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RESEARCH ON CHEMICAL INTERMEDIATES · 2019 ·Vol. 46 ·期 1 ·149-164 · IF 2.064

Imidacloprid photo-degradation on Ag/AgBr modified TiO2: critical impacts and quantitative study on mechanism

Sun Jialin,Dai Jingtao,Liu Rui,Yang Xiaowei,Chen Jian

To improve the visible-light catalytic performance of TiO 2 for practical application, Ag/AgBr modified TiO 2 was fabricated in ionic liquid–water medium via a facile hydrothermal reduction method. Imidacloprid (IMI) was employed as the target pollutant to evaluate the critical impacts on the catalytic activity of as-prepared Ag/AgBr/TiO 2 , where the factors relating to the catalyst (composition, dosage, recycle and reuse) and solution chemistry (pH and concentration, simulated wastewater samples and floodwater of rice paddy field) were studied. The results suggested that benefitting from visible-light sensitive Ag/AgBr and high specific surface area TiO 2 , Ag/AgBr/TiO 2 exhibits superior visible-light photocatalytic activity and stability to Ag/AgBr and TiO 2 . The quenching tests with various scavengers indicate that · O 2 − and h + , and · O 2 − and · OH may be the key roles in IMI photo-degradation on Ag/AgBr and on Ag/AgBr/TiO 2 , respectively. Thus, the photocatalytic performance of Ag/AgBr/TiO 2 differs from that of Ag/AgBr. Furthermore, the contribution of such active species is clarified for quantitative mechanisms study. The photo-degradation conducted in the simulated wastewater and the floodwater of rice paddy field proves favorable anti-interference capacity of Ag/AgBr/TiO 2 . The tests conducted on real wastewater sample verified that Ag/AgBr/TiO 2 can mineralize IMI promptly and almost completely.

研究领域: 环境科学 · 材料科学
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ELECTROCHIMICA ACTA · 2018 · IF 5.116

Synthesis of BiOCl-Ag/AgBr heterojunction and its photoelectrochemical and photocatalytic performance

Wei Li,Shu-ao He,Wei Xu,Ji Li,Xue-chuan Wang

In this research, a series of BiOCl-Ag/AgBr x (BAA x ) heterojunctions with surface plasmon resonance (SPR) effect of metallic Ag were synthesized by a facile one-pot solvothermal method . For the superior photosensitive effect of AgBr co-catalyst, all BAA x samples exhibited much enhanced response to visible light. For the formation of BiOCl-AgBr heterojunction and existence of metallic Ag plasma, the BAA x photocatalysts exhibited very superior interfacial charge migration, and the recombination of photoexcited electron-hole pairs could be effectively controlled. Research showed that the BAA 0.04 heterojunction exhibited the highest photocatalytic activity under visible light irradiation , and various pollutants in water system could be decomposed effectively. Furthermore, the BAA 0.04 heterojunction possessed very robust photostability, its crystal structure and photocatalytic activity almost remained unchanged after being used several times.

研究领域: 材料科学 · 环境科学 · 光化学
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Advanced Energy and Sustainability Research · 2021 ·Vol. 2 ·期 6 ·2000099 · IF 0

Defect Passivation of CsPbBr3 with AgBr for High-Performance All-Inorganic Perovskite Solar Cells

Shoulong Chen,Xiaolin Liu,Zhen Wang,Wenhui Li,Xiaoyu Gu,Jia Lin,Tieying Yang,Xingyu Gao,Aung Ko Ko Kyaw

CsPbBr 3 -based perovskite solar cells possess both high humidity and temperature tolerance, and also have excellent long-term stability in air, but the defect states in the bulk perovskite are always an obstacle for further improvement of their efficiency. Herein, a doping strategy is demonstrated in which AgBr is directly added to the precursor solution in the first step. An appropriate amount of Ag + ion doping can passivate the defects in bulk or at grain boundaries, reduce the defect density of the film, and form a pinhole-free film. Finally, the best power conversion efficiency of the solar cell reaches to 6.92% and exhibits a long-term stability in a humid environment. This work provides a simple and effective method for improving the quality of CsPbBr 3 film and the performance of CsPbBr 3 -based perovskite solar cells.

