Issue 8, 2016

An aqueous, organic dye derivatized SnO2/TiO2 core/shell photoanode

Abstract

Visible light driven water splitting in a dye-sensitized photoelectrochemical cell (DSPEC) based on a phosphonic acid-derivatized donor–π–acceptor (D–π–A) organic dye (P–A–π–D) is described with the dye anchored to an FTO|SnO2/TiO2 core/shell photoanode in a pH 7 phosphate buffer solution. Transient absorption measurements on FTO|TiO2|–[P–A–π–D] compared to core/shell, FTO|SnO2/TiO2(3 nm)|–[P–A–π–D], reveal that excitation of the dye is rapid and efficient with a decrease in back electron rate by a factor of ∼10 on the core/shell. Upon visible, 1 sun excitation (100 mW cm−2) of FTO|SnO2/TiO2(3 nm)|–[P–A–π–D] in a phosphate buffer at pH 7 with 20 mM added hydroquinone (H2Q), photocurrents of ∼2.5 mA cm−2 are observed which are sustained over >15 min photolysis periods with a current enhancement of ∼30-fold compared to FTO|TiO2|–[P–A–π–D] due to the core/shell effect. On surfaces co-loaded with both –[P–A–π–D] and the known water oxidation catalyst, Ru(bda)(pyP)2 (pyP = pyridin-4-methyl phosphonic acid), maximum photocurrent levels of 1.4 mA cm−2 were observed which decreased over an 10 min interval to 0.1 mA cm−2. O2 was measured by use of a two-electrode, collector–generator sandwich cell and was produced in low faradaic efficiencies with the majority of the oxidative photocurrent due to oxidative decomposition of the dye.

Graphical abstract: An aqueous, organic dye derivatized SnO2/TiO2 core/shell photoanode

Supplementary files

Article information

Article type
Paper
Submitted
24 אוג 2015
Accepted
03 אוק 2015
First published
05 אוק 2015

J. Mater. Chem. A, 2016,4, 2969-2975

Author version available

An aqueous, organic dye derivatized SnO2/TiO2 core/shell photoanode

K. Wee, B. D. Sherman, M. K. Brennaman, M. V. Sheridan, A. Nayak, L. Alibabaei and T. J. Meyer, J. Mater. Chem. A, 2016, 4, 2969 DOI: 10.1039/C5TA06678F

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