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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

ReS2/f-MWCNTs heterojunction for highly selective triethylamine gas sensor working at room temperature: A combined experimental and DFT study

Zhihua Zhao,Shuhan Chen,Qingsheng Shi,Chao Qiu,Lan Wu,Xinhao Zhang,Peijuan Wu,Longqi Yao

People pay more and more attention to their own health and environmental safety, which makes the monitoring and treatment of harmful amines such as triethylamine (TEA) emitted in the industrial process increasingly critical. In order to address this issue, we focus on the heterostructure construction of two-dimensional rhenium disulfide (ReS 2 ) and acid-functionalized carbon nanotubes (f-MWCNTs), using their unique electronic properties and high specific surface area for triethylamine gas detection. The findings demonstrated that, at room temperature (25°C), the ReS 2 /f-MWCNTs sensor's response to 100 ppm TEA reached 63 %. Under the same environmental conditions (25℃), the response value of the ReS 2 sensor to 100 ppm TEA is 6 %, and the sensing performance is improved by more than 10 times. In addition, the sensor has fast response recovery (73 s/46 s) and good repeatability and stability. Based on this research, we designed a simple detection device, providing a direction for the practical detection application of TEA sensors.

✓ 已验证 产品关联 DOI 高影响因子
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CHEMICAL ENGINEERING SCIENCE · 2025 · IF 4.3

Catalytic host material of NbSe2@f-Nb2C heterostructure with built-in electric field for high performance aqueous Cu-Se battery

Zhaohua Jiang,Shiyuan Fan,Huiting Xu,Huibin Liu,Sai Dong,Jing Li,Xiaoteng Yan,Zhijie Cui,Wenchao Peng,Wen Liu,Jiapeng Liu

Aqueous copper-selenium (Cu-Se) battery based on conversion mechanism have garnered interest due to their intrinsic safety features and high specific capacity. However, the slow conversion kinetics presents a challenge for its development. Herein, catalytic host material of NbSe 2 @few-layered Nb 2 C (NbSe 2 @f-Nb 2 C) heterostructure with built-in electric field (BIEF) is prepared by in situ selenization strategy for aqueous Cu-Se battery. Benefiting from the high electrical conductivity of f-Nb 2 C MXene, the high electrocatalytic performance of NbSe 2 and the spontaneous BIEF between NbSe 2 and f-Nb 2 C MXene, the Se redox reactions kinetics is enhanced and the reaction barrier is reduced. Consequently, the specific capacity of Se/NbSe 2 @f-Nb 2 C cathode can reach 1128 mAh g −1 at 0.25 A g −1 with stable cycling performance. Additionally, the conversion mechanism is investigated via comprehensive characterizations and density functional theory calculations. This study provides an innovative approach for designing high performance MXene-based catalytic host materials to enhance the conversion kinetics of aqueous Cu-Se batteries.

CAS / MDL: 7664-39-3
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ACS Catalysis · 2025 · IF 13.1

Constructing f-p-d Orbital Coupling Using Cu-Doped Frustrated Lewis Acid–Base Pairs in CeO2 to Boost CO2 Electroreduction

Fang Huang,Aihao Xu,Xiangyu Chen,Huanhuan Sun,Siyu He,Dong Wei,Boran Wang,Anxiang Guan,Xucai Yin,Jing Xu,Huibing He

The direct electrocatalytic conversion of carbon dioxide to methane using water as a medium is a reliable way to store intermittent renewable energy and solve environmental problems. However, in such multielectron/proton transfer reactions, the role of water is often overlooked. Specifically, the sluggish kinetics of water dissociation limit the effective proton supply during methane formation. Here, we propose a copper-doped CeO2 catalyst with frustrated Lewis pairs (FLPs), which can effectively reduce carbon dioxide to methane. Combined experimental analysis and theoretical calculations reveal that the synergistic interaction between Cu and FLPs forms an f-p-d gradient orbital coupling system, which significantly promotes water dissociation to generate active protons and optimizes the adsorption behavior of the *H and *COOH intermediates. Even at the large current density of −273 mA cm–2, the Faraday efficiency of Cu/CeO2-FLPs for methane was as high as 78.0%, with a conversion frequency of 15784.1 h–1 in the flow cell. This work provides a strategy for the rational design of efficient multipoint catalytic systems.

CAS / MDL: 12125-02-9 64-17-5
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ChemNanoMat · 2022 ·Vol. 8 ·期 6 ·e202200085 · IF 3.82

Electrodeposition of Amorphous Fe−P Shell on Co(OH)F Nanowire Arrays for Boosting Oxygen Evolution Electrocatalysis in Alkaline Media

Yang Gu,Chuqian Meng,Shuyue Dong,Hexin Zhu,Qian Liu,Yonglan Luo,Qingquan Kong,Tingshuai Li

High-performance earth-abundant electrocatalysts for oxygen evolution reaction (OER) are highly desirable. In this report, we successfully synthesized amorphous Fe−P shell electrodeposited on Co(OH)F nanowire arrays supported on titanium mesh (Fe−P@Co(OH)F/TM) as an efficient catalyst for OER. Such catalyst exhibits excellent OER activity with a low overpotential of 267 mV to reach the geometrical current density of 10 mA cm −2 in 1.0 M KOH. In addition, it has good electrochemical durability to maintain its activity for at least 20 h.

✓ 已验证 DOI 高影响因子
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Enhancing Ionic Conductivity and Electrochemical Stability of Li3PS4 via Zn, F Co-Doping for All-Solid-State Li–S Batteries

Yuan Gao,Jing Gao,Zhibin Zhang,Yue Wu,Xiaolin Sun,Fuhua Zhao,Yuan Zhang,Depeng Song,Wenyan Si,Qing Zhao,Xun Yuan,Jianfei Wu

Sulfide solid-state electrolytes have garnered considerable attention owing to their notable ionic conductivity and mechanical properties. However, achieving an electrolyte characterized by both high ionic conductivity and a stable interface between the electrode and electrolyte remains challenging, impeding its widespread application. In this work, we present a novel sulfide solid-state electrolyte, Li3.04P0.96Zn0.04S3.92F0.08, prepared through a solid-phase reaction, and explore its usage in all-solid-state lithium sulfur batteries (ASSLSBs). The findings reveal that the Zn, F co-doped solid-state electrolyte exhibits an ionic conductivity of 1.23 × 10–3 S cm–1 and a low activation energy (Ea) of 9.8 kJ mol–1 at room temperature, illustrating the aliovalent co-doping’s facilitation of Li-ion migration. Furthermore, benefiting from the formation of a LiF-rich interfacial layer between the electrolyte and the Li metal anode, the Li/Li3.04P0.96Zn0.04S3.92F0.08/Li symmetrical cell exhibits critical current densities (CCDs) of up to 1 mA cm–2 and maintains excellent cycling stability. Finally, the assembled ASSLSBs exhibit an initial discharge capacity of 1295.7 mAh g–1 at a rate of 0.05 C and at room temperature. The cell maintains a capacity retention of 70.5% for more than 600 cycles at a high rate of 2 C, representing a substantial improvement compared to the cell with Li3PS4. This work provides a new idea for the design of solid-state electrolytes and ASSLSBs.

✓ 已验证 DOI 高影响因子
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SEPARATION AND PURIFICATION TECHNOLOGY · 2023 · IF 8.6

Enhanced charge separation and O2 activation over an anion-rich photocatalyst Ba3(BO3)(CO3)F for metronidazole removal in water

Lidan Xie,Wenyi Huang,Guoqiang Jiang,Yi Liu,Mude Zhu,Yi Tang,Xueqin Chen,Xiaoyun Fan

The wide occurrence of metronidazole (MNZ) in aquatic environment has aroused increasing concern to the potential adverse effects on human health. Combining different motifs into a photolytic material to achieve high photocatalytic efficiency is regarded as one of the main strategies during photocatalytic process. Herein, a triple anions contained photocatalyst , Ba 3 (BO 3 )(CO 3 )F (BBCF), exhibited excellent removal efficiency of MNZ (92.6%) in 15 min, which was 5.87 times higher than that of commercial P25. The excellent removal efficiency could be attributed to the strong electronegativity of the F − , and the π-conjugated triangles structure of (BO 3 ) 3− and (CO 3 ) 2− , which made BBCF facilitate the transport of photogenerated electrons, thus accelerating the accumulation of active h + . Meanwhile, the appropriate reduction potential of BBCF accounted for the outstanding productivity of O 2 – . h + and O 2 – were proved as the dominant reactive species for MNZ degradation. The degradation products were analyzed by LC-TOF-MS, and the toxicity of the intermediate was evaluated to be lower than that of parent MNZ molecule. Moreover, BBCF showed the universal application of degrading oxytetracycline (OTC), methylene blue (MB). Therefore, anion-rich BBCF catalyst with high catalytic activity has a potential application prospect for degrading harmful pollutants in practical water environment.

✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2016 · IF 4.803

A thermostability gel polymer electrolyte with electrospun nanofiber separator of organic F-doped poly-m-phenyleneisophthalamide for lithium-ion battery

Weimin Kang,Nanping Deng,Xiaomin Ma,Jingge Ju,Lei Li,Xiaohong Liu,Bowen Cheng

In this study, the F-doped poly-m-phenyleneisophthalamide (PMIA) solution was synthesized by low temperature polymerization method and spun to be three-dimensional nanofibrous membranes by electrospinning. The Energy Dispersive X-Ray Spectroscopy and Fourier Transform Infrared Spectroscopy investigations verified that F was successfully doped in PMIA membrane. The X-ray diffraction patterns showed the crystallinity degree of PMIA membrane decreased with the addition of F. The morphology, pore size and aperture distribution tests manifested that the average diameter of F-PMIA fibers became finer and their distribution was more uniform than these of PMIA fibers. The electrolyte uptake, preserving liquid electrolyte, thermal stability and shrinkage resistance of the F-dopoed membrane were also significantly enhanced than that of pure PMIA membrane. The F-PMIA membrane could be acted as matrix to prepare gel polymer electrolyte. Finally, the F-doped PMIA membrane was used in the assembled coin cells to test the properties including the electronic conductivity , battery interfacial characteristics, electrochemical stability windows and cycle performances of battery. The lower electronic conductivity and interfacial resistance , higher electrochemical stability window (5.7   V) of F-doped PMIA membranes were obtained when comparing to the pure PMIA and commercial polyethylene membrane. The cell exhibited high first-cycle discharge capacity with 145   mAh   g −1 and excellent cycling stability with good capacity retention of 93.1% and coulombic efficiency of 99.3% after 100 cycles.

✓ 已验证 DOI 高影响因子
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JOURNAL OF LUMINESCENCE · 2022 · IF 4.171

Versatile phosphor-in-glass based on Sn–F–P–O matrix with ultra-high color rendering for white LEDs/LDs

Chenfei Xiang,Xiuping Wu,Yanjie Zhang,Zihan Zhao,Desheng Li,Hao Song,Bing Li

White light with excellent color rendering property has been highly required for comfortable and healthy illumination. A facile strategy to achieve high color rendering index (Ra >90) in practical applications is using near ultraviolet chips as excitation sources combined with RGB phosphors. However, achieving high color rendering with both blue chips and near-ultraviolet (NUV) chips for commercial phosphors dispersed in phosphor-in-glass (PiGs) materials is still a big challenge. In this work, the PiG based on the ultra-low melting point Sn–F–P–O glass with commercial green (Lu 3 Al 5 O 12 :Ce 3+ ) and red (Sr x Ca 1-x AlSiN 3 :Eu 2+ ) phosphors has been successfully fabricated by one-step sintering method. The phase identification and distribution of monochromatic red phosphor in glass (R-PiG) and green phosphor in glass (G-PiG) were investigated in detail. The Sn 2+ ions in Sn–F–P–O matrix show the intense blue emission bands centered at 420 nm under the excitation of NUV chips (365 nm). Notably, the polychromatic red/green phosphor in glasses (R/G-PiGs) are versatile and exhibited excellent color rendering (Ra = 93, Ra = 95, Ra = 92, respectively) properties excited by both blue chips, NUV chips and laser diodes (WLD). The working temperature of R/G-PiGs is stable at ∼33 °C and ∼55 °C when employed in WLEDs/WLDs (1 W), which greatly prevented the phenomenon of “thermal quenching” for the phosphors caused by high temperature. Thus, the versatile R/G-PiG with ultra-high color rendering and excellent thermal properties indicates its promising application in high-power white LEDs/LDs.

