电催化剂
材料科学
化学工程
催化作用
法拉第效率
碳纳米纤维
碳纤维
热解
微观结构
镍
纳米纤维
电化学
纳米技术
无机化学
碳纳米管
电极
化学
复合材料
冶金
有机化学
物理化学
工程类
复合数
作者
Yicheng Wang,Qiyu Zhang,Shuo Wen,Chenxu Wang,Ayeza Ayeza,Yating Zhang,Chao Hu
出处
期刊:Chemcatchem
[Wiley]
日期:2024-12-12
卷期号:17 (5)
被引量:2
标识
DOI:10.1002/cctc.202401662
摘要
Abstract The utilization of renewable energy for electrocatalytic CO 2 reduction (CO 2 RR) represents a significant advancement in green carbon conversion technologies. Single atom catalysts (SACs) featuring a transition metal‐nitride‐carbon (M‐N x ‐C) architecture exhibit catalytic activity for the reduction of CO 2 to CO. However, the impact of the morphology of carbon supports, particularly their pore structure, on the electrocatalytic performance of CO 2 RR warrants further investigation. In this study, we fabricated a series of Ni‐based SACs supported by porous carbon nanofibers through electrospinning and sacrificial template method. We examined variations in microstructure of these porous carbon nanofiber carriers at different pyrolysis temperatures and elucidated their effects on CO 2 RR catalytic performance. The catalyst obtained at 1000 °C demonstrated efficient electrocatalysis for converting CO 2 to CO due to its large specific surface area, abundant hierarchical pore structure, and high content of Ni‐N x species resulting from both the sacrificial template method and high‐temperature pyrolysis. A Faradaic efficiency exceeding 90% was sustained across potentials ranging from −0.7 V to −1.3 V (versus RHE), with a peak efficiency reaching 96.1% at −1.0 V (versus RHE). Kinetic analysis indicated that this sample exhibited the highest reaction kinetics alongside minimal charge transfer resistance.
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