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Ag-AgCl
JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Durable ZIF-8/Ag/AgCl/TiO2 decorated PAN nanofibers with high visible light photocatalytic and antibacterial activities for degradation of dyes

Yifei Zhan,Jianwu Lan,Jiaojiao Shang,Lin Yang,Xinmei Guan,Wenxu Li,Siqi Chen,Ying Qi,Shaojian Lin

A ZIF-8/Ag/AgCl/TiO 2 modified PAN nanofibrous mat was successfully fabricated via stepwise in-situ growth method. The morphology and composition of the resultant ZIF-8/Ag/AgCl/TiO 2 modified PAN nanofibrous mat were confirmed by emission scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (DRS) and electrochemical impedance spectroscopy (EIS), respectively. Next, methylene blue (MB) was employed as a contaminant to evaluate photocatalytic activity of prepared composite photocatalysts under visible light and natural sunlight irradiation. As expected, the ZIF-8/Ag/AgCl/TiO 2 decorated PAN nanofibrous mat exhibited high photocatalytic activity under both light sources, owing to the synergistic effect among ZIF-8, Ag/AgCl and TiO 2 . The degradation efficiency of the targeted PAN nanofibrous mat under visible light could reach to 98.02% within 120 min towards 20 mL of 50 mg/L MB aqueous solution. Most importantly, the fabricated ZIF-8/Ag/AgCl/TiO 2 modified PAN nanofibrous mat exhibited outstanding recyclability, the corresponding degradation efficiencies were up to 90.16% after five cycles and approximately 80% after ten cycles, respectively. Additionally, the resultant nanofibrous mat showed a long-term stability against acid and alkaline, and excellent antimicrobial performance against S. aureus and E. coli .

CAS / MDL: 693-98-1
研究领域: 材料科学 · 环境科学 · 生物学
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APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING · 2019 ·Vol. 125 ·期 2 ·1-10 · IF 1.784

Enhancement in photocatalytic performance of Ag–AgCl decorated with h-WO3 and mechanism insight

Chai Chen,Liu Jianxin,Wang Yawen,Zhang Xiaochao,Duan Donghong,Fan Caimei,Wang Yunfang

A h-WO 3 decorated Ag–AgCl composite was prepared through facile precipitation and photoreduction methods and demonstrated to be a highly efficient and stable photocatalyst for the degradation of Rhodamine B (RhB) under visible light. Ag–AgCl/h-WO 3 exhibited much improved photocatalytic performance was elucidated from the physical–chemical properties of AgCl and h-WO 3 and the surface plasmon resonance effect of the Ag particles. The techniques of X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), X-ray photoelectron spectrometry (XPS) and photocurrent were used to characterize crystalline phases, morphology, composition and separation efficiency between electrons (e − ) and holes (h + ) of the synthesized composite photocatalyst. XPS results confirmed the existence of W 5+ and W 6+ on the surface of h-WO 3 sample, which favored electrons transfer between AgCl and Ag, and generated superoxide radical for the degradation of RhB. The active species trapping experiments results further demonstrated that the formation of superoxide radical during the system. Finally, the underlying photocatalytic mechanism for the removal of RhB by Ag–AgCl/h-WO 3 composite was examined.

CAS / MDL: 7783-03-1
研究领域: 材料科学 · 环境科学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

Multifunctional polydopamine-carboxymethyl cellulose composite gels with Ag/AgCl/ZnO heterojunction to enhance sunlight-responsive photocatalytic activity

