聚丙烯腈
纳米纤维
光催化
材料科学
罗丹明B
降级(电信)
静电纺丝
化学工程
催化作用
异质结
盐酸四环素
纳米技术
复合材料
化学
聚合物
有机化学
光电子学
四环素
工程类
电信
计算机科学
生物化学
抗生素
作者
Ran Tao,Shuhua Yang,Changlu Shao,Xinghua Li,Xiaowei Li,Shuai Liu,Jian Zhang,Yichun Liu
标识
DOI:10.1021/acsanm.9b00428
摘要
Flexible photocatalysts stand out from numerous photocatalysts because of their foldable, reusable, and mechanically stable properties. Here, g-C3N4/Ag3PO4/PAN nanofibers were prepared by immobilizing Ag3PO4 nanoparticles on electrospun g-C3N4/PAN nanofibers through the room-temperature in situ synthesis method. Compared with g-C3N4/PAN and Ag3PO4/PAN, the g-C3N4/Ag3PO4/PAN nanofibers exhibited better photocatalytic performance. The degradation rates of Rhodamine B and tetracycline hydrochloride of g-C3N4/Ag3PO4/PAN nanofibers were 8.8 and 12.9 times higher than those of g-C3N4/PAN nanofibers, while 3.1 and 6.5 times higher than those of Ag3PO4/PAN nanofibers, respectively. In addition, the oxygen evolution rate of g-C3N4/Ag3PO4/PAN nanofibers was 1.9 times better than that of g-C3N4/PAN and 5.8 times better than that of Ag3PO4/PAN. The improved photocatalytic performance of g-C3N4/Ag3PO4/PAN was likely because of the existence of Z-scheme g-C3N4/Ag3PO4 heterojunction with efficient charge separation. Furthermore, g-C3N4/Ag3PO4/PAN nanofibers had a better photochemical stability than Ag3PO4/PAN, which was probably due to the inhibited of Ag3PO4 photocorrosion by the transfer of electrons from Ag3PO4 to g-C3N4. These photocatalysts could be easily separated and reused due to their extra long nanofibrous mat structures and flexible properties. This work provided a new road to design and fabricate flexible self-supporting photocatalysts for pollutants degradation and energy conversion.
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