CERAMICS INTERNATIONAL
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2025
·
IF 5.6
Han Xu,Gangsong Huang,Wenting Zhou,Xuan Miao,Hongjun Ji,Mingyu Li,Yufeng Li
In the realm of electronic packaging advancements, the utilization of metal to ceramic joints has garnered significant attention. This manuscript details the development of a specific glass solder with excellent wettability and a thermal expansion coefficient of 8.1 × 10 −6 °C −1 , comprising 35Bi 2 O 3 -30B 2 O 3 -15ZnO-20SiO 2 (mol.%). This design achieves reliable connection of the Al 2 O 3 ceramics and Kovar alloy in an atmospheric environment. The interface reaction between the glass solder, Al 2 O 3 ceramics, and oxidized Kovar alloy resulted in the formation of ZnAl 2 O 4 particles and Bi spheres at the joints. The enhancement in joint shear strength was primarily attributed to the nanoscale, dispersed ZnAl 2 O 4 particles. However, the presence of microscale Bi spheres, with a lower elastic modulus than the glass solder, initiated cracks during shear deformation, thereby compromising the integrity of the joint. Optimization of brazing temperatures enabled control over the ZnAl 2 O 4 and Bi sphere phases within the joints, yielding a peak shear strength of 51.7 ± 8.9 MPa at 650 °C. This study highlights the achievement of high-performance metal-ceramic bonding through tailored interface reactions and optimized joint microstructures.
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高影响因子
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
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2025
·
IF 4.9
Nannan Huang,Shuhao Liang,Xiangyang Liang,Huining Chai,Yingjie Sun,Lili Lyu,Weiqiang Tan
The interfacial compatibility of heterojunction photocatalysts critically governs the interaction modes between constituent materials. Herein, a flower-like Bi-BDC-NH 2 /Ag 2 CO 3 heterostructure was fabricated via a simple ion-exchange solution method, serving as a robust photocatalyst for the efficient photocatalytic reduction of Cr(VI) in simulated wastewater under visible-light irradiation. Ag 2 CO 3 nanosheets were in-situ grown on the surface of three-dimensional Bi-BDC-NH 2 , forming an Ag 2 CO 3 -on-Bi-BDC-NH 2 type II heterojunction that establishes intimate interfacial contact, significantly accelerating the charge and mass transport dynamics. In comparison with pure Bi-BDC-NH 2 and Ag 2 CO 3 , the optimal Bi-BDC-NH 2 /Ag 2 CO 3 -50 (with a weight ratio of 0.5:1) exhibited dramatically enhanced photocatalytic activity, achieving 99% Cr(VI) reduction within 2 hours under visible light (>420 nm, 150 W xenon lamp). Mechanistic investigations, including energy band structure analysis, radical trapping experiments, and photoelectrochemical measurements, revealed that the heterojunction interface significantly promotes the separation and transfer of photogenerated electron-hole pairs. This work provides valuable insights into the rational design of MOF-based heterojunction photocatalysts and their applications in environmental remediation.
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Science China-Technological Sciences
·
2025
·Vol. 68
·期 8
·1-11
·
IF 4.9
Yang Ping-an,Zhao Chensong,Luo Jiufei,Zou Lihua,Liu Zhongbang,Gui Yingang,Zhou Zhihao
This study develops a flexible strain sensor with electromagnetic interference (EMI) shielding, hydrophobicity, and acid/alkali resistance by integrating a bi-ordered porous structure with a micro-raised surface. The structure, mimicking lotus leaves, is fabricated using magnetic field-assisted freezing orientation and laser ablation on graphene (Gr)/Fe nanowire (NW)-infused aerogel and polydimethylsiloxane. The sensor, with a Gr to Fe NW ratio of 9:1, shows a high gauge factor of 85.19 in the 0–30% tensile strain. These values are 304%, 430%, 702%, and 1226% of the samples with Gr to Fe NWs ratios of 7:1, 5:1, 3:1, and 1:1, respectively. It achieves an EMI shielding efficiency (SE) of 20.02 dB and a specific SE of 807.48 dB cm 2 /g in the 8.2–12.4 GHz range, 150% higher than isotropic samples. The sensor exhibits a contact angle of 155.76°, maintaining hydrophobic stability under stretching and showing excellent resistance to acid and alkali. Additionally, the sensor can be integrated into wearable devices like gloves for gesture recognition, machine hand manipulation, and controlling neon bulbs, demonstrating potential for applications in field robotics and human-robot interaction.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2025
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IF 21.1
Tong Sun,Kuan Wang,Yuan-Xiao Du,Jian-Gang Chen,Xin-Peng Li,Zhen-Hong He,Xiaodong Hao,Weitao Wang,Huan Wang,Zhao-Tie Liu
