Source abstract
Abstract
Abstract 2D MoS2 has emerged as a promising alternative to Pt‐based catalysts for hydrogen evolution reaction (HER) due to its low cost and earth abundance. However, insufficient active sites of basal plane and poor conductivity become the foremost factors restricting the catalytic performance of MoS2. Here, a facile strategy is presented to enhance the HER performance of MoS2 by converting its 2D structure into 1D/2D heterostructures of Mo6Te6/MoS2(1−x)Te2x by the in situ tellurization. As‐prepared 1D/2D heterostructures exhibit excellent HER performance with the Tafel slope of ≈56 mV dec−1 (only one‐third of that for pristine MoS2). The enhanced HER catalytic activity is attributed to more Te/S vacancies introduced by tellurization, which serve as the active sites as suggested by theoretical calculations. Besides, the formation of highly conductive well‐aligned quasi‐1D Mo6Te6 nanobelts facilitate charge transport in HER. Previous work provides a facile approach to construct mixed dimensional materials, and opens up a new avenue to the properties modulation of 2D transition metal chalcogenides.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering iChEM Xiamen University Xiamen 361005 China
Department Key Lab of Organic Optoelectronics & Molecular Engineering Department of Chemistry Tsinghua University Beijing 100084 China
State Key Laboratory of Information Photonics and Optical Communications Beijing University of Posts and Telecommunications Beijing 100876 China
National Center for Electron Microscopy in Beijing Key Laboratory of Advanced Materials (MOE) The State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing 100084 China
Funding
National Natural Science Foundation of China · China Postdoctoral Science Foundation
References (20)
Show source-provided references