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用于将一氧化碳快速选择性电还原为甲酸盐的封装氧化铋的金属有机框架衍生碳纳米棒。

Metal-Organic Framework-Derived Carbon Nanorods Encapsulating Bismuth Oxides for Rapid and Selective CO Electroreduction to Formate.

作者信息

Deng Peilin, Yang Fan, Wang Zhitong, Chen Shenghua, Zhou Yinzheng, Zaman Shahid, Xia Bao Yu

机构信息

Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, Wuhan National Laboratory for Optoelectronics, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan, 430074, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2020 Jun 26;59(27):10807-10813. doi: 10.1002/anie.202000657. Epub 2020 Apr 28.

Abstract

Carbon dioxide (CO ) conversion is promising in alleviating the excessive CO level and simultaneously producing valuables. This work reports the preparation of carbon nanorods encapsulated bismuth oxides for the efficient CO electroconversion toward formate production. This resultant catalyst exhibits a small onset potential of -0.28 V vs. RHE and partial current density of over 200 mA cm with a stable and high Faradaic efficiency of 93 % for formate generation in a flow cell configuration. Electrochemical results demonstrate the synergistic effect in the Bi O @C promotes the rapid and selective CO reduction in which the Bi O is beneficial for improving the reaction kinetics and formate selectivity, while the carbon matrix would be helpful for enhancing the activity and current density of formate production. This work provides effective bismuth-based MOF derivatives for efficient formate production and offers insights in promoting practical CO conversion technology.

摘要

二氧化碳(CO₂)转化在缓解过量CO₂水平并同时生产有价值的产品方面具有广阔前景。这项工作报道了用于高效电催化CO₂转化生成甲酸盐的碳纳米棒包裹氧化铋的制备。在流动池配置中,这种所得催化剂相对于可逆氢电极(RHE)表现出-0.28 V的小起始电位和超过200 mA cm⁻²的分电流密度,并且对于甲酸盐生成具有93 %的稳定且高的法拉第效率。电化学结果表明Bi₂O₃@C中的协同效应促进了快速且选择性的CO₂还原,其中Bi₂O₃有利于改善反应动力学和甲酸盐选择性,而碳基质有助于提高甲酸盐生产的活性和电流密度。这项工作为高效生产甲酸盐提供了有效的铋基金属有机框架衍生物,并为推动实际的CO₂转化技术提供了见解。

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