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CARBON · 2024 · IF 10.5

Synergistic magnetic/dielectric loss and layered structural design of Ni@carbon fiber/Ag@graphene fiber/polydimethylsiloxane composite for high-absorption EMI shielding

Lu Xu,Ranran Si,Qi Ni,Jiaan Chen,Jiale Zhang,Qing-Qing Ni

Simultaneously achieving excellent shielding effectiveness (SE) and high absorption rate of flexible electromagnetic interference (EMI) shielding materials has become a growing demand for the new generation of highly integrated electronic devices. This study constructed a double-layer polydimethylsiloxane (PDMS) EMI shielding composite film, with the upper layer using Ni-plated carbon fiber (Ni@CF) as the high absorption loss part and the lower layer using Ag-plated graphene fiber (Ag@GF) as the reflection attenuation part. Due to the synergistic magnetic/dielectric loss effect in the upper layer, high electrical conductivity in the lower layer, and the shielding mechanism of “absorption-reflection-reabsorption” induced by the double-layer structure, this composite film achieves efficient EMI shielding performance and high absorption characteristics in the X-band. The EMI SE values of the 2 mm thick film containing 0.03 wt% Ni@CF and 1.2 wt% Ag@GF reach 33.7 dB, while shielding effectiveness of reflection ( SE R ) and absorption ( SE A ) is 0.8 dB and 32.9 dB, respectively. This result means that the composite film only reflects 17.2 % of the microwaves while shielding 99.9 % and absorbs nearly 82.7 %, exhibiting a significant absorption-dominated shielding mechanism. This flexible and efficient shielding film with a high absorption rate suits portable and wearable intelligent electronic products to reduce secondary electromagnetic pollution.

研究领域: 材料科学 · 电子工程
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

Effects of high entropy combined with Cu/Ag doping on the thermoelectric properties of Bi2Sr2Co2Oy ceramics

Yingying Xu,Mengyao Li,Yingjiu Zhang,Hongzhang Song,Haoshan Hao

A series of Bi 2 Sr 2 Co 2 O y (BSCO), Bi 2 (Sr 2/3 Ba 2/3 Ca 2/3 )Co 2 O y (BSBCCO), Bi 1.9 Cu 0.1 (Sr 2/3 Ba 2/3 Ca 2/3 )Co 2 O y (BCSBCCO) and Bi 1.8 Ag 0.2 (Sr 2/3 Ba 2/3 Ca 2/3 )Co 2 O y (BASBCCO) ceramic samples were prepared to optimize the thermoelectric properties of BSCO by high entropy doping combined with Cu/Ag doping. High entropy doping improves the carrier mobility significantly, due to a sintering effect in liquid phase and an additional conduction path. Cu/Ag acceptor doping increases the carrier concentration and Seebeck coefficients. Both them enhance the electrical transport performance of doped samples effectively. Specially, the random distribution of several different cations caused by high entropy doping and Cu/Ag doping can enhance the phonon scattering, which greatly reduces the thermal conductivity of doped samples. Finally, the thermoelectric figure of merit ( ZT ) value of the BASBCCO sample is improved to 0.36 at 923 K on the basis of high entropy doped BSBCCO ( ZT  = 0.28 at 923 K), which is twice that of the pristine sample.

研究领域: 材料科学 · 热电材料
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Journal of Materials Chemistry A · 2024 · IF 10.7

Synergistic vacancy defects and bandgap engineering in an Ag/S co-doped Bi2O3-based sulfur oxide catalyst for efficient hydrogen evolution

Zhengjie Su,Xinru Wu,Dong-Hau Kuo,Baoqian Yang,Binghong Wu,Longyan Chen,Pengkun Zhang,Jinguo Lin,Dongfang Lu,Xiaoyun Chen

Herein, an Ag/S co-doped Bi2O3-based sulfur oxide catalyst was prepared via a facile green method. The Ag/S–Bi2O3 catalyst with suitable Ag/S doping demonstrated super visible light photocatalytic hydrogen evolution (PHE) at 7.52 mmol g−1 h−1, with an apparent quantum efficiency (AQE) of 8.67% at 420 nm. Ag/S co-doping can adjust the energy band structure of an oxidation type Bi2O3 catalyst, converting it into a visible light hydrogen production catalyst suitable for hydrogen production. Sulfur doping adjusts the content of oxygen vacancies to enhance the surface active sites, and the introduction of noble metal silver endows the catalyst with more excellent electrical conductivity and electron trapping ability. Thus, Bi2O3 with Ag/S co-doping produced a suitable energy band structure, enhanced the content of oxygen vacancies and the number of surface active sites, and endowed the catalyst with excellent electrical conductivity and electron trapping ability, significantly producing catalysts with excellent visible light PHE activity. Furthermore, Ag/S–Bi2O3-3 exhibited super visible light PHE activity and excellent stability and persistence and is expected to play a potential role in the field of PHE reactions (PHERs).

CAS / MDL: 62-55-5
研究领域: 材料科学 · 催化化学
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TALANTA · 2024 · IF 5.6

A highly sensitive and selective SERS sensors based on Au@PATP@Ag@ZIF-8 for the detection of phosphate in water

Yueshou Zhang,Lichun Yang,Yulin Xu,Haiting Ren,Shi Yin,Yan Sun,Yongjun Hu

Rapid and sensitive detection of phosphate is of great significance for ensuring water safety and preventing eutrophication. In this study, we prepared Au@PATP@Ag NRs core-shell structures using 4-aminothiophenol (PATP) as an internal standard signal molecule to enhance the stability of the SERS signal. Based on the phosphate-induced decomposition of ZIF-8 and the protective effect of ZIF-8 on the internal Au@PATP@Ag NRs, a phosphate SERS sensor (Au@PATP@Ag@ZIF-8) with high sensitivity, selectivity and stability was designed. This method exhibited a good linear range of 0.1–125 μM and a detection limit of 30 nM. Furthermore, the developed sensor (Au@PATP@Ag@ZIF-8) was effectively applied to assess PO 4 3− in tap water samples, achieving recoveries between 97.44% and 104.54%. With its simple, fast and sensitive features, this method of phosphate detection in water provides a direction for the research and practical application of phosphate detection.

研究领域: 环境科学 · 分析化学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2020 · IF 3.99

Ordered mesoporous Ag/CeO2 nanocrystalline via silica-templated solution combustion for enhanced photocatalytic performance

Zhichao Shang,Zhongxiang Yang,Yang Xiao,Xiaohong Wang

The various ordered mesoporous Ag/CeO 2 catalysts were successfully prepared using a facile silica-templated solution combustion synthesis method (TSCS). Utilizing X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Brunauer-Emmett-Teller (BET), photoluminescence (PL) and UV–vis diffuse reflectance spectrometry (DRS), etc., the morphological, structural, crystalline, surface and optical properties of Ag/CeO 2 were investigated. It was found that the removal of the template (SiO 2 ) resulted in the formation of ultrafine mesoporous Ag/CeO 2 composites, and the specific surface area increased to 98.6 m 2 /g. The 15 % Ag/CeO 2 composite showed the best photocatalytic performance (97 % at 120 min), which was approximately 10 times higher as compared to the conventional SCS (Solution Combustion Synthesized) CeO 2 . In addition, a mechanism of the photocatalytic degradation of Rhodamine B (RhB) was proposed, where the reactive species ·O 2 − and h + played important roles in the degradation of pollutants.

研究领域: 材料科学 · 环境科学 · 催化
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CHEMOSPHERE · 2019 · IF 5.108

Degradation of bisphenol a using peroxymonosulfate activated by WO3@MoS2/Ag hollow nanotubes photocatalyst

Ying Zeng,Na Guo,Xingjian Xu,Yong Yu,Quanying Wang,Na Wang,Xuerong Han,Hongwen Yu

WO 3 @MoS 2 /Ag (HW@MA) hollow tubes were successfully engineered to photodegrade bisphenol A (BPA) combined with peroxymonosulfate (PMS) for the first time. XRD, XPS, TEM and SEM were conducted. The HW@MA tubes present excellent photocatalytic performance on the removal of BPA. The intermediate products of BPA were investigated by GC-MS analysis and the degradation pathway was proposed. To explore the transferred mechanism of photoproduced carriers, the electron paramagnetic resonance (EPR) technique was carried out. The results revealed that the superoxide radical ( O 2 − ), hydroxyl radical ( OH), sulfate radical ( SO 4 − ) were the main active radicals. Moreover, the formed schottky junctions enhanced the separation efficiency of photoinduced electron-hole pairs. Besides, the effect of the photocatalysts’ dosage, PMS concentration, pH of the initial solution and co-existing anions on the BPA degradation were investigated.

