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Yujun Si,Jianzhang Li,Junbo Zhong,Jun Zeng,Shengtian Huang,Wei Yuan,Minjiao Li,Jie Ding 한국물리학회 2016 Current Applied Physics Vol.16 No.3
(BiO)2CO3/BiOI heterojunctions were prepared in-situ by a pore impregnating method using HI aqueous solution. The specific surface area, structure, morphology, and charge separation properties of the heterostructures prepared were characterized by BrunauereEmmetteTeller (BET) method, X-ray diffraction (XRD), scanning electron microscopy (SEM), and surface photovoltage (SPV) spectroscopy, respectively. The active species were investigated using scavengers. The photocatalytic activities of (BiO)2CO3/BiOI heterojunctions towards discoloration of rhodamine B (RhB) under simulated sun light irradiation were evaluated. Benefiting from enhanced charge separation efficiency, the composite photocatalysts exhibit higher photocatalytic performance than the pure BiOI. Finally, the possible reason was discussed.
Qi Yang,Junbo Zhong,Jian zhang Li,Jiufu Chen,Zhen Xiang,Tao Wang,Minjiao Li 한국물리학회 2017 Current Applied Physics Vol.17 No.4
The inherent drawbacks of Bi2O3 greatly limit the practical application of Bi2O3, thus it is crucial to boost the photocatalytic activity of Bi2O3, and therefore NiO was employed to couple with Bi2O3. In this paper, NiO/Bi2O3 heterostructures with improved sunlight driven -photocatalytic activity were constructed by a pore impregnating method. The samples were studied by Brunauer -Emmett- Teller (BET) method, X-ray diffraction (XRD), UVeVis diffuse reflectance spectroscopy (DRS), high-resolution transmission electron microscopy (HRTEM), surface photovoltage (SPV) spectroscopy and electron spin-resonance (ESR) spectroscopy. The photocatalytic activities of NiO/Bi2O3 heterostructures toward discoloration of methyl orange (MO) aqueous solutions were evaluated. The results display that the presence of NiO in the heterojuctions increases the specific surface area, the absorbance in the visible light region, the separation rate of the photo-induced charge pairs and the formation of $O2 in the photocatalytic system.