vol.30, issue.1, pp.107-111, 2011.
DOI : 10.1016/j.bios.2011.08.038

M. K. Manthey, S. G. Pyne, and R. J. Truscott, Addition of Aliphatic and Aromatic Amines to Catechol in Aqueous Solution Under Oxidizing Conditions, Australian Journal of Chemistry, vol.42, issue.3, pp.365-373, 1989.
DOI : 10.1071/CH9890365

R. F. Klein, L. M. Bargas, V. Horak, and M. Navarro, Spontaneous rearrangement in Corey's reaction, Tetrahedron Letters, vol.29, issue.8, pp.29-851, 1988.
DOI : 10.1016/S0040-4039(00)82464-8

A. A. Kutyrev, Nucleophilic reactions of quinones, Tetrahedron, issue.38, pp.47-8043, 1991.
DOI : 10.1016/s0040-4020(01)91002-6

B. Liu, L. Burdine, and T. Kodadek, Chemistry of Periodate-Mediated Cross-Linking of 3,4-Dihydroxylphenylalanine-Containing Molecules to Proteins, Journal of the American Chemical Society, vol.128, issue.47, pp.15228-15235, 2006.
DOI : 10.1021/ja065794h

D. 107-nematollahi and M. Hesari, Electrochemical synthesis of amino-substituted 1,2-benzoquinone derivatives, Journal of Electroanalytical Chemistry, vol.577, issue.2, pp.197-203, 2005.
DOI : 10.1016/j.jelechem.2004.11.031

D. Nematollahi, E. Tammari, S. Sharifi, and M. Kazemi, Mechanistic study of the oxidation of catechol in the presence of secondary amines by digital simulation of cyclic voltammograms, Electrochimica Acta, vol.49, issue.4, pp.591-595, 2004.
DOI : 10.1016/j.electacta.2003.09.013

M. I. Aveldano and H. Sprecher, Very long chain (C24 to C36) polyenoic fatty acids of the n- 3 and n-6 series in dipolyunsaturated phosphatidylcholines from bovine retina, Journal of Biological Chemistry, vol.262, issue.3, pp.1180-1186, 1987.

S. Saito and J. Kawabata, Synergistic Effects of Thiols and Amines on Antiradical Efficiency of Protocatechuic Acid, Journal of Agricultural and Food Chemistry, vol.52, issue.26, pp.8163-8168, 2004.
DOI : 10.1021/jf048970j

M. Nikolantonaki, I. Chichuc, P. L. Teissedre, and P. Darriet, Reactivity of volatile thiols with polyphenols in a wine-model medium: Impact of oxygen, iron, and sulfur dioxide, Analytica Chimica Acta, vol.660, issue.1-2, pp.102-109, 2010.
DOI : 10.1016/j.aca.2009.11.016

M. Nikolantonaki, M. Jourdes, K. Shinoda, P. L. Teissedre, S. Quideau et al., Identification of Adducts between an Odoriferous Volatile Thiol and Oxidized Grape Phenolic Compounds: Kinetic Study of Adduct Formation under Chemical and Enzymatic Oxidation Conditions, Journal of Agricultural and Food Chemistry, vol.60, issue.10, pp.60-2647, 2012.
DOI : 10.1021/jf204295s

S. Haemers, G. J. Koper, and G. Frens, Effect of Oxidation Rate on Cross-Linking of Mussel Adhesive Proteins, Biomacromolecules, vol.4, issue.3, pp.632-640, 2003.
DOI : 10.1021/bm025707n

S. Ito, Encapsulation of a reactive core in neuromelanin, Proceedings of the National Academy of Sciences, vol.96, issue.4, pp.14647-14648, 2006.
DOI : 10.1111/j.1471-4159.2005.03638.x

A. Corani, A. Huijser, A. Iadonisi, A. Pezzella, V. Sundstro@bullet-m et al., Bottom-Up Approach to Eumelanin Photoprotection: Emission Dynamics in Parallel Sets of Water-Soluble 5,6-Dihydroxyindole-Based Model Systems, The Journal of Physical Chemistry B, vol.116, issue.44, pp.13151-13158, 2012.
DOI : 10.1021/jp306436f

J. Liebscher, R. Mro-wczyn-ski, H. A. Scheidt, C. Filip, !. Ha et al., Structure of Polydopamine: A Never-Ending Story?, Langmuir, vol.29, issue.33, pp.29-10539, 2013.
DOI : 10.1021/la4020288

C. T. Buehler and M. J. , Polydopamine and eumelanin: from structure?property relationships to a unified tailoring strategy, Accounts of chemical research, vol.118, issue.12, pp.47-3541, 2014.