The photocatalytic conversion of CO₂ into value-added chemicals using solar energy is a crucial strategy for achieving carbon neutrality. However, existing semiconductor catalyst systems suffer from suboptimal conversion efficiencies due to inefficient charge separation and transfer. The precise modulating surface microenvironment of semiconductor catalyst contributes an effective approach to address these limitations in photocatalytic applications. This study proposes a precise dual-modification strategy to modulate the surface microenvironment by incorporating Co 2+ incorporation and in situ generating Bi sub-nanoclusters in ultrathin BiOCl nanosheets. This approach synergistically establishes spin-polarization effects and interfacial ohmic contacts, while enhancing the intrinsic built-in electric field. Consequently, it drives efficient charge separation and transfer. Mechanistic analyses via theoretical simulations and in situ experiments reveal that the engineered spin polarization facilitates electron transfer through aligned magnetic moments, while the formed ohmic contact eliminates interfacial potential barriers, collectively lowering the energy barrier for CO 2 * and COOH* formation. The optimized 3 %Co-BBOC catalyst demonstrates exceptional CO₂-to-CO conversion performance with a production rate of 58.25 μmol·g −1 ·h −1 , representing a 6.6-fold enhancement over pristine BiOCl. The present work elucidates a dual-functional synergistic mechanism of modulating the surface microenvironment by integrating spin manipulation and interfacial engineering, providing fundamental insights for designing advanced photocatalytic systems with optimized charge transport and surface reaction dynamics.
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MICROCHIMICA ACTA
·
2025
·Vol. 192
·期 11
·1-16
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IF 5.3
Feng Luping,Li Xinfeng,Wang Jianghong,Chen Enjun,Fan Yujie,Jin Leyao,Tang Peisong,Zhang Lixiang
A visible-light-powered photoelectrochemical (PEC) sensor was devised for chlorpyrifos (CPs) determination using metallic Bi-decorated BiVO 4 nanosheets (Bi@BiVO 4 NSs) with localized surface plasmon resonance (SPR) synthesized via a one-step hydrothermal method. It was observed that Bi@BiVO 4 -based PEC sensors exhibit significantly enhanced PEC responses over pristine BiVO 4 due to the collaborative effect of metallic Bi’s SPR phenomenon and BiVO 4 ’s visible-light-driven properties. Furthermore, the addition of CPs selectively suppresses the photocurrent signal of the sensor due to the in-situ formation of Bi-CPs complexes, which hindered electron transfer through specific chelation reactions between Bi sites and CPs. The designed PEC sensor achieved high-sensitivity detection of CPs, with a linear concentration range from 0.02 to 20 ppb and a detection limit of 0.01 ppb. These attributes may offer a blueprint for developing diverse PEC sensing systems to monitor various environmental pesticide contaminants like CPs by synergistic integration of visible-light-responsive BiVO 4 and SPR-active metallic Bi. Graphical
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高影响因子
ELECTROCHIMICA ACTA
·
2025
·
IF 5.6
Liu Yang,Zihao Fan,Fujun Cui,Taolong Wu,Tingxu Fang,Yujie Guo,Li Tian,Bo Pang,Gaohong He,Xuemei Wu
Vanadium redox flow battery (VRFB) is promising large-scale energy storage technology for renewable energies, while the sluggish kinetics of vanadium redox reaction restricts the efficiency at high current density. Herein, the strategy of boosting V 2+ /V 3+ redox reaction by atomic Bi active sites decorated graphite felt electrode derived from bismuth-based metal−organic framework (Bi-MOF) is proposed. Bi-MOF, dispersing abundant Bi metal sites on porous carrier, helps the Bi atoms to form atomic active sites easily by coordinating with N through the nitrogen source mediated carbonization process. Porous nanobundles of atomic Bi catalyst uniformly bind to the graphite felt, exhibiting over 2 folds increase in specific surface area, higher V 2+ /V 3+ redox peak currents and reversibility, and one order of magnitude lower of charge-transfer resistance. The atomic Bi active sites decorated graphite felt negative electrode achieves high VRFB performance even with the vanadium ions heavily permeable Nafion membrane, showing 13.1 % higher energy efficiency at 200 mA cm –2 (80.2 % vs. 70.9%), 68.1% increase in electrolyte utilization comparing to the pristine graphite felt, and keeping stable during 1500 charge/discharge cycles. The performance is superior to the reported metal−organic frameworks (MOFs)-derived catalyst decorated electrodes.
