RSC Advances
·
2013
·Vol. 4
·期 1
·510-515
·
IF 2.562
Huan Wang,Baoqing Shentu,Zhixue Weng
A one-pot synthetic approach for the preparation of poly(2,6-dimethyl-1,4-phenylene oxide)/polystyrene (PPO/PS) alloy in aqueous medium was developed. The method was based on the combination of the oxidative coupling polymerization of 2,6-dimethylphenol (DMP) to form PPO in the presence of a reactive swelling agent, styrene (St), and in situ reverse atom transfer radical polymerization (RATRP) of St initiated by 2,2′-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (AIBI) in alkaline aqueous solution. The complex of CuCl2 and 4-dimethylaminopyridine (DMAP) was utilized as the catalyst to catalyze the two types of polymerization mentioned above. Oxygen was employed as the sole oxidant to synthesize PPO. The introduction of St during the oxidative polymerization of DMP could increase the molecular weight of PPO. Finally thermodynamically compatible PPO/PS alloy was successfully prepared.
研究领域:
高分子化学
·
材料科学
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2018
·Vol. 29
·期 21
·18566-18572
·
IF 2.324
Zhang Wenna,Zhang Wenwen,Xue Zexu,Xue Yu,Xu Jingkun,Chen Shuai,Zhang Ge
Poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) is a hotspot among current researched conducting polymers and its conductivity could be significantly enhanced by post-treatment with dimethyl sulphoxide (DMSO). In this work, five S and Se analogues of 3,4-ethylenedioxythiophene (EDOT) were synthesized, and chemically oxidative polymerized (COP) to obtain corresponding free-standing films of Poly(3,4-ethylenedioxythiophene)s:poly(4-styrenesulfonate) (PEDOTs:PSS). The effect of chalcogen substitution on the physicochemical properties and conductive performances of PEDOT:PSS film have been demonstrated. In contrast to the conductivities about 10 −2 –10 −1 S cm −1 for PEDOT:PSS and poly(3,4-ethylenedioxyselenophene):poly(4-styrenesulfonate) (PEDOS:PSS), other PEDOTs:PSS films had the conductivities about 10 −4 –10 −5 S cm −1 . The conductive enhancement effect of DMSO second-doping is suitable for PEDOTs:PSS films except the all-sulfur analogs of PEDOT:PSS (PEDTT:PSS and PEDTS:PSS), and the critical role of the presence of the O atoms in the ethylene bridges and the S atom in the thiophene ring has been illustrated. This work may help understand the structure-performance relationship of PEDOT family and the further development of PEDOTs in areas where the PEDOT seems monotonous and the high conductivity is not necessary, such as antistatic coating, anticorrosive coating, multi-colored electrochromics and so on.
✓ 已验证
产品关联
DOI
高影响因子
MICROCHIMICA ACTA
·
2014
·Vol. 182
·期 3
·823-829
·
IF 3.719
Wang Jinshou,Shi Zhen,Jin Jing,Liu Qi,Zhang Shenghui
A three-dimensionally ordered macroporous (3DOM) film of polycysteine (poly-Cys) was used to modify a glassy carbon electrode (GCE) to result in a sensor for 4-aminophenol. The new electrode was used to study the behavior of 4-aminophenol by cyclic voltammetry and differential pulse voltammetry. In comparison to a bare GCE and a GCE modified with poly-Cys without using template, this electrode displays a larger peak current which may be attributed to the structure of poly-Cys and the large surface area of the macroporous structure. The anodic peak current at a working voltage of 195 mV is linearly related to the concentration of 4-aminophenol in two concentration intervals: 0.02 to 20 μM and 20 to 200 μM, respectively. The detection limit is 8 nM (at an S/N ratio of 3). The method was successfully applied to the determination of 4-aminophenol in spiked water samples.
A glassy carbon electrode modified with three-dimensionally ordered macroporous polycysteine film was developed to serve as a sensor for determination of 4-aminophenol. The modified electrode presents lower detection limit, wider linear range and long-term stability for the determination of 4-aminophenol.