研究领域: 材料科学 · 能源技术 · 光电子学
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INORGANIC CHEMISTRY · 2023 · IF 4.6

Acceleration of Photocatalytic CO2 Reduction at Intimate Interface in AgBr/BiOBr Heterojunctions via a Co-anion Strategy

Jing Xie,Jianguo Huang,Dilireba Turgan,Zhenjiang Lu,Jindou Hu,Yue Feng,Yali Cao

Constructing heterojunctions with strong interfacial interactions can accelerate the transfer and separation of photogenerated charge carriers. However, finding a simple strategy to construct tightly connected heterojunctions remains a major challenge. In this work, AgBr/BiOBr S-scheme heterojunctions were designed via a straightforward co-anionic strategy without using a solvent. The experimental results indicate that the AgBr/BiOBr heterojunction with a close contact interface can extend the use of visible light, accelerate the separation, and induce the transfer of photoelectrons and holes while maintaining an excellent redox capacity. Undoubtedly, the photocatalytic reduction rate of carbon dioxide to carbon monoxide by 1.0 AgBr/BiOBr is 87.73 μmol·g–1·h–1 (quantum efficiency is 0.57%), which is 12.15 times and 4.45 times higher than that of pure AgBr and BiOBr, respectively. The present work provides insights into a simple strategy for the preparation of strongly interacting interfacial heterojunctions for photocatalytic CO2 reduction.

CAS / MDL: 10035-06-0
研究领域: 材料科学 · 环境科学 · 化学
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APPLIED CATALYSIS A-GENERAL · 2017 · IF 4.339

Fabrication of an all solid Z-scheme photocatalyst g-C3N4/GO/AgBr with enhanced visible light photocatalytic activity

Xuli Miao,Xiaoping Shen,Jiajia Wu,Zhenyuan Ji,Jiheng Wang,Lirong Kong,Miaomiao Liu,Chunsen Song

In this work, an excellent ternary visible-light all solid Z-scheme photocatalytic heterojunction of g-C 3 N 4 /GO/AgBr has been prepared by the attachment of graphene oxide (GO) to the surface of g-C 3 N 4 , followed by in-situ growth of AgBr nanoparticles on GO sheets. The g-C 3 N 4 /GO/AgBr heterojunction exhibits excellent photocatalytic efficiency for RhB degradation, which is about 17.5, 7.9, 3.5, 4.0 and 2.2 times as high as that of P25, g-C 3 N 4 , AgBr, g-C 3 N 4 /GO and g-C 3 N 4 /AgBr heterojunction, indicating the introduction of GO into the system largely improved the capability of the photocatalysis since GO acted as the charge transmission bridge between g-C 3 N 4 and AgBr. Moreover, the photocatalytic performance of g-C 3 N 4 /GO/AgBr just showed a slight decrease after 4 degradation cycles, demonstrating a high stability of the g-C 3 N 4 /GO/AgBr photocatalyst. The photocatalytic mechanism investigation indicated that O 2 − and h + are the major active species in the photocatalytic process. It is expected that the GO-inserted Z-scheme photocatalytic heterojunction could be applied to practical pollutant degradation.

CAS / MDL: 7782-42-5
研究领域: 材料科学 · 环境科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2019 ·Vol. 30 ·期 16 ·15754-15765 · IF 2.195

Photocatalytic performance of Ag/AgBr modified TiO2: critical impacts and wastewater sample study

Sun Jialin,Huang Dejia,Liu Rui,Dai Jingtao,Chen Jian

To improve the visible-light photocatalytic performance of TiO 2 for practical application, Ag/AgBr modified TiO 2 was fabricated in ionic liquid–water medium via a facile hydrothermal-reduction method. The visible-light catalytic activity of as-prepared Ag/AgBr/TiO 2 was measured using tetracycline (TC) as the target pollutant. Characterizations by various techniques (SEM–EDS, XRD, XPS and DRS) and the quenching experiments with scavengers for possible active species (h + , • O 2 − and ·OH) were executed to probe the mechanism underlying the photocatalytic performance. Critical impacts from the catalyst and solution chemistry were evaluated in the mediums of TC solution, simulated wastewater and real wastewater sample. The results suggested that: (1) benefitting from the visible-light sensitive Ag/AgBr and high specific surface area TiO 2 , Ag/AgBr/TiO 2 exhibits fair stability and remarkable visible-light photocatalytic activity; (2) under optimized conditions, Ag/AgBr/TiO 2 provides higher visible-light catalytic activity than Ag/AgBr and TiO 2 ; (3) the coexisting inorganic ions with high concentration in the simulated wastewater sample depress TC photo-degradation, and the impacts varies with the species of inorganic ions; (4) COD removal rate about 65.5% in real wastewater sample proves that Ag/AgBr/TiO 2 can mineralize TC promptly and almost completely.

