Advancing electrocatalytic nitrogen fixation: insights from molecular systems

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL
Jonas C. Peters
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Abstract

Nitrogen fixation has a rich history within the inorganic chemistry community. In recent years attention has (re)focused on developing electrocatalytic systems capable of mediating the nitrogen reduction reaction (N2RR). Well-defined molecular catalyst systems have much to offer in this context. This personal perspective summarizes recent progress from our laboratory at Caltech, pulling together lessons learned from a number of studies we have conducted, placing them within the broader context of thermodynamic efficiency and selectivity for the N2RR. In particular, proton-coupled electron transfer (PCET) provides an attractive strategy to achieve enhanced efficiency for the multi-electron/proton reduction of N2 to produce NH3 (or NH4+), and electrocatalytic PCET (ePCET) via an ePCET mediator affords a promising means of mitigating HER such that the N2RR can be achieved in a catalytic fashion.

Abstract Image

推进电催化固氮:从分子系统的见解
固氮在无机化学界有着悠久的历史。近年来,氮还原反应(N2RR)的电催化系统的开发成为人们关注的焦点。在这种情况下,定义良好的分子催化剂系统可以提供很多东西。这篇个人观点总结了我们在加州理工学院实验室的最新进展,汇集了我们从许多研究中吸取的经验教训,将它们置于N2RR的热力学效率和选择性的更广泛背景下。特别是,质子耦合电子转移(PCET)提供了一种有吸引力的策略,可以提高N2多电子/质子还原生成NH3(或NH4+)的效率,而通过ePCET介质的电催化PCET (ePCET)提供了一种有希望的减轻HER的方法,使N2RR可以以催化方式实现。
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Faraday Discussions
Faraday Discussions 化学-物理化学
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期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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