氧化还原
700页
光系统I
自愈水凝胶
光系统
化学
电化学
电子转移
光系统II
光合反应中心
接受者
光化学
电子受体
阳极
光合作用
电极
无机化学
物理化学
高分子化学
物理
生物化学
凝聚态物理
作者
Volker Hartmann,Tim Kothe,Sascha Pöller,Eithar El-Mohsnawy,Marc M. Nowaczyk,Nicolas Plumeré,Wolfgang Schuhmann,Matthias Rögner
摘要
The improvement of Z-scheme inspired biophotovoltaics is achieved by fine tuning the properties of redox hydrogels applied as immobilization and electron conducting matrices for the photosystem-protein complexes. The formal potentials of the redox hydrogels are adjusted to the respective redox sites in the photosystems for optimized electron transfer without substantial voltage loss. The anode is based on photosystem 2 (PS2) integrated in a phenothiazine modified redox hydrogel with a formal potential of -1 mV vs. SHE, which is 59 mV more positive than the QB acceptor site in PS2. The cathode is based on photosystem 1 (PS1) contacted via an Os-complex based redox hydrogel with a formal potential of 395 mV vs. SHE, i.e. 28 mV more negative than the primary P700 electron acceptor of PS1. The potential difference between the two redox hydrogels is 396 mV. An open circuit voltage (VOC) of 372.5 ± 2.1 mV could be achieved for the biophotovoltaic cell. The maximum power output is 1.91 ± 0.56 μW cm(-2) and the conversion efficiency (η) is 4.5 × 10(-5), representing a 125-fold improvement in comparison to the previously proposed device exploiting the photosynthetic Z-scheme for electrical energy production.
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