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CHEMOSPHERE · 2020 · IF 5.778

High efficient reduction of 4-nitrophenol and dye by filtration through Ag NPs coated PAN-Si catalytic membrane

Ping Li,Yixing Wang,Hairong Huang,Shuai Ma,Hu Yang,Zhen-liang Xu

Catalytic membrane plays an important role in environmental remedy. In this study, we reported an Ag coated membrane (PAN-Si-Cu-Ag) with a high catalytic activity to reduce 4-nitrophenol (4-NP) and methyl orange (MO) from water. The best performance is 99% reduction degree and 280 L m −2 .h −1 .bar −1 flux for (4-NP) reduction at 4-NP: NaBH 4  = 1:50 (mM) during a 12-h filtration. The reduction degree for MO is above 90% and the flux is about 230 L m −2 ·h −1 ·bar −1 , which is almost the best report till now. The Ag coated membrane was prepared by metal displacement-epitaxial growth on silica covalent grafted PAN membrane (PAN-Si). Silica atoms were used as linker to ensure the good adhesion between polymer and metal NPs, the loss amount of Ag NPs from the coated catalytic membrane is loss about 2 μg/cm 2 after one month storage. Cheap metal NPs were firstly reduced on the surface of PAN-Si membrane and then used to displace Ag ions. Thus the obtained catalytic membrane showed a very high loading (28%). Finally, the catalytic filtration mechanism of 4-NP was distinguished by Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and adsorption measurement.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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TALANTA · 2020 · IF 5.339

An electrochemiluminescence sensor for 17β-estradiol detection based on resonance energy transfer in α-FeOOH@CdS/Ag NCs

Yixin Liu,Binxiao Li,Yuanyuan Yao,Beibei Yang,Tongtong Tian,Yan Miao,Baohong Liu

An electrochemiluminescence (ECL) resonance energy transfer system is constructed for 17β-estradiol (E2) detection using α [email protected] nanospheres as the ECL-active substrates and Ag NCs as an efficient quencher. CdS QDs loaded onto three-dimensional (3D) urchin-like α-FeOOH nanospheres (α [email protected] nanospheres) exhibited excellent ECL responses, which is attributed to dual-amplification of α-FeOOH frameworks. The 3D hierarchical structure of the α-FeOOH nanospheres provided abundant sites for loading ECL-active species, thus significantly improving the ECL performance of substrates; While Fe 3+ presented on surface of α-FeOOH nanospheres could be reduced to Fe 2+ in negative potentials, after which might activate persulfate in a Fenton-like process, resulting in more sulfate free radicals for more effective ECL responses via electron transfer reactions. Additionally, Ag nanoclusters (Ag NCs) stabilized by single stranded oligonucleotide were introduced as quenching probes for CdS QDs owing to the well-matched donor-acceptor spectrum for efficient energy transfer, which makes them appropriate for detection of E2. The proposed strategy displayed a desirable dynamic range from 0.01 to 10 pg mL −1 with a limit of detection of 0.003 pg mL −1 . The proposed strategy based on the ECL-RET strategy offered an ideal way for E2 detection, and also revealed an alternative platform for detection of other small molecules.

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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2021 · IF 4.291

Optimization of Fe3O4/SiO2/N-TiO2/Ag/AgCl core-shell nanomaterial and its properties, repeatability and photocatalytic mechanism

Ao Li,Linbei Xie,Sijie Zhou,Min Zhang,Yi Ding,Ping Wang

In this study, the magnetic core-shell nanomaterial Fe 3 O 4 /SiO 2 /N-TiO 2 /Ag/AgCl (FSNT/Ag/AgCl) that efficiently degraded methyl orange (MO) was produced. The dosages of tetrabutyl titanate (TBOT), urea and AgNO 3 were optimized by response surface methodology (RSM). Scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy analysis (XPS), energy dispersive spectrometer (EDS), X-ray diffractometer (XRD), fourier transform infrared spectrometer (FT-IR), and UV–vis diffuse reflectance spectrum (UV–vis DRS) were used to characterize the nanomaterial. The particle size of FSNT/Ag/AgCl was 91.98 nm, and it presented a core-shell structure with Fe 3 O 4 as the core, SiO 2 and N-TiO 2 wrapped in Fe 3 O 4 , and Ag/AgCl deposited on the outermost layer. Performance and mechanism research experiments showed that under the optimized conditions of 1 g/L FSNT/Ag/AgCl, pH = 9, temperature of 35℃ and initial MO concentration of 10 mg/L, about 90 % of MO was degraded in 20 min. The mineralization rate was 35.2 % within 120 min. Holes (h + ) and superoxide anions (·O 2 − ) were the main active substances in the whole photocatalytic degradation. FSNT/Ag/AgCl could be recovered by magnet. After 5 repeated experiments, the degradation rate of MO within 100 min still reached 88.5 %. This work provides a recyclable core-shell nanomaterial for faster degradation of dye wastewater.

CAS / MDL: 78-10-4
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JOURNAL OF MATERIALS SCIENCE · 2020 ·Vol. 55 ·期 35 ·16683-16696 · IF 3.553

Flexible wire-shaped symmetric supercapacitors with Zn–Co layered double hydroxide nanosheets grown on Ag-coated cotton wire

Qi Jiqiu,Ruan Chenya,Hu Rui,Sui Yanwei,He Yezeng,Meng Qingkun,Wei Fuxiang,Ren Yaojian,Wei Wenqing

Flexible wire-shaped supercapacitors have attracted wide interest due to the increasing demand for portable and wearable electronics. Due to the complex functioning atmosphere of wearable electronics, their mechanical stability and electrochemical stability under different bending states are required. In this work, the self-made Ag-coated cotton wire was adopted as the collector and zinc–cobalt layered double hydroxide nanosheets were successfully electrodeposited on this wire (Ag-CW@ZnCo-LDH) by a facile chronopotentiometry with a constant current of 0.02A. Ag-CW@ZnCo-LDH electrode displayed a high specific capacitance of 1732.4 F g −1 at 1 A g −1 and 61.7% of capacitance retention after 2000 cycles at 10 A g −1 . Flexible wire-shaped symmetric supercapacitor was fabricated by two same Ag-CW@ZnCo-LDH electrodes, which exhibited a working potential window of 1.2 V. The as-assembled WSSC showed a good electrochemical performance with specific capacitance of 16.3 F g −1 and energy density of 1.33 Wh kg −1 at power density of 1224 W kg −1 . In addition, its CV curves barely deviated at all bending angles, manifesting the outstanding mechanical stability and great potential for practical application.

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JOURNAL OF NANOPARTICLE RESEARCH · 2020 ·Vol. 22 ·期 9 ·1-11 · IF 2.132

A highly sensitive electrochemical sensor based on nanoflower-like MoS2-Ag-CNF nanocomposites for the detection of VB2

Lin Jiaxin,Mei Qianwen,Duan Yingchun,Yu Chenhong,Ding Yaping,Li Li

The sensitive determination of VB 2 has broad analytical applications. In this work, a novel VB 2 electrochemical sensor based on the hydrothermal method was constructed to uniformly grow molybdenum disulfide and silver nanoparticles on the surface of electrospun carbon fiber. MoS 2 -Ag-CNF was characterized by scanning electron microscope, EDS spectrum, TEM analysis, cyclic voltammetry, differential pulse voltammetry, and electrochemical impedance spectroscopy. The sensor exhibited a high sensitivity of 0.05 to 40 μΜ with a fast response time and a low detection limit of 0.02 μM. The electrode also showed outstanding selectivity toward various interferences. These results indicate that the MoS 2 -Ag-CNF nanocomposites may be promising electrode materials for electrochemical biosensing. Graphical abstract

CAS / MDL: 62-56-6
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TALANTA · 2020 · IF 5.339

SERS-active Au@Ag core-shell nanorod (Au@AgNR) tags for ultrasensitive bacteria detection and antibiotic-susceptibility testing

Liyan Bi,Xiao Wang,Xiaowei Cao,Luying Liu,Congcong Bai,Qingyin Zheng,Jaebum Choo,Lingxin Chen

There is a challenge to obtain an ultrasensitive and rapid approach to detect bacteria and identify resistance. As a powerful bioanalytical tool, surface-enhanced Raman scattering (SERS) in bacterial detection have attracted increasing attentions. Herein, we developed a SERS-active [email protected] core-shell nanorod ( [email protected] ) tag platform for ultrasensitive bacteria detection and antibiotic-susceptibility testing (AST). The platform established that surface enhanced Raman scattered Rhodamine 6G (R6G) absorption at 1517 cm −1 had a good linearity (RI = 3865 + 193logC; R 2  = 0.97) with logarithm of E. coli concentration over a range of 10 7 –10 2  CFU (colony forming unit)/mL with limit of detection as low 10 2  CFU/mL. When E. coli was exposed to ampicillin at minimum inhibitory concentration (MIC, 4 μg/mL), Raman spectroscopy showed the obvious variation between ampicillin-susceptible E. coli (Amp − - E. coli ) and the ampicillin-resistant E. coli (Amp + - E. coli ). Combined with principal component analysis (PCA) statistical analysis, the Raman intensity variation mentioned above allows to obtain rapid antibiotic resistance testing (<3.5 h). In addition, E.coli spiked into blood from C57BL/6 mice can be identified clearly, indicating the potential for point-of-care diagnostics.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2020 · IF 3.99

