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配位调控热解合成超细FeNi/(FeNi)S纳米团簇/氮、硫共掺杂石墨碳纳米片作为高效双功能氧电催化剂

Coordination regulated pyrolysis synthesis of ultrafine FeNi/(FeNi)S nanoclusters/nitrogen, sulfur-codoped graphitic carbon nanosheets as efficient bifunctional oxygen electrocatalysts.

作者信息

Meng Hong-Ling, Lin Shi-Yi, Feng Jiu-Ju, Zhang Lu, Wang Ai-Jun

机构信息

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Sciences, College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua 321004, China.

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Sciences, College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua 321004, China.

出版信息

J Colloid Interface Sci. 2022 Mar 15;610:573-582. doi: 10.1016/j.jcis.2021.11.101. Epub 2021 Nov 22.

Abstract

Design of advanced carbon nanomaterials with high-efficiency oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activities is still imperative yet challenging for searching green and renewable energies. Herein, we synthesized ultrafine FeNi/(FeNi)S nanoclusters encapsulated in nitrogen, sulfur-codoped graphitic carbon nanosheets (FeNi/(FeNi)S/N,S-CNS) by coordination regulated pyrolyzing the mixture of the metal precursors, dithizone and g-CN at 800 °C. The as-prepared FeNi/(FeNi)S/N,S-CNS exhibited distinct electrocatalytic activity and stability for the ORR with positive onset (E) and half-wave (E) potentials (E = 0.97 V; E = 0.86 V) and OER with the small overpotential (η = 283 mV) at 10 mA cm in the alkaline media, outperforming commercial Pt/C and RuO catalysts. This research provides some constructive guidelines for preparing efficient, low-cost and stable nanocatalysts for electrochemical energy devices.

摘要

设计具有高效氧还原反应(ORR)和析氧反应(OER)活性的先进碳纳米材料对于寻找绿色和可再生能源而言仍然至关重要且具有挑战性。在此,我们通过在800℃下对金属前驱体、双硫腙和g-CN的混合物进行配位调控热解,合成了封装在氮、硫共掺杂石墨碳纳米片中的超细FeNi/(FeNi)S纳米团簇(FeNi/(FeNi)S/N,S-CNS)。所制备的FeNi/(FeNi)S/N,S-CNS在碱性介质中对ORR表现出独特的电催化活性和稳定性,其起始(E)和半波(E)电位为正(E = 0.97 V;E = 0.86 V),对OER在10 mA cm时过电位较小(η = 283 mV),性能优于商业Pt/C和RuO催化剂。该研究为制备用于电化学能量装置的高效、低成本和稳定的纳米催化剂提供了一些建设性的指导方针。

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