JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2026
·
IF 4.6
Jinling Wu,Runmiao Chen,Pengjing Yin,Yuanzhen Zhou,Jieli Tang,Chengbin Du,Qi Xue
S-modified MnO 2 /Ni(OH) 2 hollow nanosheets were constructed for enhanced UOR. • Requires 1.30 V at 10 mA cm −2 and remains stable for 48 h. • MnO 2 phase transformation promotes the generation of Ni 3+ active species. • S-modification enhances urea adsorption while suppressing competitive OH − adsorption. The urea oxidation reaction (UOR) provides an alternative anodic process for electrochemical hydrogen generation, but developing catalysts with high activity and sustained performance remains challenging. In this study, we report an S-modified nickel-based catalyst with a hollow nanosheet architecture (α/γ-MnO 2 /Ni(OH) 2 -S), demonstrating enhanced UOR performance in alkaline media. α/γ-MnO 2 /Ni(OH) 2 -S attains a current density of 10 mA cm −2 at a potential of 1.30 V and maintains reliable durability for 48 h without significant degradation. The improved activity and durability are associated with the hollow nanosheet structure, the phase transformation of MnO 2 , and S-modification, which facilitate mass transport and charge transfer, modulate the electronic structure of Ni(OH) 2 to promote the formation of Ni 3+ active species, and enhance the electrochemical response to urea at different concentrations. This research establishes a practical avenue for constructing advanced nickel-based UOR catalysts through rational structural optimization, phase regulation, and surface modification. Download: Download high-res image (125KB) Download: Download full-size image
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高影响因子
CHEMICO-BIOLOGICAL INTERACTIONS
·
2026
·
IF 5.2
Xuguang Mi,Jianhua Fu,Lei Liu,Lingshan Wang,Shiling Chen,Mengxue Wu,Chunxue Niu,Yan Wang,Lixin Cao,Lin Wang,Ling Deng,Xiaodan Lu,Xiuying Lin
Bisphenol S (BPS), as an environmental pollutant, poses a potential threat to reproductive system health. In this study, we added BPS to primary human endometrial stromal cells (hEnSCs) to detect the acute injury it causes and its long-term effects on the endometrium. The results showed that short-term treatment with BPS can significantly promote oxidative stress and apoptosis of hEnSCs, while long-term treatment can cause excessive senescence of hEnSCs and reduced receptivity. In addition, the culture medium of senescent cells treated with BPS can induce senescence of young hEnSCs. Studies have reported that secondary senescence can be alleviated, and we utilised the autophagy activator Rapa to treat secondary senescence of hEnSCs. We found that Rapa can inhibit the senescence of young cells induced by the culture medium of senescent cells treated with BPS. Therefore, autophagy activated by Rapa can attenuate the secondary senescence of hEnSCs induced by BPS-treated culture medium.
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PubMed
高影响因子
ADVANCED FUNCTIONAL MATERIALS
·
2026
·
IF 19.9
Sibo Wang,Yue Zhang,Wanlong Wu,Quanwei Jiang,Hua-Yu Shi,Xiaoqi Sun
Aqueous Zn─S batteries are promising energy storage systems with high theoretical capacity and low cost. However, the direct conversion between S and ZnS at the cathode suffers extremely sluggish reaction kinetics, which further decay rapidly upon the increase of current density and active material loading. Facing these challenges, we herein present a bi-directional redox mediator strategy and identify a self-adjusted Cu-based candidate. It possesses two redox couples whose potentials are on either side of the thermodynamic redox potential of S/ZnS reaction while between its kinetic oxidation and reduction potentials. These alignments enable the bi-directional mediator to catalyze the charge and discharge processes using either redox couple, respectively. As a result, the sulfur cathode reaches a high capacity of 1629 mAh g −1 at 0.1 A g −1 . It also maintains 880 mAh g −1 after 500 cycles at 1 A g −1 , superior to rapid decay to 148 mAh g −1 after only 28 cycles with the mediator free cathode. Furthermore, with a high sulfur loading of 7.3 mg cm −2 and lean electrolyte of 7 µL mg S −1 , the Zn─S battery achieves a high areal capacity over 10 mAh cm −2 .
