水热法制备镍负载硫磷双掺杂石墨烯电极及其电催化析氢性能研究

朱桂生1, 章明美2, 邵守言1, 黄春霞1, 黄诚1*, 刘洪2

化工新型材料 ›› 2022, Vol. 50 ›› Issue (1) : 89 -93.

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化工新型材料 ›› 2022, Vol. 50 ›› Issue (1) : 89-93. DOI: 10.19817/j.cnki.issn1006-3536.2022.01.018
新材料与新技术

水热法制备镍负载硫磷双掺杂石墨烯电极及其电催化析氢性能研究

    朱桂生1, 章明美2, 邵守言1, 黄春霞1, 黄诚1*, 刘洪2
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Study on the preparation of Ni/SPG electrode by hydrothermal method and its electrocatalytic hydrogen evolution performance

  • Zhu Guisheng1, Zhang Mingmei2, Shao Shouyan1, Huang Chunxia1, Huang Cheng1, Liu Hong2
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摘要

设计一种高活性、高稳定性的非贵金属基催化剂,对电催化析氢的应用具有重要意义。以硫酸和植酸为硫磷掺杂剂,采用水热法合成了硫磷共掺杂石墨烯(SPG);随后,采用简单的醇热法制备了直接生长在SPG上的Ni基纳米材料(Ni/SPG)。制备的Ni/SPG电催化剂表现出杰出的析氢性能,其阻抗极低(0.48Ω),电化学活性表面积极好(32.62m2/g),起始过电位低(115mV),并且具有优秀的Tafel斜率(115mV/dec)和良好的循环稳定性(5000个循环伏安循环)。这些显著的电催化性能归因于S和P双掺杂石墨烯产生更多暴露的活性中心和表面缺陷,使得小晶粒尺寸的Ni均匀地分散在其表面,并促进了它们之间的电子传输。

Abstract

It is of great significance to design a non-noble metal based catalyst with high activity and stability for the application of electrocatalytic hydrogen evolution.Sulfur phosphorus co-doped graphene (SPG) was successfully synthesized via a simple hydrothermal method using sulfuric acid and phytic acid as dopants.Subsequently,the nickel based nanomaterials grown directly on SPG (named Ni/SPG) were prepared by a simple alcohol thermal method.The prepared Ni/SPG electrocatalyst demonstrated excellent hydrogen evolution performance,such as very low impedance (0.48Ω),active electrochemical surface (32.62m2/g),low initial overpotential (115mV),excellent Tafel slope (115mV/dec) and good cycle stability,and so on.These remarkable electrocatalytic properties were attributed to the more exposed active centers and surface defects of S and P co-doped graphene,which made the Ni with small size evenly dispersed on its surface and promoted the electronic transmission between them.

关键词

硫磷双掺杂石墨烯 / / 析氢反应 / 电催化

Key words

sulphur and phosphorus co-doped graphene / nickel / hydrogen evolution reaction / electrocatalysis

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水热法制备镍负载硫磷双掺杂石墨烯电极及其电催化析氢性能研究[J]. 化工新型材料, 2022, 50(1): 89-93 DOI:10.19817/j.cnki.issn1006-3536.2022.01.018

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基金资助

中国博士后基金资助(2017M621656));江苏省博士后基金资助(1701170C);镇江市前瞻性重点研发计划项目资助(GY2019011)

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