研究领域: 环境科学 · 材料科学 · 化学工程
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Catalysis Science & Technology · 2022 ·Vol. 12 ·期 5 ·1628-1636 · IF 6.177

Photothermal synergy for efficient dry reforming of CH4 by an Ag/AgBr/CsPbBr3 composite

Peng Gao,Peng Wang,Xiaolei Liu,Zihao Cui,Yaqiang Wu,Xiaohan Zhang,Qianqian Zhang,Zeyan Wang,Zhaoke Zheng,Hefeng Cheng,Yuanyuan Liu,Ying Dai,Baibiao Huang

Dry reforming of CH4 by photothermal catalysis is considered to be a promising approach to produce syngas. It can not only store useful chemical energy, but also consume CO2 and CH4 to mitigate the greenhouse effect. Herein, we anchor Ag/AgBr on CsPbBr3 through an in situ ion exchange route to construct a composite material, which exhibits an excellent photothermal synergistic effect in the dry reforming of CH4. The CO production rate of the 7 wt% Ag/AgBr/CsPbBr3 composite through photothermal catalysis is 456.15 μmol g−1 h−1, which is approximately 79 times and 195 times higher than that through pure thermal catalysis and pure photocatalysis, respectively. Moreover, the CO production rate of 7 wt% Ag/AgBr/CsPbBr3 is 7.25 times higher than that of pristine CsPbBr3. The mutual promotion of the thermochemical and photochemical processes significantly improves the energy utilization efficiency and reaction kinetics, leading to high photothermal catalytic efficiency. This work indicates that the inorganic halide perovskite shows excellent photothermal catalytic activity, and provides an alternative way to extend the application range of perovskite materials.

研究领域: 催化化学 · 能源材料科学
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Molecular Catalysis · 2017 · IF 0

Fabrication of Ag/AgBr/Ga2O3 heterojunction composite with efficient photocatalytic activity

Qing Liu,Zebin Yu,Mingjie Li,Yanping Hou,Lei Sun,Li Wang,Zhenbo Peng,Dongmei Chen,Yuxin Liu

A novel Ag/AgBr/Ga 2 O 3 composite with heterojunction microstructure was synthesized by using chemical deposition followed by UV reduction method. High resolution transmission electron microscopy showed that Ga 2 O 3 microparticles were tightly attached with Ag/AgBr to form a heterojunction. UV–vis diffuse reflectance spectra revealed that light response capability of Ga 2 O 3 was enhanced significantly when combined with Ag/AgBr. The degradation efficiency of methyl orange within 30   min under UV light irradiation with Ag/AgBr/Ga 2 O 3 , Ag/AgBr and Ga 2 O 3 were 89%, 74% and 48%, respectively. Ag/AgBr/Ga 2 O 3 not only showed excellent photocatalytic activity under UV light, but also exhibited efficient photocatalysis capacity under visible light. Furthermore, the mechanism of charge separation in the heterojunction under UV light irradiation was proposed.

CAS / MDL: 12024-21-4
研究领域: 材料科学 · 化学 · 环境科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2016 · IF 3.014

Thermo-responsive PNIPAM@AgBr/CSs composite photocatalysts for switchable degradation of tetracycline antibiotics

Pengwei Huo,Zhefei Ye,Huiqin Wang,Qingfeng Guan,Yongsheng Yan

In this work, thermo-responsive PNIPAM@AgBr/CSs composite photocatalysts were successfully fabricated by grafting method. The thermo-responsive composite photocatalysts were further characterized by SEM, EDS , XRD , FT-IR, DRS and PL , the results demonstrated that the surface of CSs was successfully loaded with AgBr and further grafted with PNIPAM, and the grafted PNIPAM not only obtained the thermo-responsive performance, but also synergistically enhanced visible light photocatalytic activity toward degradation of tetracycline (TC) antibiotics. The influenced factors of photocatalytic degradation were also investigated, the results showed that the dosage of PNIPAM and the reacted temperature were obviously affected the degradation rate of TC. Lastly, the photocatalytic degradation mechanism of as-obtained thermo-sensitive photocatalyst was also discussed in detail. This work might offer a way to obtain the intelligently composite materials for switchable photocatalytic processes.

研究领域: 环境科学 · 材料科学
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NEW JOURNAL OF CHEMISTRY · 2014 ·Vol. 39 ·期 2 ·1132-1138 · IF 3.159

The preparation and properties of a g-C3N4/AgBr nanocomposite photocatalyst based on protonation pretreatment

