Dissolution of BiVO4 Photoanodes Revealed by Time-Resolved Measurements under Photoelectrochemical Conditions
Author(s) -
Siyuan Zhang,
Martin Rohloff,
Olga Kasian,
Andrea M. Mingers,
Karl J. J. Mayrhofer,
Anna Fischer,
Christina Scheu,
Serhiy Cherevko
Publication year - 2019
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.9b07220
Subject(s) - dissolution , photoelectrochemistry , photoelectrochemical cell , electrolyte , water splitting , electrode , chemistry , stoichiometry , analytical chemistry (journal) , inorganic chemistry , materials science , electrochemistry , catalysis , environmental chemistry , photocatalysis , biochemistry
Photocorrosion imposes a fundamental limit to the longevity of devices that harvest energy from photons. As one of the best performing electrode materials for photoelectrochemical water oxidation reaction, BiVO4 undergoes photocorrosion with various postulated mechanisms under debate. We present time-resolved dissolution measurements to advance the mechanistic understanding, enabled by the recent development in illuminated scanning flow cell coupled to inductively coupled plasma mass spectrometry. The contact dissolution of predominantly V was distinguished from the stoichiometric photoelectrochemical dissolution of Bi and V. The citrate electrolyte was utilized to form soluble complexes with dissolved Bi and to act as hole scavengers that provide photocurrents at a wide range of potentials. The photoelectrochemical dissolution rates remain similar between 0.4 and 1.6 V vs reversible hydrogen electrode and become lower at the open circuit potential, 0.2 V. The time-resolved measurements support oxidation ...
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom