...
首页> 外文期刊>International journal of hydrogen energy >Polysulfide functionalized reduced graphene oxide for electrocatalytic hydrogen evolution reaction and supercapacitor applications
【24h】

Polysulfide functionalized reduced graphene oxide for electrocatalytic hydrogen evolution reaction and supercapacitor applications

机译:Polysulfide functionalized reduced graphene oxide for electrocatalytic hydrogen evolution reaction and supercapacitor applications

获取原文
获取原文并翻译 | 示例

摘要

Functionalized carbon based 2D materials are promising candidates for low cost and environment friendly electrocatalyst for hydrogen evolution reaction (HER) and super -capacitor applications. To overcome the limitations posed by the noble metals and tran-sition metal based composites, we have successfully synthesized metal free polysulfide functionalized reduced graphene oxide (GPS) in a simple chemical route. Structure and morphology of the material are characterized via XRD, FTIR, Raman, TEM, XPS measure-ments. The material behaves as an efficient HER electrocatalyst in acidic medium as well as energy storage device. It shows an onset potential of 97 mV and overpotential of 254 mV to reach a high current density of 10 mA/cm2. DFT calculations are carried out to understand the structural stability and identification of active sites of the material. Boosting catalytic activity via increasing the number of active sites is an elegant approach. In this material we have used the S atoms of polysulfide polymer to facilitate hydrogen adsorption and desorption, thus improving the hydrogen evolution ability. The supecapacitor attains the high specific capacitance 347 F/g at the current density of 1 A/g. The origin of such per-formances is due to synergistic effect of both the graphene network and the polysulfide functionalizations. (c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号