TY - JOUR
T1 - Particle Size Dependent Trap States of Photoexcited Carriers in Anatase TiO2 Nanoparticles
AU - Naniwa, Shimpei
AU - Kato, Kosaku
AU - Yamamoto, Akira
AU - Yoshida, Hisao
AU - Yamakata, Akira
N1 - Funding Information:
This work was supported by Grant-in-Aid for JSPS Fellows (20J12388) and for Challenging Research (Exploratory, 20K21108), Basic Research (B) (19H02820), Transformative Research Areas (A) (Dynamic Exciton: 20H05838), Young Scientist (20K15386) from the Japan Society for the Promotion of Science (JSPS), and by the Program for Element Strategy Initiative for Catalysts & Batteries (ESICB, JPMXP0112101003) commissioned by the MEXT of Japan, ENEOS Hydrogen Trust Fund, and the Yakumo Foundation for Environmental Science, Izumi Science and Technology Foundation.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2022
Y1 - 2022
N2 - Heterogeneous photocatalysis is a promising technology for artificial photosynthesis and environmental remediation. The development of efficient photocatalysts requires a better understanding of trap states of photoexcited carriers since it determines the reactivity of the carriers. Although the surface morphology as well as coordination environment of surface atoms should depend on the size of photocatalyst nanoparticles, how the trap states change with the particle size remains unclear. Here we found that the depth of electron traps on anatase TiO2 particles decreases with increasing their particle size. It was shown that most photoexcited electrons are deeply trapped in the midgap states (3.1 to 0.7 eV from the conduction band minimum) in ultrafine nanoparticles (6.3 nm), but a part of electrons survived as free electrons in the conduction band when particle size was increased to 14.5 nm by annealing. Further increase to 28.6 nm exhibits only free electrons. These results show that an increase in the particle size decrease the density of deep electron traps, allowing photoexcited electrons to survive without being trapped even in the microsecond region. Our results identify particle size as a determining factor of trap states of photoexcited carriers in anatase TiO2 nanoparticles.
AB - Heterogeneous photocatalysis is a promising technology for artificial photosynthesis and environmental remediation. The development of efficient photocatalysts requires a better understanding of trap states of photoexcited carriers since it determines the reactivity of the carriers. Although the surface morphology as well as coordination environment of surface atoms should depend on the size of photocatalyst nanoparticles, how the trap states change with the particle size remains unclear. Here we found that the depth of electron traps on anatase TiO2 particles decreases with increasing their particle size. It was shown that most photoexcited electrons are deeply trapped in the midgap states (3.1 to 0.7 eV from the conduction band minimum) in ultrafine nanoparticles (6.3 nm), but a part of electrons survived as free electrons in the conduction band when particle size was increased to 14.5 nm by annealing. Further increase to 28.6 nm exhibits only free electrons. These results show that an increase in the particle size decrease the density of deep electron traps, allowing photoexcited electrons to survive without being trapped even in the microsecond region. Our results identify particle size as a determining factor of trap states of photoexcited carriers in anatase TiO2 nanoparticles.
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U2 - 10.1021/acs.jpcc.2c08125
DO - 10.1021/acs.jpcc.2c08125
M3 - Article
AN - SCOPUS:85148670814
SN - 1932-7447
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
ER -