D. R. Dreyer, D. J. Miller, B. D. Freeman, D. R. Paul, and C. W. Bielawski, Elucidating the Structure of Poly(dopamine), Langmuir, vol.28, issue.15, pp.28-6428, 2012.
DOI : 10.1021/la204831b

S. Hong, Y. S. Na, S. Choi, I. T. Song, W. Y. Kim et al., Non-Covalent Self-Assembly and Covalent Polymerization Co-Contribute to Polydopamine Formation, Advanced Functional Materials, vol.24, issue.22, pp.22-4711, 2012.
DOI : 10.1002/jcc.10189

A. Pezzella, L. Panzella, A. Natangelo, M. Arzillo, and A. Napolitano, d'Ischia, M. 5, 6- Dihydroxyindole tetramers with " anomalous " interunit bonding patterns by oxidative coupling of 5, 5', 6, 6'-tetrahydroxy-2, 7'-biindolyl: emerging complexities on the way toward an improved model of eumelanin buildup, The Journal of organic chemistry, issue.24, pp.72-9225, 2007.

B. P. Lee, J. L. Dalsin, and P. Messersmith, Synthesis and Gelation of DOPA-Modified Poly(ethylene glycol) Hydrogels, Biomacromolecules, vol.3, issue.5, pp.1038-1047, 2002.
DOI : 10.1021/bm025546n
URL : http://bimat.org/assets/pdf/nu_02_03lee.pdf

L. Panzella, G. Gentile, G. D-'errico, D. Vecchia, N. F. Errico et al., Atypical Structural and ?-Electron Features of a Melanin Polymer That Lead to Superior Free-Radical-Scavenging Properties, Angewandte Chemie International Edition, issue.48, pp.52-12684, 2013.

S. Chatterjee, R. Prados-rosales, S. Tan, B. Itin, A. Casadevall et al., Demonstration of a common indole-based aromatic core in natural and synthetic eumelanins by solid-state NMR, Org. Biomol. Chem., vol.28, issue.34, pp.12-6730, 2014.
DOI : 10.1021/la204831b

H. Lee, N. F. Scherer, and P. B. Messersmith, Single-molecule mechanics of mussel adhesion, Proceedings of the National Academy of Sciences, vol.17, issue.14, pp.12999-13003, 2006.
DOI : 10.1063/1.1143970

R. A. Zangmeister, T. A. Morris, and M. J. Tarlov, Characterization of Polydopamine Thin Films Deposited at Short Times by Autoxidation of Dopamine, Langmuir, vol.29, issue.27, pp.29-8619, 2013.
DOI : 10.1021/la400587j

T. Young, An Essay on the Cohesion of Fluids, Philosophical Transactions of the Royal Society of London, vol.95, issue.0, pp.65-87, 1805.
DOI : 10.1098/rstl.1805.0005

A. Lafuma and D. Qu?r?, Superhydrophobic states, Nature Materials, vol.2, issue.7, pp.457-460, 2003.
DOI : 10.1038/nmat857

L. Gao and T. J. Mccarthy, Contact Angle Hysteresis Explained, Langmuir, vol.22, issue.14, pp.6234-6237, 2006.
DOI : 10.1021/la060254j

J. M. Andanson and A. Baiker, Exploring catalytic solid/liquid interfaces by in situ attenuated total reflection infrared spectroscopy, Chemical Society Reviews, vol.134, issue.12, pp.4571-4584, 2010.
DOI : 10.1039/b919544k
URL : https://hal.archives-ouvertes.fr/hal-01629788

G. Binnig, C. F. Quate, and C. Gerber, Atomic force microscope. Physical review letters, p.930, 1986.

. Bernsmann, Melanin made by dopamine oxidation: Thin films and interactions with polyelectrolytes multilayers, 2010.
URL : https://hal.archives-ouvertes.fr/tel-00502190

P. Drude, Ueber die Gesetze der Reflexion und Brechung des Lichtes an der Grenze absorbirender Krystalle, Annalen der Physik und Chemie, vol.23, issue.12, pp.584-625, 1887.
DOI : 10.1002/andp.18822510202