Jiayin Wang,Chongjun Huang,Yilong Tu,Zhanye Chen,Yiqing Zhao,Yu Ke

Carboxymethyl cellulose (CMC) gel is an ideal substrate for supporting sunlight responsive photocatalysts, but the photocatalytic disinfection activity decreased due to the light-shielding effect of the gel. In order to enhance the formation of active oxygen species, polydopamine (PDA) was introduced in CMC gels to function as an intermediate to connect two semiconductors inside the gels via its quinhydrone charge-transfer complexation. CMC/PDA gel with a double-network was formed via chemical crosslinking and reversible hydrogen bonding between prepolymerized PDA and CMC, then Ag/AgCl, ZnO and Ag/AgCl/ZnO photocatalysts were formed in situ in CMC/PDA gel, respectively. Ag/AgCl/ZnO heterojunction loaded composite gel displayed a remarkable photocatalytic degradation activity, with a weight ratio of the degraded methyl orange divided by composite gels up to 0.00090 under sunlight irradiation for 30 min. Ag/AgCl/ZnO loaded gel presented the bactericidal rate of 99.9 % against E. coli and 99.8 % against S. aureus . The inhibition zone of Ag/AgCl/ZnO loaded composite gel with dopamine mass of 100 mg increased under 6 h of sunlight compared with 24 h in dark against both E. coli and S. aureus . The biocompatible Ag/AgCl/ZnO loaded composite gel with pH-responsive swelling property and sunlight-responsive antibacterial activity promised to broaden the application of CMC-based antibacterial gels.

研究领域: 材料科学 · 环境科学 · 生物学
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Catalysts · 2020 ·Vol. 10 ·期 7 ·746 · IF 3.52

Facile Synthesis of Porous Hexapod Ag@AgCl Dual Catalysts for In Situ SERS Monitoring of 4-Nitrothiophenol Reduction

Yuxiang Lu,Jikai Mao,Zelin Wang,Yazhou Qin,Jianguang Zhou

Controllable morphological metal catalytic materials have always been a focus in research. In the previous work, hexapod AgCl was successfully synthesized. In this paper, hexapod Ag@AgCl microstructures with diverse Ag contents are prepared through NaBH4reduction. They are characterized by scanning electron microscopy (SEM) and the element distribution is proved by an energy dispersive X-ray spectrometer (EDS). They are porous dendritic microstructures with a large specific surface area and a rough surface, which display high catalytic performance and surface-enhanced Raman spectroscopy (SERS) activity. Furthermore, the hexapod Ag@AgCl microstructure is devoted as a dual catalyst to monitor the reduction of 4-nitrothiophenol (4-NTP) to 4-aminothiophenol (4-ATP) in situ using SERS. Ultraviolet–visible (UV–Vis) spectroscopy was employed to evaluate the catalytic performance of the hexapod Ag@AgCl microstructures. The consequences show that the velocity of reaction became faster with a corresponding increase in silver content and the reaction mechanism was cleared. In addition to preparing a good catalyst, this work also promotes the combination of micro-nano materials and spectroscopy technology.Keywords:Ag@AgCl microstructure;in situ monitoring;surface-enhanced Raman spectroscopy;4-nitrothiophenol reduction

研究领域: 材料科学 · 光谱学
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CHEMICAL ENGINEERING JOURNAL · 2018 · IF 6.735

Rapid synthesis of Ag/AgCl@ZIF-8 as a highly efficient photocatalyst for degradation of acetaminophen under visible light

Gongduan Fan,Xiaomei Zheng,Jing Luo,Huiping Peng,Hui Lin,Minchen Bao,Liang Hong,Jinjin Zhou

The presence of acetaminophen (ACT) used for painkillers has attracted great attention in the world, which have potentially adverse effects on aquatic lives and human beings. Advanced oxidation technology applied to water repair has received increasing concerns in recent years. In this study, photodegradation ACT in aqueous solution over Ag/AgCl@ZIF-8 synthesised by a simple stirring method was investigated under visible light irradiation. The prepared photocatalyst was characterized by powder X-ray diffraction (XRD), field emission scanning electron microscopy (SEM) and UV-visible diffuse reflectance spectra (UV-vis). The degradation rates of ACT under different parameters were studied to get the optimal operating conditions in water. Results showed that the photodegradation process fitted pseudo-first order model well. 99% ACT degradation achieved when Ag/AgCl@ZIF-8 was delivered to the solution compared with ZIF-8 and Ag/AgCl with the maximum value of constant ( k app ). The degradation rate obviously slowed down when the initial concentration of ACT increased to 2 mg/L while it increased with the increasing of dosage of photocatalyst. In contrast, pH has little effect on the degradation of ACT over Ag/AgCl@ZIF-8. The Ag/AgCl@ZIF-8 showed high efficiency for degradation after three repeated cycles which demonstrated the prepared photocatalyst has high stability. The O 2 − turned out to be the main active group during the photodegradation process responsible for the disappearance of ACT. Intermediate products analysis results by LC-MS showed that photolysis was the first step of photocatalytic degradation for ACT followed by a ring cleavage.

