过电位
催化作用
二氧化碳电化学还原
材料科学
碳纤维
吸附
介孔材料
纳米技术
化学工程
钴
二氧化碳
无机化学
化学
有机化学
电极
一氧化碳
电化学
复合材料
物理化学
复合数
工程类
作者
Shucheng Yang,Zihe Zhou,Wei Li-xin,Si-Qi Li,Song Liu
标识
DOI:10.1002/cphc.202300502
摘要
Abstract Molecular catalysts stabilized on a support material, also called heterogeneous molecular catalysts, exhibit excellent performance in carbon dioxide reduction reaction (CO 2 RR). Different support in these electrocatalysts can have a substantial influence on the activity, making support control one tool to enhance the CO 2 RR performance. However, a systematic understanding of the support effects is lacking. Taking cobalt phthalocyanine (CoPc) immobilized onto different carbon materials as examples, we demonstrate that the surface area, pore structure and the morphology of the as‐prepared heterogeneous molecular catalysts can influence the CO 2 transfer and adsorption, and then change the CO 2 RR activity. In contrast to the other four materials, CoPc/mesoporous carbon (MC) can efficiently convert carbon dioxide to carbon monoxide at minimal overpotential (−0.8 V vs. RHE) due to its special nanostructure and pore distribution. The results of this study suggest that the performance of electrocatalytic reduction of carbon dioxide can be improved by changing different substrates.
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