D. P. Woodruff and T. A. Delchar, Modern techniques of surface science, 1994.

K. L. Johnson, K. Kendall, and A. D. Roberts, Surface Energy and the Contact of Elastic Solids, Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences, vol.324, issue.1558, pp.301-313, 1971.
DOI : 10.1098/rspa.1971.0141

E. Charrault, C. Gauthier, P. Marie, and R. Schirrer, Experimental and Theoretical Analysis of a Dynamic JKR Contact, Langmuir, vol.25, issue.10, pp.25-5847, 2009.
DOI : 10.1021/la803434b
URL : https://hal.archives-ouvertes.fr/hal-00430706

M. Moreno-couranjou, N. Blondiaux, R. Pugin, L. Houerou, V. Gauthier et al., Cover Picture: Plasma Process. Polym. 7???2014, Cover Picture: Plasma Process. Polym. 7? 2014, pp.617-617, 2014.
DOI : 10.1002/ppap.201470026

J. Sedò, J. Saiz-poseu, F. Busqué, and D. Ruiz-molina, Catechol-Based Biomimetic Functional Materials, Advanced Materials, vol.113, issue.5, pp.653-701, 2013.
DOI : 10.1021/jp9019574

F. Bernsmann, B. Frisch, C. Ringwald, and V. Ball, Protein adsorption on dopamine???melanin films: Role of electrostatic interactions inferred from ??-potential measurements versus chemisorption, Journal of Colloid and Interface Science, vol.344, issue.1, pp.54-60, 2010.
DOI : 10.1016/j.jcis.2009.12.052

B. Zhu and S. Edmondson, Polydopamine-melanin initiators for Surface-initiated ATRP, Polymer, vol.52, issue.10, pp.2141-2149, 2011.
DOI : 10.1016/j.polymer.2011.03.027

J. Ryu, S. H. Ku, H. Lee, and C. B. Park, Mussel-Inspired Polydopamine Coating as a Universal Route to Hydroxyapatite Crystallization, Advanced Functional Materials, vol.31, issue.13, pp.2132-2139, 2010.
DOI : 10.1073/pnas.0605552103

F. Bernsmann, A. Ponche, . Ch, J. Ringwald, J. Hemmerlé et al., Characterization of Dopamine???Melanin Growth on Silicon Oxide, The Journal of Physical Chemistry C, vol.113, issue.19, pp.8234-8242, 2009.
DOI : 10.1021/jp901188h
URL : https://hal.archives-ouvertes.fr/hal-00430678

S. Gidanian and P. J. Farmer, Redox behavior of melanins: direct electrochemistry of dihydroxyindole-melanin and its Cu and Zn adducts, Journal of Inorganic Biochemistry, vol.89, issue.1-2, pp.54-60, 2002.
DOI : 10.1016/S0162-0134(01)00405-6

S. Ito and K. Wakamatsu, Chemistry of Mixed Melanogenesis???Pivotal Roles of Dopaquinone, Photochemistry and Photobiology, vol.123, issue.3, pp.582-592, 2008.
DOI : 10.1016/S0304-4165(00)00080-5

M. Ischia, A. Napolitano, A. Pezella, P. Meredith, and T. Sarna, Chemical and Structural Diversity in Eumelanins: Unexplored Bio-Optoelectronic Materials, Angewandte Chemie International Edition, vol.84, issue.512, pp.3914-3921, 2009.
DOI : 10.1111/j.1600-0773.1984.tb01975.x

F. Bernsmann, J. Voegel, and V. Ball, Different synthesis methods allow to tune the permeability and permselectivity of dopamine???melanin films to electrochemical probes, Electrochimica Acta, vol.56, issue.11, pp.3914-3919, 2011.
DOI : 10.1016/j.electacta.2011.02.028

Y. Li, M. Liu, C. Xiang, Q. Xie, and S. Yao, Electrochemical quartz crystal microbalance study on growth and property of the polymer deposit at gold electrodes during oxidation of dopamine in aqueous solutions, Thin Solid Films, vol.497, issue.1-2, pp.270-278, 2006.
DOI : 10.1016/j.tsf.2005.10.048

J. Jiang, L. Zhu, L. Zhu, B. Zhu, and Y. Xu, Surface Characteristics of a Self-Polymerized Dopamine Coating Deposited on Hydrophobic Polymer Films, Langmuir, vol.27, issue.23, pp.14180-14187, 2011.
DOI : 10.1021/la202877k

