光催化
材料科学
异质结
纳米纤维
可见光谱
氢
光电子学
化学工程
纳米技术
化学
催化作用
工程类
生物化学
有机化学
作者
Tianjin Zhang,Lijiao Chen,Changlai Yuan,Mingwei Su,Xiao Liu,Shuya Huang,Mingfang Jiang,Kaiyuan Su,Dezhi Wang
标识
DOI:10.1016/j.jphotochem.2022.114192
摘要
• Nanofibres heterojunction were synthesized by electrospinning and heat-treat. • The rate of the optimum heterojunction is 1.7 times than mechanical mixing. • The negative shift of band edge is the reason for the enhancement of activity. In this paper, g–C 3 N 4 /K 0.5 Na 0.5 NbO 3 nanofibers heterojunction were synthesized via electrospinning and facile heat-treat method. According to XRD, Raman, SEM, TEM and XPS analysis, a heterojunction structure was formed in g–C 3 N 4 /K 0.5 Na 0.5 NbO 3 nanofibers. Electrochemical impedance spectroscopy and transient photocurrent analysis indicated that 20 wt % g–C 3 N 4 /K 0.5 Na 0.5 NbO 3 had the best interfacial charge transfer reaction and high separation efficiency of photogenerated carriers. The rate of photocatalytic hydrogen evolution is 96.3 μmol·g −1 ·h −1 , which is 1.7 times that of simple mechanical mixed powders. This is attributed to the fact that the valence band maximum and conduction band minimum of g–C 3 N 4 /K 0.5 Na 0.5 NbO 3 nanofibers heterojunction are more negative than the mechanical mixed powders, and the difference value between them reaches the maximum when the content of g–C 3 N 4 is 20 wt %.
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