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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Ag NP catalysis of Cu ions in the preparation of AgCu NPs and the mechanism of their enhanced antibacterial efficacy

Fang Zhou,Yan Zhu,Longlai Yang,De-Quan Yang,Edward Sacher

Aqueous dispersions of AgCu nanoparticles (NPs), with enhanced antibacterial efficacy, have been prepared through the catalyzed reduction of Cu ions by PVP/PVA-stabilized Ag nanoparticles at 85 °C. The effects of Cu concentration and heating time on NP morphology and antibacterial efficacy were investigated, using TEM, UV-Vis and FTIR spectroscopies , and antibacterial evaluations. The enhanced antibacterial performance of these NPs was correlated with Ag ion release. We propose a simple model of AgCu NP formation, and an enhanced antibacterial efficacy mechanism involving Ag ion release, in which AgCu NPs formation plays a role to control of Ag ion release.

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CHEMOSPHERE · 2019 · IF 5.108

Aggregation and dissolution of engineering nano Ag and ZnO pretreated with natural organic matters in the simulated lung biological fluids

Laijin Zhong,Xin Hu,Zhaoming Cao,Hongwei Wang,Yijun Chen,Hong-zhen Lian

The increasing application of engineered nanoparticles such as silver nanoparticles (nAg) and zinc oxide nanoparticles (nZnO), results in their accumulation in environmental media. The environmental natural organic matter (NOM) adsorbed by these nanoparticles may have great effects on the aggregation and dissolution of metall ions, which are interesting and important for the assessment of the inhalation risks of these airborne suspended NOM-coated nanoparticles to humans. Therefore, the aggregation and dissolution of nAg and nZnO pretreated with citric acid (CA), tartaric acid (TA) and fulvic acid (FA) in simulated lung biological fluids (artificial lysosomal fluid (ALF) and Gamble Solution) were investigated. The surface properties, morphology and size of the NOM-treated ENPs changed, but the crystalline phase was relatively stable when observed using surface-enhanced Raman scattering , transmission electron microscope , and X-ray diffraction. NOM treatment had no significant influence on the particle size of NOM-treated nAg and nZnO except for a decrease in the size of CA-treated nAg, and it could not promote the aggregation of NOM-treated nAg and nZnO except for the aggregation of TA-treated nAg in Gamble Solution or TA-treated nZnO in ALF. CA- and FA-treatments promoted the release of Zn 2+ and Ag + , respectively, while no promotion was observed after TA-treatment. Therefore, NOM affects the release of Zn 2+ and Ag + from NOM-treated nAg and nZnO but does not promote the aggregation of NOM-treated nAg and nZnO, which influences the inhalation risk-based assessment.

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Small · 2026 · IF 11.8

Density Modulated (Co-W)@Ag Core-Shell Microspheres as Magnetic Fillers of Liquid Metal E-GaIn for Soft Intelligent Systems

Puyue Xia,Zhaomeng Wang,Sining Fan,Wenhao Zhang,Ziying Li,Wei Xu,Weixin Guo,Geng Wei,Yangguang Shi,Li Zhang,Leyi Chen,Shaolong Tang

Through innovative composition and structural design, this study develops core-shell microspheres featuring Co-W alloy cores and Ag shells. Their formation relies on the synergistic effect of solid-liquid interface dewetting, principle of energy minimization, and marangoni effect. These microspheres serve as functional fillers within liquid metal (LM) matrix to create magnetic liquid metal (MLM) with magnetism and enhanced conductivity. We focus on the physical mechanism of density matching, achieved by using high-density W to align the density of Co-W cores with that of liquid Ag. This strategy effectively suppresses the upward buoyancy of cores during spheroidization. Furthermore, finite element simulations elucidate the critical role of the marangoni effect in promoting the formation of this core-shell structure. Experimental results verify that density matching significantly improves the encapsulation quality of Ag shells, thereby endowing the fillers with exceptional resistance against LM corrosion. Finally, the versatility of this MLM is validated across the magnetically actuated liquid-metal soft robot, refreshable liquid-metal blackboard, self-healing circuits, and magnetic liquid-metal strain sensor. These diverse applications underscore the immense potential of MLM as the robust candidate for modern soft intelligent systems.