Ag nanoparticles supported on MgAl-LDH decorated wood veneer with enhanced flame retardancy, water repellency and antimicrobial activity

Tailong Cai,Xiaoyuan Shen,Erzhuo Huang,Yutao Yan,Xiaoping Shen,Fengqiang Wang,Zhe Wang,Qingfeng Sun

Wood is an important and ubiquitous material applied in building and decorative applications, but it is easily invaded by fire, water and microorganisms. In this study, a new Ag nanoparticles supported on MgAl-LDH decorated wood veneer is successfully developed via simple hydrothermal reaction and silver mirror reaction. This unique wood veneer shows excellent flame retardancy under a continuous open flame, and super water repellency with a large water contact angle of 156°. In addition, the wood veneer has admirable antimicrobial activity (e.g. Staphylococcus aureus and Escherichia coli ). This paper presents a novel route of synthesizing a well-designed wood based composite with enhanced flame retardancy, water repellency and antimicrobial activity, which greatly broadens the application range of wood.

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SENSORS AND ACTUATORS B-CHEMICAL · 2020 · IF 7.1

Sensitive electrochemiluminescence aptasensor for chlorpyrifos detection based on resonance energy transfer between MoS2/CdS nanospheres and Ag/CQDs

Jianhui Liu,Peipei Chen,Fangquan Xia,Zhen Liu,Hanbiao Liu,Jiangle Yi,Changli Zhou

A "signal on" aptasensor was fabricated for chlorpyrifos detection by a highly efficient electrochemiluminescence resonance energy transfer (ECL-RET) strategy between MoS 2 /CdS nanospheres and silver/carbon quantum dots (Ag/CQDs). Compared with the conventional MoS 2 /CdS nanosheets, the MoS 2 /CdS nanospheres have a larger specific surface area and electron density, which makes the catalytic effect on K 2 S 2 O 8 stronger and has higher luminescence intensity. As a receptor, through the synergistic effect of Ag NPs and CQDs, it has a very wide absorption band between 300 and 600 nm. The absorption band and the emission spectrum of MoS 2 /CdS completely overlap, and the high quantum yield of Ag/CQDs can achieve efficient energy resonance transfer. The proposed ECL aptasensor provided a linear range from 10 nM to 1.0 fM for chlorpyrifos detection and the detection limit of 0.35 fM (S/N = 3) under optimal experimental conditions. The method was successfully applied to the detection of chlorpyrifos in fruit and vegetable samples with satisfactory results.

CAS / MDL: 16940-66-2 6132-04-3
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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

Transition metal dichalcogenides in alliance with Ag ameliorate the interfacial connection between Li anode and garnet solid electrolyte

Zhen Sun,Yanqing Lai,Na Lv,Liangxing Jiang,Ming Jia,Jie Li,Weizhai Bao,Fangyang Liu

Solid-state batteries (SSBs) exhibit a promising prospect due to their potential in terms of safety and energy densities . As an oxide electrolyte, cubic garnet solid electrolyte (cubic-Li 7 La 3 Zr 2 O 12 ) attracts wide attention due to the high ionic conductivity . However, the problem of poor contact between garnet solid electrolyte and lithium impairs the development of solid electrolytes. Herein, we demonstrate an effective modification method to cope with the interface issue between electrolyte and Li metal by introducing an Ag@WSe 2 composite layer. By applying this method, the interfacial resistance between the garnet electrolyte and Li metal is reduced to ~12.5 Ω cm 2 , which is nearly 150 times lower than the value of 1900 Ω cm 2 before modification. The WSe 2 acts as a framework to immobilize Ag, while Ag forms an Ag–Li alloy with lithium for lithium ions transportation. And other Ag@TMDs (transition metal dichalcogenides) composites have also been proven to have similar effects. In addition, the Li | Ag@WSe 2 -LLZO | LFP full cell demonstrates a satisfactory capacity and excellent cycle stability (500 cycles with 90% capacity retention rate) at room temperature .