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry A
·
2022
·Vol. 10
·期 42
·22791-22802
·
IF 14.511
Xing-Ye Chen,Muhammad Ishaq,Nafees Ahmad,Rong Tang,Zhuang-Hao Zheng,Ju-Guang Hu,Zheng-Hua Su,Ping Fan,Guang-Xing Liang,Shuo Chen
The existence of various detrimental defects inside the absorber layer is a major obstacle limiting the performance of kesterite Cu2ZnSn(S,Se)4 (CZTSSe) thin-film solar cells. Cationic substitution is a viable strategy for overcoming this challenge and has drawn tremendous research attention. In this work, a dual-cation substituted CZTSSe involving Ag and Ti to separately occupy partial Cu and Sn lattice sites is proposed. Under 6% Ag and 1% Ti dual-cation substitution, the champion CZTSSe device delivers a highly interesting efficiency of 12.73%, accompanied by an outstanding VOC of 530 mV. Further investigation demonstrates that Ag introduction can improve the density and crystallinity of CZTSSe thin films while decreasing the concentration of CuZn acceptor defects. Further Ti substitution can effectively eliminate fine grains and reduce the defect density of CuSn and [2CuZn + SnZn] defects, as well as the core level defects. This work explores the synergistic effect of Ag, Ti dual-cation substitution in CZTSSe solar cells for the first time, and the clarified device performance improvement mechanism opens up promising possibilities for the bright development of CZTSSe thin-film photovoltaic technology.
研究领域:
材料科学
·
光伏技术
·
半导体物理
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2025
·
IF 4.1
Qing Fu,Xuhuai Fu,Jinzhou Feng,Jing Wang,Jinyu Jiang,Shijia Ding,Daobin Han,Manxia Wang
Neuromyelitis optica spectrum disorder (NMOSD) is a central nervous system demyelinating disease that typically causes severe visual impairment and paralysis, and the aquaporin-4 antibodies (AQP4-IgG) serve as its specific diagnostic marker. In patients presenting with typical NMOSD symptoms, a positive AQP4-IgG result is sufficient to confirm the diagnosis. However, current clinical methods for detecting AQP4-IgG suffer from limited sensitivity, time-consuming procedures, and labor-intensive workflows, underscoring the urgent need for more efficient and reliable diagnostic approaches. To address these limitations, we report a novel electrochemical biosensor leveraging a hierarchical ZIF-67@PDA@PtCu nanozyme for ultrasensitive and rapid AQP4-IgG detection. ZIF-67@PDA@PtCu, a composite material consisting of a ZIF-67 core coated with polydopamine (PDA) and further decorated with PtCu nanoparticles, was utilized as a signal amplification component. The PtCu alloy nanoflowers demonstrated exceptional catalytic activity, which was further amplified by the sturdy ZIF-67 framework that enabled the integration of additional functional materials. In parallel, PDA enhanced the synergy between the unsaturated edge sites of the metal-organic framework and the outstanding catalytic properties of the PtCu alloy, thereby boosting the overall performance of the system. The integration of graphene oxide (GO) and gold nanoparticles (AuNPs) enhanced electrical conductivity. This configuration enabled efficient electrochemical (EC) signal generation, facilitating the detection of AQP4-IgG with high stability, a broad detection range of 0.1–80 U mL −1 , and an impressively low detection limit of 0.05 U mL −1 . Our findings offer a novel approach for the early diagnosis of NMOSD and provide valuable insights into the detection of other antibody-dependent neuroimmune disorders.
研究领域:
免疫学
·
神经病学
·
生物医学工程
✓ 已验证
产品关联
DOI
高影响因子
Nature Communications
·
2024
·Vol. 15
·期 1
·1-12
·
IF 14.7
Wei Shengjie,Ma Wenjie,Sun Minmin,Xiang Pan,Tian Ziqi,Mao Lanqun,Gao Lizeng,Li Yadong
Constructing atom-pair engineering and improving the activity of metal single-atom nanozyme (SAzyme) is significant but challenging. Herein, we design the atom-pair engineering of Zn-SA/CNCl SAzyme by simultaneously constructing Zn-N 4 sites as catalytic sites and Zn-N 4 Cl 1 sites as catalytic regulator. The Zn-N 4 Cl 1 catalytic regulators effectively boost the peroxidase-like activities of Zn-N 4 catalytic sites, resulting in a 346-fold, 1496-fold, and 133-fold increase in the maximal reaction velocity, the catalytic constant and the catalytic efficiency, compared to Zn-SA/CN SAzyme without the Zn-N 4 Cl 1 catalytic regulator. The Zn-SA/CNCl SAzyme with excellent peroxidase-like activity effectively inhibits tumor cell growth in vitro and in vivo. The density functional theory (DFT) calculations reveal that the Zn-N 4 Cl 1 catalytic regulators facilitate the adsorption of * H 2 O 2 and re-exposure of Zn-N 4 catalytic sites, and thus improve the reaction rate. This work provides a rational and effective strategy for improving the peroxidase-like activity of metal SAzyme by atom-pair engineering.