Yu Feng,Jianchao Shen,Qifeng Cai,Hui Yang,Qianhong Shen

A novel method was proposed to fabricate a g-C3N4/AgBr nanocomposite photocatalyst by loading AgBr nanoparticles onto the g-C3N4 matrix, which was protonated under hydrothermal conditions in the presence of sulfuric acid. X-ray diffraction (XRD), Fourier transform infrared spectra (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), UV-vis diffuse reflectance spectra (DRS), electrochemical impedance spectroscopy (EIS), electron paramagnetic resonance (EPR), photoluminescence (PL) and reactive species trapping measurement were adopted to analyze the structure and properties of the g-C3N4/AgBr nanocomposite photocatalyst. The photocatalytic activities of the as-prepared samples were also evaluated by decomposing methyl orange (MO) in aqueous solution under visible light illumination. The results show that the protonation pretreatment of a g-C3N4 matrix can not only provide growth sites for AgBr grains, but also increase the porosity of the g-C3N4 matrix. Therefore, the AgBr nanoparticles can be uniformly loaded onto the surface of the g-C3N4 matrix, and the specific surface area of the composite can be increased obviously. As a result, the best photodegradation rate of MO over g-C3N4/AgBr nanocomposite photocatalyst is 33.8 and 2.1 times higher than that over pure g-C3N4 and AgBr samples, respectively. Combining the results of EIS Nyquist plots, EPR spectroscopy, reactive species trapping measurement and ˙OH trapping PL spectra, a Z-scheme charge transfer mechanism is proposed.

研究领域: 材料科学 · 环境科学 · 光催化技术
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Electron-buffer-mediated dual Z-scheme ZnSe/Ag2Se/AgBr heterojunction for efficient CO2 photocatalytic reduction

Ting Liang,Jingwen Wei,Shiming Zhang,Jinhang Yang,Jiangli Sun,Zuji Li,Zhihong Li,Zebin Yu,Shuangfei Wang,Yanping Hou

Design of photocatalysts with high-efficiency for sunlight utilization is one of the prerequisites for CO 2 photoreduction . Besides, modulating a stable electron-donating environment to meet the energy barrier for CO 2 reduction to CO is crucial. In this work, the ZnSe/Ag 2 Se/AgBr (ZAA) heterojunction was fabricated by growing the ZnSe on the AgBr surface accompanied by in-situ generation of Ag 2 Se between the two components by hydrothermal process. Results showed that the ZAA exhibited excellent light response ability over the full wavelength range. X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) demonstrated that the charge transfer of the ZAA conformed to dual Z-scheme mechanism, with the Ag 2 Se acting as an electron transfer bridge, which in turn acted as an electron reservoir to accelerate electron transfer, facilitating carriers’ separation. The highest CO yield of 54.14 µmol/g/h was obtained from the optimal ZAA-2, which was 11.76 and 10.44 times of pure ZnSe and Ag 2 Se, respectively. This work demonstrated the feasibility of a dual Z-scheme heterostructure with full spectrum response for offering stable electron-donating environment and improving electron transfer for enhanced photocatalytic activity.

研究领域: 材料科学 · 环境科学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2018 · IF 11.698

Visible-light Ag/AgBr/ferrihydrite catalyst with enhanced heterogeneous photo-Fenton reactivity via electron transfer from Ag/AgBr to ferrihydrite

Yanping Zhu,Runliang Zhu,Lixia Yan,Haoyang Fu,Yunfei Xi,Huijun Zhou,Gangqiang Zhu,Jianxi Zhu,Hongping He

Herein, we have reported an effective strategy to solve the rate-limiting step in a heterogeneous Fenton reaction, i.e., the generation of Fe(II) from Fe(III), which also inevitably consumes a large amount of H 2 O 2 . For the first time, a novel heterogeneous photo-Fenton catalyst - Ag/AgBr/ferrihydrite (Ag/AgBr/Fh) was successfully developed by combing AgBr with ferrihydrite (Fh) and then in-situ generating Ag nanoparticles on the surface of AgBr/Fh. This strategy can introduce photo-generated electrons from semiconductor-based plasmonic photocatalysts to heterogeneous Fenton catalysts and significantly increase the efficiency to degrade contaminants. The presence of both AgBr and Ag nanoparticles was proved by a combination of structural characterization studies (i.e., XRD, SEM, TEM, and XPS). Under visible light irradiation, the generated Fe(II) on the samples and the degradation rate constants of bisphenol A (BPA) followed the same order: Ag/AgBr/Fh > AgBr/Fh > Fh, which could be attributed to the accelerated reduction of Fe(III) to Fe(II) by the photo-generated electrons from AgBr and Ag nanoparticles, and also profit from the strong electron trapping ability of Ag nanoparticles in separating the electron-hole pairs of AgBr. The Ag/AgBr/Fh system could produce more hydroxyl radicals (•OH), and its catalytic performance was less affected by decreasing H 2 O 2 concentration, which suggested a more efficient utilization of H 2 O 2 . The Ag/AgBr/Fh system exhibits relatively high photo-Fenton reactivity even at neutral pH. In addition, a much lower Fe 3+ dissolution indicates that a large portion of the contribution is from the direct heterogeneous Fenton reaction in this system.

CAS / MDL: 65-85-0 99-96-7
研究领域: 环境科学 · 催化 · 光化学 · 水处理
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