SnSe 2 quantum dot sensitized solar cells prepared employing molecular metal chalcogenide as precursors

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Electronic SnSe 2 quantum dot sensitized solar cells prepared employing molecular metal chalcogenide as precursors Xuechao Yu, Jun Zhu,* Yaohong Zhang, Jian Weng, Linhua Hu and Songyuan Dai* Key Laboratory of Novel Thin Film Solar Cells, Institute of Plasma Physics, Chinese Academy of Sciences, P.O. Box 1126, Hefei, Anhui 230031, China. E-mail: zhujzhu@gmail.com, sydai@ipp.ac.cn; Fax: +86-551-5591377; Tel: +86-551-5591377 Experimental details (N 2 H 4 ) 3 (N 2 H 5 ) 4 Sn 2 Se 6 complex was synthesized using a literature method 1. In detail, elemental tin (10 mmol) is dissolved in a mixture of 1M Se/N 2 H 4 and N 2 H 4 (10ml) and after stirring for 3h, a clear yellow solution of the complex is formed. Alternatively, it can be synthesized from SnSe 2 and Se by dissolving them in N 2 H 4 solution. Note that hydrazine is a highly toxic chemical and must be handled with great care. The colloidal TiO 2 nanoparticles were prepared by hydrolysis of titanium tetraisopropoxide as described elsewhere by our group 2 and were anatase phase. The TiO 2 paste was printed on transparent conducting glass sheets (TEC-8, LOF) by using a screen-printing technique, and sintered in air at 510 C for 30 min to form a nanostructured TiO 2 electrode. The film thickness was about 10 μm, which was determined by a profilometer (XP-2, AMBIOS Technology Inc., USA). The TiO 2 films were not rinsed after MCC adsorption, and dried with air. To prepare SnSe 2 sensitized photoanodes, the MCC deposited TiO 2 films were annealed at 250 o C under Ar atmosphere for 60 min, and then cooled to room temperature. The electrolyte for the sensitized solar cells consists of anhydrous lithium iodide, iodine, 3-methoxypropionitrile (MePN) purchased from Fluka, and 1,2-dimethyl-3-propylimidazolium iodide (DMPII), methylbenzimidazole (MBI) obtained from Aldrich. The counter electrode was platinized by spraying H 2 PtCl 6 solution to FTO glass and fired in air at 420 C for 20 min. Then, it was placed directly on the top of the quantum dot-sensitized TiO 2 film. The gap between the two electrodes was sealed by thermal adhesive films (Surlyn, Dupont). The electrolyte was filled from a hole made on the counter electrode, which was later sealed by a cover glass and thermal adhesive films. The total active electrode area of the solar cells was 0.25 cm 2. Thermogravimetric analysis data were acquired using Shimadzu DTG-60H/DSC-60 thermal analyzer at a heating rate of 10 o C/min under slow nitrogen flow. Powder X-ray diffraction patterns were collected using a MXPAHF diffractometer with Cu K α X-ray source operating at 40 kv and 40 ma and Vantec 2000 area detector. High Resolution Transmission Electron Microscopy imaging was carried out using JEM-2010 with a carbon-coated copper grid (Ted Pella). Incident photon-to-electron conversion efficiency of SnSe 2 quantum dots sensitized solar cell was recorded under monochromatic irradiation by the use of a setup for the IPCE measurement (PEC-S2012, Peccell), which consisted of a 150 W Xe lamp and a monochromator (Instruments S. A. Triax 180). The photovoltaic performance, including short-circuit current (J sc ), open-circuit voltage (V oc ), fill factor (FF), and energy conversion efficiency (η) of the quantum dots sensitized solar cell

Electronic was measured with a Keithley model 2420 digital source meter controlled by test point software under a xenon lamp (Oriel, USA) with an AM 1.5 filter.

Electronic The amount of SnSe 2 on the TiO 2 photoanodes can be increased by repeating the MCC adsorption and annealing procedures for more times and the corresponding XRD patterns were shown in Figure S1. Figure S1. XRD of SnSe 2 sensitized TiO 2 powders with different deposition cycles

Electronic Figure S2. TG of (N 2 H 4 ) 3 (N 2 H 5 ) 4 Sn 2 Se 6 complex capped TiO 2 film

Electronic Table S1 Photovoltaic data sets of SnSe 2 quantum dots sensitized TiO 2 solar cells with room temperature aging in dark J sc (ma cm -2 ) V oc (V) FF η(%) as prepared 0.77 0.37 0.43 0.12 15 days aging 0.67 0.33 0.39 0.089 References 1. D. B. Mitzi, Inorg.Chem., 2005, 44, 3755-3761. 2. H. Tian, L. Hu, C. Zhang, W. Liu, Y. Huang, L. Mo, L. Guo, J. Sheng and S. Dai, The Journal of Physical Chemistry C, 2010, 114, 1627-1632.