Sr2NiWO6 Double Perovskite Oxide as a Novel Visible-Light-Responsive Water Oxidation Photocatalyst

被引:57
|
作者
Idris, Ahmed Mahmoud [1 ,2 ,3 ]
Liu, Taifeng [4 ]
Shah, Jafar Hussain [1 ,2 ,3 ]
Malik, Anum Shahid [1 ,2 ,3 ]
Zhao, Dan [5 ]
Han, Hongxian [1 ,2 ]
Li, Can [1 ,2 ]
机构
[1] Chinese Acad Sci, State Key Lab Catalysis, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Div Solar Energy, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Henan Univ, Natl & Local Joint Engn Res Ctr Appl Technol Hybr, Collaborat Innovat Ctr Nano Funct Mat & Applicat, Kaifeng 475004, Peoples R China
[5] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
water oxidation; double perovskite oxide semiconductor; visible light; water splitting; solar fuel; ONE-STEP SYNTHESIS; DRIVEN Z-SCHEME; OXYGEN EVOLUTION; DUAL-COCATALYSTS; BAND-STRUCTURE; EFFICIENT; O-2; H-2; NANOPARTICLES; DEPENDENCE;
D O I
10.1021/acsami.0c05576
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Screening of stable visible-light-responsive water oxidation semiconductor photocatalysts is highly desired for the development of photocatalytic water splitting systems. Herein, a visible-light-absorbing Sr2NiWO6 double perovskite oxide photocatalyst was successfully prepared via a conventional solid-state reaction method. The intrinsic Sr2NiWO6 shows photocatalytic oxygen evaluation reaction (OER) activity of 60 mu mol h(-1) g(-1), even without loading any cocatalysts. The DFT calculation indicates that the Ni species on the surface is the active site for the OER. The photocatalytic OER activity was further improved by loading Pt and RuO2 dual redox cocatalysts on the surface of Sr2NiWO6 to achieve a photocatalytic OER activity of 420 mu mol h(-1) g(-1), which corresponds to a remarkable apparent quantum efficiency (AQE) of 8.6% (lambda approximate to 420 nm). The result indicates that Sr2NiWO6 is one of the best double perovskite oxide-based photocatalysts for the photocatalytic OER, and the activity is even comparable to the benchmark BiVO4-based photocatalyst. The improvement of the photocatalytic OER activity is due to the provision of more active redox sites as well as the synergetic effect of the dual redox cocatalysts in facilitating charge separation and transfer. This work demonstrates that double perovskite oxides may serve as a novel class of efficient and stable oxide-based semiconductor photocatalysts for water splitting.
引用
收藏
页码:25938 / 25948
页数:11
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