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非晶化激活的铜铟核壳纳米粒子用于电化学 CO 还原稳定合成气生产。

Amorphization-Activated Copper Indium Core-Shell Nanoparticles for Stable Syngas Production from Electrochemical CO Reduction.

机构信息

Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, 325035, P. R. China.

Institute of New Materials and Industrial Technology, Wenzhou University, Wenzhou, 325035, P. R. China.

出版信息

ChemSusChem. 2022 Dec 7;15(23):e202201350. doi: 10.1002/cssc.202201350. Epub 2022 Oct 26.

Abstract

Electrochemical carbon dioxide reduction reaction (CO RR) refers to the conversion of carbon dioxide into compounds with added value through electrolysis. It is still a great challenge to design and manufacture efficient CO RR catalysts for desired products. Producing syngas via CO RR is an environmentally friendly way to reduce CO in the atmosphere and the dependence on fossil fuels. Herein, a new class of Cu/In O nanoparticles (NPs) with controlled phases and structures were successfully prepared as superior electrocatalysts for CO RR, where the CO/H ratios in syngas on Cu/In O NPs/C-H remained about 1 : 2 at a broad potential range and the total faradaic efficiency of H and CO always remained about 90 %. Electronic structural analysis revealed that the excellent performance was attributed to the electronic interaction between amorphous In O and Cu. This work broadens the horizons for designing and preparing fascinating electrocatalysts for CO RR.

摘要

电化学二氧化碳还原反应(CO RR)是指通过电解将二氧化碳转化为具有附加值的化合物。设计和制造高效的 CO RR 催化剂以获得所需产物仍然是一个巨大的挑战。通过 CO RR 生产合成气是减少大气中 CO 和对化石燃料依赖的一种环保方式。在此,成功制备了一类具有可控相和结构的 Cu/In O 纳米颗粒(NPs),作为 CO RR 的优异电催化剂,在宽电位范围内,Cu/In O NPs/C-H 上合成气的 CO/H 比约为 1∶2,H 和 CO 的总法拉第效率始终约为 90%。电子结构分析表明,优异的性能归因于非晶态 In O 和 Cu 之间的电子相互作用。这项工作拓宽了设计和制备迷人的 CO RR 电催化剂的视野。

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