This paper describes a solvothermal approach to synthesize CuInS2 quantum dots (QDs) and demonstrates their application as a potential electron accepting material for polymer-based hybrid solar cells, for the first time. The CuInS2 QDs with a size of 2-4 nm are synthesized by the solvothermal method with 4-bromothiophenol (HSPh) as both reduction and capping agents, and characterized by XRD, XPS, TEM, FT-IR, cyclic voltammetry (CV), and absorption and photoluminescence spectra. Results reveal that the CuInS2 QDs result from the solvothermal decomposition of a soluble organic sodium salt as an intermediate precursor formed by simple reactions among CuCl2, InCl3, HSPh and Na2S at room temperature; they have an ionization potential (IP) of -5.8 eV and an electron affinity (EA) of -4.0 eV and can quench effectively the luminescence of poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene vinylene) (MEH-PPV). Due to the favorable IP and EA positions with respect to MEH-PPV, the CuInS2 QDs act as an effective electron acceptor for the hybrid solar cells based on MEH-PPV/CuInS2-QDs blends with a wide spectral response extending from 300 to 900 nm, by allowing the efficient charge separation for neutral excited states produced either on the polymer or on the QDs. The MEH-PPV/CuInS2-QDs solar cells exhibit a promising open circuit voltage (V-oc) of 0.62 V under the monochromic illumination of 15.85 mW cm(-2) at 470 nm. The charge transfer processes in the solar cells are also described

This paper presents a solvothermal strategy for chemical modification of TiO(2) nanoparticles with carboxylic acids. Solvothermal reaction between the TiO(2) nanoparticles and carboxylic acid molecules in an autoclave at 100 degrees C provides carboxylic acid-modified TiO(2) particles with a modification efficiency much higher than the conventional immersion method. TiO(2) nanoparticles were prepared by hydrolysis of titanium isopropoxide in nitric acid solution; the modified nanoparticles were characterized by powder X-ray diffraction pattern, scanning electron microscopy, absorption and Fourier transform infrared spectra, and thermogravimetric analysis. Results show that the binding form of the modifier molecules on TiO(2) surface is in a bidentate chelating mode, the crystalline phase composition and morphological structure of the preformed TiO(2) nanoparticles are not affected by the solvothermal reaction, and the surface coverage of the modifier molecules can be adjusted by the weight ratio of modifier/TiO(2) during feeding. It is evident that the reaction processes in the solvothermal strategy involve the formation of double hydrogen bondings between carboxylic acid molecule and TiO(2) at the same Ti site and the coordination at solvothermal temperature by dehydration from the hydrogen bondings. The solvothermal strategy for modifying TiO(2) nanoparticles is expected to find potential applications in many fields; for example, our results demonstrate that the photovoltaic performance of the TiO(2) nanoparticles can be improved by the solvothermal modification even with an insulating modifier and controlled by the modifier coverage.