A Nonmetal Plasmonic Z-Scheme Photocatalyst with UV- to NIR-Driven Photocatalytic Protons Reduction

被引:465
作者
Zhang, Zhenyi [1 ]
Huang, Jindou [1 ]
Fang, Yurui [2 ]
Zhang, Mingyi [3 ]
Liu, Kuichao [1 ]
Dong, Bin [1 ]
机构
[1] Dalian Nationalities Univ, Sch Phys & Mat Engn, Key Lab New Energy & Rare Earth Resource Utilizat, State Ethn Affairs Commiss, 18 Liaohe West Rd, Dalian 116600, Peoples R China
[2] Dalian Univ Technol, Sch Phys & Optoelect Technol, Key Lab Mat Modificat Laser Electron & Ion Beams, Minist Educ, Dalian 116024, Peoples R China
[3] Harbin Normal Univ, Sch Phys & Elect Engn, Minist Educ, Key Lab Photon & Elect Bandgap Mat, Harbin 150025, Peoples R China
基金
中国国家自然科学基金;
关键词
INTERFACIAL CHARGE-TRANSFER; HEXAGONAL SNS2 NANOSHEETS; TUNGSTEN-OXIDE NANOWIRES; ENERGY-STORAGE ABILITY; STATE Z-SCHEME; VISIBLE-LIGHT; HYDROGEN GENERATION; SOLID-STATE; COMPOSITE PHOTOCATALYSTS; CHEMICAL ENERGY;
D O I
10.1002/adma.201606688
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ultrabroad-spectrum absorption and highly efficient generation of available charge carriers are two essential requirements for promising semiconductor-based photocatalysts, towards achieving the ultimate goal of solar-to-fuel conversion. Here, a fascinating nonmetal plasmonic Z-scheme photocatalyst with the W18O49/g-C3N4 heterostructure is reported, which can effectively harvest photon energies spanning from the UV to the nearinfrared region and simultaneously possesses improved charge-carrier dynamics to boost the generation of long-lived active electrons for the photocatalytic reduction of protons into H-2. By combining with theoretical simulations, a unique synergistic photocatalysis effect between the semiconductive Z-scheme charge-carrier separation and metal-like localized-surface-plasmon-resonance-induced "hot electrons" injection process is demonstrated within this binary heterostructure.
引用
收藏
页数:9
相关论文
共 49 条
[1]   Carbon-based H2-production photocatalytic materials [J].
Cao, Shaowen ;
Yu, Jiaguo .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY C-PHOTOCHEMISTRY REVIEWS, 2016, 27 :72-99
[2]   Polymeric Photocatalysts Based on Graphitic Carbon Nitride [J].
Cao, Shaowen ;
Low, Jingxiang ;
Yu, Jiaguo ;
Jaroniec, Mietek .
ADVANCED MATERIALS, 2015, 27 (13) :2150-2176
[3]   g-C3N4-Based Photocatalysts for Hydrogen Generation [J].
Cao, Shaowen ;
Yu, Jiaguo .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2014, 5 (12) :2101-2107
[4]   Fabrication and characterization of novel Z-scheme photocatalyst WO3/g-C3N4 with high efficient visible light photocatalytic activity [J].
Chen, Shifu ;
Hu, Yingfei ;
Jiang, Xiaoliang ;
Meng, Sugang ;
Fu, Xianliang .
MATERIALS CHEMISTRY AND PHYSICS, 2015, 149 :512-521
[5]   Study on the separation mechanisms of photogenerated electrons and holes for composite photocatalysts g-C3N4-WO3 [J].
Chen, Shifu ;
Hu, Yingfei ;
Meng, Sugang ;
Fu, Xianliang .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2014, 150 :564-573
[6]   Semiconductor-based Photocatalytic Hydrogen Generation [J].
Chen, Xiaobo ;
Shen, Shaohua ;
Guo, Liejin ;
Mao, Samuel S. .
CHEMICAL REVIEWS, 2010, 110 (11) :6503-6570
[7]   A Plasmonic Molybdenum Oxide Hybrid with Reversible Tunability for Visible-Light-Enhanced Catalytic Reactions [J].
Cheng, Hefeng ;
Qian, Xufang ;
Kuwahara, Yasutaka ;
Mori, Kohsuke ;
Yamashita, Hiromi .
ADVANCED MATERIALS, 2015, 27 (31) :4616-4621
[8]   Surfactant-Free Nonaqueous Synthesis of Plasmonic Molybdenum Oxide Nanosheets with Enhanced Catalytic Activity for Hydrogen Generation from Ammonia Borane under Visible Light [J].
Cheng, Hefeng ;
Kamegawa, Takashi ;
Mori, Kohsuke ;
Yamashita, Hiromi .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (11) :2910-2914
[9]   Mediator-free Z-scheme photocatalytic system based on ultrathin CdS nanosheets for efficient hydrogen evolution [J].
Huang, Yi ;
Liu, Yang ;
Zhu, Dongyang ;
Xin, Yani ;
Zhang, Bin .
JOURNAL OF MATERIALS CHEMISTRY A, 2016, 4 (35) :13626-13635
[10]   A Hierarchical Z-Scheme CdS-WO3 Photocatalyst with Enhanced CO2 Reduction Activity [J].
Jin, Jian ;
Yu, Jiaguo ;
Guo, Daipeng ;
Cui, Can ;
Ho, Wingkei .
SMALL, 2015, 11 (39) :5262-5271