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桑叶一步热解转化后进行电化学处理:制备负载M(M = Pt、Au)纳米颗粒的氮掺杂碳纳米多孔结构作为析氢反应的高效电催化剂

One-Step Pyrolysis Transformation of Mulberry Leaves Followed by Electrochemical Treatment: Preparing of M (M = Pt, Au) Nanoparticles Incorporated Nitrogen-Doped Carbon Nanoporous Structures as Efficient Electrocatalyst for Hydrogen Evolution Reaction.

作者信息

Guan Lihao, Li Changqing, Sun Fengzhan, Hu Lianglu, Gao Feng, Lin Yuqing

机构信息

Department of Chemistry, Capital Normal University, Beijing 100048, China.

College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, China.

出版信息

J Nanosci Nanotechnol. 2018 Dec 1;18(12):8289-8295. doi: 10.1166/jnn.2018.16375.

DOI:10.1166/jnn.2018.16375
PMID:30189949
Abstract

To facilely develop low-cost and efficient hydrogen evolution electrocatalysts, catalyst with low content of platinum on nitrogen-doped carbon nanoporous structures were prepared for hydrogen evolution reaction (HER). This study firstly demonstrated the one-step pyrolysis transformation of conveniently accessible mulberry leaves to obtain nitrogen-doped nanoporous carbons (N-NPCs) for hydrogen evolution reaction. After electrochemical treatment, the obtained N-NPCs-ET with Pt as counter electrode exhibited an unexpected high hydrogen evolution activity, which had low onset overpotential of 100 mV and a Tafel slope of 60 mV dec-1. N-NPCs-ET maintained catalytic activity for at least 10 h in 0.5 M H2SO4 solution. The enhanced HER performance was relevant to the incorporation of Pt nanoparticles, which were dissolved from anodic Pt counter electrode in acid media and precipitated into cathodic N-NPCs surface again. Moreover, for the first time, we found that with a gold electrode as the counter electrode, Au nanoparticles could be incorporated into N-NPCs by electrochemical treatments and the formed Au nanoparticles decorated N-NPCs possessed efficient catalytic activity toward HER.

摘要

为了简便地开发低成本且高效的析氢电催化剂,制备了氮掺杂碳纳米多孔结构上铂含量低的催化剂用于析氢反应(HER)。本研究首次展示了通过一步热解转化方便可得的桑叶来获得用于析氢反应的氮掺杂纳米多孔碳(N-NPCs)。经过电化学处理后,以铂作为对电极得到的N-NPCs-ET表现出意想不到的高析氢活性,其起始过电位低至100 mV,塔菲尔斜率为60 mV dec-1。N-NPCs-ET在0.5 M H2SO4溶液中保持催化活性至少10小时。析氢性能的增强与铂纳米颗粒的掺入有关,这些铂纳米颗粒在酸性介质中从阳极铂对电极溶解,然后再次沉淀到阴极N-NPCs表面。此外,我们首次发现,以金电极作为对电极时,通过电化学处理金纳米颗粒可以掺入N-NPCs中,并且形成的金纳米颗粒修饰的N-NPCs对析氢具有高效的催化活性。

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