Direct Light-Driven Water Oxidation by a Ladder-Type Conjugated Polymer Photoanode
Author(s) -
Pauline Bornoz,
Mathieu S. Prévot,
Xiaoyun Yu,
Néstor Guijarro,
Kevin Sivula
Publication year - 2015
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.5b05724
Subject(s) - chemistry , conjugated system , polymer , chemical engineering , nanotechnology , photochemistry , organic chemistry , engineering , materials science
A conjugated polymer known for high stability (poly[benzimidazobenzophenanthroline], coded as BBL) is examined as a photoanode for direct solar water oxidation. In aqueous electrolyte with a sacrificial hole acceptor (SO3(2-)), photoelectrodes show a morphology-dependent performance. Films prepared by a dispersion-spray method with a nanostructured surface (feature size of ∼20 nm) gave photocurrents up to 0.23 ± 0.02 mA cm(-2) at 1.23 VRHE under standard simulated solar illumination. Electrochemical impedance spectroscopy reveals a constant flat-band potential over a wide pH range at +0.31 VNHE. The solar water oxidation photocurrent with bare BBL electrodes is found to increase with increasing pH, and no evidence of semiconductor oxidation was observed over a 30 min testing time. Characterization of the photo-oxidation reaction suggests H2O2 or •OH production with the bare film, while functionalization of the interface with 1 nm of TiO2 followed by a nickel-cobalt catalyst gave solar photocurrents of 20-30 μA cm(-2), corresponding with O2 evolution. Limitations to photocurrent production are discussed.
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