中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
2D Porous TiO2 Single-Crystalline Nanostructure Demonstrating High Photo-Electrochemical Water Splitting Performance

文献类型:期刊论文

作者Butburee, Teera5,6,7; Bai, Yang5,6; Wang, Huanjun4,5,6; Chen, Hongjun5,6; Wang, Zhiliang5,6; Liu, Gang1,8; Zou, Jin2; Khemthong, Pongtanawat7; Lu, Gao Qing Max3; Wang, Lianzhou5,6
刊名ADVANCED MATERIALS
出版日期2018-05-24
卷号30期号:21页码:8
关键词2D ion-exchange pore-forming porous single-crystalline TiO2 films water splitting
ISSN号0935-9648
DOI10.1002/adma.201705666
通讯作者Liu, Gang(gangliu@imr.ac.cn) ; Wang, Lianzhou(l.wang@uq.edu.au)
英文摘要Porous single crystals are promising candidates for solar fuel production owing to their long range charge diffusion length, structural coherence, and sufficient reactive sites. Here, a simple template-free method of growing a selectively branched, 2D anatase TiO2 porous single crystalline nanostructure (PSN) on fluorine-doped tin oxide substrate is demonstrated. An innovative ion exchange-induced pore-forming process is designed to successfully create high porosity in the single-crystalline nanostructure with retention of excellent charge mobility and no detriment to crystal structure. PSN TiO2 film delivers a photocurrent of 1.02 mA cm(-2) at a very low potential of 0.4 V versus reversible hydrogen electrode (RHE) for photo-electrochemical water splitting, closing to the theoretical value of TiO2 (1.12 mA cm(-2)). Moreover, the current-potential curve featuring a small potential window from 0.1 to 0.4 V versus RHE under one-sun illumination has a near-ideal shape predicted by the Gartner Model, revealing that the charge separation and surface reaction on the PSN TiO2 photoanode are very efficient. The photo-electrochemical water splitting performance of the films indicates that the ion exchange-assisted synthesis strategy is effective in creating large surface area and single-crystalline porous photoelectrodes for efficient solar energy conversion.
资助项目Australian Research Council ; National Natural Science Foundation of China[51629201] ; National Natural Science Foundation of China[51422210] ; Major Basic Research Program, Ministry of Science and Technology of China[2014CB239401] ; NANOTEC Thailand, Royal Thai Government Scholarship
WOS研究方向Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics
语种英语
WOS记录号WOS:000434032600003
出版者WILEY-V C H VERLAG GMBH
资助机构Australian Research Council ; National Natural Science Foundation of China ; Major Basic Research Program, Ministry of Science and Technology of China ; NANOTEC Thailand, Royal Thai Government Scholarship
源URL[http://ir.imr.ac.cn/handle/321006/128124]  
专题金属研究所_中国科学院金属研究所
通讯作者Liu, Gang; Wang, Lianzhou
作者单位1.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Liaoning, Peoples R China
2.Univ Queensland, Mat Engn & Ctr Microscopy & Microanal, St Lucia, Qld 4072, Australia
3.Univ Surrey Guildford, Surrey GU2 7XH, England
4.Tsinghua Univ, Dept Chem Engn, Beijing Key Lab Green React Engn & Technol, Beijing 100084, Peoples R China
5.Univ Queensland, Australian Inst Bioengn & Nanotechnol, Nanomat Ctr, St Lucia, Qld 4072, Australia
6.Univ Queensland, Sch Chem Engn, St Lucia, Qld 4072, Australia
7.NSTDA, Natl Nanotechnol Ctr NANOTEC, Klongluang 12120, Pathumthani, Thailand
8.Univ Sci & Technol China, Sch Mat Sci & Engn, 72 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
推荐引用方式
GB/T 7714
Butburee, Teera,Bai, Yang,Wang, Huanjun,et al. 2D Porous TiO2 Single-Crystalline Nanostructure Demonstrating High Photo-Electrochemical Water Splitting Performance[J]. ADVANCED MATERIALS,2018,30(21):8.
APA Butburee, Teera.,Bai, Yang.,Wang, Huanjun.,Chen, Hongjun.,Wang, Zhiliang.,...&Wang, Lianzhou.(2018).2D Porous TiO2 Single-Crystalline Nanostructure Demonstrating High Photo-Electrochemical Water Splitting Performance.ADVANCED MATERIALS,30(21),8.
MLA Butburee, Teera,et al."2D Porous TiO2 Single-Crystalline Nanostructure Demonstrating High Photo-Electrochemical Water Splitting Performance".ADVANCED MATERIALS 30.21(2018):8.

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来源:金属研究所

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