Spinel Indium Sulfide Precursor for the Phase-Selective Synthesis of Cu-In-S Nanocrystals with Zinc-Blende, Wurtzite, and Spinel Structures

被引:69
作者
Lei, Shuijin [1 ,2 ]
Wang, Chunying [1 ,2 ]
Liu, Lei [1 ]
Guo, Donghai [1 ]
Wang, Chuanning [1 ]
Tang, Qingliu [1 ]
Cheng, Baochang [1 ,2 ]
Xiao, Yanhe [1 ,2 ]
Zhou, Lang [1 ,2 ]
机构
[1] Nanchang Univ, Sch Mat Sci & Engn, Nanchang 330031, Jiangxi, Peoples R China
[2] Nanchang Univ, Sch Photovolta Engn, Nanchang 330031, Jiangxi, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
Cu-In-S; nanocrystals; zinc-blende; wurtzite; spinel; CUIN5S8; THIN-FILMS; CUINS2; NANOCRYSTALS; ELECTRICAL-PROPERTIES; SOLAR-CELLS; GROWTH-MECHANISM; SINGLE-CRYSTALS; NANOPARTICLES; AGIN5S8; CHALCOPYRITE; PARTICLES;
D O I
10.1021/cm400848f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Group I-III-VI ternary chalcogenides have attracted extensive attention as important functional semiconductors. Among them, Cu-In-S compounds have seen strong research interest due to their potential applications in high-efficiency solar cells. However, the controllable synthesis of Cu-In-S nanostructures with different phases is always difficult. In this research, zinc-blende CuInS2, wurtzite CuInS2, and spinel CuIn5S8 could be selectively synthesized using spinel In3-xS4 as the precursor by a simple solvothermal method. X-ray powder diffraction was used to determine the phase and crystal structure, and transmission electron microscopy was employed to characterize the morphologies of the as-prepared samples. Experiments showed that the acidity-basicity of the reaction system and the coordination and reducibility of the capping ligands were crucial to the final phases of the products. The UV-vis-NIR spectra of the three phases all exhibited a broad-band absorption over the entire visible light and extending into the near-infrared region, and the zinc-blende, wurtzite, and spine! Cu-In-S nanocrystals showed band gaps of 1.55, 1.54, and 1.51 eV, respectively, which indicates their potential applications in thin-film solar cells.
引用
收藏
页码:2991 / 2997
页数:7
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