研究领域:
材料科学
·
催化
·
纳米技术
·
生物化学
·
理论化学
✓ 已验证
DOI
高影响因子
JOURNAL OF POLYMER RESEARCH
·
2013
·Vol. 20
·期 7
·1-9
·
IF 2.019
Xu Jingmei,Ren Chunli,Cheng Hailong,Ma Li,Wang Zhe
Double fluoride 2,5-bis(4-fluorophenyl)-1,3,4-oxadiazole (BFO) monomer was synthesized. Copolymerization of BFO, 2,2-bis(4-hydroxypheny)propane (bisphenol A) and 3′3-disulfonate-4′4-dichloro dipheny sulfone (SDCDPS) at different molar ratio resulted in a new poly (aryl ether sulfone) containing 1, 3, 4-oxadiazole polymers (SPAESO). The structures of monomer BFO and copolymer were confirmed by FT-IR and 1 H NMR. The TEM pictures showed that the ion clusters were formed and distributed evenly in SPAESO copolymer matrix. The sulfonated polyoxadiazole membranes exhibited excellent thermal, dimensional and oxidative stability and lower methanol diffusion coefficient. The proton conductivity of SPAESO-3 was 7.5 × 10 −2 Scm −1 at 120 °C while the methanol permeability coefficient of SPAESO-3 was only 2.23 × 10 −7 cm 2 S −1 at 25 °C. According to the comprehensive performance, the sulfonated polyoxadiazole membranes may be the alternative materials as proton exchange membrane for PEMFC at medium-high temperature operation.
研究领域:
高分子化学
·
燃料电池技术
·
功能材料科学
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2017
·Vol. 41
·期 14
·6475-6488
·
IF 3.269
Shaojun Yuan,Jing Zhang,Zhenyi Yang,Shengwei Tang,Bin Liang,Simo O. Pehkonen
Chelating 1,2,3-triazole-4-carboxylic acids were successfully introduced onto the cross-linked PGMA microsphere surfaces by the combination of ring-opening reactions and the click chemistry process between the alkynyl groups of propiolic acid (PA) and the epoxy groups on the surfaces of the PGMA microspheres. The resultant PA-conjugated PGMA microspheres were found to be an effective adsorbent for Pb(II) removal from aqueous solutions. Success in each functionalization step was ascertained by ATR-FTIR, XPS and SEM characterization. Batch and column adsorption experiments were performed to determine the adsorption kinetics, adsorption isotherms and thermodynamics of Pb(II) ions on the as-synthesized microspheres. The Langmuir-fitted maximum adsorption capacity for Pb(II) ions was found to be 69.41 mg g−1 at a solution pH of 5.0, together with the adsorption equilibrium being achieved within 60 min. The thermodynamic studies demonstrated an endothermic and spontaneous adsorption process of Pb(II) ions on the PA-conjugated PGMA microspheres. Column adsorption studies revealed the decrease in the adsorption capacities of the breakthrough and exhaustion points with increasing flow rate. The postulated adsorption mechanism was attributed to the electrostatic interactions from carboxylic groups and chelation or coordination of Pb(II) ions from the triazole moieties, which was facilitated to form a pluralistic potential trap for Pb(II) ions, as confirmed by XPS characterization.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2025
·
IF 2.5
Huanjing Chen,Wanqiao Bai,Hongmei Chai,Loujun Gao
To achieve the rapid and sensitive detection of trace methyl parathion (MP) in river water and edible agricultural products, the catalytic composite material zirconium hydroxide (Zr(OH)4)/zeolite imidazolate framework-90 (ZIF-90) was prepared by a one-step synthesis method. The composite was further incorporated with a conductive poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) hydrogel to prepare a modified electrode. Then, an electrochemical sensing method based on the PEDOT:PSS/Zr(OH)4/ZIF-90 composite was successfully established for the analysis and detection of MP. The component ratio of the composite material, modification amount and pH value of the detection substrate were optimized. The electrochemical properties of the composite modified electrode were evaluated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques, and the results confirmed that it had good electrochemical properties. The electrochemical response of the established sensing method to MP showed a good linear relationship in the concentration range of 1–250 µmol L−1, and its detection limit and sensitivity reached 0.74 µmol L−1 and 0.09 µA µmol−1 L−1, respectively. The interference of common coexisting ions on the detection performance of the PEDOT:PSS/Zr(OH)4/ZIF-90 modified electrode was further investigated, and it was applied for the quantitative analysis of MP in actual river water and apple samples. The electrochemical sensing method developed in this work provides a new way for the efficient detection of MP residues in environmental water and agricultural products.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2020
·
IF 8.247
Linbin Tang,Jianhua Zhang,Zhi Li,Xiaohao Liu,Qunjie Xu,Haimei Liu,YongGang Wang,Yongyao Xia,Zifeng Ma
Symmetric sodium ion full batteries with high energy density are expected to become promising storage devices. Na 7 V 4 (P 2 O 7 ) 4 (PO 4 )/C can be assembled into a high energy density symmetric full battery due to 3.85 V operating voltage as a cathode and 0.94 V operating voltage as an anode. Here, the as-prepared Na 7 V 4 (P 2 O 7 ) 4 (PO 4 )/C-GA (graphene aerogel) displays excellent electrochemical behavior as both cathode and anode . As the cathode, it can deliver a reversible capacity of 91.4 mA h g −1 at 1C (1C = 92.8 mA h g −1 ) and even shows 74 mA h g −1 capacity at 100C. Meanwhile, an ultra-long cycling property is obtained (77.2% capacity retention after 5000 cycles at 20C). As the anode, it can output 92.4 mA h g −1 at 25 mA g −1 and has a 79.2% capacity retention after 300 cycles at 50 mA g −1 . Interestingly, the symmetric full battery assembled with NVPP/C-GA outputs an initial 81.9 mA h g −1 capacity, a high 2.84 V working voltage, and 232.6 Wh kg −1 energy density at 25 mA g −1 . Therefore, our work shows potential application prospects of the symmetric full battery with Na 7 V 4 (P 2 O 7 ) 4 (PO 4 )/C-GA in energy storage systems .
