材料科学
聚酰亚胺
光催化
钼酸铵
傅里叶变换红外光谱
光致发光
结晶度
偏钒酸铵
硫脲
X射线光电子能谱
钼
光化学
化学工程
锌
钒
有机化学
纳米技术
图层(电子)
光电子学
复合材料
催化作用
化学
冶金
工程类
作者
Chenghai Ma,Jun Zhou,Haoyue Zhu,Weiwei Yang,Jianguo Liu,Ying Wang,Zhigang Zou
标识
DOI:10.1021/acsami.5b01356
摘要
A novel two-dimensional hybrid polymer photocatalyst black-MoO3/polyimide was synthesized by one-pot thermopolymerization of monomers, ammonium molybdate, and thiourea at mild temperatures. Thiourea and ammonium molybdate as fluxing agents promote the formation of black molybdenum oxide (BMO) on polyimide (PI) and enhance the crystallinity of PI. It is confirmed by X-ray photoelectron spectroscopy, electron paramagnetic resonance, and Fourier transform infrared that the strong interaction between BMO and PI leads to the formation of a Mo–N coordination bond through the coordination of N atoms of heptazine units to the unsaturated Mo atoms of BMO and results in a large number of Mo5+ cations in BMO/PI. UV–vis and photoluminescence reveal that the visible light absorption of BMO/PI was increased and the separation efficiency of photogenerated electron/hole obviously was significantly enhanced, which facilitates the improvement of the photocatalytic activity of BMO/PI. This work provides a new approach to synthesizing efficient inorganic–organic hybrid semiconductor photocatalysts.
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