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Efficient electrochemical reduction of CO to C-2 products on the transition metal and boron co-doped black phosphorene
Kong, Lingyi5,6; Chen, Zhe4; Cai, Qinghai3,5,6; Yin, Lichang1,2; Zhao, Jingxiang5,6
刊名CHINESE CHEMICAL LETTERS
2022-04-01
卷号33期号:4页码:2183-2187
关键词CO reduction Electrocatalysis Multi-carbon products Density functional theory 2D black phosphorene
ISSN号1001-8417
DOI10.1016/j.cclet.2021.09.010
通讯作者Yin, Lichang(lcyin@imr.ac.cn) ; Zhao, Jingxiang(xjz_hmily@163.com)
英文摘要The synthesis of high-value multi-carbon products through the electrochemical reduction of carbon monoxide (COER) is one of the promising avenues for carbon utilization and energy storage, in which searching for efficient electrocatalysts that exhibit moderate CO intermediate binding strength and low kinetic barrier for C-C coupling is a key issue. Herein, by means of comprehensive density functional theory (DFT) computations, we theoretically designed three synergistic coupling catalysts by co-doping transition metal (TM = Fe, Co and Ni) and boron (B) into the two-dimensional black phosphorene (BP), namely TM-B@BP for COER to C-2 products. DFT computations and ab initio molecular dynamics simulations reveal the good stability and high feasibility of these proposed TM-B@BP catalysts for practical applications and future experimental synthesis. More interestingly, high-value ethylene (C2H4), ethane (C2H6) and ethanol (C2H5OH) products can be obtained on these three designed electrocatalysts with ultra-small limiting potentials (-0.20 similar to-0.41 V) and low kinetic energy barriers of C-C coupling (0.52 similar to 0.91 eV). Meanwhile, the competitive one-carbon (C-1) products and hydrogen evolution reaction can also be effectively suppressed. The promising activity and selectivity of these three designed electrocatalysts render them ideal candidates for CO electroreduction, thus providing a cost-effective opportunity to achieve a sustainable production of high value C-2 chemicals and fuels. (c) 2021 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
WOS研究方向Chemistry
语种英语
出版者ELSEVIER SCIENCE INC
WOS记录号WOS:000789375500089
内容类型期刊论文
源URL[http://ir.imr.ac.cn/handle/321006/173884]  
专题金属研究所_中国科学院金属研究所
通讯作者Yin, Lichang; Zhao, Jingxiang
作者单位1.Huaibei Normal Univ, Dept Phys & Elect Informat, Huaibei 235000, Peoples R China
2.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
3.Heilongjiang Prov Collaborat Innovat Ctr Cold Reg, Harbin 150025, Peoples R China
4.Westlake Univ, Ctr Artificial Photosynth Solar Fuels, Sch Sci, Hangzhou 310024, Peoples R China
5.Harbin Normal Univ, Key Lab Photon & Elect Bandgap Mat, Minist Educ, Harbin 150025, Peoples R China
6.Harbin Normal Univ, Coll Chem & Chem Engn, Harbin 150025, Peoples R China
推荐引用方式
GB/T 7714
Kong, Lingyi,Chen, Zhe,Cai, Qinghai,et al. Efficient electrochemical reduction of CO to C-2 products on the transition metal and boron co-doped black phosphorene[J]. CHINESE CHEMICAL LETTERS,2022,33(4):2183-2187.
APA Kong, Lingyi,Chen, Zhe,Cai, Qinghai,Yin, Lichang,&Zhao, Jingxiang.(2022).Efficient electrochemical reduction of CO to C-2 products on the transition metal and boron co-doped black phosphorene.CHINESE CHEMICAL LETTERS,33(4),2183-2187.
MLA Kong, Lingyi,et al."Efficient electrochemical reduction of CO to C-2 products on the transition metal and boron co-doped black phosphorene".CHINESE CHEMICAL LETTERS 33.4(2022):2183-2187.
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