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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.
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页码:349 / 363
页数:15
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