Metal–semiconductor ternary hybrids for efficient visible-light photocatalytic hydrogen evolution. Issue 27 (21st June 2018)

• Record Type: Journal Article
• Authors: Wi, Dae Han; Park, Se Young; Lee, Seunghoon; Sung, Jiha; Hong, Jong Wook; Han, Sang Woo
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 27(2018)
• Page Start: 13225
• Page End: 13235
• Publication Date: 2018-06-21
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8ta03462a
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : A high-performance solar energy conversion platform was constructed by the intimate coupling of two different complementary semiconductors and morphology-controlled plasmonic metal nanocrystals in a controlled manner. Abstract : Solar-driven production of chemical fuels through photocatalysis holds great promise for addressing the ever-increasing energy and environmental issues. However, its practical application is limited due to low light harvesting efficiency, fast charge recombination, and low stability of current photocatalysts. Here, we introduce a high-performance solar energy conversion platform constructed by the intimate coupling of two different complementary semiconductors (MoS2 and CdS) and morphology-controlled plasmonic metal nanocrystals (concave cubic Au nanocrystals) in a controlled manner. The sequential Au nanocrystal anchoring and CdS growth on two-dimensional exfoliated MoS2 nanosheets successfully yielded intimately coupled plasmonic metal–semiconductor ternary hybrids. The prepared hybrid photocatalysts exhibited superb hydrogen evolution capability under visible-light irradiation, which can be attributed to the synergistic integration of the advantages of semiconductor–semiconductor coupling, such as the broadening of light absorption and the retardation of charge recombination, and plasmon energy transfer from Au nanocrystals to semiconductors via the hot electron transfer mechanism.