CAS / MDL: 693-98-1
研究领域: 环境科学 · 材料科学
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Synergistic effect of Z-scheme junction and core–shell architecture over NH2-MIL-125@Ag@AgCl ternary heterojunction for cooperative CO and H2O2 production

Haopeng Jiang,Xiaohui Yu,Jinhe Li,Lele Wang,Weikang Wang,Chunxia Wu,Liyong Tang,Qinqin Liu

Herein, a NH 2 -MIL-125(Ti)@Ag@AgCl (NM@Ag@AgCl) stacked core–shell heterojunction with Z-scheme carrier transfer mechanism was developed to fulfil the goal of synchronous reactions of CO 2 reduction and H 2 O oxidation. In detail, the NM@Ag@AgCl was obtained by in-situ loading the AgCl as the shell-inorganic semiconductor on the octahedral NM as the core-organic semiconductor, followed by in-situ transforming part of the AgCl shell into the plasmonic Ag nanoparticles using a photo-reduction method. As a result, the interface effects of core–shell architecture majorized by the Ag electronic mediator can favor the transmission of photogenerated carriers and reduce electron transport resistance; while the plasmonic Ag mediated Z-scheme mode with a giant internal electronic field provided a strong driving force to recombine the carriers with weak redox ability, reserving the carrier with strong redox ability on the NH 2 -MIL-125-core and AgCl-shell for the simultaneous reactions. The CO and H 2 O 2 yields of the optimal NM@Ag@AgCl were 6.02 and 5.43 μmol⋅g −1 ⋅h −1 , which were 3.31 and 4.02 times that of the NM, respectively. This study furnishes a novel thread for the design of core–shell organic–inorganic heterojunction with high interfacial charge transfer for realizing the simultaneous reactions.

CAS / MDL: 10312-55-7 7761-88-8
研究领域: 材料科学 · 环境科学 · 化学工程
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CERAMICS INTERNATIONAL · 2018 · IF 3.057

Preparation of Ag@AgCl/g-C3N4/TiO2 porous ceramic films with enhanced photocatalysis performance and self-cleaning effect

Xiang Lv,Tianhe Wang,Wei Jiang

We report a novel method to prepare translucent and stable Ag@AgCl/g-C 3 N 4 /TiO 2 ceramic films having strong photocatalytic activities and self-cleaning capabilities under light irradiation. Colloidal silica was used as an inorganic binder and P25 TiO 2 was added as a hydrophilicity enhancer without which a smooth coating was not achievable. Ag@AgCl of particle size around 30 nm, was synthesized by in-situ oxidation of nano-silver particles in porous g-C 3 N 4 /TiO 2 films. Optimal conditions for Ag@AgCl/g-C 3 N 4 /TiO 2 preparation in terms of strongest photocatalysis were established by tests on Rhodamine B degradation under visible and full spectral irradiations. A good adhesion strength of the porous films on glass substrate was achieved. Stability and reusability of the films were assessed by cycling tests. Possible photocatalytic mechanisms are proposed based on the basis of trapping experiments. Systematic characterization of the film suggests that the in-situ oxidation is an effective and practical method to produce nanoscale Ag@AgCl.