V. Ball, J. Gracio, M. Vila, M. K. Singh, M. H. Metz-boutigue et al., Cations as Oxidants, Langmuir, vol.29, issue.41, pp.12754-12761, 2013.
DOI : 10.1021/la4029782

]. H. Lee, S. M. Dellatore, W. M. Miller, and P. B. Messersmith, Mussel-Inspired Surface Chemistry for Multifunctional Coatings, Science, vol.39, issue.7, pp.426-430, 2007.
DOI : 10.1038/nrc1391
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2601629/pdf

D. R. Dreyer, D. J. Miller, B. D. Freeman, D. R. Paul, and C. W. Bielawski, Perspectives on poly(dopamine), Chemical Science, vol.113, issue.426, pp.3796-3802, 2013.
DOI : 10.1021/jp901188h

M. E. Lynge, R. Van-der-westen, A. Postma, and B. Städler, Polydopamine???a nature-inspired polymer coating for biomedical science, Nanoscale, vol.11, issue.12, pp.4916-4928, 2012.
DOI : 10.1038/nm1314

H. J. Nam, J. Cha, S. H. Lee, and W. J. Yoo, A new mussel-inspired polydopamine phototransistor with high photosensitivity: signal amplification and light-controlled switching properties, Chem. Commun., vol.5, issue.12, pp.1458-1461, 2014.
DOI : 10.1021/am302833j

M. Ambrico, P. F. Ambrico, A. Cardone, N. F. Della-vecchia, T. Ligonzo et al., Engineering polydopamine films with tailored behaviour for next-generation eumelanin-related hybrid devices, J. Mater. Chem. C, vol.100, issue.5, pp.1018-1028, 2013.
DOI : 10.1063/1.3688491

V. Ball, J. Gracio, M. Vila, M. K. Singh, M. Metz-boutigue et al., Cations as Oxidants, Langmuir, vol.29, issue.41, pp.12754-12761, 2013.
DOI : 10.1021/la4029782

M. Arzillo, G. Mangiapia, A. Pezzella, R. K. Heenan, A. Radulescu et al., Eumelanin Buildup on the Nanoscale: Aggregate Growth/Assembly and Visible Absorption Development in Biomimetic 5,6-Dihydroxyindole Polymerization., Biomacromolecules, vol.13, issue.8, pp.2379-2390, 2012.
DOI : 10.1021/bm3006159

Y. Zhang, B. Thingholm, K. N. Goldie, R. Ogaki, and B. Städler, Assembly of Poly(dopamine) Films Mixed with a Nonionic Polymer, Langmuir, vol.28, issue.51, pp.17585-17592, 2012.
DOI : 10.1021/la304080c

Y. Zhang, B. M. Teo, A. Postma, F. Ercole, R. Ogaki et al., -isopropylacrylamide) as a Component in Poly(dopamine) Films, The Journal of Physical Chemistry B, vol.117, issue.36, pp.10504-10512, 2013.
DOI : 10.1021/jp407106z

A. Chassepot and V. Ball, Human serum albumin and other proteins as templating agents for the synthesis of nanosized dopamine-eumelanin, Journal of Colloid and Interface Science, vol.414, pp.97-102, 2014.
DOI : 10.1016/j.jcis.2013.10.002

V. Ball and C. Surf, Impedance spectroscopy and zeta potential titration of dopa-melanin films produced by oxidation of dopamine, Colloids and Surfaces A: Physicochemical and Engineering Aspects, vol.363, issue.1-3, pp.92-97, 2010.
DOI : 10.1016/j.colsurfa.2010.04.020

J. Riesz, J. Gilmore, and P. Meredith, Quantitative Scattering of Melanin Solutions, Biophysical Journal, vol.90, issue.11, pp.4137-4144, 2006.
DOI : 10.1529/biophysj.105.075713
URL : https://doi.org/10.1529/biophysj.105.075713

F. Bernsmann, A. Ponche, C. Ringwald, J. Hemmerlé, J. Raya et al., Characterization of Dopamine???Melanin Growth on Silicon Oxide, The Journal of Physical Chemistry C, vol.113, issue.19, pp.8234-8242, 2009.
DOI : 10.1021/jp901188h
URL : https://hal.archives-ouvertes.fr/hal-00430678

F. Ponzio, V. Ball, and C. Surf, Persistence of dopamine and small oxidation products thereof in oxygenated dopamine solutions and in ???polydopamine??? films, Colloids and Surfaces A: Physicochemical and Engineering Aspects, vol.443, pp.540-543, 2014.
DOI : 10.1016/j.colsurfa.2013.12.027

