过电位
催化作用
材料科学
剥脱关节
塔菲尔方程
过渡金属
金属
纳米工程
纳米技术
化学工程
化学
物理化学
电化学
冶金
有机化学
石墨烯
工程类
电极
作者
Leyla Najafi,Sebastiano Bellani,Reinier Oropesa‐Nuñez,Rosaria Brescia,Mirko Prato,Lea Pasquale,Cansunur Demirci,Filippo Drago,Beatriz Martín‐García,Jan Luxa,Liberato Manna,Zdeněk Sofer,Francesco Bonaccorso
出处
期刊:Small
[Wiley]
日期:2020-11-23
卷期号:16 (50)
被引量:22
标识
DOI:10.1002/smll.202003372
摘要
Abstract The nanoengineering of the structure of transition metal dichalcogenides (TMDs) is widely pursued to develop viable catalysts for the hydrogen evolution reaction (HER) alternative to the precious metallic ones. Metallic group‐5 TMDs have been demonstrated to be effective catalysts for the HER in acidic media, making affordable real proton exchange membrane water electrolysers. Their key‐plus relies on the fact that both their basal planes and edges are catalytically active for the HER. In this work, the 6R phase of TaS 2 is “rediscovered” and engineered. A liquid‐phase microwave treatment is used to modify the structural properties of the 6R ‐TaS 2 nanoflakes produced by liquid‐phase exfoliation. The fragmentation of the nanoflakes and their evolution from monocrystalline to partly polycrystalline structures improve the HER‐activity, lowering the overpotential at cathodic current of 10 mA cm −2 from 0.377 to 0.119 V. Furthermore, 6R ‐TaS 2 nanoflakes act as ideal support to firmly trap Pt species, which achieve a mass activity (MA) up 10 000 A g Pt −1 at overpotential of 50 mV (20 000 A g Pt −1 at overpotentials of 72 mV), representing a 20‐fold increase of the MA of Pt measured for the Pt/C reference, and approaching the state‐of‐the‐art of the Pt mass activity.
科研通智能强力驱动
Strongly Powered by AbleSci AI