研究领域: 材料科学 · 环境科学
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Materials · 2015 ·Vol. 8 ·期 5 ·2043-2053 · IF 2.651

Biochemical Synthesis of Ag/AgCl Nanoparticles for Visible-Light-Driven Photocatalytic Removal of Colored Dyes

Xiyun Zhao,Jie Zhang,Binsong Wang,Amir Zada,Muhammad Humayun

Photocatalytic removal of organic pollution such as waste colored dyes was a promising technique for environment technique. However, effective photocatalysts were needed to enhance the photocatalytic efficiency. Ag/AgCl was regarded as high performance catalyst for photocatalytic degradation. Ag/AgCl nanoparticles were biochemically prepared with metabolin of living fungi which was used as reductant and characterized by X-Ray diffraction (XRD), UV-visible spectroscopy and transmission electron microscopy (TEM). The Ag/AgCl nanoparticle composites showed spherical aggregation shape with an average size of about 3–5 nm which is well inside the quantum regime. The UV-visible study showed that Ag/AgCl nanoparticles had strong visible light absorption and exhibited excellent visible-light-driven photocatalytic performance. Photocatalytic results indicated that the obtained Ag/AgCl nanoparticles were suitable for photocatalytic removal of RhB dye under visible light irradiation. The excellent photocatalytic activities could be attributed to the quantum size nanoparticles and the Plasmon resonance of Ag/AgCl composites.

研究领域: 环境科学 · 生物化学 · 材料科学
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Surfaces and Interfaces · 2025 · IF 6.3

Synthesis and application of UiO-66-NO2@Ag/AgCl nanocomposite as photocatalysts for water remediation

Xiao Ling,Xiaofeng Guo,Ke Wang,Ziming Huang,Zhixuan Mo,Huibo Qin,Linhai Duan,Xiuhong Meng,Hui Wang

Photocatalytic degradation of organic pollutants in water represents a highly promising strategy for environmental remediation. However, conventional photocatalysts are hampered by their inefficient employment of visible light energy and the propensity of photoinduced charge carriers to undergo recombination. To overcome these limitations, Z-scheme photocatalyst UiO-66-NO 2 @ Ag/AgCl (UiO@Ag-X, where X denotes the Ag/AgCl content) composites were designed and prepared. The crystal structure, morphology, photocatalytic performance, light absorption capacity, and carrier separation efficiency were systematically tested. Optical and electrochemical measurements revealed that the incorporation of Ag/AgCl enhanced the segregation and transfer efficiency of charge, which is crucial for boosting photocatalytic activity. These improvements directly contributed to the enhanced degradation efficiency observed in subsequent experiments. In experiments using methyl violet (MV) as the model pollutant, the photocatalytic degradation performance of UiO@Ag-X samples was evaluated. Among these samples, UiO@Ag-50 achieved a remarkable degradation efficiency under light irradiation. Moreover, the corresponding kinetic rate constant was about 0.04724 min -1 , which was higher than that of UiO-66-NO 2 . Quenching experiments were employed to investigate the mechanisms related to photocatalysis. The results show that hydroxyl radicals play an important role in the degradation of MV.

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2015 · IF 7.435

Synthesis of flower-like Ag/AgCl-Bi2MoO6 plasmonic photocatalysts with enhanced visible-light photocatalytic performance

Xiaoxuan Li,Siman Fang,Lei Ge,Changcun Han,Ping Qiu,Weilong Liu

A novel plasmonic photocatalysts of Ag/AgCl-Bi 2 MoO 6 was successfully synthesized via a simple and mild wet-chemical process. The physical and photophysical properties of the as-prepared Ag/AgCl-Bi 2 MoO 6 samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscope (TEM), Ultraviolet–visible diffuse reflection spectroscopy (DRS), electron spin resonance (ESR), photoluminescence emission spectra (PL) and surface photovoltage spectroscopy (SPV). The interaction between Ag/AgCl and Bi 2 MoO 6 has been investigated by X-ray photoelectron spectroscopy (XPS) analysis, and which is facile to the electron transfer between Ag/AgCl and Bi 2 MoO 6 and result in the enhancing photocatalytic activity of Ag/AgCl-Bi 2 MoO 6 composite. The photocatalytic experiments indicate that the Ag/AgCl species can efficiently promote the separation efficiency of photo-generated charge carriers in Bi 2 MoO 6 , and consequently improve the RhB photodegradation activity. The 20   wt% Ag/AgCl-Bi 2 MoO 6 sample shows the highest photocatalytic activity, the degradation constant of 20   wt% Ag/AgCl-Bi 2 MoO 6 was as high as 4 times to that of pure Bi 2 MoO 6 . A possible catalytic mechanism for Ag/AgCl-Bi 2 MoO 6 is proposed, which can be attributed to the surface plasmon resonance (SPR) effect from Ag/AgCl species.