F. Ponzio, Role of surfactants in the control of dopamine???eumelanin particle size and in the inhibition of film deposition at solid???liquid interfaces, Journal of Colloid and Interface Science, vol.431, pp.176-179, 2014.
DOI : 10.1016/j.jcis.2014.06.025

C. Bain, E. Troughton, Y. Tao, J. Evall, G. Whitesides et al., Formation of monolayer films by the spontaneous assembly of organic thiols from solution onto gold, Journal of the American Chemical Society, vol.111, issue.1, pp.321-335, 1989.
DOI : 10.1021/ja00183a049

J. Sagiv and J. , Organized monolayers by adsorption. 1. Formation and structure of oleophobic mixed monolayers on solid surfaces, Journal of the American Chemical Society, vol.102, issue.1, pp.92-98, 1980.
DOI : 10.1021/ja00521a016

B. Lee, P. Messersmith, J. Israelachvili, and J. Waite, Mussel-Inspired Adhesives and Coatings, Annual Review of Materials Research, vol.41, issue.1, pp.99-132, 2011.
DOI : 10.1146/annurev-matsci-062910-100429
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207216/pdf

H. Lee, N. Scherer, and P. Messersmith, Single-molecule mechanics of mussel adhesion, Proceedings of the National Academy of Sciences, vol.17, issue.14, pp.12999-13003, 2006.
DOI : 10.1063/1.1143970

F. Zucca, G. Giaveri, M. Gallorini, A. Albertini, M. Toscani et al., The Neuromelanin of Human Substantia Nigra: Physiological and Pathogenic Aspects, Pigment Cell Research, vol.53, issue.3, pp.610-617, 2004.
DOI : 10.1016/S0892-0362(02)00218-0

H. Lee, S. Dellatore, W. Miller, and P. Messersmith, Mussel-Inspired Surface Chemistry for Multifunctional Coatings, Science, vol.39, issue.7, pp.426-430, 2007.
DOI : 10.1038/nrc1391
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2601629/pdf

V. Ball, I. Nguyen, M. Haupt, C. Oehr, C. Arnoult et al., The reduction of Ag+ in metallic silver on pseudomelanin films allows for antibacterial activity but does not imply unpaired electrons, Journal of Colloid and Interface Science, vol.364, issue.2, pp.359-365, 2011.
DOI : 10.1016/j.jcis.2011.08.038

Y. Liu, A. K. Lu, and L. , Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields, Chemical Reviews, vol.114, issue.9, pp.5057-5115, 2014.
DOI : 10.1021/cr400407a

J. Sedó, J. Saiz-poseu, F. Busqué, and D. Ruiz-molina, Catechol-Based Biomimetic Functional Materials, Advanced Materials, vol.113, issue.5, pp.653-701, 2013.
DOI : 10.1021/jp9019574

M. Lynge, R. Van-der-westen, A. Postma, and B. Städler, Polydopamine???a nature-inspired polymer coating for biomedical science, Nanoscale, vol.11, issue.12, pp.4916-4928, 2011.
DOI : 10.1038/nm1314

V. Ball, D. Frari, D. Michel, M. Buehler, M. Toniazzo et al., Deposition Mechanism and Properties of Thin Polydopamine Films for High Added Value Applications in Surface Science at the Nanoscale, BioNanoScience, vol.133, issue.1, pp.16-35, 2012.
DOI : 10.1021/ja1100189

D. Dreyer, D. Miller, B. Freeman, D. Paul, and C. Bielawski, Perspectives on poly(dopamine), Chemical Science, vol.113, issue.426, pp.3796-3802, 2013.
DOI : 10.1021/jp901188h

V. Ball, Physicochemical perspective on ???polydopamine??? and ???poly(catecholamine)??? films for their applications in biomaterial coatings (Review), Biointerphases, vol.9, issue.3, p.30801, 2014.
DOI : 10.1116/1.4875115

P. Meredith and T. Sarna, The physical and chemical properties of eumelanin, Pigment Cell Research, vol.77, issue.6, pp.572-594, 2006.
DOI : 10.1007/s007020200055

V. Ball, J. Gracio, M. Vila, M. Singh, M. Metz-boutigue et al., Cations as Oxidants, Langmuir, vol.29, issue.41, pp.12754-12761, 2013.
DOI : 10.1021/la4029782