研究领域:
材料科学
·
电化学
·
能源存储
✓ 已验证
DOI
高影响因子
RSC Advances
·
2025
·Vol. 15
·期 14
·10884-10895
·
IF 4.6
Yanling Wu,Xi Tang,Hui He,Qingyuan Luo,Wenkai Fu,Qinggao Hou,Haijun Zhang
Developing high-performance, multifunctional non-precious metal catalysts is essential for enhancing the efficiency of future energy utilization. In this study, four types of magnetic, recyclable Co3Fe7/CoFe2O4 incorporated porous carbon composite catalysts were synthesized using citric acid as the carbon source and ammonium chloride (NH4Cl) as the salt medium. Iron and cobalt salts, in four different proportions, were uniformly incorporated using freeze-drying technology and subsequently processed through in situ calcination. Among the synthesized catalysts, Co3Fe7/CoFe2O4@NC-1, demonstrated outstanding catalytic reduction performance, with a reaction rate constant (k) of 0.031 min−1, along with excellent cycle stability for 4-NP. The resulting Co3Fe7/CoFe2O4@NC-3 catalyst exhibited good ORR activity in an alkaline medium (Eonset = 0.99 V, E1/2 = 0.83 V, JL = −5.2 mA cm−2), along with long-term durability and resistance to methanol poisoning. These hybrid materials hold promise as non-precious metal electrocatalysts for fuel cell ORRs and introduce a new class of catalytic candidates for 4-NP reduction.
研究领域:
材料科学
·
催化化学
·
能源科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MOLECULAR THERAPY
·
2024
·
IF 12.1
Liqing Ke,Qifei He,Jing Qu,Xiyue Wang,Kaibo Li,Xun Gong,Lan Li,Jiake Xu,Qiuliyang Yu,Hao Yu,Xuefei Lin,Jian Li,Nguan Soon Tan,Wei Sun,Liang Li,Peng Zhang,Wenxiang Cheng
Despite recent advances, rheumatoid arthritis (RA) patients remain refractory to therapy. Dysregulated overproduction of angiopoietin-like protein 4 (ANGPTL4) is thought to contribute to the disease development. ANGPTL4 was initially identified as a regulator of lipid metabolism, which is hydrolyzed to N-terminal and C-terminal (cANGPTL4) fragments in vivo . cANGPTL4 is involved in several non-lipid-related processes, including angiogenesis and inflammation. This study revealed that the level of ANGPTL4 was markedly elevated in the sera and synovial tissues from patients with RA versus controls. The administration of a neutralizing antibody against cANGPTL4 (anti-cANGPTL4 Ab) resulted in the inhibition of inflammatory processes and bone loss in animal models of collagen-induced arthritis and adjuvant-induced arthritis (AIA). Transcriptomic and proteomic profiling of synovial tissues from an AIA model indicated that the anti-cANGPTL4 Ab inhibited fibroblast-like synoviocyte (FLS) immigration and inflammatory-induced osteoclastogenesis. Mechanistically, the anti-cANGPTL4 Ab has been shown to inhibit TNF-α-induced inflammatory cascades in RA-FLS through the sirtuin 1/nuclear factor-κB signaling pathway. Moreover, the anti-cANGPTL4 Ab was found to block FLS invasion- and immigration-induced osteoclast activation. Collectively, these findings identify ANGPTL4 as a prospective biomarker for the diagnosis of RA, and targeting cANGPTL4 should represent a potential therapeutic strategy.
研究领域:
免疫学
·
风湿病学
·
分子生物学
·
药理学
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）