| Literature DB >> 31488721 |
Degao Wang1, Fujun Niu1,2, Michael J Mortelliti1, Matthew V Sheridan3, Benjamin D Sherman4, Yong Zhu5, James R McBride6, Jillian L Dempsey1, Shaohua Shen2, Christopher J Dares3, Fei Li7,5, Thomas J Meyer7.
Abstract
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.Entities:
Keywords: NiO; artificial photosynthesis; core/shell; mediator; water oxidation
Year: 2019 PMID: 31488721 PMCID: PMC7293597 DOI: 10.1073/pnas.1821687116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205