| Literature DB >> 24336404 |
Longb Liao1, Qiuhui Zhang2, Zhihua Su1, Zhongzheng Zhao3, Yanan Wang1, Yang Li1, Xiaoxiang Lu1, Dongguang Wei4, Guoying Feng5, Qingkai Yu6, Xiaojun Cai7, Jimin Zhao8, Zhifeng Ren9, Hui Fang10, Francisco Robles-Hernandez11, Steven Baldelli7, Jiming Bao12.
Abstract
The generation of hydrogen from water using sunlight could potentially form the basis of a clean and renewable source of energy. Various water-splitting methods have been investigated previously, but the use of photocatalysts to split water into stoichiometric amounts of H2 and O2 (overall water splitting) without the use of external bias or sacrificial reagents is of particular interest because of its simplicity and potential low cost of operation. However, despite progress in the past decade, semiconductor water-splitting photocatalysts (such as (Ga1-xZnx)(N1-xOx)) do not exhibit good activity beyond 440 nm (refs 1,2,9) and water-splitting devices that can harvest visible light typically have a low solar-to-hydrogen efficiency of around 0.1%. Here we show that cobalt(II) oxide (CoO) nanoparticles can carry out overall water splitting with a solar-to-hydrogen efficiency of around 5%. The photocatalysts were synthesized from non-active CoO micropowders using two distinct methods (femtosecond laser ablation and mechanical ball milling), and the CoO nanoparticles that result can decompose pure water under visible-light irradiation without any co-catalysts or sacrificial reagents. Using electrochemical impedance spectroscopy, we show that the high photocatalytic activity of the nanoparticles arises from a significant shift in the position of the band edge of the material.Entities:
Year: 2013 PMID: 24336404 DOI: 10.1038/nnano.2013.272
Source DB: PubMed Journal: Nat Nanotechnol ISSN: 1748-3387 Impact factor: 39.213