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Nanomaterials · 2020 ·Vol. 10 ·期 5 ·883 · IF 4.324

Highly Efficient Mesoporous Core-Shell Structured Ag@SiO2 Nanosphere as an Environmentally Friendly Catalyst for Hydrogenation of Nitrobenzene

Bonan Zhao,Zhipeng Dong,Qiyan Wang,Yisong Xu,Nanxia Zhang,Weixing Liu,Fangning Lou,Yue Wang

The size-uniformed mesoporous Ag@SiO2nanospheres’ catalysts were prepared in one-pot step via reducing AgNO3by different types of aldehyde, which could control the size of Ag@SiO2NPs and exhibit excellent catalytic activity for the hydrogenation of nitrobenzene. The results showed that the Ag core size, monitored by different aldehydes with different reducing abilities, together with the ideal monodisperse core-shell mesoporous structure, was quite important to affect its superior catalytic performances. Moreover, the stability of Ag fixed in the core during reaction for 6 h under 2.0 MPa, 140 °C made this type of Ag@SiO2catalyst separable and environmentally friendly compared with those conventional homogeneous catalysts and metal NPs catalysts. The best catalyst with smaller Ag cores was prepared by strong reducing agents such as CH2O. The conversion of nitrobenzene can reach 99.9%, the selectivity was 100% and the catalyst maintained its activity after several cycles, and thus, it is a useful novel candidate for the production of aniline.Keywords:mesoporous;Ag@SiO2;catalyst;hydrogenation;nitrobenzene

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ACS Applied Bio Materials · 2020 · IF 0

Au Film–Au@Ag Core–Shell Nanoparticle Structured Surface-Enhanced Raman Spectroscopy Aptasensor for Accurate Ochratoxin A Detection

Xiaohui Jing,Lin Chang,Lixia Shi,Xiaohong Liu,Yuan Zhao,Wei Zhang

As a powerful toxin that could cause fatal death, the detection of ochratoxin A (OTA) has gained much attention in the fields of environmental and food sciences. In this study, an internal standard (IS) aptasensor was synthesized through a facile and scalable method to enhance the sensitivity and quantativity of OTA detection. The substrates were formed through hybridization of modified aptamers on Au@Ag core–shell nanoparticles (NPs) and Au films at a silicon surface. Incorporated with 4-ATP and 4-NTP as an internal standard, OTA recognition of such aptamers could cause NP release and signal losses. Utilizing the strong peaks at 1078 and 1335 cm–1, which represent 4-ATP and 4-NTP, respectively, the intensity ratio of I1078/I1335 could delegate the OTA concentration in a ratiometric manner. Therefore, the highest ratio of I1078/I1335 represents the lowest concentration of OTA, and a lower ratio means a higher OTA concentration. Quantitatively, the high consistency for OTA detection was achieved through correction of signal losses by IS references with an R2 of 0.993 and RSD of 0.94%, and the OTA detection limit of 5 pM was achieved. Herein, such an IS aptasensor provides a reliable and scalable detection platform for various molecules in a continuous and high-throughput manner and holds great promise in future quantitative SERS measurements.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2020 · IF 7.489

Visible light photocatalytic degradation of tetracycline with porous Ag/graphite carbon nitride plasmonic composite: Degradation pathways and mechanism

Weicheng Xu,Shufeng Lai,Suresh C. Pillai,Wei Chu,Yun Hu,Xueding Jiang,Mingli Fu,Xiaolian Wu,Fuhua Li,Hailong Wang

Ag/g-C 3 N 4 plasmonic photocatalysts with porous structure (Ag/PCN) were successfully synthesized via a thermal exfoliation strategy and photo-reduction method. Owing to the combined merits of porous structure and surface plasmon resonance effect of silver nanoparticles, the Ag/PCN catalysts exhibited excellent photocatalytic performance for the degradation of antibiotic agents. With the optimal Ag loading, the Ag/PCN-2 catalyst exhibited the optimal catalytic activity for TC degradation under visible light, which shows about 11.8 times enhancement in the photocatalytic removal efficiency as compared to pure g-C 3 N 4 , respectively. This phenomenon can be attributed to the increased specific surface area, broadened visible light absorption and improved charge separation. The radical quenching results confirmed that h + and O 2 − radicals were the major active species during removal of TC. The degradation of TC is increased with the increment of Ag/PCN-2 catalysts, and the optimum catalyst was found to be 1.67 g/L. The hindering effect of selected of anions (Cl − , CO 3 − , H 2 PO 4 − ) was found to follow the order H 2 PO 4 − > CO 3 − > Cl − . Ag/PCN-2 sample also possessed high stability after six cycles of reuses. Furthermore, the possible degradation pathways of TC and photocatalytic mechanism over Ag/PCN-2 were proposed in detail.

CAS / MDL: 60-54-8
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