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The TiO 2 –Catechol Complex: Coupling Type II Sensitization with Efficient Catalysis of Water Oxidation
Author(s) -
Tachan Zion,
Hod Idan,
Zaban Arie
Publication year - 2014
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201301249
Subject(s) - overpotential , catalysis , water splitting , photochemistry , materials science , oxygen evolution , adsorption , catechol , redox , inorganic chemistry , electrochemistry , chemical engineering , photocatalysis , chemistry , organic chemistry , electrode , engineering
Two main requirements must be fulfilled in order to construct an efficient TiO 2 ‐based photo‐electrochemical water splitting cell. One is the expansion of the cell's spectral response, usually by the attachment of a sensitizing dye monolayer on the surface of the TiO 2 . The second involves the incorporation of a water oxidation catalyst that reduces the overpotential for the oxygen evolution reaction. These requirements are often achieved by the co‐adsorption of both the dye and the catalyst on the TiO 2 , or by a covalent attachment of the catalyst to the dye molecule. Here, the possibility to use a single material that acts as a sensitizer and a catalyst is presented. The use of a catechol molecule to form a type II charge transfer complex with TiO 2 widens the absorption of the system into the visible region. The TiO 2 ‐catechol complex is highly catalytic toward the oxidation of water to oxygen, reducing the electrocatalytic reaction overpotential by 500 mV compared to bare TiO 2 . A suggested catalytic mechanism for the water oxidation reaction is described. This methodology opens a new path for type II charge transfer complexes to be utilized as catalysts/light absorbers in water splitting systems based on TiO 2 or other metal oxides.