A variety of adsorbates have been combined with TiO2 to form surface complexes that enable the absorption of visible
light through a ligand-to-metal charge transfer (LMCT) process. However,
proteins have not been investigated as a complex ligand for the LMCT
sensitization of TiO2. In this study, we employed albumin
as a model protein and investigated an albumin/TiO2 LMCT
complex for visible light photocatalysis. We confirmed the surface
adsorption of albumin on TiO2 using various analytical
methods such as Fourier transform infrared (FTIR) spectroscopy, zeta-potential
analysis, X-ray photoelectron spectroscopy (XPS), and electron energy-loss
spectroscopy (EELS). The LMCT process occurs between the highest occupied
molecular orbital (HOMO) level of albumin to the conduction band of
TiO2. The surface complex of albumin and TiO2 induced significant reductive conversion of Cr(VI) to Cr(III) and
production of H2O2 from O2 reduction
under visible light irradiation (λ > 420 nm). In contrast,
surface
fluorination of TiO2 (F-TiO2) hindered the complex
formation with albumin, which markedly decreased the visible light
reactivity. We also confirmed that reaction parameters such as the
mass ratio of albumin to TiO2, irradiation wavelengths,
initial pH, and temperature considerably influenced the activity of
the albumin/TiO2 complex.
Can a robot be a personal dating coach? Even with the increasing amount of conversational data on the internet, the implementation of conversational robots remains a challenge. In particular, a detailed and professional counseling log is expensive and not publicly accessible. In this paper, we develop a robot dating coaching system leveraging corpus from online communities. We examine people's perceptions of the dating coaching robot with a dialogue module. 97 participants joined to have a conversation with the robot, and 30 of them evaluated the robot. The results indicate that participants thought the robot could become a dating coach while considering the robot is entertaining rather than helpful.
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