基于氢酶及其模拟物的生物启发光驱动氢进化系统

IF 5 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Sustainable Energy & Fuels Pub Date : 2024-08-30 DOI:10.1039/D4SE00423J
Rahat Gupta and Amlan K. Pal
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引用次数: 0

摘要

通过开发可持续的可再生能源,可以解决日益严重的能源危机问题。自然界存在的氢化酶及其活性位点为我们提供了模仿制氢反应途径和机制的蓝图。本研究深入总结了利用 4d/5d-T 金属复合物、量子点和有机染料作为光敏剂(PSs)以及氢酶模拟物作为催化剂的光催化制氢方法。本综述的重点是精心设计光敏剂和催化剂,以提高人工光合作用系统的整体催化活性。文章讨论了光诱导电子转移过程中的路径,包括催化剂的活性位点,以指导设计稳健高效的光催化制氢系统。讨论了催化剂和 PS 的还原电位、自由能值的变化以及密度泛函理论 (DFT) 计算,以评估光诱导电子转移过程的热力学可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Bioinspired photo-driven hydrogen evolution systems based on hydrogenases and their mimics

The ever-growing problem of the energy crisis can be addressed with the development of sustainable and renewable sources of energy. The naturally occurring hydrogenases with their active sites provide us with a blueprint to mimic the reaction pathway and mechanism of hydrogen production. This work presents an in-depth summary of the photocatalytic hydrogen production employing 4d/5d-T-metal complexes, quantum dots, and organic dyes as photosensitizers (PSs) and hydrogenase mimics as catalysts. This review is focused on the careful design of both the PSs and catalysts to enhance the overall catalytic activity of artificial photosynthetic systems. The paths followed during the photoinduced electron transfer including the active sites of the catalysts, are discussed to guide the design of robust and efficient photocatalytic hydrogen production systems. The reduction potentials of the catalysts and PSs, change in the free energy values and density functional theory (DFT) calculations are discussed to assess the thermodynamic feasibility of the photoinduced electron transfer processes.

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来源期刊
Sustainable Energy & Fuels
Sustainable Energy & Fuels Energy-Energy Engineering and Power Technology
CiteScore
10.00
自引率
3.60%
发文量
394
期刊介绍: Sustainable Energy & Fuels will publish research that contributes to the development of sustainable energy technologies with a particular emphasis on new and next-generation technologies.
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