Integrating the plasmonic effect and p-n heterojunction into a novel Ag/Ag2O/PbBiO2Br photocatalyst: Broadened light absorption and accelerated charge separation co-mediated highly efficient visible/NIR light photocatalysis

被引:166
|
作者
Guo, Hai [1 ]
Niu, Cheng-Gang [1 ]
Huang, Da-Wei [2 ]
Tang, Ning [1 ]
Liang, Chao [1 ]
Zhang, Lei [1 ]
Wen, Xiao-Ju [1 ]
Yang, Yang [1 ]
Wang, Wen-Jun [1 ]
Zeng, Guang-Ming [1 ]
机构
[1] Hunan Univ, Coll Environm Sci Engn, Key Lab Environm Biol Pollut Control, Minist Educ, Changsha 410082, Hunan, Peoples R China
[2] Minist Environm Protect PRC, South China Inst Environm Sci, Guangzhou 510655, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Surface plasmon resonance; P-n heterojunction; Photocatalysis; Tetracycline; Z-SCHEME PHOTOCATALYST; POSSIBLE DEGRADATION PATHWAYS; IN-SITU SYNTHESIS; FULL-SPECTRUM UV; CARBON NITRIDE; TETRACYCLINE DEGRADATION; CR(VI) REDUCTION; MINERALIZATION ACTIVITY; OXYGEN ACTIVATION; PERFORMANCE;
D O I
10.1016/j.cej.2018.11.229
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Among several factors that influence the effectiveness of a semiconductor mediated photocatalysis, efficient charge separation and broadened light absorption are regarded as two of the most important parameters. Herein, a series of plasmonic p-n heterojunction Ag/Ag2O/PbBiO2Br photocatalysts with wide spectrum responses were successfully fabricated through a facile precipitation-calcination method. The obtained samples display exceptional photocatalytic performance for the degradation of tetracycline (TC), and the results reveal that the 10 wt% Ag/Ag2O/PbBiO2Br exhibits the optimal activity, which can efficiently decompose 84.4% of TC after 90 min of visible light irradiation. While under NIR light irradiation, the TC removal ratio can still reach 50.9% with 240 min. Besides, no significant deterioration in the degradation performance is observed even after four cycling runs. The photoactivity enhancement of Ag/Ag2O/PbBiO2Br can be credited to the synergistic effect between the local surface plasmon resonance (LSPR) effect of metallic Ag and the p-n heterojunction of Ag2O/PbBiO2Br, which not only greatly broadens the light utilization, but also remarkably accelerates the charge separation. The radical trapping experiments and the ESR measurements ascertains that center dot O-2 (-), h(+) and center dot OH play a critical role in the degradation of TC under visible light irradiation, while center dot O-2(-) and h(+) become the major reactive species in NIR light-driven reaction. According to the experimental results, the plausible reaction mechanisms for TC degradation over Ag/Ag2O/PbBiO2Br composite are proposed under both visible and NIR light irradiation. This work provides some guidance for rational construction of novel plasmonic p-n heterojunction photocatalysts to meet ever-increasing environmental requirements.
引用
收藏
页码:349 / 363
页数:15
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