TY - JOUR
T1 - Tube-like ternary α-Fe2O3@SnO 2@Cu2O sandwich heterostructures
T2 - Synthesis and enhanced photocatalytic properties
AU - Tian, Qingyong
AU - Wu, Wei
AU - Sun, Lingling
AU - Yang, Shuanglei
AU - Lei, Mei
AU - Zhou, Juan
AU - Liu, Ying
AU - Xiao, Xiangheng
AU - Ren, Feng
AU - Jiang, Changzhong
AU - Roy, Vellaisamy A.L.
PY - 2014/8/13
Y1 - 2014/8/13
N2 - Heterogeneous photocatalysis is of great interest for environmental remediation applications. However, fast recombination of photogenerated electron-hole pair and a low utilization rate of sunlight hinder the commercialization of currently available semiconductor photocatalysts. In this regard, we developed a unique ternary single core-double shell heterostructure that consists of α-Fe2O3@SnO2@Cu 2O. This heterostructure exhibits a tube-like morphology possessing broad spectral response for the sunlight due to the combination of narrow bandgap and wide bandgap semiconductors forming a p-n heterojunction. To fabricate such a short nanotube (SNT), we used an anion-assisted hydrothermal route for deposition of α-Fe2O3, a seed-mediated deposition strategy for SnO2, and finally an aging process to deposit a Cu2O layer to complete the tube-like ternary α-Fe 2O3@SnO2@Cu2O single core-double shell heterostructures. The morphology, composition, and photocatalytic properties of those ternary core-shell-shell heterostructures were characterized by various analytical techniques. These ternary heterostructures exhibited enhanced photocatalytic properties on the photodegradation of the organic dye of Rhodamine B (RhB) under simulated sunlight irradiation. The origin of enhanced photocatalytic activity is due to the synergistic effect of broad spectral response by combining narrow bandgap and wide bandgap semiconductors and, hence, an efficient charge separation of photogenerated electron-hole pairs facilitated through the p-n heterojunction. Furthermore, our unique structure provides an insight on the fabrication and controlled preparation of multilayer heterostructural photocatalysts that have intriguing properties.
AB - Heterogeneous photocatalysis is of great interest for environmental remediation applications. However, fast recombination of photogenerated electron-hole pair and a low utilization rate of sunlight hinder the commercialization of currently available semiconductor photocatalysts. In this regard, we developed a unique ternary single core-double shell heterostructure that consists of α-Fe2O3@SnO2@Cu 2O. This heterostructure exhibits a tube-like morphology possessing broad spectral response for the sunlight due to the combination of narrow bandgap and wide bandgap semiconductors forming a p-n heterojunction. To fabricate such a short nanotube (SNT), we used an anion-assisted hydrothermal route for deposition of α-Fe2O3, a seed-mediated deposition strategy for SnO2, and finally an aging process to deposit a Cu2O layer to complete the tube-like ternary α-Fe 2O3@SnO2@Cu2O single core-double shell heterostructures. The morphology, composition, and photocatalytic properties of those ternary core-shell-shell heterostructures were characterized by various analytical techniques. These ternary heterostructures exhibited enhanced photocatalytic properties on the photodegradation of the organic dye of Rhodamine B (RhB) under simulated sunlight irradiation. The origin of enhanced photocatalytic activity is due to the synergistic effect of broad spectral response by combining narrow bandgap and wide bandgap semiconductors and, hence, an efficient charge separation of photogenerated electron-hole pairs facilitated through the p-n heterojunction. Furthermore, our unique structure provides an insight on the fabrication and controlled preparation of multilayer heterostructural photocatalysts that have intriguing properties.
KW - iron oxide
KW - multilayer heterostructure
KW - p-n heterojunction
KW - photocatalytic activity
UR - http://www.scopus.com/inward/record.url?scp=84906269115&partnerID=8YFLogxK
U2 - 10.1021/am5029439
DO - 10.1021/am5029439
M3 - Article
AN - SCOPUS:84906269115
SN - 1944-8244
VL - 6
SP - 13088
EP - 13097
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 15
ER -