Photo-deposition of AgO thin films on TiO2 substrate for (P-N) hetero-junction applications: Considering the degree of contamination

被引:2
|
作者
Nezzal, Hala [1 ]
Rahmane, Saad [2 ]
Temam, Elhachmi Guettaf [2 ]
Al-Abri, Mohammed [3 ]
Kyaw, Htet Htet [3 ]
Gasmi, Brahim [2 ]
Althamthami, Mohammed [2 ]
Ben Temam, Hachemi [2 ]
Hu, Jinguang [4 ]
机构
[1] Phys Lab Photon & Multifunct Nanomat, BP 145, Biskra 07000, Algeria
[2] Biskra Univ, Phys Lab Thin Films & Applicat, BP 145, Biskra 07000, Algeria
[3] Sultan Qaboos Univ, Nanotechnol Res Ctr, POB 33, Muscat 123, Oman
[4] Univ Calgary, Dept Chem & Petr Engn, Calgary, AB, Canada
关键词
Photo-deposition; Sol-gel; Dip coating; MB; AMX; Photodegradation; ANATASE TIO2; PHOTOCATALYSIS; DEGRADATION;
D O I
10.1016/j.jallcom.2024.177331
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study explored the development of photocatalytic heterostructures via the P-N junction formation between TiO2 and AgO. TiO2 thin films were fabricated on glass substrates through dip coating. Subsequently, photodeposition of AgO was achieved under sunlight irradiation using varying AgNO3 concentrations (0.5-2.5 g/L). The films were characterized using XRD, SEM, EDX, UV-vis, and water droplet tests. Samples with concentrations below 2 g/L uniquely exhibited the anatase phase, while a significant prominence of AgO was observed in the film prepared with a 2 g/L AgNO3 concentration. Silver nitrate contamination loads had a significant impact on the particle size and the overall morphological characteristics of the heterojunctions. The band gap values were 3.52 eV for the anatase substrate, whereas the band gaps of the photodeposited films decreased from 2.44 to 1.98 eV. Despite all films being hydrophilic, a rise in water droplet contact angle was observed in the heterojunctions compared to the pure TiO2. Photodegradation of methylene blue under sunlight irradiation demonstrated exceptional efficiency (>90 %) for the 2 g/L AgNO3 heterojunction in 6 hours, maintaining high photocatalytic activity over multiple cycles (>77 %). This same configuration achieved a 50 % degradation of amoxicillin within 2 hours. This investigation addresses water contamination issues while offering a straightforward production method for efficient P-N junction co-catalysts.
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页数:14
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