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

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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 N-oxide (PNO) derivative as an efficient electron transfer relay between an organic light absorber and molecular water oxidation catalyst on a nanoparticle TiO2 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 via multi-step electron transfer. The integrated photoanode exhibited a 1 sun current density of 3 mA cm−2 in the presence of Na2SO3 and a highly stable photocurrent density of >0.5 mA cm−2 at 0.4 V vs. 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.

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Zhu, Y., Liu, G., Zhao, R., Gao, H., Li, X., Sun, L., & Li, F. (2022). Photoelectrochemical water oxidation improved by pyridine N-oxide as a mimic of tyrosine-Z in photosystem II. Chemical Science, 13(17), 4955–4961. https://doi.org/10.1039/d2sc00443g

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