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教授

博士生导师

硕士生导师

主要任职:Professor

性别:男

毕业院校:奥地利University of Graz

学位:博士

所在单位:环境学院

学科:环境工程. 环境科学. 水科学与技术

办公地点:大连理工大学环境学院

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Unique three dimensional architecture using a metal-free semiconductor cross-linked bismuth vanadate for efficient photoelectrochemical water oxidation

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论文类型:期刊论文

发表时间:2016-06-01

发表刊物:NANO ENERGY

收录刊物:EI、SCIE

卷号:24

页面范围:148-157

ISSN号:2211-2855

关键字:Solar water oxidation; Bismuth vanadate; Graphene; Carbon nitride; Photoelectrochemical

摘要:In this study, we report a unique design of nano-porous bismuth vanadate (BiVO4) photoelectrode decorated with graphene linked carbon nitride (GCN) nanosheets and their potential application in solar driven photoelectrochemical water oxidation. Especially, an integrated sandwich-like heterojunction with highly interconnected porous structure, comprising two dimensional GCN sheets and three dimensional BiVO4 was successfully synthesized with significantly enhanced photoelectrochemical activity. The prepared photoelectrode achieves up to 1.98 mA cm(-2) (1.23 V vs RHE) under AM 1.5G solar light irradiation, 2.06 times compared with pristine BiVO4 (0.96 mA cm(-2) at 1.23 V vs RHE). After deposition of cobalt phosphate nanoparticles as water-oxidation electrocatalyst, a plateau photocurrent of 3.42 mA cm(-2) (1.23 V vs RHE) with a maximum photo-conversion efficiency of 1.28% was achieved on the prepared photoanode. The highly improved photoelectrochemical performance can be attributed to suitable band matching facilitating efficient charge separation between GCN and BiVO4 as well as the desirable incorporation of rational designed dimensionality-dependent heterojunction for promoted solar energy utilization. More importantly, the combined experimental results and computational simulations reveal that the strong donor-acceptor coupling between GCN sheets and porous BiVO4 facilitates the separation and transfer of photoinduced electron-hole pairs, accounting for the highly promoted photoelectrochemical performance. (C) 2016 Elsevier Ltd. All rights reserved.