Improving the stability of photosystem I-based bioelectrodes for solar energy conversion

被引:33
作者
Wolfe, Kody D. [1 ]
Dervishogullari, Dilek [2 ]
Passantino, Joshua M. [3 ]
Stachurski, Christopher D. [2 ]
Jennings, G. Kane [3 ]
Cliffel, David E. [2 ]
机构
[1] Vanderbilt Univ, Interdisciplinary Mat Sci & Engn Program, 221 Kirkland Hall, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Dept Chem, Box 1583, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Dept Chem & Biomol Engn, 221 Kirkland Hall, Nashville, TN 37235 USA
基金
美国国家科学基金会;
关键词
Photosystem I; Reactive oxygen species; Stability; Protein electronics; PHOTOCURRENT GENERATION; ELECTRON-TRANSFER; CYTOCHROME-C; COMPLEXES; GRAPHENE; CELLS; ARCHITECTURES; ORIENTATION; PERFORMANCE; POLYMERS;
D O I
10.1016/j.coelec.2019.09.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Isolated photosystem I (PSI) has been integrated into numerous technologies for solar energy conversion. Interest in PSI is a consequence of its high internal quantum efficiency, thermal stability, ease of extraction, and adaptability. While there has been success in improving performance to elevate PSI biohybrid technologies toward a practical realm, the stability of PSI bioelectrodes is also of critical importance. Commercial solar energy conversion technologies are expected to achieve lifetimes of the order of ten years; however, many research-scale PSI bioelectrodes have only been tested for tens of days. Key areas affecting PSI bioelectrode stability include the effects of reactive oxygen species, immobilization strategies, and the environment within solid-state PSI biohybrid photovoltaics. At the current state, further investigation of long-term stability is necessary in enabling the development of PSI bioelectrodes for both photoelectrochemical cells and solid-state biohybrid photovoltaics.
引用
收藏
页码:27 / 34
页数:8
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