Facet-Specific Ligand Interactions on Ternary AgSbS2 Colloidal Quantum Dots

被引:20
作者
Choi, Hyekyoung [1 ]
Kim, Sungwoo [1 ,3 ]
Luther, Joseph M. [2 ]
Kim, Sang-Wook
Shin, Dongwoon [1 ,4 ]
Beard, Matthew C. [2 ]
Jeong, Sohee [1 ,4 ]
机构
[1] Korea Inst Machinery & Mat, Nanoconvergence Syst Res Div, Daejeon 34103, South Korea
[2] Natl Renewable Energy Lab, Chem & Mat Sci Ctr, Golden, CO 80401 USA
[3] Ajou Univ, Dept Mol Sci & Technol, Suwon 16499, South Korea
[4] Korea Univ Sci & Technol UST, Dept Nanomech, Daejeon 34113, South Korea
关键词
AgSbS2; I-V-VI2; quantum dots; surface chemistry; ternary; SOLAR-CELLS; SURFACE-CHEMISTRY; SIZE-CONTROL; NANOCRYSTALS; HALIDE; RECOMBINATION; SOLIDS; ACIDS; SHAPE;
D O I
10.1002/chem.201703681
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Silver dimetal chalcogenide (Ag-V-VI2) ternary quantum dots (QDs) are emerging lead-free materials for optoelectronic devices due to their NIR band gaps, large absorption coefficients, and superior electronic properties. However, thin film-based devices of the ternary QDs still lag behind due to the lack of understanding of the surface chemistry, compared to that of lead chalcogenide QDs even with the same crystal structure. Herein the surface ligand interactions of AgSbS2 QDs, synthesized with 1-dodecanethiol used as a stabilizer, are studied. For nonpolar (100) surfaces, it is suggested that the thiolate ligands are associated with the crystal lattices, thus preventing surface oxidation by protecting sulfur after air-exposure, as confirmed through optical and surface chemical analysis. Otherwise, silver rich (111) surfaces are passivated by thiolate ligands, allowing ligand exchange processes for the conductive films. This in-depth investigation of the surface chemistry of ternary QDs will prompt the performance enhancement of their optoelectronic devices.
引用
收藏
页码:17707 / 17713
页数:7
相关论文
共 41 条
[1]  
Bernechea M, 2016, NAT PHOTONICS, V10, P521, DOI [10.1038/NPHOTON.2016.108, 10.1038/nphoton.2016.108]
[2]   Photoconductive thin films of AgSbS2 with cubic crystalline structure in solar cells [J].
Capistran-Martinez, Jesus ;
Nair, P. K. .
PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE, 2015, 212 (12) :2869-2876
[3]   Colloidal Quantum Dot Solar Cells [J].
Carey, Graham H. ;
Abdelhady, Ahmed L. ;
Ning, Zhijun ;
Thon, Susanna M. ;
Bakr, Osman M. ;
Sargent, Edward H. .
CHEMICAL REVIEWS, 2015, 115 (23) :12732-12763
[4]   The Chemical Environments of Oleate Species within Samples of Oleate-Coated PbS Quantum Dots [J].
Cass, Laura C. ;
Malicki, Michal ;
Weiss, Emily A. .
ANALYTICAL CHEMISTRY, 2013, 85 (14) :6974-6979
[5]   Supersonically Spray-Coated Colloidal Quantum Dot Ink Solar Cells [J].
Choi, Hyekyoung ;
Lee, Jong-Gun ;
Mai, Xuan Dung ;
Beard, Matthew C. ;
Yoon, Sam S. ;
Jeong, Sohee .
SCIENTIFIC REPORTS, 2017, 7
[6]   Increased open-circuit voltage in a Schottky device using PbS quantum dots with extreme confinement [J].
Choi, Hyekyoung ;
Kim, Jun Kwan ;
Song, Jung Hoon ;
Kim, Youngjo ;
Jeong, Sohee .
APPLIED PHYSICS LETTERS, 2013, 102 (19)
[7]   Steric-Hindrance-Driven Shape Transition in PbS Quantum Dots: Understanding Size-Dependent Stability [J].
Choi, Hyekyoung ;
Ko, Jae-Hyeon ;
Kim, Yong-Hyun ;
Jeong, Sohee .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (14) :5278-5281
[8]  
Chuang CHM, 2014, NAT MATER, V13, P796, DOI [10.1038/nmat3984, 10.1038/NMAT3984]
[9]   EVIDENCE FOR SPATIALLY INDIRECT RECOMBINATION IN GA0.52IN0.48P [J].
DELONG, MC ;
OHLSEN, WD ;
VIOHL, I ;
TAYLOR, PC ;
OLSON, JM .
JOURNAL OF APPLIED PHYSICS, 1991, 70 (05) :2780-2787
[10]   High-Quality CuInS2/ZnS Quantum Dots for In vitro and In vivo Bioimaging [J].
Deng, Dawei ;
Chen, Yuqi ;
Cao, Jie ;
Tian, Junmei ;
Qian, Zhiyu ;
Achilefu, Samuel ;
Gu, Yueqing .
CHEMISTRY OF MATERIALS, 2012, 24 (15) :3029-3037