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Journal of Biomedical Nanotechnology · 2022 ·Vol. 18 ·期 8 ·2001-2009 · IF 3.641

Poly-Lactide-Co-Glycolide-Polyethylene Glycol-Ginsenoside Rg3-Ag Exerts a Radio-Sensitization Effect in Non-Small Cell Lung Cancer

Ma Jun,Yu Da-Hai,Zhao Di,Huang Teng,Dong Min,Wang Ting,Yin Hai-Tao

Radiotherapy is an effective anti-cancer therapy for patients with non-small cell lung cancer (NSCLC), however, the prognosis is unsatisfactory owing to radio-resistance and toxicity. It is crucial to improve radiotherapy efficacy. Ag nanoparticles (NPs) and ginsenoside Rg3 (Rg3) exerted antitumor and radio-sensitization effects. Therefore, we investigated whether poly-lactide-co-glycolide-polyethylene glycol (PLGA-PEG)-Rg3-Ag will function as a noninvasive, tracing, radiotherapy sensitizer. The morphology of NPs was visualized with transmission electron microscopy (TEM). The drug loading content, encapsulation efficiency, and cumulative drug release of Rg3 was determined by HPLC. Cellular uptake of NPs in A549 and SPCA-1 was measured by immunostaining. The radio-sensitization effect of PLGA-PEG-Rg3-Ag in vitro was determined in A549 by detecting proliferation, colony formation, and apoptosis with CCK-8, clonogenic survival assay, and flow cytometry, while in vivo was determined in nude mice by testing the body weight and tumor volume. PLGA-PEG-Rg3-Ag exerted radio-sensitization effect by reducing cell proliferation and colony formation while enhancing cell apoptosis in A549; reduced tumor volume in nude mice. PLGA-PEG-Rg3-Ag exhibits radio-sensitization effects in NSCLC.

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RSC Advances · 2020 ·Vol. 10 ·期 55 ·33299-33306 · IF 3.119

Selective determination of Ag+ in the presence of Cd2+, Hg2+ and Cu2+ based on their different interactions with gold nanoclusters

Rentian Guan,Lixia Tao,Yingying Hu,Cong Zhang,Yongping Wang,Min Hong,Qiaoli Yue

In this work, a fluorescence method was developed for selective detection of Ag+ in the presence of Cd2+, Hg2+, and Cu2+ based on gold nanoclusters (AuNCs). That is, bovine serum albumin (BSA) templated AuNCs with double emission peaks were synthesized using BSA as a protective agent. AuNCs with uniform distribution and average size between 2.0 and 2.2 nm were synthesized using a green and simple method, and showed bright orange-red fluorescence under ultraviolet light. AuNCs have two emission peaks at 450 nm and 630 nm with an excitation wavelength of 365 nm. Under alkaline conditions, Cd2+ can combine with the surface sulfhydryl groups of BSA–AuNCs to form Cd–S bonds, which cause AuNCs to aggregate, resulting in an increase in fluorescence intensity at 630 nm. Conversely, due to the d10–d10 metal affinity interaction, the addition of Hg2+ can reduce the fluorescence peak at 630 nm. Ag+ was reduced to Ag0 by gold nuclei in AuNCs, forming a stable hybrid Au@ AgNCs species with blue-shifted and enhanced fluorescence. Finally, the paramagnetic behavior of Cu2+ combined with BSA causes the excited electrons of the gold cluster to lose their energy via ISC, eventually leading to simultaneous quenching of the two emission peaks. The results show that the limit of detection (LOD) of Ag+, Hg2+, Cd2+ and Cu2+ is 1.19 μM, 3.39 μM, 1.83 μM and 5.95 μM, respectively.

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ANALYTICAL SCIENCES · 2025 · IF 2

Enhancing peroxidase-like activity of Cu/Ag nanoclusters nanozyme by G/C-rich sequence for colorimetric determination of ochratoxin A

Xia Shaojie,Yang Zhenyuan,Sun Xiaohui,Huang Junjie,Peng Kuan,Wang Yonghong

Ochratoxin A (OTA), a highly toxic mycotoxin, extensively contaminates a wide range of food commodities. Given increasing demands for sensitive and user-friendly detection platforms, we developed a colorimetric OTA biosensor leveraging copper-silver nanoclusters (Cu/Ag NCs), whose peroxidase-like activity is augmented via G/C-rich DNA hybridization. The system employs two tailored DNA strands: a template strand featuring a cytosine-rich domain for NC synthesis flanked by terminal recognition segments and an enhancer strand containing a guanine-rich signal amplification domain and a complementary linker. Upon OTA binding with the aptamer, the apt-template complex dissociates, facilitating template-enhancer hybridization to form G/C-rich double-stranded DNA. This structural transition substantially enhances the peroxidase-like activity of DNA-Cu/Ag NCs, accelerating the oxidation of 3,3′,5,5′-tetramethylbenzidine by H 2 O 2 while simultaneously amplifying the colorimetric signal. Quantitative OTA detection is accomplished by monitoring this dynamic color response. The biosensor demonstrates a semi-log linear detection range from 5.0 nM to 1.0 μM with a detection limit of 5.0 nM. Furthermore, the specific test has high selectivity for other common mycotoxins, and its applicability has been validated through real sample analysis, suggesting that the DNA-Cu/Ag NCs biosensor used for OTA detection holds promising practical applications in food samples. Graphical abstract

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Molecular Catalysis · 2025 · IF 4.9

Charge transfer mechanism in Z-scheme ternary heterojunction photocatalysts of AgCl/CoWO4/Ag and its role in enhancing photocatalytic performance

Junlong Zhang,Jie Wei,Long Yang,Ao Cao,Zehao Sun,Youxin Yuanfeng,Xuyu Shen,Bing Chen,Guogang Chen

With the rapid advancement of modern industry and population growth, unrestrained discharge of industrial effluent and domestic sewage has caused severe environmental pollution, which poses a severe challenge to human habitat. Owing to the unique eco-friendly characteristics, photocatalytic technology has emerged as a highly promising approach in the wastewater treatment very recently. Z-scheme heterojunction ternary photocatalysts of “ x · AgCl/ y · CoWO₄/Ag” were ingeniously designed and developed in this study, exhibiting exceptionally high photocatalytic activity for degrading micropollutants in wastewater compared with single-component photocatalysts. For instance, photocatalytic activity of AgCl/CoWO₄/Ag (reflected by the reaction kinetic parameter k ) is 7.7 times that of AgCl and 313 times that of CoWO₄, respectively. The experimental results and analysis revealed a typical Z-scheme charge transfer mechanism in these ternary photocatalyst heterojunctions, thereby confirming the structural characteristics of Z-scheme heterojunction. Furthermore, the ternary photocatalysts retained the reaction activity with virtually no change after undergoing five cycles of catalytic experiments, highlighting its excellent stability. Consequently, an underlying mechanism was proposed herein to account for the enhanced photocatalytic properties. It is believed that such ternary Z-scheme heterojunction materials expand halide-based heterojunction construction methods and promise significant implications for environmental remediation.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2020 · IF 4.65

The influences of graphene oxide (GO) and plasmonic Ag nanoparticles modification on the SERS sensing performance of TiO2 nanosheet arrays

Maofeng Zhang,Haoran Sun,Xin Chen,Hongyang Zhou,Liangzhong Xiong,Wei Chen,Zihai Chen,Zhiyong Bao,Yucheng Wu

