Bifunctional PdPt bimetallenes for formate oxidation‐boosted water electrolysis

Author:

Liu Xi‐Lai1,Jiang Yu‐Chuan1,Huang Jiang‐Tao2,Zhong Wei1,He Bin2ORCID,Jin Pu‐Jun1,Chen Yu1ORCID

Affiliation:

1. Key Laboratory of Macromolecular Science of Shaanxi Province, Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education), Shaanxi Key Laboratory for Advanced Energy Devices, Shaanxi Engineering Lab for Advanced Energy Technology, School of Materials Science and Engineering Shaanxi Normal University Xi'an Shaanxi PR China

2. College of New Materials and New Energies Shenzhen Technology University Shenzhen Guangdong PR China

Abstract

AbstractSmall‐molecule electrooxidation‐boosted water electrolysis (WE) is an energy‐saving method for hydrogen (H2) production. Herein, PdPt bimetallenes (PdPt BMLs) are obtained through the simple galvanic replacement reaction. PdPt BMLs reveal 2.93‐fold enhancement in intrinsic electroactivity and 4.53‐fold enhancement in mass electroactivity for the formate oxidation reaction (FOR) with respect to Pd metallenes (Pd MLs) at 0.50 V potential due to the synergistic effect. Meanwhile, the introduction of Pt atoms also considerably increases the electroactivity of PdPt BMLs for hydrogen evolution reaction (HER) with respect to Pd MLs in an alkaline medium, which even exceeds that with the use of commercial Pt nanocrystals. Inspired by the outstanding FOR and HER electroactivity of bifunctional PdPt BMLs, a two‐electrode FOR‐boosted WE system (FOR‐WE) is constructed by using PdPt BMLs as the cathode and the anode. The FOR‐WE system only requires an operational voltage of 0.31 V to achieve H2 production, which is 1.48 V lower than that (ca. 1.79 V) with the use of the traditional WE system.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Materials Chemistry,Energy (miscellaneous),Materials Science (miscellaneous),Renewable Energy, Sustainability and the Environment

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3