催化作用
沸石咪唑盐骨架
研磨
法拉第效率
电化学
X射线吸收光谱法
化学
化学工程
钴
二氧化碳电化学还原
材料科学
无机化学
吸收光谱法
金属有机骨架
一氧化碳
物理化学
电极
吸附
有机化学
冶金
工程类
物理
量子力学
作者
Zhangsen Chen,Gaixia Zhang,Qingmin Hu,Yi Zheng,Siyi Cao,Guozhu Chen,Cuncheng Li,Teak D. Boyko,Ning Chen,Weifeng Chen,Tom Regier,James J. Dynes,Jian Wang,Hsiao‐Tsu Wang,Jigang Zhou,Shuhui Sun
标识
DOI:10.1002/sstr.202200031
摘要
Zeolitic imidazolate framework (ZIF‐8)‐derived single‐atom catalysts (SACs) are widely studied in many catalytic reactions such as hydrogen evolution reaction (HER), oxygen reduction reaction (ORR), and CO 2 reduction reactions (CO 2 RR). Grinding procedures involved in the synthesis of ZIF‐8‐derived SACs could affect the catalytic performance but are less evaluated in the literature. Herein, a series of ZIF‐8‐derived cobalt SACs (C–Co–ZIFs) with different grinding processes to investigate the impact of the grinding degrees on the performance of the electrochemical reduction reaction of CO 2 (ECO 2 RR) is presented. The moderate grinding process affords a boost in CO Faradaic efficiency (FE, around 15% higher than that of the original C–Co–ZIF) and the highest current densities among all the samples. The variations in the electronic structure of the Co active sites in the ground catalysts are confirmed by X‐Ray absorption spectroscopy (XAS) and X‐Ray emission spectroscopy (XES) for improved catalytic performance. The increased micropores in the moderately ground catalyst provide more exposed active sites while the increased meso‐ and macropores promote the mass transfer, benefiting the ECO 2 RR performance. It suggests that the impact of grinding processes on the synthesis of ZIF‐8‐derived SACs should be considered for the evaluation of the catalytic performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI