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SENSORS AND ACTUATORS B-CHEMICAL · 2022 · IF 9.221

Au@Ag@ZIF-8 multifunction probe with internally o-phenylenediamine encoding for the colorimetric, fluorescence, and SERS multi-mode optical detection of reactive sulfur species

Xia Zhou,Xiaoling Lin,Haiqiu Huang,Ping Li,Jiamin Wu,Xueqin Huang,Huaihong Cai,Hai Han,Junxia Zheng,Haibo Zhou

Visual, highly selective, and sensitive detection of sulfur dioxide (SO 2 ) and its derivatives (SO 3 2- ) in vitro/in vivo is of great significance in maintaining cell homeostasis. A new Au@Ag@ZIF-8 optical sensor with o-phenylenediamine (OPD) internal coding surface-enhanced Raman scattering (SERS) tags based on the free radical reaction was synthesized for multi-mode detection of sulfite . First, Co 2+ is oxidized to Co 3+ . Second, the oxidoreduction between SO 3 2- and Co 3+ produces SO 4 -• and Co 2+ to complete the cycle. The resulting SO 4 -• is further reacted with the chromogenic substrate OPD to form the polymer. Due to the UV–vis absorbance of OPD polymer being stronger than that of OPD, but the fluorescence intensity is lower, and their Raman peaks are obviously different, this sensor can be used for the detection of SO 3 2- through colorimetric, fluorescence, and Raman multi-mode. The main advantages are as follows: (1) high selectivity; (2) achieve fast, visual, and highly sensitive detection of SO 3 2- , and the low limit of detection (LOD) is 1 nM; (3) improve the reliability of detection and expands the detection range (1 nM-800 μM); (4) demonstrate the applicability in recognizing SO 3 2- in HeLa cells to provide accurate information on the dynamic distribution of sulfur in cells.

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Acta Biomaterialia · 2022 · IF 10.633

Preparation of epigallocatechin gallate decorated Au-Ag nano-heterostructures as NIR-sensitive nano-enzymes for the treatment of osteoarthritis through mitochondrial repair and cartilage protection

Shibo Xu,Linna Chang,Xingjun Zhao,Yanan Hu,Yiyi Lin,Zhenhua Chen,Xiuli Ren,Xifan Mei

Osteoarthritis (OA), a widespread degenerative disease characterized by cartilage destruction, has emerged as a public health challenge in the current aging society. In addition to applied steroids and surgery, near-infrared (NIR) sensitive nano-enzyme for the treatment of osteoarthritis through mitochondrial repair and cartilage protection is attractive and promising. In this study, a NIR sensitive multifunctional heterostructure (EGCG (Epigallocatechin gallate) decorated Au-Ag nano-jars ( [email protected] )) was introduced as an enzyme-sensitive active nanoplatform for the treatment of osteoarthritis. Molecular biology results indicated that [email protected] possesses intrinsic properties of anti-oxidative stress and was able to reduce the apoptosis rate of chondrocytes by 83.3%. The area of the intra-articular joint cavity injected with [email protected] can be elevated to 46.6 °C under NIR to promote the release of EGCG further to induce cartilage regeneration. X-ray radiography and section staining showed that [email protected] reduced cartilage damage and decreased OARSI scores by approximately 52% after 8 weeks of treatment in a surgically induced OA model. The results demonstrated that this multifunctional enzyme-like nanoplatform with a synergistic NIR sensitive property to facilitate cartilage migration and regeneration repair provides a promising OA treatment strategy. Statement of significance 1. NIR-sensitive nano-enzyme is gaining much attention in the field of biomedical materials . 2. EGCG decorated Au-Ag nano-heterostructures were utilized as NIR-sensitive nano-enzymes for the treatment of osteoarthritis through mitochondrial repair and cartilage protection. 3. The obtained multifunctional Au-Ag nano-heterostructures are promising for osteoarthritis treatment.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Constructing Ag decorated ZnS1-x quantum dots/Ta2O5-x nanospheres for boosted tetracycline removal: Synergetic effects of structural defects, S-scheme heterojunction, and plasmonic effects

Jing Liu,Min Ma,Xin Yu,Changhui Xin,Mingxue Li,Shijie Li

Constructing S-scheme charge transfer pathways is often considered to be an efficient strategy for boosting interfacial charge separation for high-performance photocatalysis, especially for ultrawide bandgap tantalum-based semiconductors. In this work, defects-mediated S-scheme ZnS 1-x quantum dots (QDs)/Ta 2 O 5-x composites decorated with Ag were prepared by the modified solvothermal and photoreduction methods and employed for visible-light photocatalytic toxic tetracycline degradation. Compared with commercial Ta 2 O 5 , pristine Ta 2 O 5-x microspheres, and ZnS 1-x QDs , the prepared Ag/ZnS 1-x /Ta 2 O 5-x -1.0% composite showed the highest visible-light photocatalytic performance, and the corresponding reaction rate constant reached as high as approximately 0.02605 min −1 , which was 5.97 times of ZnS 1-x QDs, 2.63 times of Ta 2 O 5-x , and far better than that of commercial Ta 2 O 5 . The main reactive species, photocatalytic mechanism and degradation pathways were also studied. The highly enhanced photocatalytic performance of the Ag/ZnS 1-x quantum dots/Ta 2 O 5-x composites could be mainly attributed to the formation of Ag modified S-scheme heterostructures and highly increased surface areas. Current work indicates a high-performance tantalum-based composite for dealing with persistent organic pollutants.

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CERAMICS INTERNATIONAL · 2020 · IF 3.83

Enhanced the photocatalytic activity of B–C–N–TiO2 under visible light:Synergistic effect of element doping and Z-scheme interface heterojunction constructed with Ag nanoparticles

Weiwen Wang,Hui Zhao,Peng Pan,Kang Xue,Zisheng Zhang,Jihai Duan

In order to enhance the photocatalytic activity of TiO 2 under visible light, Ag nanoparticles were introduced into tridoped B–C–N–TiO 2 (TT) catalyst by photoreduction deposition. Ag/B–C–N–TiO 2 (ATT) catalysts with the functions of reducing band gap and carrier recombination were prepared. At the same time, the effect of the amount of Ag on the photocatalytic performance of ATT catalyst was investigated. Through XRD , XPS , PL and other characterization methods, the (211)/(101)/Ag interface heterojunction mechanism similar to the traditional Z-scheme heterojunction was proposed. The intervention of Ag nanoparticles changed the P–N interface heterojunction between (211)/(101) to the (211)/(101)/Ag Z-scheme interface heterojunction. The results show that ATT catalyst exhibits the highest photocatalytic activity when the molar amount of Ag is 0.005% with the MB degradation rate of the ATT catalyst (0.01707 min −1 ), which is 14.59 times of TiO 2 (0.00117 min −1 ) and 2.02 times of TT (0.00847 min −1 ). In addition, the four cycles efficiencies of ATT for MB degradation were all above 94.00%.This study reveals the possibility of construction of Z-scheme heterojunctions between precious metal nanoparticles and different interfaces of TiO 2 , and provides a reference for the construction of Z-scheme interface heterojunctions.

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

A novel “off-on-off” fluorescent-nanoprobe based on B, N co-doped carbon dots and MnO2 nanosheets for sensitive detection of GSH and Ag+

Jun Zhang,Huan Yang,Shuang Pan,Hui Liu,Xiaoli Hu

In this study, a new “off-on-off” fluorescence strategy for detecting glutathione (GSH) and silver ions (Ag + ) is presented. The constructed nanoprobe is composed of B, N co-doped carbon dots (B, N-CDs) and manganese dioxide nanosheets (MnO 2 nanosheets), where MnO 2 nanosheets serve as a kind of efficient fluorescence quencher . The sensing mechanism of the system is based on the inner filter effect (IFE) and destruction-protection strategy. The assay strategy includes three processes: fluorescence quenching of B, N-CDs by MnO 2 nanosheets, the deconstruction of MnO 2 nanosheets by GSH, the combination between GSH and Ag + . The MnO 2 nanosheets are reduced to Mn 2+ because of the addition of GSH and restoring the fluorescence intensity of the system, while the formation of the complex between GSH and Ag + inhibit the reduction of MnO 2 nanosheets on account of the addition of Ag + , leading to the decrease in fluorescence of the probe. This strategy allows the quantitative detection of GSH and Ag + with detection limit of 0.32 μmol·L −1 and 0.24 μmol·L −1 , respectively. Moreover, this approach displays good sensitivity, selectivity and broad linear range, which could be broadly applicable for practical applications.

CAS / MDL: 70-18-8 7761-88-8
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2020 · IF 7.489

Compositional and morphological engineering of in-situ‐grown Ag nanoparticles on Cu substrate for enhancing oxygen reduction reaction activity: A novel electrochemical redox tuning approach

Hao Lei,Samarjeet Singh Siwal,Xiaoying Zhang,Qibo Zhang

Silver nanoparticles (NPs) developed on a copper substrate, Ag NPs/Cu, are synthesized by a novel and facile galvanic replacement method performed in Ethaline deep eutectic solvent (DES). It reveals that the Ag NPs could be well dispersed on the Cu support via an in-situ electrochemical oxidation-reduction (ECO-ECR) activation process, which deliver significantly enhanced activity and stability for the oxygen reduction reaction (ORR) in alkaline media. The in-situ redox tuning triggers a reversible phase transformation of the formed initially Ag NPs, Ag ↔ Ag 2 O, with surface reconstruction and gives rise to a strong metal-support interaction with tailored atomic/electronic structures, resulting in enhanced ORR activity. Impressively, the introduction of Ni II ions can regulate the galvanic replacement kinetics by mediating the diffusion of Ag I ions and subsequent growth of Ag on the Cu surface in Ethaline, leading to the formation of uniformly distributed Ag NPs. Coupled with redox activation, the optimal Ag-Ni 1 NPs/Cu_ECO-ECR exhibits ORR activity similar to that of the commercial state-of-the-art Pt/C catalyst, and better long-term durability (95% activity retention after 30,000 s), cyclic stability performance, and anti-poisoning capacity for methanol (96% after 3300 s), suggesting it a promising ORR electrocatalyst for practical application.

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ACS Applied Materials & Interfaces · 2020 · IF 8.758

In Situ Recyclable Surface-Enhanced Raman Scattering-Based Detection of Multicomponent Pesticide Residues on Fruits and Vegetables by the Flower-like MoS2@Ag Hybrid Substrate

Ying Chen,Hongmei Liu,Yiran Tian,Yuanyuan Du,Yi Ma,Shuwen Zeng,Chenjie Gu,Tao Jiang,Jun Zhou

Pesticides, extensively used in agriculture production, have received enormous attention because of their potential threats to the environment and human health. Hence, in this study, a kind of highly sensitive and stable hybrid surface-enhanced Raman scattering (SERS)-active substrates constructed with flower-like two-dimensional molybdenum sulfide and Ag (MoS2@Ag) has been developed, and then the above substrate was sequentially utilized in the recyclable detection of pesticide residues on several kinds of fruits and vegetables. In the first place, the excellent photocatalytic performance of the MoS2@Ag hybrid substrate was demonstrated, which was attributed to the inhibition of electron–hole combination after the formation of Schottky barrier between the Ag NPs and MoS2 matrix. Thereafter, two calibration curves with ultra-low limits of detection (LOD) as 6.4 × 10–7 and 9.8 × 10–7 mg/mL were established for the standard solutions of thiram (tetramethylthiuram disulfide, TMTD) and methyl parathion (MP), and then the recyclable assay of their single and mixed residues on eggplant, Chinese cabbage, grape, and strawberry was successfully realized. It is interesting to note that the detection recoveries from 95.5 to 63.1% for TMTD and 92.3 to 62.6% for MP are greatly dependent on the size and surface roughness of these foods. In a word, the MoS2@Ag composite matrix shows attractive SERS and photocatalysis performance, and it is expected to have the potential application on food safety monitoring.

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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.

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JOURNAL OF MATERIALS SCIENCE · 2020 ·Vol. 55 ·期 31 ·15238-15251 · IF 3.553

Microstructures, electrical behavior and energy storage properties of Ag@shell/PVDF-based polymers: different effects between an organic polydopamine shell and inorganic zinc oxide shell

Guan Lizhu,Weng Ling,Zhang Xiaorui,Wu Zijian,Li Qiong,Liu Lizhu

Two kinds of 1D core–shell nanorods silver@polydopamine (Ag@PDA) and silver@zinc oxide (Ag@ZnO) were successfully synthesized and doped into polyvinylidene fluoride (PVDF) to fabricate composites. The different surface modification effects between the organic PDA shell and inorganic ZnO shell on structure and dielectric properties of PVDF composites were investigated. Results indicated that the ZnO shell showed a crystalline structure, while the PDA shell is amorphous. Due to the difference in crystal structure of the coating shell, the Ag@ZnO/PVDF composites showed a better dielectric performance than the Ag@PDA/PVDF composites, while the Ag@PDA/PVDF showed excellent mechanical properties. The crystallized structure of ZnO not only promoted the crystal conversion of PVDF molecules, but also effectively limited the movement of charge carriers in composites. In the case of 10wt% fillers' content and before breakdown strength, the energy storage densities of Ag@PDA/PVDF and Ag@ZnO/PVDF composites are 79.53% and 209.2% higher than that of pure PVDF films, respectively. Moreover, the charge/discharge efficiency of Ag@ZnO/PVDF composite is also higher than that of pure PVDF and Ag@PDA/PVDF composite. When testing at 1800 kV/cm electrical strength, the energy storage density of Ag@ZnO/PVDF composite increases to 4.02 J/cm 3 .

CAS / MDL: 62-31-7 5970-45-6
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BIOSENSORS & BIOELECTRONICS · 2019 · IF 9.518

In-situ reduction of Ag+ on black phosphorene and its NH2-MWCNT nanohybrid with high stability and dispersibility as nanozyme sensor for three ATP metabolites

Ting Xue,Yingying Sheng,Jingkun Xu,Yingying Li,Xinyu Lu,Yifu Zhu,Xuemin Duan,Yangping Wen

The environmental stability, water-processibility and life-span of black phosphorene (BP) severely limit the application of its electronic devices in aqueous system containing oxygen. We reported the controllable preparation of in-situ reduction and deposition of silver nanoparticles on the BP surface and its amino-functionalized multi-walled carbon nanotubes (NH 2 -MWCNT) nanocomposite . With the addition of both NH 2 -MWCNT and Ag + , the BP-based nanocomposite was prepared by ultrasonic-assisted liquid-phase exfoliation and was dispersed in carboxymethyl cellulose sodium (CMC) aqueous solution. The morphology, microstructure, and electrochemical properties of the nanohybrid were characterized. NH 2 -MWCNT-BP-AgNPs showed high environmental stability, good water-processibility, satisfactory life-spans, superior electrocatalytic capacity with enzyme-like kinetic characteristics. The nanohybrid was applied as electrochemical sensors for single/simultaneous analysis of uric acid (UA), xanthine (XT) and hypoxanthine (HX). Excellent voltammetric responses for simultaneous determination in linear ranges of 0.1–800 μM with a limit of detection (LOD) of 0.052 μM for UA, 0.5–680 μM with a LOD of 0.021 μM for XT, and 0.7–320 μM with a LOD of 0.025 μM for HX under optimal conditions. Besides, the developed nanozyme sensor was employed for simultaneous voltammetric analysis of UA, XT and HX in real samples with acceptable recoveries. This work will provide theoretical guidance and experimental support for the preparation and application of two-dimensional materials, nanozymes and sensing devices.

CAS / MDL: 872-50-4 69-93-2
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CHEMOSPHERE · 2023 · IF 8.8

One-pot synthesis of 2D Ag/BiOCl/Bi2O2CO3 S-scheme heterojunction with oxygen vacancy for photocatalytic disinfection of Fusarium graminearum in vitro and in vivo

Yunlei Zhou,Zhuangzhuang Wang,Huanshun Yin,Xiaoting Cui,Ying Tian,Zhen Qiao,Suo Wang,Runye Hu,Wenjing Lv,An Mao,Jun Wang

2D Ag/BiOCl/Bi 2 O 2 CO 3 S-scheme heterojunction was prepared with oxygen vacancy (OVs) via one-pot hydrothermal method. The XRD and XPS analysis indicated the synthesized sample contained Ag nanoparticles (AgNPs) instead of Ag ions. The SEM and HRTEM pictures showed that BiOCl/Bi 2 O 2 CO 3 nanosheets were modified with AgNPs. Compared with AgNPs, BiOCl, and Bi 2 O 2 CO 3 , Ag/BiOCl/Bi 2 O 2 CO 3 exhibited highly photocatalytic inactivation of pathogenic fungi ( Fusarium graminearum ) due to the wide light absorption range and S-scheme heterojunction structure, which improved the production and transfer of photogenerated carrier, and enhanced the separation of photogenerated e − /h + pairs. In addition, the improved photocatalytic disinfection against Fusarium graminearum of Ag/BiOCl/Bi 2 O 2 CO 3 was verified in Sedeveria Letizia plant . Furthermore, active species capture assay and ESR experiments disclosed the involvement of OVs, h + , ∙O 2 − , ∙OH, and – for Fusarium graminearum destruction during photocatalysis process. The S-scheme heterojunction was proved via oxygen vacancy, which was extensively beneficial to increase charge transmission and separation efficiency. Our work proposed Ag/BiOCl/Bi 2 O 2 CO 3 was an efficient and ecological fungicide to inactive Fusarium graminearum in vitro and vivo for crop disease .

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

Silver ions-regulated two-stage photoluminescence transformations of glutathione-capped gold nanoclusters from near-infrared (NIR) to visible region: Anti-galvanic reaction and Ag deposition

De-Yan Qi,Chong Wang,Qi-Yu Liang,Hong-Wei Li,Yuqing Wu

In the present study, glutathione-capped gold nanoclusters (AuNCs@GSH) were prepared by an improved hydrothermal method , which showed near-infrared (NIR) emission centered at 805 nm. Besides, Ag + can induce the NIR emission transformations in a two-stage mode under different concentration ranges of Ag + . At the first stage (0.50–15 μM), a new emission at 615 nm was generated while the original NIR emission was quenched upon Ag + addition; at the second stage (15–120 μM), it shifted to 720 nm gradually along with more Ag + addition, which realized precise regulation of the emission range of metal nanoclusters from red to NIR region. The in-depth mechanism investigation revealed the transformations in both stages originated from the anti-galvanic reaction (AGR) of AuNCs toward Ag + and Ag deposition. In detail, the first stage was attributed to the formation of bimetallic gold and silver nanoclusters (Au-AgNCs); while the second stage ascribed to the Ag deposition-induced size growth and composition changes of Au-AgNCs. Therefore, the present study supplies a simple and rapid method for preparing NIR-emitted AuNCs and provides a facile approach to regulate the photoluminescence ranges based on the AGR and Ag deposition.

CAS / MDL: 70-18-8 16903-35-8
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