Advanced Ultrathin RuPdM (M = Ni, Co, Fe) Nanosheets Electrocatalyst Boosts Hydrogen Evolution

过电位 电催化剂 材料科学 分解水 电解 过渡金属 电化学 催化作用 化学工程 电子转移 纳米技术 电解水 化学 光化学 物理化学 光催化 电极 工程类 电解质 生物化学
作者
Dan Zhang,Huan Zhao,Bolong Huang,Bin Li,Hongdong Li,Yi Han,Zuochao Wang,Xueke Wu,Yue Pan,Yingjun Sun,Xuemei Sun,Jianping Lai,Lei Wang
出处
期刊:ACS central science [American Chemical Society]
卷期号:5 (12): 1991-1997 被引量:78
标识
DOI:10.1021/acscentsci.9b01110
摘要

The hydrogen evolution reaction (HER) is one of the most significant reactions in the electrolysis water process, and electrocatalysts which possess high mass activity and excellent stability are the most important driving factors to improve the efficiency of HER. As for the efficient commercially electrocatalyst, Pt/C is limited in development because of its high cost. Therefore, the study of non-Pt high-efficiency catalysts is particularly important at this moment. Here, we creatively report for the first time a kind of RuPdM (M= Ni, Co, Fe) ultrathin nanosheets (NSs), which exhibit extraordinary electrochemical properties for HER under alkaline conditions. The overpotential of optimized trimetallic Ru38Pd34Ni28 ultrathin NSs is only 20 mV (10 mA cm–2), and the mass activity reaches 6.15 A mg–1noble metal at −0.07 V vs RHE. It can be compared to Pt-based electrocatalysts, which have the highest mass activity currently reported. The durability tests also prove that the stability of the electrocatalyst is outstanding. DFT calculations disclose that the flexible modulation of electronic structures of RuPd ultrathin NSs is achieved by utilizing the additional 3d transition metals Fe, Co, and Ni. In particular, the Ni-3d bands act as the continuous electron-supply center for Ru to ensure an efficient electron transfer toward the adsorbates. Meanwhile, the stable Pd sites are critical for coupling the O-2pπ orbital in the initial H2O splitting with a facile barrier. This work will open up a new era of non-Pt materials for alkaline hydrogen evolution toward practical application.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
李晨阳发布了新的文献求助10
1秒前
星辰大海应助科研通管家采纳,获得10
1秒前
乐乐应助科研通管家采纳,获得10
1秒前
1秒前
斯文败类应助科研通管家采纳,获得10
1秒前
科研通AI2S应助科研通管家采纳,获得10
1秒前
LWW应助科研通管家采纳,获得30
1秒前
pluto应助科研通管家采纳,获得20
1秒前
shinysparrow应助科研通管家采纳,获得20
1秒前
英姑应助科研通管家采纳,获得10
1秒前
思源应助科研通管家采纳,获得10
1秒前
zzz4743应助科研通管家采纳,获得30
1秒前
香蕉觅云应助科研通管家采纳,获得30
1秒前
Hao应助科研通管家采纳,获得10
1秒前
科研通AI2S应助科研通管家采纳,获得10
1秒前
丹霞应助科研通管家采纳,获得10
1秒前
CipherSage应助科研通管家采纳,获得10
1秒前
充电宝应助科研通管家采纳,获得10
1秒前
隐形曼青应助科研通管家采纳,获得10
1秒前
传奇3应助想查文献采纳,获得10
2秒前
慕青应助欧阳娜娜采纳,获得30
2秒前
2秒前
3秒前
4秒前
美丽的含羞草完成签到,获得积分20
4秒前
5秒前
所所应助激动的砖家采纳,获得10
5秒前
清欢发布了新的文献求助10
5秒前
是容与呀发布了新的文献求助10
5秒前
6秒前
7秒前
7秒前
xxs应助科研鸟采纳,获得10
7秒前
Lucas应助宋1234采纳,获得10
8秒前
8秒前
开心榴莲大王完成签到 ,获得积分10
9秒前
小宇发布了新的文献求助10
9秒前
SciGPT应助w-w采纳,获得10
9秒前
9秒前
科研通AI2S应助hola采纳,获得10
9秒前
高分求助中
One Man Talking: Selected Essays of Shao Xunmei, 1929–1939 1000
Yuwu Song, Biographical Dictionary of the People's Republic of China 800
Multifunctional Agriculture, A New Paradigm for European Agriculture and Rural Development 600
The Illustrated History of Gymnastics 500
Division and square root. Digit-recurrence algorithms and implementations 500
Hemerologies of Assyrian and Babylonian Scholars 500
Bernd Ziesemer - Maos deutscher Topagent: Wie China die Bundesrepublik eroberte 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2492882
求助须知:如何正确求助?哪些是违规求助? 2151305
关于积分的说明 5494733
捐赠科研通 1871863
什么是DOI,文献DOI怎么找? 930816
版权声明 563437
科研通“疑难数据库(出版商)”最低求助积分说明 497735