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AgBr/BiOBr
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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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 22 ·26465-26479 · IF 2.478

The fast degradation for tetracycline over the Ag/AgBr/BiOBr photocatalyst under visible light

Zhu Wanrong,Song Jimei,Wang Xule,Lu Yun,Hu Gang,Yang Jie

A series of Ag/AgBr/BiOBr photocatalysts with different weight contents of Ag/AgBr were successfully constructed via a simple precipitation method in 80 °C water bath. Photocatalysts were characterized by XRD, XPS, SEM, TEM, N 2 Adsorption-Desorption (BET), and UV–Vis Diffuse Reflectance Spectroscopy (DRS). Compared with BiOBr and Ag/AgBr, all the composite photocatalysts show the prominent photocatalytic activity for the degradation of tetracycline (TC). Especially, 1:5Ag/AgBr/BiOBr (20%) has the highest reaction rate constant (kapp = 0.20 min −1 ). Moreover, according to the results of radical scavengers runs, ·OH and h + acted as the main reactive species in the degradation process. Based on above, a possible photocatalytic mechanism for organics degradation over Ag/AgBr/BiOBr was proposed. Interestingly, the redox cycle between O 2 /·O 2 − and Br − /Br 0 assisted with the surface plasmon resonance (SPR) effect of silver dramatically promotes the separation and transfer of electron–hole pairs, and improves the photocatalytic activity of the as-obtained composite samples.

研究领域: 环境科学 · 材料科学 · 光催化技术
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NEW JOURNAL OF CHEMISTRY · 2020 ·Vol. 44 ·期 33 ·14180-14188 · IF 3.288

A comparative study in single- and binary-contaminant systems: the photodegradation of tetracycline and imidacloprid on flower-shaped Ag/AgBr/BiOBr under visible-light irradiation

Jingjing Zhang,Jingtao Dai,Jian Chen

To compare photodegradation processes in single- and binary-contaminant systems, a representative antibiotic (tetracycline) and insecticide (imidacloprid) were employed as two contaminants of emerging concern. Ag/AgBr modified BiOBr was synthesized hydrothermally in an ionic-liquid/water medium and characterized via various techniques to support mechanistic studies. As-prepared flower-shaped Ag/AgBr/BiOBr exhibits superior photocatalytic activity to Ag/AgBr and BiOBr. Parallel experiments were conducted in single-contaminant systems to optimize the solution chemistry for comparison studies; these suggested that the photodegradation rate (DR) is highest at 1.0 g L−1 at catalyst dosages ranging from 0.6 to 1.4 g L−1, while raising the initial concentration reduces the DR. Additionally, electrostatic interactions between the reactants and photocatalyst cause DR fluctuations at different pH values. In the mechanistic studies, the contributions of the dominant active species (˙O2− and h+) were analysed quantitatively through quenching tests with scavengers. Furthermore, electrostatic interactions between the reactants and the active species result in non-equilibrated contributions from ˙O2− and h+ in single-contaminant systems. Comparison studies distinctly demonstrated a synergistic effect in binary-contaminant systems, which is caused by the mutually complementary utilization of h+ and ˙O2− during the photodegradation of tetracycline and imidacloprid.

研究领域: 环境科学 · 催化材料
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JOURNAL OF HAZARDOUS MATERIALS · 2021 · IF 10.588

Surface modification of BiOBr/TiO2 by reduced AgBr for solar-driven PAHs degradation: Mechanism insight and application assessment

Xianbo Sun,Weiyu He,Xiaodi Hao,Haodong Ji,Wen Liu,Zhengqing Cai

A novel solar active AgBr/BiOBr/TiO 2 catalyst was synthesized by a facile coprecipitation method for solar-driven water remediation . The synthesized material composed of flower-like TiO 2 nanoparticles loaded on BiOBr nanosheets and with homogeneous surface distributed Ag/AgBr nanoparticles. The internal electric field between BiOBr/TiO 2 heterojunction greatly facilitated the charge carrier migration; the introduction of narrow band gap semiconductors (AgBr and BiOBr) promoted the visible light adsorption; and the Ag/AgBr nanoparticles acted as photosensitizer to further improve the light utilization. The new material showed 7.6- and 4.0-times activity of pure TiO 2 and BiOBr under solar light, and the contribution of reactive species on anthracene degradation followed the order of h + > O 2 • − > •OH. The degradation mechanism and pathway were proposed based on intermediates analysis and DFT calculation. The QSAR analysis revealed that the environmental risks of contaminants were greatly reduced during the photocatalysis process but some intermediates were still toxic. The high photocatalytic activity, stability and adaptability all indicated that this new material owns great application potential for cost-effective photocatalytic remediation of persistent organic contaminants under solar light.

研究领域: 环境科学 · 材料科学
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BIOELECTROCHEMISTRY · 2021 · IF 5.373

A label-free photoelectrochemical immunosensor for prostate specific antigen detection based on Ag2S sensitized Ag/AgBr/BiOBr heterojunction by in-situ growth method

Qiying Zhu,Canguo Li,Huiqin Chang,Meng Jiang,Xiaokai Sun,Wei Jing,Haowei Huang,Di Huang,Ling Kong,Zhiwei Chen,Feng Sang,Xiuzhen Zhang

Prostate cancer is one of the most common cancers in the world, and its early detection is vital to saving the lives of patients. In this research, a novel label-free photoelectrochemical immunosensor was designed for sensitive detection of prostate specific antigen (PSA). Ag 2 S sensitized on Ag/AgBr/BiOBr heterojunction could effectively inhibit photogenic holes recombination and improve photocurrent response and sensitivity. Ascorbic acid was an effective electron donor, which can effectively eliminate photo-generated holes. The photocurrent reduced linearly with the logarithm of PSA concentration ranged from 0.001 to 50 ng·mL −1 and the limit of detection was 0.25 pg·mL −1 . The designed sensor had the advantages of wide linear range, good stability, high reproducibility, and good selectivity. This study not only provided a method for efficient and sensitive detection of PSA, but also provided valuable reference ideas for the detection of other tumor markers.

研究领域: 医学 · 生物技术
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