Affiliation:
1. State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan Provincial Key Lab of Fine Chemistry School of Chemical Engineering and Technology Hainan University Haikou 570228 P. R. China
2. Key Laboratory of Electrochemical Energy Storage and Energy Conversion of Hainan Provinc School of Chemistry and Chemical Engineering Hainan Normal University Haikou 571158 P. R. China
Abstract
AbstractElectrochemical 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.
Funder
National Natural Science Foundation of China
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
32 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献