Visible-light-induced electron transfer between alternating stacked layers of tungstate and titanate mediated by excitation of intercalated dye molecules

Literature Information

Publication Date 2013-11-05
DOI 10.1039/C3CP53579G
Impact Factor 3.676
Authors

Fuminao Kishimoto, Dai Mochizuki, Kozue Kumagai, Masato M. Maitani, Eiichi Suzuki, Yuji Wada


View Original

Abstract

Visible-light-induced electron transfer from a tungstate to a titanate layer was demonstrated to be mediated by excited rhodamine B (RhB) intercalated by ion exchange between the two layers. The distance of only 1 nm between the layers provides a large contact area that enables the efficient mediation of electron transfer by RhB.

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Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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