Boron doping induced strong anchor effect between bimetal NiCo alloy and carbon support for efficient electrocatalytic nitrate reduction to ammonia.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2024-11-18 DOI:10.1002/cssc.202401979
Meng Zhang, Xuetao Cheng, Yun Duan, Junxiang Cheng, Yan-Qin Wang
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引用次数: 0

Abstract

The electrochemical reduction of nitrate to ammonia presents a promising alternative to the conventional Haber-Bosch process. In this study, a bimetallic NiCo alloy embedded in metal-organic framework derived carbon layer with B doping electrocatalyst NiCo@BC was first successfully developed, which exhibits excellent electrochemical nitrate reduction to ammonia (ENO3RR) performance. In-depth in situ experiments and a machine-learning potential (MLP)-based simulation reveal that B doping within the carbon layer has a crucial anchor effect that induces strong binding between bimetal NiCo alloy and carbon support. Moreover, B doping leads to a decrease in the coordination numbers around the metals, which results in a reduction of the excessively strong intermediates adsorption in the ENO3RR process, thereby significantly enhancing catalytic activity. The fabrication strategy of this electrocatalyst provides a new avenue on ENO3RR research.

硼掺杂诱导双金属镍钴合金与碳支撑之间产生强烈的锚定效应,从而实现高效电催化硝酸盐还原成氨。
通过电化学方法将硝酸盐还原成氨是传统哈伯-博施工艺的一种很有前景的替代方法。本研究首次成功开发了一种嵌入金属有机框架衍生碳层的双金属镍钴合金,其掺杂硼的电催化剂 NiCo@BC,表现出优异的电化学硝酸盐还原成氨(ENO3RR)性能。深入的原位实验和基于机器学习电位(MLP)的模拟显示,碳层中的硼掺杂具有关键的锚定效应,可诱导双金属镍钴合金与碳支撑之间的强结合。此外,掺杂硼还会导致金属周围的配位数减少,从而减少 ENO3RR 过程中过强的中间产物吸附,从而显著提高催化活性。这种电催化剂的制备策略为 ENO3RR 研究提供了一条新途径。
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来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
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