Ultrathin Nitrogen-Doped Carbon Encapsulated Ni Nanoparticles for Highly Efficient Electrochemical CO2 Reduction and Aqueous Zn-CO2 Batteries

被引:48
作者
Wang, Fangyuan [1 ]
Wang, Guan [1 ]
Deng, Peilin [1 ]
Chen, Yao [1 ]
Li, Jing [1 ]
Wu, Daoxiong [1 ]
Wang, Zhitong [1 ]
Wang, Chongtai [2 ]
Hua, Yingjie [2 ]
Tian, Xinlong [1 ]
机构
[1] Hainan Univ, Sch Chem Engn & Technol, State Key Lab Marine Resource Utilizat South China, Hainan Prov Key Lab Fine Chem, Haikou 570228, Peoples R China
[2] Hainan Normal Univ, Sch Chem & Chem Engn, Key Lab Electrochem Energy Storage & Energy Conver, Haikou 571158, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2 electrochemical reduction; core-shell structures; electronic effect; N-doped carbon shells; Zn-CO2; batteries; CATALYTIC PERFORMANCE; FLOW CELL; ELECTROREDUCTION; ELECTROCATALYSTS; METHANOL; DIOXIDE; SITES; METAL;
D O I
10.1002/smll.202301128
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical CO2 reduction reaction (CO2RR), powered by renewable electricity, has attracted great attention for producing high value-added fuels and chemicals, as well as feasibly mitigating CO2 emission problem. Here, this work reports a facile hard template strategy to prepare the Ni@N-C catalyst with core-shell structure, where nickel nanoparticles (Ni NPs) are encapsulated by thin nitrogen-doped carbon shells (N-C shells). The Ni@N-C catalyst has demonstrated a promising industrial current density of 236.7 mA cm(-2) with the superb FECO of 97% at -1.1 V versus RHE. Moreover, Ni@N-C can drive the reversible Zn-CO2 battery with the largest power density of 1.64 mW cm(-2), and endure a tough cycling durability. These excellent performances are ascribed to the synergistic effect of Ni@N-C that Ni NPs can regulate the electronic microenvironment of N-doped carbon shells, which favor to enhance the CO2 adsorption capacity and the electron transfer capacity. Density functional theory calculations prove that the binding configuration of N-C located on the top of Ni slabs (Top-Ni@N-C) is the most thermodynamically stable and possess a lowest thermodynamic barrier for the formation of COOH* and the desorption of CO. This work may pioneer a new method on seeking high-efficiency and worthwhile electrocatalysts for CO2RR and Zn-CO2 battery.
引用
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页数:8
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