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Crystalline phase engineering in WO3/g-C3N4 composites for improved photocatalytic performance under visible light
Author(s) -
Junmei Liang,
Yuhui Li,
Jing Zhang,
Chun Li,
Yang Xia,
Xuebing Chen,
Fangfang Wang,
Changdong Chen
Publication year - 2020
Publication title -
materials research express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.383
H-Index - 35
ISSN - 2053-1591
DOI - 10.1088/2053-1591/ab96fe
Subject(s) - photocatalysis , materials science , monoclinic crystal system , semiconductor , phase (matter) , composite material , hexagonal phase , composite number , visible spectrum , surface photovoltage , chemical engineering , crystal structure , crystallography , optoelectronics , catalysis , chemistry , organic chemistry , physics , quantum mechanics , spectroscopy , engineering
The photocatalytic performance of a semiconductor material is significantly related to its crystalline phase, thus, crystalline phase engineering is of importance for designing the semiconductor composites fabricated between two semiconductor materials. In this work, WO 3 /g-C 3 N 4 composites was taken as an example, we designed and prepared the WO 3 /g-C 3 N 4 composites with different crystalline phases of WO 3 . The important role of the crystalline phase of WO 3 , which is hexagonal phase (h-WO 3 ), monoclinic phase (m-WO 3 ), and mixed phases of h-WO 3 and m-WO 3 on the morphology, photoabsorption property, charge separation efficiency, and photocatalytic activity of the WO 3 /g-C 3 N 4 composites were systematically investigated. By evaluating the photocatalytic degradation of RhB, it is found that the highest photocatalytic activity was achieved by WO 3 /g-C 3 N 4 with 25 wt% h-WO 3 and 75% g-C 3 N 4 (H1G3). The enhanced photocatalytic performance of H1G3 was mainly attributed to the improvement in the separation efficiency of photogenerated electron-hole pairs, which was confirmed by surface photovoltage results. Our work sheds a light on the design of composite photocatalysts based on semiconductor oxides.

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