| Literature DB >> 32282192 |
Takayoshi Oshima1,2, Shunta Nishioka1,2,3, Yuka Kikuchi4, Shota Hirai1, Kei-Ichi Yanagisawa5, Miharu Eguchi6, Yugo Miseki7, Toshiyuki Yokoi8, Tatsuto Yui4, Koji Kimoto5, Kazuhiro Sayama7, Osamu Ishitani1, Thomas E Mallouk3,9, Kazuhiko Maeda1.
Abstract
Sensitization of a wide-gap oxide semiconductor with a visible-light-absorbing dye has been studied for decades as a means of producing H2 from water. However, efficient overall water splitting using a dye-sensitized oxide photocatalyst has remained an unmet challenge. Here we demonstrate visible-light-driven overall water splitting into H2 and O2 using HCa2Nb3O10 nanosheets sensitized by a Ru(II) tris-diimine type photosensitizer, in combination with a WO3-based water oxidation photocatalyst and a triiodide/iodide redox couple. With the use of Pt-intercalated HCa2Nb3O10 nanosheets further modified with amorphous Al2O3 clusters as the H2 evolution component, the dye-based turnover number and frequency for H2 evolution reached 4580 and 1960 h-1, respectively. The apparent quantum yield for overall water splitting using 420 nm light was 2.4%, by far the highest among dye-sensitized overall water splitting systems reported to date. The present work clearly shows that a carefully designed dye/oxide hybrid has great potential for photocatalytic H2 production, and represents a significant leap forward in the development of solar-driven water splitting systems.Entities:
Year: 2020 PMID: 32282192 DOI: 10.1021/jacs.0c02053
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419