Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 37, Pages 19067-19089Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ta02458f
Keywords
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Funding
- National Key R&D Program of China [2021YFA1500900]
- Fundamental Research Funds for Central Universities [531119200209]
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This article discusses two-dimensional transition metal dichalcogenides as a promising material for the environmentally friendly and efficient hydrogen fuel production. The strategies for activating the basal planes of these materials are classified into internal and external regulations, leading to increased catalytic activities. The article also provides personal perspectives on the challenges and opportunities in this emerging field.
The hydrogen evolution reaction (HER) presents an environmentally friendly, efficient, and cost-effective way to produce hydrogen fuel. Recently, two-dimensional (2D) transition metal dichalcogenides (TMDCs) have emerged as a fascinating class of HER materials. Their atomically thin nature acts as an interface with the possibility of maximum exposure of nearly all active sites to the reaction environment. However, for most non-metallic TMDCs, as exemplified by 2H-MoS2, 1T-PtSe2, and 1T '-ReSe2, their basal planes are usually HER-inert except for minor edges. Based on their rich chemistry, significant progress has been recently made to activate the basal planes for HER. This review provides an overview of the current activating strategies. They can be classified into internal and external regulations, depending on whether the pristine structure is altered or not. The former directly creates more active sites through doping, vacancies, phases, grain boundaries (GBs), and superlattices. On the other hand, the latter indirectly promotes the activity utilizing external methods such as the electric field, strain, substrates, and heterostructures. We discuss each strategy's principles and characteristics and highlight their enhanced catalytic activities. We finally provide personal perspectives on the challenges and opportunities in this emerging field, including a joint strategy, a phase-engineering strategy, electrical-electrocatalytic coupling, as well as the potential of single-atom-layer catalysis.
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