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Yunchang Fan,Yafang Tian,Lei Yang,Yanhe Nie,Xinjia Wei,Haibao Zhu
Two types of poly(ionic liquids) (PILs), namely linear PILs (LPILs) and reticulated cross-linked network PILs (RPILs), were synthesized and evaluated for the adsorption of gold thiosulfate complex ([Au(S 2 O 3 ) 2 ] 3− ) from thiosulfate solutions. Experimental results showed that the adsorption of [Au(S 2 O 3 ) 2 ] 3− on the PILs followed the pseudo-second-order kinetic model, indicating that the adsorption process was dominated by chemical adsorption. In terms of adsorption thermodynamics, the bromide-based LPIL fitted the Hill adsorption model, whereas the other PILs followed to the Freundlich model. The main interactions between the PILs and [Au(S 2 O 3 ) 2 ] 3− were electrostatic attraction and anion – π interactions, and ion exchange dominated the gold adsorption process. The RPILs exhibited higher gold adsorption capacities than the LPILs. However, gold desorption was more readily achieved with LPILs, primarily owing to their weaker affinity for gold species. In addition, the perchlorate-based LPIL showed good adsorption selectivity and recyclability toward [Au(S 2 O 3 ) 2 ] 3− . This study provides a promising strategy for the efficient separation and recovery of gold from thiosulfate media.
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高影响因子
VETERINARY MICROBIOLOGY
·
2026
·
IF 2.8
Leyu Hu,Lexi Gao,Xingwei Fu,Zesheng Rong,Yue Cheng,Yuhan Hou,Lu Han,Xin Ran,Guiwen Guan,Ting Zhou,Lingling Chang,Xiaomin Zhao,Qian Du,Yong Huang,Dewen Tong,Mingjun Zhu
PEDV infection induces intracellular iron accumulation in host cells. • Iron promotes CoV replication by enhancing Fe-S cluster-dependent RdRp activity. • TEMPOL suppresses CoV replication by disrupting viral Fe-S cluster integrity. • TEMPOL exhibits broad-spectrum anti-CoV activity in vitro and in vivo. • TEMPOL effectively counteracts iron-exacerbated viral pathogenesis in vivo. Coronaviruses (CoVs) can cause severe respiratory and enteric diseases, posing major threats to human health and the livestock industry. However, the host metabolic mechanisms underlying viral replication remain unclear. Using porcine epidemic diarrhea virus (PEDV) as the primary model, this study investigated the role of iron metabolism in CoV replication and its mechanisms. Our results showed that PEDV infection markedly induced intracellular iron accumulation, while exogenous iron supplementation enhanced viral replication and iron chelation suppressed it. Mechanistically, iron enhances viral replication by promoting the formation of iron-sulfur (Fe-S) clusters, essential cofactors for the viral RNA-dependent RNA polymerase (RdRp). Based on these findings, we further evaluated the antiviral activity of TEMPOL, a small molecule targeting viral Fe-S clusters. TEMPOL reduced RdRp activity and effectively inhibited PEDV replication. Moreover, TEMPOL exhibited broad-spectrum antiviral activity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), infectious bronchitis virus (IBV), and porcine deltacoronavirus (PDCoV). Importantly, TEMPOL effectively reversed FAC-promoted viral pathogenesis, alleviating tissue lesions and clinical symptoms across multiple CoV animal models. Collectively, this study reveals a key role of iron metabolism in CoV replication and suggests that targeting viral Fe-S clusters may provide a novel strategy for anti-CoV therapy against diverse CoVs.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Feng Zhu,Haibin Niu,Xiaoming Li,Shaoqing Zhang,Xiutao Yang,Hongwen Yu,Guopeng Zhu
Hydrogen production via photocatalytic water splitting holds great promise for efficient solar energy conversion. While ZnIn₂S₄ (ZIS) exhibits a suitable band structure for visible-light-driven hydrogen production, its practical application is significantly limited by low charge separation efficiency and poor stability. This work pioneers an acousto-hydrothermal strategy utilizing high-frequency ultrasonic atomization to synthesis structurally optimized ZIS. Systematic characterization reveals that ultrasonic cavitation compresses crystal lattices to enhance Zn 3d-S 3p orbital hybridization, assembles nanosheets with a 20 % increased surface area, leading to enhanced charge separation efficiency. The optimized ZIS demonstrates significantly enhanced photocatalytic activity and stability. It achieves a remarkable hydrogen evolution rate of 51.8 mmol g⁻¹ h⁻¹ under 455 nm visible light irradiation, representing an 86 % improvement over pristine ZIS. After a 15 h reaction, the catalytic system produces 8.3 mmol of H₂ (185.9 mL at standard conditions). This work presents an innovative strategy for designing nanosheet-based materials to achieve high-efficiency photocatalytic hydrogen evolution.
