电子转移
氧化还原
背景(考古学)
电化学
极化子
化学
电极
聚合物
马库斯理论
导电聚合物
电子传输链
化学物理
纳米技术
材料科学
动力学
物理化学
电子
反应速率常数
有机化学
物理
生物
古生物学
量子力学
生物化学
作者
N. Samali Weliwatte,Olja Simoska,Daniel Powell,Miharu Koh,Matteo Grattieri,Luisa Whittaker‐Brooks,Carol Korzeniewski,Shelley D. Minteer
标识
DOI:10.1149/1945-7111/ac84b2
摘要
Poor electrochemical communication between biocatalysts and electrodes is a ubiquitous limitation to bioelectrocatalysis efficiency. An extensive library of polymers has been developed to modify biocatalyst-electrode interfaces to alleviate this limitation. As such, conducting redox polymers (CRPs) are a versatile tool with high structural and functional tunability. While charge transport in CRPs is well characterized, the understanding of charge transport mechanisms facilitated by CRPs within decisively complex photobioelectrocatalytic systems remains very limited. This study is a comprehensive analysis that dissects the complex kinetics of photobioelectrodes into fundamental blocks based on rational assumptions, providing a mechanistic overview of charge transfer during photobioelectrocatalysis. We quantitatively compare two biohybrids of metal-free unbranched CRP (polydihydroxy aniline) and photobiocatalyst (intact chloroplasts), formed utilizing two deposition strategies ( “mixed” and “layered” depositions). The superior photobioelectrocatalytic performance of the “ layered” biohybrid compared to the “ mixed” counterpart is justified in terms of rate ( D app ), thermodynamic and kinetic barriers (H ≠ , E a ), frequency of molecular collisions ( D 0 ) during electron transport across depositions, and rate and resistance to heterogeneous electron transfer ( k 0 , R CT ). Our results indicate that the primary electron transfer mechanism across the biohybrids, constituting the unbranched CRP, is thermally activated intra- and inter-molecular electron hopping, as opposed to a non-thermally activated polaron transfer model typical for branched CRP- or conducting polymer (CP)-containing biohybrids in literature. This work underscores the significance of subtle interplay between CRP structure and deposition strategy in tuning the polymer-catalyst interfaces, and the branched/unbranched structural classification of CRPs in the bioelectrocatalysis context.
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