材料科学
法拉第效率
催化作用
电化学
电催化剂
铜
二氧化碳电化学还原
一氧化碳
化学工程
吸附
氧化还原
原位
复合数
氧化物
碳纤维
产量(工程)
联轴节(管道)
还原(数学)
纳米技术
选择性
工作(物理)
金属有机骨架
多相催化
电极
配体(生物化学)
选择性催化还原
无机化学
氧化铜
二氧化碳
合成气
选择性还原
纳米晶
乙醇
乙醇燃料
作者
Ziyu Yu,Jian Wang,Mingzheng Gu,Qiao Chen,Xiaojun Zhang
标识
DOI:10.1021/acsami.6c03213
摘要
The electrocatalytic carbon dioxide reduction reaction (CO2RR) offers a promising approach for the conversion of carbon dioxide into valuable C2 chemicals and fuels. Nevertheless, challenges persist in attaining high selectivity, stability, and yield. Dual-phase copper-based catalysts, particularly cuprous oxide (Cu2O), exhibit potential owing to their favorable carbon monoxide adsorption and carbon-carbon (C-C) coupling capabilities. However, they encounter problems such as structural instability, agglomeration, and insufficient Faradaic efficiency (FE) for C2 products. This study addresses these limitations by proposing an innovative strategy for the oriented growth of in situ coordinated metal-organic framework (MOF) shells on spherical Cu2O. Through the control of ligand density on the Cu2O surface, a Cu2O@Cu-BTC composite catalyst was synthesized, integrating the advantages of Cu2O and MOFs. The MOF shell not only stabilizes the Cu2O core against agglomeration, but also creates a Cu(I)-O coordination microenvironment that enhances C-C coupling efficiency. Electrochemical evaluations reveal exceptional performance. The low-coordination copper sites at the Cu2O@Cu-BTC-0.5 interface achieve a high FE of 58.5% for ethanol (C2H5OH) production, along with a yield of 454.73 μmol cm-2 in neutral media, and improved structural durability. This work emphasizes the crucial role of tailored coordination environments in MOF-based composite catalysts for optimizing CO2RR pathways, presenting a feasible strategy to promote the scalable production of C2 products with high selectivity and stability.
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