电催化剂
碳纤维
催化作用
材料科学
法拉第效率
镍
电化学
选择性
化学工程
电解质
纳米颗粒
金属有机骨架
无机化学
纳米技术
电极
复合数
化学
冶金
复合材料
有机化学
物理化学
工程类
吸附
作者
Minglong Guo,Shengjun Du,Guangxing Yang,Qiao Zhang,Zhiting Liu,Feng Peng
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2024-06-06
卷期号:38 (12): 11043-11050
被引量:2
标识
DOI:10.1021/acs.energyfuels.4c01580
摘要
Electrochemical CO2 reduction reaction (ECO2RR) represents a promising approach for attaining a neutral carbon cycle and the sustainable production of value-added chemicals. However, fabricating nonprecious metals catalysts with high selectivity within a broad potential window and excellent stability under tough electrolytic conditions remains a great challenge. Herein, we developed an in situ confining strategy to prepare metal–organic frameworks derived N-doped carbon-wrapped nickel nanoparticles for ECO2RR to CO. The optimal Ni-MOF@NC exhibited a remarkable Faradaic efficiency (FE) of 99% and a partial current density of −26.3 mA/cm2 toward CO at −1.0 V (vs RHE). The CO FE maintained a high value of over 90% within a wide potential range of −0.8 to −1.4 V (vs RHE). The well-designed control experiments reveal that the high catalytic activity is attributed to the N-doped carbon layer encapsulating the Ni particles. Furthermore, benefiting from the protective carbon–nitrogen shell, the Ni-MOF@NC composite exhibited robust durability under a high local alkaline environment. This work offers a promising design principle for constructing N-doped carbon-wrapped nickel electrocatalysts for ECO2RR with high catalytic activity and CO selectivity.
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