钯基催化剂上电催化CO2与HCOOH的相互转化

Guiru Zhang , Xianxian Qin , Chengwei Deng , Wen-Bin Cai , Kun Jiang
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引用次数: 6

摘要

电化学储能和向可持续碳中和循环转化是当今社会非常关注的问题。从这个角度来看,我们强调通过电催化CO2还原反应(CO2RR)和甲酸氧化反应(FAOR)实现二氧化碳和甲酸之间的相互转化是实现这一目标的有效途径。根据Pd对FAOR和CO2RR可逆驱动的独特催化性质,我们首先阐明了Pd表面上这两种逆转反应之间的密切机理关系。其次,简要总结了近年来钯基双功能催化剂的研究进展及其优化策略,包括优先面暴露的几何结构工程、晶体有序金属间化合物的构建、通过金属或类金属掺杂微调活性和中毒中间体结合强度的电子结构操纵。最后,提出了我们在微观和宏观尺度上对高效的CO2 - HCOOH相互转换回路的设计原则的观点。
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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Electrocatalytic CO2 and HCOOH interconversion on Pd-based catalysts

Electrochemical energy storage and conversion toward sustainable carbon neutrality cycle is of great interest in today's society. In this perspective, we highlight the interconversion between carbon dioxide and formic acid by means of electrocatalytic CO2 reduction reaction (CO2RR) and formic acid oxidation reaction (FAOR) as an effective way to achieve that goal. In line with the distinctive catalytic nature of Pd to reversibly drive both FAOR and CO2RR, we first illustrate the intimate mechanistic relation between these two reversed reactions over Pd surfaces. Next, recent advances in developing Pd-based bifunctional catalysts and relevant optimization strategies are briefly summarized, including geometric structure engineering with preferential facet exposure, construction of crystallographic ordering intermetallic, electronic structure manipulation through metal or metalloid doping to fine tune the binding strength for active and poisoning intermediates. At the end, our viewpoints on the design principles at both microscopic and macroscopic scales are offered toward an efficient CO2 and HCOOH interconversion loop.

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