biostudies-literatureFu ZJapan Society for the Promotion of Science321-327https://www.ebi.ac.uk/biostudies/studies/S-EPMC9841978biostudies-literatureUnknown127(1)Chemical conversion of materials is completed in milliseconds or seconds by assembling atoms over semiconductor photocatalysts. Bandgap-excited electrons and holes reactive on this time scale are key to efficient atom assembly to yield the desired products. In this study, attenuated total reflection of infrared and near-infrared light was applied to characterize and quantify the electronic absorption of TiO₂ photocatalysts excited in liquid. Nanoparticles of rutile or anatase were placed on a diamond prism, covered with liquid, and irradiated by steady UV light through the prism. Electrons excited in rutile particles (JRC-TIO-6) formed small polarons characterized by a symmetric absorption band spread over 10000-700 cm^-1 with a maximum at 6000 cm^-1. Electrons in anatase particles (JRC-TIO-7) created large polarons and produced an asymmetric absorption band that gradually strengthened at wavenumbers below 5000 cm^-1 and sharply weakened at 1000 cm^-1. The absorption spectrum of large electron polarons in TIO-7 was compared with the absorption reported in a Sr-doped NaTaO₃ photocatalyst, and it was suggested that excited electrons were accommodated as large polarons in NaTaO₃ photocatalysts efficient for artificial photosynthesis. UV-light power dependence of the absorption bands was observed in N₂-exposed decane liquid to deduce electron-hole recombination kinetics. With light power density <i>P</i> > 200 W m^-2 (TIO-6) and 2000 W m^-2 (TIO-7), the polaron absorptions were enhanced with absorbance being proportional to <i>P</i>^1/2. The observed 1/2-order power law suggested recombination of multiple electrons and holes randomly moving in each particle. Upon excitation with smaller <i>P</i>, the power-law order increased to unity. The unity-order power law was interpreted with recombination of an electron and a hole that were excited by the same photon. In addition, an average lifetime of 1 ms was estimated with electron polarons in TIO-6 when weakly excited at <i>P</i> = 20 W m^-2 to simulate solar-light irradiation.The journal of physical chemistry. BInfrared and Near-Infrared Spectrometry of Anatase and Rutile Particles Bandgap Excited in Liquid.PMC984197822H0034419H0091518KK0161Fu ZOnishi HfalseInfrared and Near-Infrared Spectrometry of Anatase and Rutile Particles Bandgap Excited in Liquid.Chemical conversion of materials is completed in milliseconds or seconds by assembling atoms over semiconductor photocatalysts. Bandgap-excited electrons and holes reactive on this time scale are key to efficient atom assembly to yield the desired products. In this study, attenuated total reflection of infrared and near-infrared light was applied to characterize and quantify the electronic absorption of TiO₂ photocatalysts excited in liquid. Nanoparticles of rutile or anatase were placed on a diamond prism, covered with liquid, and irradiated by steady UV light through the prism. Electrons excited in rutile particles (JRC-TIO-6) formed small polarons characterized by a symmetric absorption band spread over 10000-700 cm^-1 with a maximum at 6000 cm^-1. Electrons in anatase particles (JRC-TIO-7) created large polarons and produced an asymmetric absorption band that gradually strengthened at wavenumbers below 5000 cm^-1 and sharply weakened at 1000 cm^-1. The absorption spectrum of large electron polarons in TIO-7 was compared with the absorption reported in a Sr-doped NaTaO₃ photocatalyst, and it was suggested that excited electrons were accommodated as large polarons in NaTaO₃ photocatalysts efficient for artificial photosynthesis. UV-light power dependence of the absorption bands was observed in N₂-exposed decane liquid to deduce electron-hole recombination kinetics. With light power density <i>P</i> > 200 W m^-2 (TIO-6) and 2000 W m^-2 (TIO-7), the polaron absorptions were enhanced with absorbance being proportional to <i>P</i>^1/2. The observed 1/2-order power law suggested recombination of multiple electrons and holes randomly moving in each particle. Upon excitation with smaller <i>P</i>, the power-law order increased to unity. The unity-order power law was interpreted with recombination of an electron and a hole that were excited by the same photon. In addition, an average lifetime of 1 ms was estimated with electron polarons in TIO-6 when weakly excited at <i>P</i> = 20 W m^-2 to simulate solar-light irradiation.2023-01-01T00:00:00Z2023 Jan2025-04-18T15:18:36.054Z2025-04-07T01:53:54.631ZS-EPMC98419783654279610.1021/acs.jpcb.2c07433