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Biomimetic Approach to Confer Redox Activity to Thin Chitosan Films
Author(s) -
Kim Eunkyoung,
Liu Yi,
Shi XiaoWen,
Yang Xiaohua,
Bentley William E.,
Payne Gregory F.
Publication year - 2010
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.200902428
Subject(s) - catechol , chitosan , redox , quartz crystal microbalance , electrochemistry , electron transfer , materials science , electrode , cyclic voltammetry , ferrocene , chemical engineering , inorganic chemistry , photochemistry , organic chemistry , chemistry , adsorption , engineering , metallurgy
Electron transfer in biology occurs with individual or pairs of electrons, and is often mediated by catechol/ o ‐quinone redox couples. Here, a biomimetic polysaccharide‐catecholic film is fabricated in two steps. First, the stimuli‐responsive polysaccharide chitosan is electrodeposited as a permeable film. Next, the chitosan‐coated electrode is immersed in a solution containing catechol and the electrode is biased to anodically‐oxidize the catechol. The oxidation products covalently graft to the chitosan films as evidenced by electrochemical quartz crystal microbalance (EQCM) studies. Cyclic voltammetry (CV) measurements demonstrate that the catechol‐modified chitosan films are redox‐active although they are non‐conducting and cannot directly transfer electrons to the underlying electrode. The catechol‐modified chitosan films serve as a localized source or sink of electrons that can be transferred to soluble mediators (e.g., ferrocene dimethanol and Ru(NH 3 ) 6 Cl 3 ). This electron source/sink is finite, can be depleted, but can be repeatedly regenerated by brief (30 s) electrochemical treatments. Further, the catechol‐modified chitosan films can i) amplify currents associated with the soluble mediators, ii) partially‐rectify these currents in either oxidative or reductive directions (depending on the mediator), and iii) switch between regenerated‐ON and depleted‐OFF states. Physical models are proposed to explain these novel redox properties and possible precedents from nature are discussed.