TY - JOUR
T1 - A stable dye-sensitized photoelectrosynthesis cell mediated by a NiO overlayer for water oxidation
AU - Wang, Degao
AU - Niu, Fujun
AU - Mortelliti, Michael J.
AU - Sheridan, Matthew V.
AU - Sherman, Benjamin D.
AU - Zhu, Yong
AU - McBride, James R.
AU - Dempsey, Jillian L.
AU - Shen, Shaohua
AU - Dares, Christopher J.
AU - Li, Fei
AU - Meyer, Thomas J.
N1 - Publisher Copyright:
© 2020 National Academy of Sciences. All rights reserved.
PY - 2020/6/9
Y1 - 2020/6/9
N2 - In the development of photoelectrochemical cells for water splitting or CO2 reduction, a major challenge is O2 evolution at photoelectrodes that, in behavior, mimic photosystem II. At an appropriate semiconductor electrode, a water oxidation catalyst must be integrated with a visible light absorber in a stable half-cell configuration. Here, we describe an electrode consisting of a light absorber, an intermediate electron donor layer, and a water oxidation catalyst for sustained light driven water oxidation catalysis. In assembling the electrode on nanoparticle SnO2/TiO2 electrodes, a Ru(II) polypyridyl complex was used as the light absorber, NiO was deposited as an overlayer, and a Ru(II) 2,2′-bipyridine-6,6′-dicarboxylate complex as the water oxidation catalyst. In the final electrode, addition of the NiO overlayer enhanced performance toward water oxidation with the final electrode operating with a 1.1 mA/cm2 photocurrent density for 2 h without decomposition under one sun illumination in a pH 4.65 solution. We attribute the enhanced performance to the role of NiO as an electron transfer mediator between the light absorber and the catalyst.
AB - In the development of photoelectrochemical cells for water splitting or CO2 reduction, a major challenge is O2 evolution at photoelectrodes that, in behavior, mimic photosystem II. At an appropriate semiconductor electrode, a water oxidation catalyst must be integrated with a visible light absorber in a stable half-cell configuration. Here, we describe an electrode consisting of a light absorber, an intermediate electron donor layer, and a water oxidation catalyst for sustained light driven water oxidation catalysis. In assembling the electrode on nanoparticle SnO2/TiO2 electrodes, a Ru(II) polypyridyl complex was used as the light absorber, NiO was deposited as an overlayer, and a Ru(II) 2,2′-bipyridine-6,6′-dicarboxylate complex as the water oxidation catalyst. In the final electrode, addition of the NiO overlayer enhanced performance toward water oxidation with the final electrode operating with a 1.1 mA/cm2 photocurrent density for 2 h without decomposition under one sun illumination in a pH 4.65 solution. We attribute the enhanced performance to the role of NiO as an electron transfer mediator between the light absorber and the catalyst.
KW - Artificial photosynthesis
KW - Core/shell
KW - Mediator
KW - NiO
KW - Water oxidation
UR - https://www.scopus.com/pages/publications/85086146607
U2 - 10.1073/pnas.1821687116
DO - 10.1073/pnas.1821687116
M3 - 文章
C2 - 31488721
AN - SCOPUS:85086146607
SN - 0027-8424
VL - 117
SP - 12564
EP - 12571
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 23
ER -