催化作用
二氧化碳
联轴节(管道)
二氧化碳电化学还原
甘油
化学
氧化还原
偶联反应
还原(数学)
电化学
光化学
无机化学
化学工程
材料科学
有机化学
物理化学
一氧化碳
电极
冶金
几何学
数学
工程类
作者
Thi-Hong-Hanh Le,Yong Zuo,Manjunath Chatti,Martina Rizzo,Andrea Griesi,Abinaya Annamalai,Simone Lauciello,Luca Leoncino,Mirko Prato,Silvia Dante,Ilka Kriegel,Giorgio Divitini,Michele Ferri,Liberato Manna
标识
DOI:10.1002/ange.202502617
摘要
Glycerol ElectroOxidation Reaction (GEOR) is a promising alternative to the Oxygen Evolution Reaction (OER) in electrolyzers, overcoming the inherent challenges of high energy demand and low‐value output of water oxidation. Here, we designed a non‐noble metal‐based electrocatalyst (CuO@NiBiOx, CNBO) for selective and efficient GEOR. The CNBO‐catalyst demonstrated high selectivity and achieved nearly 100% GEOR Faradaic efficiency (FE), 80% of which is conveyed into formic acid (FA). Bismuth incorporation modified the structure of the mixed oxide, increasing the surface concentration of Ni(III) species and enhancing the GEOR activity. In‐situ studies confirmed the formation of NiOOH, which is identified as the active site for GEOR and suggests an indirect GEOR mechanism. This study demonstrates the potential of GEOR to replace OER in Carbon dioxide reduction reaction (CO2RR) electrolyzers. Depending on the selected CO2RR catalyst (Ag or Sn), we could obtain either an easy‐to‐separate mixture of high‐added value products (CO and FA) or a single product (FA) with FEFA > 85% at both electrodes. Moreover, we demonstrate that replacing OER with GEOR in a CO2RR‐electrolyzer can save up to 25% of the electrolysis energy input while the co‐production of FA at both electrodes halves the energy per mole required for its electrosynthesis.
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