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单壁碳纳米管中残余镍纳米颗粒的部分热雾化用于高效的CO电还原

Partial thermal atomization of residual Ni NPs in single-walled carbon nanotubes for efficient CO electroreduction.

作者信息

Zhang Fengwei, Zhang Han, Zhao Yang, Li Jingjing, Guan Chong, Li Jijie, Wang Xuran, Mu Yuewen, Zan Wen-Yan, Zhu Sheng

机构信息

Institute of Crystalline Materials, Institute of Molecular Science, Key Lab of Materials for Energy Conversion and Storage of Shanxi Province, Key Laboratory of Chemical Biology and Molecular Engineering of Education Ministry, Shanxi University Taiyuan 030006 P. R. China

Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences Dalian 116023 Liaoning P. R. China.

出版信息

Chem Sci. 2024 Nov 25;15(48):20565-20572. doi: 10.1039/d4sc07291j. eCollection 2024 Dec 11.

DOI:10.1039/d4sc07291j
PMID:39600498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11587534/
Abstract

CO electroreduction (CORR) is an important solution for converting inert CO into high value-added fuels and chemicals under mild conditions. The decisive factor lies in the rational design and preparation of cost-effective and high-performance electrocatalysts. Herein, we first prepare a novel f-SWNTs-650 catalyst a facile partial thermal atomization strategy, where the residual Ni particles in single-walled carbon nanotubes (SWNTs) are partially converted into atomically dispersed NiN species. CORR results show that the competitive evolution hydrogen reaction (HER) predominates on pristine SWNTs, while f-SWNTs-650 switches the CO reduction product to CO, achieving a CO faradaic efficiency (FE) of 97.9% and a CO partial current density ( ) of -15.6 mA cm at -0.92 V RHE. Moreover, FE is higher than 95% and remains at -10.0 mA cm at -0.82 V RHE after 48 h potentiostatic electrolysis. Combined with systematic characterization and density functional theory (DFT) calculations, the superior catalytic performance of f-SWNTs-650 is attributed to the synergistic effect between the NiN sites and adjacent Ni NPs, that is, Ni NPs inject electrons into NiN sites to form electron-enriched Ni centers and reduce the energy barrier for CO activation to generate the rate-limiting *COOH intermediate, thus implementing the efficient electroreduction of CO.

摘要

CO电还原(CORR)是在温和条件下将惰性CO转化为高附加值燃料和化学品的重要解决方案。决定性因素在于合理设计和制备具有成本效益的高性能电催化剂。在此,我们首先通过一种简便的部分热原子化策略制备了一种新型的f-SWNTs-650催化剂,其中单壁碳纳米管(SWNTs)中的残留Ni颗粒部分转化为原子分散的NiN物种。CORR结果表明,在原始SWNTs上竞争性析氢反应(HER)占主导,而f-SWNTs-650将CO还原产物转变为CO,在-0.92 V(相对于可逆氢电极,RHE)时实现了97.9%的CO法拉第效率(FE)和-15.6 mA cm⁻²的CO分电流密度(jCO)。此外,在48 h恒电位电解后,在-0.82 V(RHE)时FE高于95%,jCO保持在-10.0 mA cm⁻²。结合系统表征和密度泛函理论(DFT)计算,f-SWNTs-650的优异催化性能归因于NiN位点与相邻Ni纳米颗粒之间的协同效应,即Ni纳米颗粒向NiN位点注入电子以形成富电子的Ni中心并降低CO活化的能垒以生成限速的*COOH中间体,从而实现CO的高效电还原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/70d22f303088/d4sc07291j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/ebd9b5bd12ae/d4sc07291j-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/a46062b41341/d4sc07291j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/11d2b923b102/d4sc07291j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/8ec3012be398/d4sc07291j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/70d22f303088/d4sc07291j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/ebd9b5bd12ae/d4sc07291j-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/a46062b41341/d4sc07291j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/11d2b923b102/d4sc07291j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/8ec3012be398/d4sc07291j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b4/11632820/70d22f303088/d4sc07291j-f4.jpg

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