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Nitrate Radical Facilitates Indirect Benzyl Alcohol Oxidation on Bismuth(III) Vanadate Photoelectrodes
Author(s) -
Terry Bradley D.,
DiMeglio John L.,
Cousineau John P.,
Bartlett Bart M.
Publication year - 2020
Publication title -
chemelectrochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 59
ISSN - 2196-0216
DOI - 10.1002/celc.202000911
Subject(s) - chemistry , benzaldehyde , inorganic chemistry , catalysis , acetonitrile , benzyl alcohol , tungstate , vanadate , medicinal chemistry , vanadium , photochemistry , organic chemistry
Bismuth(III) vanadate (BiVO 4 ) films show activity for direct benzyl alcohol (PhCH 2 OH) oxidation to benzaldehyde (PhCHO) in acetonitrile solvent. Introducing tetrabutylammonium nitrate (Bu 4 NNO 3 ) drastically reduces the overpotential required to generate the PhCHO product while maintaining a high faradaic efficiency (FE) >90 %. BiVO 4 corrosion accompanies PhCH 2 OH oxidation. However, the presence of nitrate ions (NO 3 − ) results in significantly less bismuth‐ and vanadium‐ion leaching (determined by ICP‐MS analysis), as well as reduced surface roughening (determined by SEM imaging). In this reaction, it is proposed that rate‐determining NO 3 − oxidation generates a highly reactive nitrate radical (NO 3 ⋅) that reacts with PhCH 2 OH by hydrogen‐atom abstraction (HAT). NO 3 − is stoichiometrically consumed by the irreversible formation of electrochemically inert HNO 3 , characterized by an EC i mechanism, rather than a catalytic EC′ mechanism. In the presence of PhCH 2 OH, NO 3 − oxidation on BiVO 4 becomes more facile; every order of magnitude increase in PhCH 2 OH concentration shifts the NO 3 − / NO 3 ⋅ equilibrium potential negatively by 200 mV. The shift results from the introduction of a consumption pathway for the nitrate radical intermediate via a coupled chemical step with benzyl alcohol. This report is the first example of photoelectrochemical NO 3 ⋅ generation to initiate indirect PhCH 2 OH oxidation.