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通过多孔工程提高石墨烯的杂原子掺杂百分比以增强电催化活性。

Increasing the heteroatoms doping percentages of graphene by porous engineering for enhanced electrocatalytic activities.

作者信息

Li Xintong, Xu Yongsheng, Li Yang, Fan Xiaobin, Zhang Guoliang, Zhang Fengbao, Peng Wenchao

机构信息

School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China.

School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China.

出版信息

J Colloid Interface Sci. 2020 Oct 1;577:101-108. doi: 10.1016/j.jcis.2020.05.089. Epub 2020 May 24.

Abstract

Graphene based materials are considered as promising catalysts towards electro-catalytic water splitting. Heteroatoms doping and structure defects creation in graphene matrix could enhance the electro-catalytic activity effectively. In this work, a nitrogen and sulfur co-doped graphene is synthesized and then activated by KOH to involve a porous structure. The atomic ratios of doped heteroatoms are found increased surprisingly. This should be due to the better thermal stability of doped heteroatoms compared with the origin carbon atoms. More carbon atoms will be removed, thus leading to the increased heteroatoms doping percentages. The increased surface area, larger heteroatoms ratios, and abundant structure defects result in the improved catalytic activity towards electrochemical oxygen evolution reaction (OER). The overpotential for OER could achieve as early as 281 mV vs. RHE at 10 mA·cm in 1 M KOH, better than most of the metal free catalysts. The obtained sample is active over a wide pH range in electrochemical hydrogen evolution reaction (HER), thus could be used as bifunctional materials for water splitting. This work provides a simple and low-cost approach to increase the ratios of doped heteroatoms, and thus should have great potential both for carbon materials synthesis and hydrogen production.

摘要

基于石墨烯的材料被认为是用于电催化水分解的有前景的催化剂。在石墨烯基体中进行杂原子掺杂和引入结构缺陷能够有效提高电催化活性。在这项工作中,合成了氮硫共掺杂的石墨烯,然后用氢氧化钾进行活化以形成多孔结构。发现掺杂杂原子的原子比惊人地增加。这应该归因于与原始碳原子相比,掺杂杂原子具有更好的热稳定性。更多的碳原子会被去除,从而导致杂原子掺杂百分比增加。表面积的增加、更大的杂原子比例以及丰富的结构缺陷导致对电化学析氧反应(OER)的催化活性提高。在1 M氢氧化钾中,10 mA·cm时OER的过电位最早可达到相对于可逆氢电极(RHE)为281 mV,优于大多数无金属催化剂。所获得的样品在电化学析氢反应(HER)的较宽pH范围内都具有活性,因此可作为水分解的双功能材料。这项工作提供了一种简单且低成本的方法来提高掺杂杂原子的比例,因此在碳材料合成和制氢方面都应具有巨大潜力。

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