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基于ZIF-8的Fe/S/N/C催化剂用于高效氧还原反应的合理设计

Rational design of a Fe/S/N/C catalyst from ZIF-8 for efficient oxygen reduction reaction.

作者信息

Chen Danke, Fang Zhou, Ma Xu, Li Zhuoyi, Lin Hanqing, Ying Wen, Peng Xinsheng

机构信息

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, People's Republic of China.

出版信息

Nanotechnology. 2020 Nov 20;31(47):475404. doi: 10.1088/1361-6528/abaf84.

Abstract

Fe/N/C catalysts have been regarded as prospective electrocatalysts for oxygen reduction reactions (ORR). As reported, doping S into the Fe/N/C catalyst is an effective strategy to further enhance its ORR performance. Herein, a rational design is demonstrated to synthesize Fe/S/N/C catalysts with a flexible ratio of the doped Fe and S. Through atomic substitution and molecular confinement methods, Fe and S were incorporated into the ZIF-8 precursor, respectively. After further pyrolysis, the Fe/S/N/C catalyst was obtained with uniformly dispersed Fe-N, C-S-C active sites and high specific surface area. The Fe/S/N/C catalyst shows a high half-wave potential in alkaline medium, nearly 32 mV higher than the commercial Pt/C, owing to the strong synergistic effect from Fe-N and C-S-C active sites. Additionally, the Fe/S/N/C catalyst exhibits good long-term electrocatalytic durability and high endurance to methanol crossover, implying it is a suitable candidate to take the place of conventional Pt or Pt-based catalysts in electrochemical devices.

摘要

铁氮碳催化剂被认为是用于氧还原反应(ORR)的潜在电催化剂。据报道,将硫掺杂到铁氮碳催化剂中是进一步提高其ORR性能的有效策略。在此,展示了一种合理设计,以合成具有灵活掺杂铁和硫比例的铁硫氮碳催化剂。通过原子取代和分子限域方法,分别将铁和硫掺入ZIF-8前驱体中。经过进一步热解,获得了具有均匀分散的Fe-N、C-S-C活性位点和高比表面积的铁硫氮碳催化剂。由于Fe-N和C-S-C活性位点的强协同效应,铁硫氮碳催化剂在碱性介质中显示出高半波电位,比商业Pt/C高出近32 mV。此外,铁硫氮碳催化剂表现出良好的长期电催化耐久性和对甲醇渗透的高耐受性,这意味着它是在电化学装置中替代传统Pt或Pt基催化剂的合适候选者。

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