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具有增强可见光响应活性的高效Ag₂O/Bi₂O₂CO₃ p-n异质结光催化剂。

Highly efficient Ag₂O/Bi₂O₂CO₃ p-n heterojunction photocatalysts with improved visible-light responsive activity.

作者信息

Liang Na, Wang Min, Jin Lun, Huang Shoushuang, Chen Wenlong, Xu Miao, He Qingquan, Zai Jiantao, Fang Nenghu, Qian Xuefeng

机构信息

School of Chemistry and Chemical Engineering and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University , Shanghai 200240, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2014 Jul 23;6(14):11698-705. doi: 10.1021/am502481z. Epub 2014 Jul 8.

Abstract

Ag2O/Bi2O2CO3 p-n heterojunctions are prepared with commercial Bi2O2CO3 as precursor via a simple photosynthesis process. The obtained Ag2O/Bi2O2CO3 p-n heterojunctions show higher photocatalytic activity than that of pure n-Bi2O2CO3, and the obtained Ag2O/Bi2O2CO3 (AB-4) heterojunction exhibits the best photocatalytic activity under visible light (λ > 400 nm), with which Rhodamine B, methyl blue and methyl orange can be completely degraded within 12 min. Photoluminescent spectra and photoelectrochemical measurement further indicate that the Ag2O/Bi2O2CO3 p-n heterojunctions greatly enhance the charge generation and suppress the charge recombination of photogenerated electron-hole pairs, which would be beneficial to improve their photocatalytic activity.

摘要

以市售的Bi2O2CO3为前驱体,通过简单的光合成过程制备了Ag2O/Bi2O2CO3 p-n异质结。所制备的Ag2O/Bi2O2CO3 p-n异质结表现出比纯n-Bi2O2CO3更高的光催化活性,且所制备的Ag2O/Bi2O2CO3(AB-4)异质结在可见光(λ>400 nm)下表现出最佳的光催化活性,利用该异质结,罗丹明B、甲基蓝和甲基橙可在12分钟内被完全降解。光致发光光谱和光电化学测量进一步表明,Ag2O/Bi2O2CO3 p-n异质结极大地增强了电荷产生并抑制了光生电子-空穴对的电荷复合,这将有利于提高其光催化活性。

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