Abstract
Semiconductor nanocrystals, often referred to as quantum dots (QDs), exhibit unique physicochemical properties due to the quantum size effect when their size is less than 10 nm. In our previous works, we successfully synthesized Zn-Ag-In-S (ZAIS) solid solution QDs with a tunable energy gap (Eg) and then reported the photocatalytic activity for H2 evolution depending on their morphology and particle composition [1,2]. However, ZAIS QDs have limited light absorption with wavelengths less than ca. 600 nm, restricting their utilization of near-infrared light in solar light. In this study, we report the preparation of near-IR-responsive QD photocatalysts with use of Zn-Ag-In-Se (ZAISe) solid solution semiconductors. Precise controls over their morphology and particle composition enabled to vary their photocatalytic H2 evolution activity.ZAISe QDs with different compositions and particle shapes (sphere or rod) were synthesized by thermal decomposition of corresponding metal acetates and selenourea in a mixture solution of oleylamine and dodecane thiol at 250 oC. The chemical composition of QDs was controlled by varying the Zn fraction in metal precursors, ensuring nearly stoichiometric composition.The obtained QDs with a rod shape had lengths varying from ca. 10 to 100 nm, correlating with an increase in the Zn fraction. The onset wavelengths of absorption spectra of the ZAISe QDs were red-shifted from 500 nm to 900 nm with decreasing Zn fraction, indicating that the Eg of ZAISe QDs was controlled between visible and near-infrared wavelength regions.The QDs modified with dodecane thiol showed poor dispersibility in water and almost no photocatalytic activity for H2 evolution. In contrast, the surface modification of QDs with 3-mercaptopropionic acid enabled to uniformly disperse in an aqueous solution. The photocatalytic activity of ZAISe QDs was investigated for H2 evolution as a model reaction. The irradiation to ZAISe QDs in an aqueous solution containing Na2S and Na2SO3 as hole scavengers was carried out using Xe lamp light (λ> 350 nm). The H2 evolution rate exhibited a remarkable dependence on both the composition and particle shape of ZAISe QDs. The photocatalytic activity showed a tendency to increase with the enlargement of the Eg of QDs, probably due to the negative shift of conduction band minimum potential. The optimum H2 evolution activity was obtained with rod-shaped QDs having the Eg of 1.65 eV, being twice as large as that of spherical QDs with a similar Eg. This behavior can be attributed to the change of the crystal facets exposed on the QD surface. References Kameyama, T. Takahashi, T. Machida, Y. Kamiya, T. Yamamoto, S. Kuwabata, and T. Torimoto, J. Phys. Chem. C, 2015, 119, 24740-24749.Torimoto, Y. Kamiya, T. Kameyama, H. Nishi, T. Uematsu, S. Kuwabata, and T. Shibayama, ACS Appl. Mater. Interfaces 2016 , 8, 27151-27161.
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