A sensitive solid semiconductor-based surface-enhanced Raman spectroscopy (SERS) substrate can realize recyclable and portable detection of organic pollutants. In this paper, TiO 2 nanosheets (NSs) on FTO glass substrate were synthesized by a simple and controllable hydrothermal method , followed by decoration of plasmonic Ag nanoparticles (AgNPs), and further deposition of graphene oxide (GO). The GO and AgNPs co-modified TiO 2 substrate showed improved signal reproducibility, longer-term stability, and higher detection sensitivity than that of TiO 2 counterparts. Note that, the optimized TiO 2 -Ag-GO substrate can also be utilized to discriminate multiple organic pollutants with a portable Raman instrument. The limit of detection (LOD) for crystal violet (CV), rhodamine 6 G (R6G) and malachite green (MG) was 10 −9 M, 10 −8 M, and 10 −7 M, respectively. Moreover, the solid substrate was applied to discern low concentrations of CV residue (10 −8 M) on crayfish’s shell and thiram residue (10 −6 M) on grape skin. As a proof of concept, multiplex detections were also demonstrated. More significantly, the better photocatalytic degradation performance of the TiO 2 -Ag-GO makes the solid substrate reuse for 10 cycles. The solid SERS substrate may have great potential for practical applications and resource-confined detections.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2020 · IF 3.232

Chemometrics coupled 4-Aminothiophenol labelled Ag-Au alloy SERS off-signal nanosensor for quantitative detection of mercury in black tea

Zhiming Guo,Alberta Osei Barimah,Chuang Guo,Akwasi A. Agyekum,Viswadevarayalu Annavaram,Hesham R. El-Seedi,Xiaobo Zou,Quansheng Chen

Black tea like other food crops is prone to mercury ion (Hg 2+ ) contamination right from cultivation to industrial processing. Due to the dangerous health effects posed even in trace contents, sensitive detection and quantification sensors are required. This study employed the surface-enhanced Raman scattering (SERS) enhancement property of 4-aminothiophenol (4-ATP) as a signal turn off approach functionalized on Ag-Au alloyed nanoparticle to firstly detect Hg 2+ in standard solutions and spiked tea samples. Different chemometric algorithms were applied on the acquired SERS and inductively coupled plasma-mass spectrometry (ICP-MS) chemical reference data to select effective wavelengths and spectral variables in order to develop models to predict the Hg 2+ . Results indicated that Ag-Au/4-ATP SERS sensor combined with ant colony optimization partial least squares (ACO-PLS) exhibited the best correlation efficient and minimum errors for Hg 2+ standard solutions (R c  = 0.984, R p  = 0.974, RMSEC = 0.157 μg/mL, RMSEP = 0.211 μg/mL) and spiked tea samples (R c  = 0.979, R p  = 0.963, RMSEC = 0.181 μg/g and RMSEP = 0.210 μg/g). The limit of detection of the proposed sensor was 4.12 × 10 −7  μg/mL for Hg 2+ standard solutions and 2.83 × 10 −5  μg/g for Hg 2+ spiked tea samples. High stability and reproducibility with relative standard deviation of 1.14% and 0.84% were detected. The potent strong relationship between the SERS sensor and the chemical reference method encourages the application of the developed chemometrics coupled SERS system for future monitoring and evaluation of Hg 2+ in tea.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2017 · IF 2.536

Chiral recognition of phenylglycinol enantiomers based on N-acetyl-l-cysteine capped CdTe quantum dots in the presence of Ag+

