OAK

p-Si/SnO2/Fe2O3 Core/Shell/Shell Nanowire Photocathodes for Neutral pH Water Splitting

Metadata Downloads
Author(s)
Kargar, AlirezaKim, Sung JooAllameh, PanizChoi, ChulminPark, NamseokJeong, HuisuPak, YusinJung, Gun YoungPan, XiaoqingWang, DeliJin, Sungho
Type
Article
Citation
ADVANCED FUNCTIONAL MATERIALS, v.25, no.17, pp.2609 - 2615
Issued Date
2015-05
Abstract
Silicon is one of the promising materials for solar water splitting and hydrogen production; however, it suffers from two key factors, including the large external potential required to drive water splitting reactions at its surface and its instability in the electrolyte. In this study, a successful fabrication of novel p-Si/n-SnO2/n-Fe2O3 core/shell/shell nanowire (css-NW) arrays, consisting of vertical Si NW cores coated with a thin SnO2 layer and a dense Fe2O3 nanocrystals (NCs) shell, and their application for significantly enhanced solar water reduction in a neutral medium is reported. The p-Si/n-SnO2 /n-Fe2O3 css-NW structure is characterized in detail using scanning, transmission, and scanning transmission electron microscopes. The p-Si/n-SnO2 /n-Fe2O3 css-NWs show considerably improved photocathodic performances, including higher photocurrent and lower photocathodic turn-on potential, compared to the bare p-Si NWs or p-Si/n-SnO2 core/shell NWs (cs-NWs), due to increased optical absorption, enhanced charge separation, and improved gas evolution. As a result, photoactivity at 0 V versus reversible hydrogen electrode and a low onset potential in the neutral solution are achieved. Moreover, p-Si/n-SnO2 /n-Fe2O3 css-NWs exhibit long-term photoelectrochemical stability due to the Fe2O3 NCs shell well protection. These results reveal promising css-NW photoelectrodes from cost-effective materials by facile fabrication with simultaneously improved photocathodic performance and stability.
Publisher
WILEY-V C H VERLAG GMBH
ISSN
1616-301X
DOI
10.1002/adfm.201404571
URI
https://scholar.gist.ac.kr/handle/local/14726
공개 및 라이선스
  • 공개 구분공개
파일 목록

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.