Q. Wei, F. Zhang, J. Li, B. Li, and C. Zhao, Oxidant-induced dopamine polymerization for multifunctional coatings, Polymer Chemistry, vol.329, issue.9, pp.1430-1433, 2010.
DOI : 10.1039/c0py00215a

X. Du, L. Li, J. Li, C. Yang, N. Frenkel et al., UV-Triggered Dopamine Polymerization: Control of Polymerization, Surface Coating, and Photopatterning, Advanced Materials, vol.2012, issue.47, pp.8029-8033, 2014.
DOI : 10.1155/2012/985298

B. Stöckle, D. Ng, C. Meier, T. Paust, F. Bischoff et al., Precise Control of Polydopamine Film Formation by Electropolymerization, Macromolecular Symposia, vol.29, issue.1, pp.73-81, 2014.
DOI : 10.1021/la400587j

C. Chen, V. Ball, J. De-almeida-gracio, M. Singh, V. Toniazzo et al., Self-Assembly of Tetramers of 5,6-Dihydroxyindole Explains the Primary Physical Properties of Eumelanin: Experiment, Simulation, and Design, ACS Nano, vol.7, issue.2, pp.1524-1532, 2013.
DOI : 10.1021/nn305305d

I. Langmuir and V. Schaeffer, Composition of Fatty Acid Films on Water Containing Calcium or Barium Salts, Journal of the American Chemical Society, vol.58, issue.2, pp.284-287, 1936.
DOI : 10.1021/ja01293a028

S. Lin, C. Chen, I. Bdikin, V. Ball, J. Gracio et al., Tuning heterogeneous poly(dopamine) structures and mechanics: in silico covalent cross-linking and thin film nanoindentation, Soft Matter, vol.19, issue.3, pp.457-464, 2014.
DOI : 10.1109/JMEMS.2009.2039697

F. Ponzio, P. Payamyar, A. Schneider, M. Winterhalter, J. Bour et al., Polydopamine Films from the Forgotten Air/Water Interface, The Journal of Physical Chemistry Letters, vol.5, issue.19, pp.3436-3440, 2014.
DOI : 10.1021/jz501842r

D. Hönig and D. Möbius, Direct visualization of monolayers at the air-water interface by Brewster angle microscopy, The Journal of Physical Chemistry, vol.95, issue.12, pp.4590-4592, 1991.
DOI : 10.1021/j100165a003

D. Taylor, R. Thomas, and J. Penfold, Polymer/surfactant interactions at the air/water interface, Advances in Colloid and Interface Science, vol.132, issue.2, pp.69-110, 2007.
DOI : 10.1016/j.cis.2007.01.002

C. Bain, P. Claesson, D. Langevin, R. Meszaros, T. Nylander et al., Complexes of surfactants with oppositely charged polymers at surfaces and in bulk, Advances in Colloid and Interface Science, vol.155, issue.1-2, pp.32-49, 2010.
DOI : 10.1016/j.cis.2010.01.007

H. Yang, Q. Wu, L. Wan, and Z. Xu, Polydopamine gradients by oxygen diffusion controlled autoxidation, Chemical Communications, vol.33, issue.89, pp.10522-10524, 2013.
DOI : 10.1016/j.biomaterials.2012.08.011

S. Hong, C. Schaber, K. Dening, E. Appel, S. Gorb et al., Air/Water Interfacial Formation of Freestanding, Stimuli-Responsive, Self-Healing Catecholamine Janus-Faced Microfilms, Advanced Materials, vol.115, issue., Suppl, pp.7581-7587, 2014.
DOI : 10.1016/j.zool.2011.11.002

J. Beattie and A. Djerdjev, The Pristine Oil/Water Interface: Surfactant-Free Hydroxide-Charged Emulsions, Angewandte Chemie International Edition, vol.43, issue.27, pp.3568-3571, 2004.
DOI : 10.1002/anie.200453916

L. Cote, F. Kim, and J. Huang, Langmuir???Blodgett Assembly of Graphite Oxide Single Layers, Journal of the American Chemical Society, vol.131, issue.3, pp.1043-1049, 2009.
DOI : 10.1021/ja806262m

J. Shao, W. Lv, and Y. , Self-Assembly of Graphene Oxide at Interfaces, Advanced Materials, vol.3, issue.32, pp.5586-5612, 2014.
DOI : 10.1126/science.1239089