热解
催化作用
纳米颗粒
化学工程
法拉第效率
电池(电)
材料科学
电化学
碳纤维
吸附
电催化剂
无机化学
纳米技术
复合数
化学
电极
有机化学
物理化学
功率(物理)
复合材料
工程类
物理
量子力学
作者
Wenqian Yang,Ziqian Xue,Jun Yang,Jiahui Xian,Qing Lin Liu,Yanan Fan,Kai Zheng,Pei‐Qin Liao,Hui Su,Qinghua Liu,Guangqin Li,Cheng‐Yong Su
标识
DOI:10.1016/s1872-2067(23)64415-8
摘要
The selective electrochemical reduction of CO2 to CO is a promising solution for the design of carbon-neutral, sustainable processes. Achieving a highly selective single reduction product is still challenging because of the energetically favorable competing hydrogen evolution reaction. We report the fabrication of N-doped sponge-like porous graphitic carbon structures embedded with Fe nanoparticles ([email protected]) via the pre-modification of a metal-organic framework (IRMOF-3(Zn)) with carboxyferrocene, followed by pyrolysis. The as-prepared [email protected] exhibited a 96.4% CO Faradaic efficiency at –0.5 VRHE and good stability. The exceptional CO2 reduction performance is attributed to the unique structure of the composite catalyst, which provides abundant hierarchical pores that increase CO2 adsorption and mass transfer, and active Fe sites that synergistically accelerate the kinetics of CO generation. The in situ attenuated total reflectance-Fourier transform infrared analysis provided proof of the improved ability of [email protected] to accumulate the crucial intermediate *COOH compared with other pyrolyzed porous carbons. [email protected] was used in a Zn-CO2 battery that delivered a maximum power density of 3.0 mW cm–2, evidencing its potential for application in energy-converting devices.
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