研究领域: 材料科学 · 光催化 · 纳米材料 · 环境化学 · 半导体物理 · 表面科学
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JOURNAL OF HAZARDOUS MATERIALS · 2020 · IF 9.038

Efficient integration of plasmonic Ag/AgCl with perovskite-type LaFeO3: Enhanced visible-light photocatalytic activity for removal of harmful algae

Gongduan Fan,Zhong Chen,Zhongsen Yan,Banghao Du,Heliang Pang,Dingsheng Tang,Jing Luo,Jiuyang Lin

A novel plasmonic Ag/AgCl@LaFeO 3 (ALFO) photocatalyst was successfully synthesized by a simple in-situ synthesis method with enhanced photocatalytic activity under visible light for harmful algal blooms (HABs) control. The structure, morphology, chemical states, optical and electrochemical properties of the photocatalyst were systematically investigated using a series of characterization methods. Compared with pure LaFeO 3 and Ag/AgCl, ALFO-20% owned a higher light absorption capacity and lower electron–hole recombined rate. Therefore, ALFO-20% had higher photocatalytic activity with a near 100% removal rate of chlorophyll a within 150 min, whose kinetic constant was 15.36 and 9.61 times faster than those of LaFeO 3 and Ag/AgCl. In addition, the changes of zeta potential , cell membrane permeability, cell morphology, organic matter, total soluble protein, photosynthetic system and antioxidant enzyme system in Microcystis aeruginosa ( M. aeruginosa ) were studied to explore the mechanism of M. aeruginosa photocatalytic inactivation. The results showed that ALFO-20% could change the permeability and morphology of the algae cell membrane, as well as destroy the photosynthesis system and antioxidant system of M. aeruginosa . What’s more, ALFO could further degrade the organic matters flowed out after algae rupture and die, reducing the secondary pollution and avoiding the recurrence of HABs. Finally, the species of reactive oxygen species (ROS) (mainly •O 2 - and •OH) produced by ALFO were determined through quenching experiments, and a possible photocatalytic mechanism was proposed. Overall, ALFO can efficiently remove the harmful algae under the visible light, providing a promising method for controlling HABs.

CAS / MDL: 10277-43-7
研究领域: 环境科学 · 光催化技术
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ACS Applied Nano Materials · 2023 · IF 5.9

One-Pot Synthesis of Ag/AgCl Heterojunction Nanoparticles on Polyaniline Nanocone Arrays on Graphene Oxide for Microwave Absorption

Wenwen Fu,Wentong Yang,Chen Qian,Yaqin Fu,Yaofeng Zhu

Heterointerfaces in microwave absorption materials can induce dielectric polarization relaxation for superior microwave absorption capacity. Nevertheless, the construction of favorable hierarchical structures in dielectric heterogeneous materials remains a considerable challenge. Herein, Ag/AgCl heterojunction (HAg) nanoparticles are successfully decorated on polyaniline (PANI)/graphene oxide (GO) sheets through simple one-pot interfacial polymerization. The synthesized HAg/PANI/GO hybrid exhibits superior microwave absorption performance due to the multi-heterogeneous and hierarchical structures, which provides numerous interface polarizations, dipolar relaxations, and improved impedance matching. The minimum reflection loss of the optimum HAg/PANI/GO hybrid reaches −61.14 dB at 11.32 GHz with an effective absorption bandwidth of 4.77 GHz in the range from 9.70 to 14.47 GHz. This work provides ideas for producing multi-heterogeneous and hierarchical structures to reach a high microwave absorption performance.

CAS / MDL: 62-53-3
研究领域: 材料科学 · 纳米技术 · 电磁材料
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