Yuan Guo,Xiaoqing Zeng,Haiyan Yuan,Yunmei Huang,Yanmei Zhao,Huan Wu,Jidong Yang

In this study, a novel method for chiral recognition of phenylglycinol (PG) enantiomers was proposed. Firstly, water-soluble N -acetyl- l -cysteine (NALC)-capped CdTe quantum dots (QDs) were synthesized and experiment showed that the fluorescence intensity of the reaction system slightly enhancement when added PG enantiomers to NALC-capped CdTe quantum dots (QDs), but the R-PG and S-PG could not be distinguished. Secondly, when there was Ag + presence in the reaction system, the experiment result was extremely interesting, the PG enantiomers cloud make NALC-capped CdTe QDs produce different fluorescence signal, in which the fluorescence of S-PG   +   Ag +   +   NALC-CdTe system was significantly enhanced, and the fluorescence of R-PG   +   Ag +   +   NALC-CdTe system was markedly decreased. Thirdly, all the enhanced and decreased of the fluorescence intensity were directly proportional to the concentration of R-PG and S-PG in the linearly range 10 −   5 –10 −   7   mol·L −   1 , respectively. So, the new method for simultaneous determination of the PG enantiomers was built too. The experiment result of the method was satisfactory with the detection limit of PG can reached 10 −   7   mol·L −   1 and the related coefficient of S-PG and R-PG are 0.995 and 0.980, respectively. The method was highly sensitive, selective and had wider detection range compared with other methods.

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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Wearable Pressure Sensor Array with Layer-by-Layer Assembled MXene Nanosheets/Ag Nanoflowers for Motion Monitoring and Human–Machine Interfaces

Hao Zhang,Dongzhi Zhang,Bao Zhang,Dongyue Wang,Mingcong Tang

Recently, wearable sensors and electronic skin systems have become prevalent, which can be employed to detect the movement status and physiological signals of wearers. Here, a pressure sensor composed of mesh-like micro-convex structure polydimethylsiloxane (PDMS), MXene nanosheet/Ag nanoflower (AgNF) films, and flexible interdigital electrodes was designed by layer-by-layer (LBL) assembly. The unique microstructure of PDMS effectively increases the contact area and improves sensitivity. Moreover, AgNFs were introduced into the MXene as a “bridge,” and the synergistic effect of the two further enhanced the performance of the sensor. The pressure sensor has high sensitivity (191.3 kPa–1), good stability (18,000 cycles), fast response/recovery time (80 ms/90 ms), and low detection limit (8 Pa), so it can be used for all-round monitoring of the human body. Sensing arrays were integrated with a wireless transmitter as an intelligent artificial electronic skin for spatial pressure mapping and human–computer interaction sensing. Moreover, we develop a smart glove by a simple method, combining it with a 3D model for wireless accurate detection of hand poses. This provides ideas for hand somatosensory detection technology, leading to health monitoring, intelligent rehabilitation training, and personalized medicine.

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CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Fabrication of Ag@AgCl/ZnO submicron wire film catalyst on glass substrate with excellent visible light photocatalytic activity and reusability

Jiajie Yu,Dongping Sun,Tianhe Wang,Feng Li

Conventional ZnO powder catalysts possess excellent stability and photocatalytic activity, but have great difficulties for separation and regeneration after the reaction and require ultraviolet irradiation (less than 5% of solar energy), thus restricting practical applications. In this paper, unique short submicron wire-like ZnO films were successfully prepared on silicate glass substrates by calcination of spin-coated zinc acetate solution in the presence of ethanolamine (EA). A typical synthesis yields ZnO submicron wires with ca. 50–120 nm in diameter, 15–30 μm in length and 0.5–1.5 μm in height. Ag@AgCl particles were deposited on short ZnO submicron wire films by a simple impregnating-precipitation-photoreduction method. The as-prepared Ag@AgCl/ZnO film exhibited efficient photocatalytic performance under visible light irradiation and excellent self-cleaning capability under solar light. This film photocatalysts were easy to separate from the reaction, and the tests showed that the films were reusable for four times without significantly loosing efficiency. Additionally, gas chromatography–mass spectroscopy (GC–MS) was applied to investigate the degraded chemical species resulted from the photo-catalytic degradation of methylene blue (MB) and methyl orange (MO) dyes under Ag@AgCl/ZnO. A possible photocatalytic mechanism was proposed based on the photoelectrochemical measurements and radical trapping experiments.

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