Rationally constructing of a novel 2D/2D WO/Pt/g-CN Schottky-Ohmic junction towards efficient visible-light-driven photocatalytic hydrogen evolution and mechanism insight.

J Colloid Interface Sci

Institute of Green Chemistry and Chemical Technology, School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, China. Electronic address:

Published: March 2021

Effectively separating photo-generated charge carriers is usually important but difficult for the high-activity photocatalysis. Fabricating 2D/2D Schottky-Ohmic junction is more beneficial to the spatial separation and transfer of photo-induced charges at the interface of different components due to the matching of distinct two-dimension structure and band alignment, but the manipulation and mastery of junction type (Schottky-Ohmic junction and Z-scheme junction) and electronic structure is an arduous task for preparing satisfactory photocatalysts and investigating the PHE mechanism. In this work, the 2D/2D WO/Pt/g-CN (WPC) Schottky-Ohmic junction composite photocatalysts is formed via facile hydrothermal and photo-induced deposition method for employing to produce H. The optimized WPC Schottky-Ohmic junction photocatalyst exhibits remarkable photocatalytic H-release performance with ability to produce the amount of H reaches 1299.4 μmol upon exposure to visible light, which is about 1.2 and 11.5 times higher than that of WO/g-CN/Pt (WCP) (1119.4 μmol) and pure CN (113.2 μmol)), respectively. This remarkable enhancement of photocatalytic performance is ascribed to: (i) Schottky-Ohmic junction can strikingly expedite spatial charge separation and elongate electron lifetime, (ii) the 2D/2D structure can shorten the charge transportation distance, (iii) Pt with rich electron density can stably adsorb H. This work provides a successful paradigm for future fundamental research, and exquisitely designs ideal g-CN-based photocatalysts by simultaneously adjusting and optimizing material structure and electronic dynamics.

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http://dx.doi.org/10.1016/j.jcis.2020.10.123DOI Listing

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