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在硼、氮共掺杂碳纳米管上设计钴镍双原子用于将二氧化碳电还原为合成气

Designing cobalt-nickel dual-atoms on boron, nitrogen-codoped carbon nanotubes for carbon dioxide electroreduction to syngas.

作者信息

Ping Dan, Li Yapeng, Wu Shide, Zhang Zhiqiang, Liu Weitao, Wang Dingsheng, Liu Shuqing, Wang Shiwen, Yang Xuzhao, Han Guanglu, Tian Junfeng, Guo Dongjie, Qiu Huajun, Fang Shaoming

机构信息

Henan Provincial Key Laboratory of Surface & Interface Science, Henan Engineering Research Center of Technology and Equipment of Biodegradable Materials, School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002, PR China.

Henan Provincial Key Laboratory of Surface & Interface Science, Henan Engineering Research Center of Technology and Equipment of Biodegradable Materials, School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002, PR China.

出版信息

J Colloid Interface Sci. 2025 Apr;683(Pt 1):446-456. doi: 10.1016/j.jcis.2024.12.096. Epub 2024 Dec 16.

DOI:10.1016/j.jcis.2024.12.096
PMID:39693882
Abstract

Developing highly efficient electrocatalysts to produce syngas with a stable hydrogen/carbon monoxide (H/CO) ratio in a wide potential window via electrochemical carbon dioxide (CO) reduction is desperately required but still challenging. Herein, a dual-atomic site on boron, nitrogen-codoped carbon nanotubes (BCN) has been designed, containing both cobalt (CoN) and nickel (NiNB) sites. Benefiting from the structure advantage and the bifunctional Co/Ni sites, such designed catalyst (CoNi-BCN) demonstrates remarkable performance for syngas production, achieving a stable H/CO ratio of 1.5 over a broad potential window from -0.47 to -0.87 V vs. RHE. By tuning the Co/Ni molar ratio in CoNi-BCN, the H/CO ratio can be adjusted from 0.5 to 2. In addition, this electrocatalyst exhibits outstanding stability within a long-term 20 h electrolyzing. Both experimental and theoretical calculation results confirm the primary role of the Co sites in H production and the Ni sites in CO production, as well as the preferred process for H evolution. This work provides a strategy in the construction of dual-site catalysts for efficient syngas production, which is significant for practical applications.

摘要

迫切需要开发高效的电催化剂,通过电化学二氧化碳还原在宽电位窗口内以稳定的氢/一氧化碳(H/CO)比生产合成气,但这仍然具有挑战性。在此,设计了一种硼、氮共掺杂碳纳米管(BCN)上的双原子位点,包含钴(CoN)和镍(NiNB)位点。得益于结构优势和双功能Co/Ni位点,这种设计的催化剂(CoNi-BCN)在合成气生产中表现出卓越性能,在相对于可逆氢电极(RHE)从-0.47至-0.87 V的宽电位窗口内实现了1.5的稳定H/CO比。通过调节CoNi-BCN中的Co/Ni摩尔比,H/CO比可从0.5调节至2。此外,这种电催化剂在长达20小时的电解过程中表现出出色的稳定性。实验和理论计算结果均证实了Co位点在产氢和Ni位点在产一氧化碳中的主要作用,以及析氢的优先过程。这项工作为构建用于高效合成气生产的双位点催化剂提供了一种策略,对实际应用具有重要意义。

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