CAS / MDL: 70693-62-8
研究领域: 环境科学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2018 · IF 3.927

Fabrication of UV–Vis-NIR-driven photocatalysts Ag/Bi/BiOCl0.8Br0.2 with high catalytic activity

Hui Xu,Yunfang Huang,Dan Luo,Xiaomin Yang,Shao Jin,Qiyao Guo,Yuezhu Zhao,Yu Fang,Yuelin Wei,Jihuai Wu

In this work, multiple heterojunction Ag/Bi/BiOCl 0.8 Br 0.2 photocatalysts with novel porous micro-flower structure were fabricated via a facile one-step solvothermal route and characterized systematically. The TEM and HRTEM images clearly showed the heterogeneous nanostructures at the interface between Ag/Bi and BiOCl 0.8 Br 0.2 . The as-prepared Ag/Bi/BiOCl 0.8 Br 0.2 composites displayed a strong optical absorption in the region of 250–1500 nm, especially in the unexploited near infrared region which accounts for most of the sunlight. The multiple heterojunction photocatalyst exhibited an outstanding photocatalytic activity for the degradation of Rhodamine B under the UV, visible and NIR light irradiation, respectively. The highly enhanced photocatalytic activity was attributed to the synergistic effects, including the reduced band gap, the surface plasmon resonance effect, efficient charge separation of photo-generated electron-holes. On the basis of the radical species trapping experiments, the holes and superoxide radicals were confirmed to be the mainly active species involved in the degradation of Rhodamine B under the NIR light irradiation. This study provides a novel strategy for designing highly performance plasmonic photocatalysts under the whole solar light irradiation.

研究领域: 材料科学 · 环境科学
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CHINESE JOURNAL OF CATALYSIS · 2022 · IF 12.92

Efficient CO2 fixation with acetophenone on Ag-CeO2 electrocatalyst by a double activation strategy

Anxiang Guan,Yueli Quan,Yangshen Chen,Zhengzheng Liu,Junbo Zhang,Miao Kan,Quan Zhang,Haoliang Huang,Linping Qian,Linjuan Zhang,Gengfeng Zheng

The electrocarboxylation reaction is an attractive means to convert CO 2 into valuable chemicals under ambient conditions, while it still suffers from low efficiency due to the high stability of CO 2 . In this work, we report a double activation strategy for simultaneously activating CO 2 and acetophenone by silver-doped CeO 2 (Ag-CeO 2 ) nanowires, featuring as an effective electrocatalyst for electrocarboxylation of acetophenone with CO 2 . Compared to the Ag foil, Ag nanoparticles and CeO 2 nanowires, the Ag-CeO 2 nanowire catalyst allowed to reduce the onset potential difference between CO 2 and acetophenone activation, thus enabling efficient electrocarboxylation to form 2-phenyllactic acid. The Faradaic efficiency for producing 2-phenyllactic acid reached 91% at −1.8 V versus Ag/AgI. This double activation strategy of activating both CO 2 and organic substrate molecules can benefit the catalyst design to improve activities and selectivities in upgrading CO 2 fixation for higher-value electrocarboxylation.

研究领域: 化学 · 环境科学 · 材料科学
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Materials Science and Engineering B-Advanced Functional Solid-State Materials · 2024 · IF 3.9

Fabrication and properties analysis of paraffin@TiO2/Ag phase change microcapsules for thermal energy storage and photocatalysis

Jieying Su,Haitao Zhang,Yuanyuan Gong,Qinqin Xu,Maohua Hou,Bin Xu

To develop a material that can be applied in the field of thermoregulation materials for residential buildings and degradation of organic pollutants. A novel microencapsulated phase change material, paraffin@TiO 2 /Ag, was prepared using interfacial condensation technology. The paraffin@TiO 2 /Ag microcapsules' melting point and latent heat were 48.00 °C and 63.56 J/g, respectively, according to the DSC study results, and their encapsulation rate was 46.11 %. In addition, the experimental results of photocatalytic degradation of MB (methylene blue) showed that the paraffin@TiO 2 /Ag microcapsules had high photocatalytic activity for organic dyes under natural light, and the degradation rate of MB reached 99 % when the light exposure time reached 4 h. By comparing the reaction rate constant of MB by paraffin@TiO 2 microcapsules (0.98969 h −1 ) with that of MB by paraffin@TiO 2 /Ag microcapsules (1.15845 h −1 ), it was learned that the introduction of Ag nanoparticles effectively improved the photocatalytic activity of the phase change microcapsules.

