Supersensitization of CdS Quantum Dots with a Near-Infrared Organic Dye: Toward the Design of Panchromatic Hybrid-Sensitized Solar Cells

被引:135
作者
Choi, Hyunbong [2 ,3 ]
Nicolaescu, Roxana [2 ,3 ]
Paek, Sanghyun [1 ]
Ko, Jaejung [1 ]
Kamat, Prashant V. [2 ,3 ]
机构
[1] Korea Univ, Dept Adv Mat Chem, Jochiwon 339700, Chungnam, South Korea
[2] Univ Notre Dame, Radiat Lab, Notre Dame, IN 46556 USA
[3] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
基金
新加坡国家研究基金会;
关键词
quantum dot solar cells; squaraine dye; photosensitization; transient absorption spectroscopy; pulse radiolysis; photocurrent generation; CdS; MULTIPLE EXCITON GENERATION; NANOCRYSTALLINE TIO2 FILMS; SEMICONDUCTOR NANOCRYSTALS; SQUARAINE DYES; ELECTRON-TRANSFER; PHOTOCHEMISTRY; PBS; RECOMBINATION; INJECTION; RADICALS;
D O I
10.1021/nn2035022
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The photoresponse of quantum dot solar cells (QDSCs) has been successfully extended to the near-IR (NIR) region by sensitizing nanostructured TiO2-CdS films with a squaraine dye (JK-216). CdS nanoparticles anchored on mesoscopic TiO2 films obtained by successive ionic layer adsorption and reaction (SILAR) exhibit limited absorption below 500 nm with a net power conversion efficiency of similar to 1% when employed as a photoanode in QDSC. By depositing a thin barrier layer of Al2O3, the TiO2-CdS films were further modified with a NIR absorbing Squaraine dye. Quantum dot sensitized solar cells supersensitized with a squariand dye (JK-216) showed good stability during illumination with standard global AM 1.5 solar conditions, delivering a maximum overall power conversion efficiency (eta) of 3.14%. Transient absorption and pulse radiolysis measurements provide further insight Into the excited state interactions of squaraine dye with SiO2, TiO2, and TiO2/CdS/Al2O3 films and interfacial electron transfer processes. The synergy of combining semiconductor quantum dots and NIR absorbing dye provides new opportunities to harvest photons from different regions of the solar spectrum.
引用
收藏
页码:9238 / 9245
页数:8
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