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DOI | 10.1039/c7ee03650g |
Spatial control of cocatalysts and elimination of interfacial defects towards efficient and robust CIGS photocathodes for solar water splitting | |
Chen M.; Liu Y.; Li C.; Li A.; Chang X.; Liu W.; Sun Y.; Wang T.![]() | |
发表日期 | 2018 |
ISSN | 17545692 |
起始页码 | 2025 |
结束页码 | 2034 |
卷号 | 11期号:8 |
英文摘要 | Chalcopyrite thin film absorbers such as Cu(In,Ga)Se2 (CIGS) exhibit excellent solar energy conversion efficiency, particularly when coupled with CdS to form an excellent p-n junction. To advance CIGS towards an efficient photoelectrochemical (PEC) hydrogen evolution reaction (HER), a protective overlayer (typically TiO2) is needed to prevent the corrosion of CIGS and CdS in the electrolyte, and a HER catalyst (typically Pt) is required to promote the surface reaction. However, it is a great challenge to realize delicate spatial control of the HER catalyst on the surface of the protective overlayer using the traditional deposition method. The charge transport through the CdS/overlayer interface is also of vital importance but is rarely considered. Herein, through a new two-step platinization strategy, the dispersion and particle size of Pt nanoparticles are independently controlled to realize high HER catalytic activity. Moreover, defects at the CdS/TiO2 interface are passivated via an ultrathin Al2O3 insertion layer. Consequently, we have obtained a robust CIGS/CdS/Al2O3/TiO2/Pt photocathode for PEC hydrogen evolution, which yields an applied bias photon-to-current efficiency (ABPE) of 6.6% in neutral electrolyte with a long-term stability up to 8 h (4.5% drop), and an unprecedented ABPE of 9.3% in acidic electrolyte that is the highest among chalcopyrite-based photocathodes. When paired with a BiVO4 photoanode to form a PEC tandem cell, an unbiased solar-to-hydrogen conversion efficiency of 1.01% is achieved. © 2018 The Royal Society of Chemistry. |
英文关键词 | Alumina; Aluminum oxide; Bismuth compounds; Cadmium sulfide; Catalyst activity; Conversion efficiency; Copper compounds; Corrosion prevention; Corrosion protection; Electrolytes; Energy conversion; Field emission cathodes; Hydrogen; II-VI semiconductors; Particle size; Photocathodes; Photoelectrochemical cells; Semiconductor junctions; Solar absorbers; Solar energy; Surface reactions; Titanium dioxide; Chalcopyrite thin films; Hydrogen evolution reactions; Long term stability; Neutral electrolytes; Photoelectrochemicals; Photon-to-current efficiencies; Solar water splitting; Solar-to-hydrogen conversions; Solar power generation; catalyst; chemical compound; chemical reaction; efficiency measurement; electrode; electrolyte; energy efficiency; nanoparticle; particle size; platinum; solar power |
语种 | 英语 |
来源期刊 | Energy & Environmental Science
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/190184 |
作者单位 | Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin, 300072, China; Institute of Photoelectronic Thin Film Devices and Technology, Tianjin Key Laboratory of Thin Film Devices and Technology, Nankai University, Tianjin, 300071, China |
推荐引用方式 GB/T 7714 | Chen M.,Liu Y.,Li C.,et al. Spatial control of cocatalysts and elimination of interfacial defects towards efficient and robust CIGS photocathodes for solar water splitting[J],2018,11(8). |
APA | Chen M..,Liu Y..,Li C..,Li A..,Chang X..,...&Gong J..(2018).Spatial control of cocatalysts and elimination of interfacial defects towards efficient and robust CIGS photocathodes for solar water splitting.Energy & Environmental Science,11(8). |
MLA | Chen M.,et al."Spatial control of cocatalysts and elimination of interfacial defects towards efficient and robust CIGS photocathodes for solar water splitting".Energy & Environmental Science 11.8(2018). |
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