Zhao Deqiang, Wang Wenwen, Zong Wenjuan, Xiong Shimin, Zhang Qian, Ji Fangying, Xu Xuan
Key Laboratory of Three Gorges Reservoir Region's Eco-Environment Ministry of Education and National Centre for International Research of Low-Carbon and Green Buildings, Chongqing University, No. 174 Shazhengjie, Shapingba, Chongqing 400045, China.
National Centre for International Research of Low-Carbon and Green Buildings, Chongqing University, Chongqing 400045, China.
Materials (Basel). 2017 Aug 2;10(8):891. doi: 10.3390/ma10080891.
The band gaps of bismuth vanadate (BiVO₄) and bismuth sulfide (Bi₂S₃) are about 2.40 eV and 1.30 eV, respectively. Although both BiVO₄ and Bi₂S₃ are capable of strong visible light absorption, electron-hole recombination occurs easily. To solve this problem, we designed a one-step hydrothermal method for synthesizing a Bismuth sulfide (Bi₂S₃)/Bismuth vanadate (BiVO₄) heterojunction using polyvinylpyrrolidone K-30 (PVP) as a structure-directing agent, and 2-Amino-3-mercaptopropanoic acid (l-cysteine) as a sulfur source. The pH of the reaction solution was regulated to yield different products: when the pH was 7.5, only monoclinic BiVO₄ was produced (sample 7.5); when the pH was 8.0 or 8.5, both Bi₂S₃ and BiVO₄ were produced (samples 8.0 and 8.5); and when the pH was 9.0, only Bi₂S₃ was produced (sample 9.0). In sample 8.0, Bi₂S₃ and BiVO₄ were closely integrated with each other, with Bi₂S₃ particles formed on the surface of concentric BiVO₄ layers, but the two compounds grew separately in a pH solution of 8.5. Visible-light photocatalytic degradation experiments demonstrated that the degradation efficiency of the Bi₂S₃/BiVO₄ heterojunction was highest when prepared under a pH of 8.0. The initial rhodamine B in the solution (5 mg/L) was completely degraded within three hours. Recycling experiments verified the high stability of Bi₂S₃/BiVO₄. The synthesis method proposed in this paper is expected to enable large-scale and practical use of Bi₂S₃/BiVO₄.
钒酸铋(BiVO₄)和硫化铋(Bi₂S₃)的带隙分别约为2.40电子伏特和1.30电子伏特。尽管BiVO₄和Bi₂S₃都能够强烈吸收可见光,但电子 - 空穴复合很容易发生。为了解决这个问题,我们设计了一种一步水热法,以聚乙烯吡咯烷酮K - 30(PVP)作为结构导向剂,2 - 氨基 - 3 - 巯基丙酸(L - 半胱氨酸)作为硫源,合成硫化铋(Bi₂S₃)/钒酸铋(BiVO₄)异质结。调节反应溶液的pH值以产生不同的产物:当pH值为7.5时,仅生成单斜晶系的BiVO₄(样品7.5);当pH值为8.0或8.5时,Bi₂S₃和BiVO₄都生成(样品8.0和8.5);当pH值为9.0时,仅生成Bi₂S₃(样品9.0)。在样品8.0中,Bi₂S₃和BiVO₄彼此紧密结合,Bi₂S₃颗粒形成在同心BiVO₄层的表面上,但在pH为8.5的溶液中这两种化合物是分开生长的。可见光光催化降解实验表明,在pH为8.0的条件下制备的Bi₂S₃/BiVO₄异质结的降解效率最高。溶液中初始的罗丹明B(5毫克/升)在三小时内完全降解。循环实验验证了Bi₂S₃/BiVO₄的高稳定性。本文提出的合成方法有望实现Bi₂S₃/BiVO₄的大规模实际应用。