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高影响因子
ACS Sustainable Chemistry & Engineering
·
2021
·
IF 8.198
Hongbing Song,Yongjie Wang,Yule Liu,Lei Chen,Bingxiao Feng,Xin Jin,Yu Zhou,Tingting Huang,Meng Xiao,Fangmin Huang,Hengjun Gai
Three ionic liquid (IL) monomers consisting of one, two, and four benzene rings were designed with 2-phenylimidazole and polymerized with α,α′-dichloro-p-xylene (DCX) and formaldehyde dimethyl acetal (FDA) to form a series of novel poly(ionic liquid)s (PILs). In this process, the designed ILs were employed as active ionic sites, and DCX and FDA were selected as cross-linkers. Self-condensation of the cross-linker provided a large specific surface area for the hypercross-linked organic framework, while co-condensation between the cross-linker and IL introduced active sites to the framework. The obtained porous hypercross-linked PILs not only promoted CO2 capture and the selective absorption of CO2/N2 but also showed good activity for the cycloaddition of epoxide with CO2. HP-[BZPhIm]Cl-DCX-1 with a large surface area (763 m2·g–1) showed a CO2 uptake capacity of 1.47 mmol·g–1 and offered a 98.9% yield of the CO2 cycloaddition product with epichlorohydrin at 80 °C for 24 h under 0.1 MPa CO2 pressure. The designed PILs provide an important reaction for CO2 utilization.
研究领域:
材料科学
·
催化化学
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高影响因子
Small Methods
·
2026
·
IF 9.1
Pengfei Sun,Shu Zhang,Chengdong Fang,Qingquan Lin,Liubin Feng,Jiajia Chen
In this work, an agarose-polyacrylamide hydrogel electrolyte (APE) with an interpenetrating and hierarchically porous network is introduced to reconstruct solvation and interface dynamics for a high-performance Zn-S batteries. This structure results in a high ionic conductivity of 42.1 mS cm −1 and a Zn 2+ transference number of 0.64. Molecular dynamics reveal that most H 2 O and SO 4 2− are excluded from the outer Helmholtz plane, forming an optimized electric double layer on Zn surface. Consequently, a prolonged 1200 h Zn plating/stripping behavior is obtained with 1 mAh cm −2 at 1 mA cm −2 , and a high Zn plating of 20 mAh cm −2 at 5 mA cm −2 . Furthermore, APE modulates the nucleation mode of ZnS, converting the originally sluggish and non-uniform progressive nucleation into a rapid and uniform instantaneous nucleation. As a result, this hydrogel Zn-S batteries deliver a capacity of 895 mAh g −1 and 91% capacity retention within 300 cycles at 5 A g −1 .
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PubMed
高影响因子
Journal of Energy Storage
·
2026
·
IF 9.8
Ting Liu,Menghui Yin,Beibei Li,Salifu Nasir,Qiang Chen
The accelerating demand for sustainable, high-rate, and durable energy storage underscores the need for carbon electrodes that simultaneously offer balanced micro–mesoporosity for rapid ion transport and robust heteroatom functionalities for enhanced interfacial chemistry. In the present work, we convert bitumen asphaltenes and recycled cellulose acetate into N/S co-doped hierarchical carbons via ammonium persulfate-assisted co‑carbonization and KOH activation. The optimized carbon combines an ultrahigh specific surface area of 3527 m 2 g −1 , balanced micro–mesoporosity, and uniformly distributed electroactive N/S species (pyridinic/pyrrolic N, C S, SO x ), enhancing conductivity and pseudocapacitance. In three-electrode tests, the electrode delivered 382.5 F g −1 at 0.5 A g −1 with 74% retention at 10 A g −1 . The symmetric aqueous device achieved a specific capacitance of 288.2 F g −1 at 0.5 A g −1 , energy densities of 10.01 Wh kg −1 at 257.4 W kg −1 and 5.42 Wh kg −1 at 6728.3 W kg −1 , and 108.7% capacitance retention after 10,000 cycles at 5 A g −1 . This study advances sustainable energy storage by enabling low-cost, high-performance supercapacitors and promoting solid-waste recycling.
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高影响因子
ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Bo Wang,Wei Guo,Yongzhu Fu
Lithium–sulfur (Li–S) batteries are promising to enable high-energy-density storage systems; however, their commercialization is hampered by several technical challenges such as polysulfide shuttle and safety issues related to the lithium metal anode. Herein, we use anodized aluminum oxide (AAO) membranes as separators in Li–S batteries for the first time. AAO membranes are rigid and nonflammable, which is helpful for improving battery safety. The aligned and uniform channels within AAO membranes provide fast pathways for lithium ion transport, leading to low areal specific resistance due to the electroosmotic flow of lithium ions in nanoscaled channels. In addition, the AAO separator leads to low overpotential during lithium deposition/stripping in lithium symmetric cells. The Li–S cells with AAO separators show better cycling performance than those with Celgard ones, in particular, at high C rates. At the 2 C rate, the cell shows a battery performance of 480 cycles with a capacity degradation rate of 0.105%, which is much better than that when the Celgard separator is used. This work demonstrates that AAO membranes are promising separators with unique properties for improving the performance of Li–S batteries.
研究领域:
材料科学
·
能源存储
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高影响因子
INTERNATIONAL JOURNAL OF ENERGY RESEARCH
·
2022
·Vol. 46
·期 14
·19480-19492
·
IF 4.672
Jiuqing Liu,Fanli Zeng,Meng Liu,Junying He,Qihou Li,Feifei Song,Zikun Hong,Ya Chen,Lishun Bai,Chen Cheng,Zehao Chen
Summary As one of the most promising energy storage systems, the application of lithium sulfur battery is hindered by low ionic conductivity, poor thermal stability, and a serious shuttle effect of polysulfide species of commercial polyolefin separators. Herein, a kind of novel porous polyetherimide (PEI) based separator (IAPEI-4) with excellent heat resistance and electrochemical properties was prepared. Briefly, by grafting amino group (–NH 2 ) onto the surface of SiO 2 , highly dispersed amino-functionalized SiO 2 (A-SiO 2 ) were synthesized as fillers to blend PEI matrix. Based on physical characterizations of the representative IAPEI-4 separator, abundant micropores and mesopores exist in the separator, and A-SiO 2 nanoparticles are uniformly distributed in the PEI matrix. The ameliorated Li + transport channels and the uniform distribution of A-SiO 2 nanoparticles endow IAPEI-4 separator with higher ionic conductivity (1.60 mS cm −1 ) and Li + transfer number (0.63). Besides, the IAPEI-4 separator exhibits good electrochemical stability and excellent thermal stability (no shrinkage at 200°C). The Li-S cells with the IAPEI separator also show greatly enhanced electrochemical performances. After 100 cycles, its specific discharge capacity can reach 695.4 mAh g −1 at 0.2 C and its capacity retention rate is 84.8%. This simple and effective separator modification method can provide a general strategy to achieve high-performance Li-S batteries.
研究领域:
材料科学
·
能源存储技术
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高影响因子
Solar RRL
·
2019
·Vol. 4
·期 1
·1900410
·
IF 0
Qiong Yan,Shuying Cheng,Xue Yu,Hongjie Jia,Junjie Fu,Caixia Zhang,Qiao Zheng,Sixin Wu
Partial cation substitution is an effective way to inhibit defects and carrier recombination, which can improve the efficiency of Cu 2 ZnSn(S,Se) 4 (CZTSSe) solar cells. Herein, flexible Cu 2 Zn 1− x Cd x Sn(S,Se) 4 ( x = 0–15%) solar cells are fabricated on Mo foils with partial Cd substitution for Zn via a green solution-process. The best device performance can be achieved when Cd/(Zn + Cd) = 8%, with an efficiency up to 6.49% and a significantly improved device repeatability. The E U decreases from 24 to 15 meV, indicating that antisite defects and band tailings are effectively suppressed. C – V data reveal that W d and V bi are enhanced after doping Cd, resulting in a stronger built-in electric field which facilitates Fermi-level splitting and hence increases band bending of the absorber toward the junction interface. Furthermore, the mechanism of current shunting is studied using an equivalent circuit model with three parallel current pathways to fit J – V curves. The key parameters for the solar cell diode such as A , J 0 , and R sh are significantly improved by partially substituting Zn with Cd, demonstrating that current shunting loss is suppressed and the junction quality is improved, resulting in a significant improvement in device repeatability.
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