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TALANTA
·
2018
·
IF 4.244
Meichuan Liu,Hongyang Ke,Caiqin Sun,Guoqiang Wang,Yu Wang,Guohua Zhao
In the present work, a convenient signal-on electrochemical label-free aptasensor for 17β-estradiol (E2), a typical steroidal hormones endocrine disrupting chemicals , was proposed. 6-mercapto-1-hexanol (MCH) self-assembled monolayer (SAM) modified Au (MCH/Au) electrode was used as the substrate electrode. Graphene is used with bi-functions, not only to adsorb E2 binding aptamer, serving as the recognition element to E2, but also to be assembled onto MCH/Au electrode when sensing E2, to controllably turn on the electron transfer (eT), and further indicate the signal to E2 concentration. With the synergistic effect of DNase I enzyme, highly sensitive detection of E2 was achieved at this aptasensing system, with a linear range from 0.07 to 10 pM and a detection limit of 50 fM. An outstanding selectivity towards E2 was proven for the sensing system by simultaneously detecting 100-fold potential co-existing interferences. The stability and reproducibility were also evaluated to be satisfactory. Spiked real water analysis further indicated its reliability and potential in practical environmental monitoring.
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高影响因子
JOURNAL OF MOLECULAR STRUCTURE
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2025
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IF 4.7
Xingshi Li,Ruihan Zhang,Linlin Chen,Zhihui Cheng,Yaoguo Huang,Yali Zhang
A novel composite material, MIBuXATT@GO, was synthesized by functionalizing graphene oxide (GO) with a bi-ligand triazole-thione ligand, 3-methyl isobutylxanthate-4-amino-1,2,4-triazole-5-thione (MIBuXATT), for the efficient adsorption of Cu(II) ions. This modified material served as an adsorbent to enhance the selective adsorption of Cu(II) from wastewater by synergistically combining physical and chemical adsorption mechanisms. MIBuXATT@GO was characterized by XRD, SEM/EDS, and FTIR. Under the optimal conditions (pH=4, adsorbent dosage 250 mg/L, contact time 60 minutes), the maximum adsorption capacity of Cu(II) by the material is 97.24 mg/g, which is 1.3 times higher than that of GO. Meanwhile, the adsorption process of MIBuXATT@GO to Cu(II) is characterized as spontaneous endothermic chemisorption. Furthermore, the experimental results regarding metal ion adsorption selectivity indicate that MIBuXATT@GO exhibits superior selectivity for Cu(II) compared to Mn(II), Zn(II), Co(II), and Ni(II), which is an improvement over GO. The results indicate that MIBuXATT@GO is a promising adsorbent for the removal of Cu(II) ions from aqueous solutions, offering high capacity, rapid kinetics, and excellent selectivity. The adsorption mechanism was elucidated through FTIR, UV, XPS, and DFT calculations, revealing the critical role of the thiocarbonyl and triazole-thione functional groups in Cu(II) coordination. This work provides a new strategy for designing efficient adsorbents for heavy metal ion removal.
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
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IF 9.7
Jiaoping Si,Hongjing Liu,Wendong Zhang,Dengyu Jiao,Wangxing Ai,Yuerui Ma,Lihuan Feng,Xing’an Dong,Wenjie He,Peng Chen
The catalytic conversion of nitrogen oxides (NO x ) to non-toxic products has emerged as a critical strategy for air pollution control under stringent emission regulations. Photocatalytic NO x removal performance highly depends on the transmission of photogenerated electrons and the amount of reactive oxygen species (ROS) generated. Herein, the Bi/BiOCl/SrTiO 3 heterostructure photocatalyst was prepared by a simple in situ synthesis method to address the limitations of conventional NOx removal systems. Due to the synergistic effect of bismuth (Bi) surface plasmon resonance (SPR) and the built-in electric field in BiOCl/SrTiO 3 S-scheme heterojunction, Bi/BiOCl/SrTiO 3 showed strong light absorption ability and high charge separation efficiency, with the highest NO removal efficiency reaching 70 %. The enhanced electronic interaction between Bi and BiOCl/SrTiO 3 induced Bi-O covalent bonds with the BiOCl layer to facilitate fast charge separation, promoting the rapid transfer of interfacial photogenerated carriers, this process induces the activation of O 2 and H 2 O to form reactive oxygen species (ROS) to promote the oxidative removal of NO. This study provides new insights into the development of effective photocatalysts with fast charge separation by synergistic metal active sites and built-in electric field of heterojunction for air pollutant purification.
