Salt-Induced High-Density Vacancy-Rich 2D MoS 2  for Efficient Hydrogen Evolution

Emerging non-noble metal 2D catalysts, such as molybdenum disulfide (MoS ), hold great promise in hydrogen evolution reactions. The sulfur vacancy is recognized as a key defect type that can activate the inert basal plane to improve the catalytic performance. Unfortunately, the method of introducing...

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Veröffentlicht in:Advanced materials (Weinheim) 2024-04, Vol.36 (17), p.e2304808
Hauptverfasser: Man, Ping, Jiang, Shan, Leung, Ka Ho, Lai, Ka Hei, Guang, Zhiqiang, Chen, Honglin, Huang, Lingli, Chen, Tianren, Gao, Shan, Peng, Yung-Kang, Lee, Chun-Sing, Deng, Qingming, Zhao, Jiong, Ly, Thuc Hue
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Sprache:eng
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Zusammenfassung:Emerging non-noble metal 2D catalysts, such as molybdenum disulfide (MoS ), hold great promise in hydrogen evolution reactions. The sulfur vacancy is recognized as a key defect type that can activate the inert basal plane to improve the catalytic performance. Unfortunately, the method of introducing sulfur vacancies is limited and requires costly post-treatment processes. Here, a novel salt-assisted chemical vapor deposition (CVD) method is demonstrated for synthesizing ultrahigh-density vacancy-rich 2H-MoS , with a controllable sulfur vacancy density of up to 3.35 × 10  cm . This approach involves a pre-sprayed potassium chloridepromoter on the growth substrate. The generation of such defects is closely related to ion adsorption in the growth process, the unstable MoS -K-H O triggers the formation of sulfur vacancies during the subsequent transfer process, and it is more controllable and nondestructive when compared to traditional post-treatment methods. The vacancy-rich monolayer MoS exhibits exceptional catalytic activity based on the microcell measurements, with an overpotential of ≈158.8 mV (100 mA cm ) and a Tafel slope of 54.3 mV dec in 0.5 m H SO electrolyte. These results indicate a promising opportunity for modulating sulfur vacancy defects in MoS using salt-assisted CVD growth. This approach represents a significant leap toward achieving better control over the catalytic performances of 2D materials.
ISSN:0935-9648
1521-4095
DOI:10.1002/adma.202304808