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通过吡啶氧化物模拟光系统II中的酪氨酸-Z改善光电化学水氧化。

Photoelectrochemical water oxidation improved by pyridine -oxide as a mimic of tyrosine-Z in photosystem II.

作者信息

Zhu Yong, Liu Guoquan, Zhao Ran, Gao Hua, Li Xiaona, Sun Licheng, Li Fei

机构信息

State Key Laboratory of Fine Chemicals, Dalian University of Technology Dalian 116024 China

Key Laboratory of Industrial Ecology and Environmental Engineering (MOE), School of Environmental Science and Technology, Dalian University of Technology Dalian 116024 China.

出版信息

Chem Sci. 2022 Apr 1;13(17):4955-4961. doi: 10.1039/d2sc00443g. eCollection 2022 May 4.

Abstract

Artificial photosynthesis provides a way to store solar energy in chemical bonds with water oxidation as a major challenge for creating highly efficient and robust photoanodes that mimic photosystem II. We report here an easily available pyridine -oxide (PNO) derivative as an efficient electron transfer relay between an organic light absorber and molecular water oxidation catalyst on a nanoparticle TiO photoanode. Spectroscopic and kinetic studies revealed that the PNO/PNO˙ couple closely mimics the redox behavior of the tyrosine/tyrosyl radical pair in PSII in improving light-driven charge separation multi-step electron transfer. The integrated photoanode exhibited a 1 sun current density of 3 mA cm in the presence of NaSO and a highly stable photocurrent density of >0.5 mA cm at 0.4 V NHE over a period of 1 h for water oxidation at pH 7. The performance shown here is superior to those of previously reported organic dye-based photoanodes in terms of photocurrent and stability.

摘要

人工光合作用提供了一种将太阳能存储在化学键中的方法,而水氧化是制造模仿光系统II的高效且稳定的光阳极的主要挑战。我们在此报告一种易于获得的吡啶氧化物(PNO)衍生物,它作为纳米颗粒TiO光阳极上有机光吸收剂与分子水氧化催化剂之间的有效电子转移中继体。光谱和动力学研究表明,PNO/PNO˙ 对在改善光驱动电荷分离的多步电子转移方面紧密模仿了PSII中酪氨酸/酪氨酸自由基对的氧化还原行为。在NaSO存在的情况下,集成光阳极在1个太阳光照射下的电流密度为3 mA cm,并且在pH值为7的条件下,在0.4 V(相对于标准氢电极)时,经过1小时的水氧化过程,具有大于0.5 mA cm的高度稳定的光电流密度。此处所示的性能在光电流和稳定性方面优于先前报道的基于有机染料的光阳极。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7c/9067620/6ad56c7b9945/d2sc00443g-f1.jpg

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