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TOXICOLOGY AND APPLIED PHARMACOLOGY
·
2020
·
IF 3.347
Yang Zhang,Jiabei Zhou,Qin Ye,Kui Zeng,Jie Pan,Lu Chen,Yingying Wang,Bo Yang,Qiaojun He,Jianqing Gao,Su Zeng,Lushan Yu
Thioredoxin 1 (Trx1) and telomerase play key roles in the development and progression process of most tumors, and they both are promising drug therapy targets. We have, for the first time, discovered that Trx1 and telomerase had a dual-target synergistic effect. Based on that results, we designed a series of 6-dithio-2′-deoxyguanosine analogs (named as YLS00X) and verified whether they can inhibit Trx1 and telomerase simultaneously. TrxR1/Trx1 system activity and telomerase expression were significantly inhibited by 6-dithio-2′-deoxyguanosine analogs, especially YLS004. YLS004 can also cause ROS accumulation, and induce tumor cell apoptosis . The vitro antitumor activity of 6-dithio-2′-deoxyguanosine analogs using MTT assay on 11 different human cancer cells and found that human colon cancer cells(HCT116) and melanoma cells (A375) were the most sensitive cells to 6-dithio-2′-deoxyguanosine analogs treatment and vivo xenografts models also confirmed that. The serum biochemical parameters and multiple organs HE staining results of subacute experiments indicated that YLS004 might be mildly toxic to immune organs, including the thymus, spleen, and hematopoietic system . Besides, YLS004 was rapidly metabolized in the rats' blood. Our study revealed that YLS004, a Trx1 and telomerase inhibitor , has strong anti-tumor effects to colon cancer and melanoma cells and is a promising new candidate drug.
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高影响因子
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2022
·Vol. 105
·期 5
·3438-3446
·
IF 4.186
Shuting Pang,Yiping Wang,Ying Yang,Jiyang Zhang,Querui Hu,Jingjing Shi,XiongJie Li
Bi(Zn 1/2 Ti 1/2 )O 3 −BiScO 3 −PbTiO 3 (BZT−BS−PT) high Curie temperature piezoelectric ceramics were synthesized by the conventional solid-state reaction method. Systematical investigations on the sintering, piezoelectric, and dielectric properties of the piezoceramics have been conducted. It was found that the sintering temperature could be remarkably depressed by varying the compositions in BZT−BS−PT systems. For composition of 11BZT−34BS−55PT ceramic, the sintering temperature is even lowered down to 750°C without any extra additions of sintering aids. Meanwhile, the ceramic sintered at this ultralow temperature presents dense microstructure with relative density up to 97%, as well as optimal properties of piezoelectric coefficient d 33 of 336 pC/N and Curie temperature of 415°C. The mechanism of low sintering temperature may be ascribed to the low melting point bismuth-based components in BZT−BS−PT solid solutions. Furthermore, 11BZT−34BS−55PT multilayer ceramics have been co-fired at 750°C with Ag internal electrodes. The dense structures, low cost, and optimal comprehensive properties of the co-fired multilayers illustrate obvious advantages of the ultralow sintering temperature in LTCC devices, implying promising applications of this Bi(Zn 1/2 Ti 1/2 )O 3 −BiScO 3 −PbTiO 3 high Curie temperature ternary system.
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高影响因子
INORGANIC CHEMISTRY
·
2022
·
IF 5.436
Qiang Xian,Xin Xiao,Jiaping Yu,Yi Gan,Li Chen,Xinmiao He,Enchao Wang,Hui Dan,Lin Zhu,Yi Ding,Tao Duan
The immobilization of iodine waste suffers from serious iodine loss during heat treatment. Herein, we reported on the high iodine retention immobilization of simulated radioiodine-contaminated Bi0–SiO2 sorbent in B–Bi–Zn oxide glass using Bi2O3 as a stabilizer under a N2 atmosphere. The effects of the Bi2O3 content and sintering atmosphere on the iodine immobilization behaviors (iodine retention ratio, phase composition, microstructure, and chemical stability) were investigated. It was found that the decomposition of BiI3 was prevented by adding Bi2O3 and sintering in a N2 atmosphere. The iodine retention ratio in the obtained glass waste form was significantly enhanced with increasing Bi2O3 content and sintering in the N2 atmosphere due to the synergistic effect. The achieved record-high iodine retention (92.22 ± 2.6%) was much higher than that of conventional heat treatment route (18.01 ± 3.5%). The results demonstrated that iodine was effectively immobilized through the formation of stable BixOyI (Bi5O7I and BiOI). Furthermore, the obtained iodine waste form exhibited excellent compactness and chemical stability. Owing to its high iodine retention ratio, this route can be employed to effectively immobilize radioactive iodine.
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