镍
酞菁
石墨
共轭体系
材料科学
无机化学
化学
冶金
纳米技术
聚合物
复合材料
作者
Jingwei Han,Qiang Xu,Fengkun Tian,Hai Sun,Yuanyuan Qi,Guodong Zhang,Jun‐Sheng Qin,Heng Rao
出处
期刊:Chemical Science
[Royal Society of Chemistry]
日期:2024-01-01
卷期号:15 (38): 15670-15678
被引量:10
摘要
The linking chemistry between molecular catalysts and substrates is a crucial challenge for enhancing electrocatalytic performance. Herein, we elucidate the influence of various immobilization methods of amino-substituted Ni phthalocyanine catalysts on their electrocatalytic CO2 reduction reaction (eCO2RR) activity. A graphite-conjugated Ni phthalocyanine, Ni(NH2)8Pc-GC, demonstrates remarkable electrocatalytic performance both in H-type and flow cells. In situ infrared spectroscopy and theoretical calculations reveal that the graphite conjugation, through strong electronic coupling, increases the electron density of the active site, reduces the adsorption energy barrier of *COOH, and enhances the catalytic performance. As the cathode catalyst, Ni(NH2)8Pc-GC also displays remarkable charge-discharge cycle stability of over 50 hours in a Zn-CO2 battery. These findings underscore the significance of immobilization methods and highlight the potential for further advancements in eCO2RR.
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