Tailoring Polymorphic Heterostructures of MoS₂–WS₂ (1T/1T, 2H/2H) for Efficient Hydrogen Evolution Reaction

Earth-abundant and inexpensive transition metal dichalcogenides (TMDCs) with existing polymorphisms (metallic 1T phase and semiconducting 2H phase) have been proposed as alternatives to noble metals (e.g., Pt, Ir, and Ru) to achieve an efficient hydrogen evolution reaction (HER). Although the 1T phase of TMDCs (1T-TMDCs) is essential as an HER catalyst, practical application in the HER has not been realized owing to the lack of any large-scale production of the 1T-TMDC and 1T/1T-TMDC heterostructure fabrication method. Here, polymorphic TMDC–TMDC heterostructures at a 4 in. wafer scale is reported for 1T-MoS2/1T-WS2 vertical heterostructures (1T/1T-MWH) or 2H-MoS2/2H-WS2 vertical heterostructures (2H/2H-MWH) under cold plasma conditions and process temperature. Simultaneous ion-bombardment onto substrates induces a few nanosized grain boundaries with discontinuous films, resulting in exposed edges that act as catalytically active sites. The electrocatalytic performances of the prepared polymorph (1T or 2H phases of MoS2 and WS2) and polymorphic heterostructures of 1T/1T-MWH and 2H/2H-MWH are compared. 1T/1T-MWH shows the highest electrocatalytic performance owing to its metallic 1T phase and heterostructures containing alloy structures at the heterointerface. Moreover, the nanosized grains of 1T/1T-MWH preserve their original phase after 1000 HER cycles, proving their robustness and durability

Soft Template-Assisted Fabrication of Mesoporous Graphenes for High-Performance Energy Storage Systems

Graphene is a promising active material for electric double layer supercapacitors (EDLCs) due to its high electric conductivity and lightweight nature. However, for practical uses as a power source of electronic devices, a porous structure is advantageous to maximize specific energy density. Here, we propose a facile fabrication approach of mesoporous graphene (m-G), in which self-assembled mesoporous structures of poly(styrene)-block-poly(2-vinylpyridine) copolymer (PS-b-P2VP) are exploited as both mesostructured catalytic template and a carbon source. Notably, the mesostructured catalytic template is sufficient to act as a rigid support without structural collapse, while PS-b-P2VP converts to graphene, generating m-G with a pore diameter of ca. 3.5 nm and high specific surface area of 186 m2/g. When the EDLCs were prepared using the obtained m-G and ionic liquids, excellent electrochemical behaviors were achieved even at high operation voltages (0 ∼ 3.5 V), including a large specific capacitance (130.2 F/g at 0.2 A/g), high-energy density of 55.4 W h/kg at power density of 350 W/kg, and excellent cycle stability (>10,000 cycles). This study demonstrates that m-G is a promising material for high-performance energy storage devices