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Tunable Transformation Between SnS and SnO x Nanostructures via Facile Anodization and Their Photoelectrochemical and Photocatalytic Performance
Author(s) -
Bian Haidong,
Li Zebiao,
Xiao Xufen,
Schmuki Patrik,
Lu Jian,
Li Yang Yang
Publication year - 2018
Publication title -
solar rrl
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.544
H-Index - 37
ISSN - 2367-198X
DOI - 10.1002/solr.201800161
Subject(s) - materials science , heterojunction , anodizing , photocatalysis , electrolyte , band gap , nanostructure , anode , tin oxide , cadmium sulfide , sulfide , photoelectrochemistry , oxide , nanotechnology , tin , photocurrent , chemical engineering , electrode , optoelectronics , electrochemistry , catalysis , metallurgy , chemistry , engineering , aluminium , biochemistry
Anodic fabrication of tin sulfide is for the first time reported. Through a facile anodization method in a glycerol electrolyte of sodium sulfide, a range of interesting tin sulfide nanostructures are produced in a controllable manner. By changing the anodization parameters (anodization potential, water content, and electrolyte concentration), anodic nanomaterials ranging from pure SnS to SnO x can be conveniently synthesized. The fabricated SnS/SnO x multi‐heterojunction nanocomposites delivered greatly improved photoelectrochemical and photocatalytic performances, due to the presence of narrow‐bandgap SnS (≈1.56 eV) in wide‐bandgap SnO x (≈3.6 eV), which can effectively separate the photoinduced electron‐hole pairs and prolong their lifetime. The novel method reported here presents an efficient strategy to directly construct metal sulfides or sulfide/oxide heterojunctions that are directly applicable as electrode materials in photoelectrochemical cells, photovoltaic devices, sensors, and binder‐free batteries or supercapacitors.

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