光系统II
光养
活性氧
化学
析氧
氧气
光化学
光合作用
降级(电信)
光合反应中心
生物物理学
光电阴极
电化学
电极
生物化学
计算机科学
生物
物理
电信
有机化学
物理化学
量子力学
电子
作者
Fangyuan Zhao,Steffen Hardt,Volker Hartmann,Huijie Zhang,Marc M. Nowaczyk,Matthias Rögner,Nicolas Plumeré,Wolfgang Schuhmann,Felipe Conzuelo
标识
DOI:10.1038/s41467-018-04433-z
摘要
Interfacing photosynthetic proteins specifically photosystem 1 (PS1) with electrodes enables light-induced charge separation processes for powering semiartificial photobiodevices with, however, limited long-term stability. Here, we present the in-depth evaluation of a PS1/Os-complex-modified redox polymer-based biocathode by means of scanning photoelectrochemical microscopy. Focalized local illumination of the bioelectrode and concomitant collection of H2O2 at the closely positioned microelectrode provide evidence for the formation of partially reduced oxygen species under light conditions. Long-term evaluation of the photocathode at different O2 concentrations as well as after incorporating catalase and superoxide dismutase reveals the particularly challenging issue of avoiding the generation of reactive species. Moreover, the evaluation of films prepared with inactivated PS1 and free chlorophyll points out additional possible pathways for the generation of oxygen radicals. To avoid degradation of PS1 during illumination and hence to enhance the long-term stability, the operation of biophotocathodes under anaerobic conditions is indispensable.
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