CAS / MDL: 4420-74-0
研究领域: 材料科学 · 环境科学
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WATER RESEARCH · 2024 · IF 11.4

Rational regulation of post-electrodialysis electrochromic anion exchange membranes via TiO2@Ag synergistically strengthens visible-light photocatalytic anti-contamination activity

Yuyang Yao,Yueyue Lu,Jingwen Xu,Jiacheng Yu,Liang Guo,Heda Ding,Jian Li,Junbin Liao,Edison Huixiang Ang,Zhenlu Shen,Jiangnan Shen

Membrane-contamination during electrodialysis (ED) process is still a non-negligible challenge, while irreversible consumption and unsustainability have become the main bottlenecks limiting the improvement of anion exchange membranes (AEMs) anti-contamination activity. Here, we introduce a novel approach to design AEMs by chemically assembling 4-pyndinepropanol with bromomethylated poly(2,6-dimethyl-1,4-phenylene oxide) (BPPO) in an electrochromic-inspired process. Subsequently, the co-mingled TiO 2 @Ag nanosheet with the casting-solution were sprayed onto the surface of the substrate membrane to create a micrometer-thick interfacial layer. The addition of Ag nanoparticles (NPs) enhances the active sites of TiO 2 , resulting in stronger local surface plasmon resonance (LSPR) effects and reducing its energy band gap limitation (From 3.11 to 2.63 eV). Post-electrodialysis electrochromic AEMs incorporating TiO 2 @Ag exhibit synergistic enhancement of sunlight absorption, effectively suppressing photogenerated carrier binding and promoting migration. These resultant-membranes demonstrate significantly improved bacterial inhibition properties (42.0-fold increase for E. coli ) and degradation activity (7.59-fold increase for rhodamine B) compared to pure TiO 2 membranes. Importantly, they maintain photocatalytic activity without compromising salt-separation performance or stability, as the spraying process utilizes the same substrate materials. This approach to rational design and regulation of anti-contamination AEMs offers new insights into the collaborative synergy of color-changing and photocatalytic materials.

研究领域: 材料科学 · 环境工程
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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Investigation of interfacial properties of Ag–Cu/Si3N4 composite ceramic substrates by interface reaction of Si3N4 and CuO

Chaochen Chen,Fang Lei,Ying Shi,Jianjun Xie,Lei Zhang,Lingcong Fan

The surface metallization of Si 3 N 4 ceramics with the Ag–Cu conductive paste containing CuO was systematically investigated. The interfacial reactions between CuO and Si 3 N 4 promoted the surface metallization of the ceramic substrate in an argon atmosphere. The effects of Ag and Cu relative contents on the evolution of the thick film surface morphology were studied. The electrical properties and tensile strength of composite ceramic substrates were enhanced through the generation of Ag–Cu eutectic solution within the thick film layer. The effect of brazing time on the properties of Ag–Cu/Si 3 N 4 composite ceramic substrates was investigated. Mechanical testing and scanning electron microscopy (SEM) were used to analyze the interface tensile strength of the Ag–Cu/Si 3 N 4 composite substrates and the morphology of the Ag–Cu film, and the bonding mechanism of the composite ceramic substrate was studied. When the sample was brazed at 800 °C for 20 min, the maximum tensile strength of 23.6 MPa between the Ag–Cu film and ceramic substrate was obtained, the lowest resistivity of 6.22 μΩ•cm was obtained. The bonding interface between thick film layer and the ceramic substrate formed the Ag–Cu mechanical structure was benefit for improving the comprehensive performance of the Cu/Si 3 N 4 composite ceramic substrate.

CAS / MDL: 1317-38-0 7440-22-4
研究领域: 材料科学 · 陶瓷工程
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Nanoscale · 2022 ·Vol. 14 ·期 41 ·15340-15347 · IF 8.307

Heterojunction MnO2-nanosheet-decorated Ag nanowires with enhanced oxidase-like activity for the sensitive dual-mode detection of glutathione

Lin Tian,Zijun Huang,Weidan Na,Yuanyuan Liu,Shuai Wang,Yu He,Wenjing Cheng,Tianzi Huang,Zhao Li,Tongxiang Li

The biocatalytic design of nanomaterials with enzyme-like activity is considered a reliable and promising toolkit for the generation of diagnostic agents in complex biological microenvironments. However, the preparation of nanomaterials while maintaining a high catalytic activity in tumor cells (pH 6.0–6.5) poses a prominent challenge. Herein, we constructed a biomimetic enzyme-trigged dual-mode system with colorimetry at 652 nm and photothermal biosensors to detect glutathione based on hollow MnO2-nanosheet-decorated Ag nanowires (Ag@MnO2) as an oxidase-like nanozyme. As expected, Ag@MnO2 catalyzed the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) in the absence of H2O2, leading to a blue-colored oxidized TMB (oxTMB) that displayed oxidase-like activity in pH 6.0. Interestingly, the portable dual-mode colorimetry and photothermal method for GSH was developed based on the redox reaction between GSH and oxTMB. This detection method exhibited a wide linear range of 0.1–55 μM for GSH with a low detection limit of 0.08 μM. This work highlights a new insight into nanotechnology by taking advantage of biomimetic design in biological analysis.

研究领域: 生物化学 · 纳米医学 · 诊断学
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