✓ 已验证 DOI 高影响因子
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PEST MANAGEMENT SCIENCE · 2024 ·Vol. 80 ·期 10 ·5026-5034 · IF 3.8

Efficacy of steam and diatomaceous earth dust against the tropical bed bug Cimex hemipterus (F.) under laboratory and field conditions

Delong Kong,Ying Xie,Zitong Wang,Daxia Shi,Qiling Liang,Min Fan,Lingling Lyu,Xu Xu,Hui Guo,Chunsheng Jia,Changlu Wang,Desen Wang

BACKGROUND Over the past two decades, bed bugs ( Cimex spp.) have resurged as common urban pests around the world. The search for efficient and safe control measures has become a key interest among researchers, manufacturers, and pest control professionals. In this study, we evaluated and compared the efficacy of steam, diatomaceous earth (DE) dust, and a combination of both against tropical bed bugs ( Cimex hemipterus (F.)) under laboratory and field conditions. RESULTS In the laboratory study, the mortality of bed bugs after 2 days of exposure to DE dust was 100%. When bed bugs stayed on the surface of an object or in cracks, a brief steam treatment (1 s) caused 100% mortality. However, when bed bugs were hidden under a fabric cover, steam application for 10 s only caused 89 ± 6% mortality. Bed bugs that survived steam treatment exhibited reduced feeding activity. In a 14-week long study, there was no significant difference in the reduction rate of bed bugs between steam treatment and DE dust treatment. A 37-week long control study showed that steam and steam plus DE dust treatments eliminated 97–100% of the infestations. CONCLUSION Applying steam and DE dust are effective strategies for eliminating natural tropical bed bug infestations. Continuous follow-up monitoring and treatment until no bed bugs are found are crucial in completely eliminating the infestation of tropical bed bugs. © 2024 Society of Chemical Industry.

✓ 已验证 DOI PubMed 高影响因子
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GREEN CHEMISTRY · 2025 · IF 9.2

Enhanced electrocatalytic CO2 reduction to methane via synergistic Sb and F dual-doping on copper foil under pulsed potential electrolysis

Kuan Wang,Xue Jiang,Xin-Peng Li,Zhe Cao,Zhen-Hong He,Weitao Wang,Huan Wang,Xiaojuan Lai,Zhao-Tie Liu

The electrocatalytic reduction of carbon dioxide (CO2) to methane (CH4) represents a promising strategy for carbon utilization, however, achieving high selectivity and efficiency remains a significant challenge. Herein, a copper foil-based catalyst with abundant interfaces was synthesized through electrodeposition to achieve Sb and F dual doping on the copper surface (CuSbF-ED), enabling efficient methane production through pulsed CO2 electrolysis. Under the pulsed electrolysis condition, the CuSbF-ED catalyst achieved a remarkably high CH4 Faradaic efficiency of approximately 92.6% and a partial current density of 60.3 mA•cm-2 at an overpotential of -1.2 V vs RHE, representing significant advancement over the static electrolysis performance of pristine copper foil. The in situ infrared spectroscopy results revealed an enhanced coverage of key intermediates *CHO on the CuSbF-ED surface during pulsed electrolysis. Theoretical calculations further confirmed that the CuSbF-ED structure with Sb and F dual doping stabilizes *CO intermediates and promotes the formation and adsorption of *CHO intermediates. Under the pulsed electrolysis conditions, the stabilized Cu species on CuSbF-ED surface facilitate the further conversion of adsorbed *CHO and *CH2O intermediates by deep hydrogenation processes toward high CH4 selectivity. The present research highlights Sb-F dual doping combined with pulsed potential electrolysis as a promising approach for the efficient and selective electroreduction of CO2 to CH4, contributing to sustainable carbon management

CAS / MDL: 10025-91-9 1341-49-7
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COMPOSITES PART B-ENGINEERING · 2025 · IF 14.2

Enhanced electromagnetic wave absorption in (SiO2–C)f/(CrZrHfNbTa)C–Si3N4–SiBCN composite by defect engineering and gradient permittivity modulation

Yang Hu,Dewei Ni,Bowen Chen,Feiyan Cai,Xiaoyu Wang,Yanmei Kan,Yusheng Ding,Shaoming Dong

Structure and stealth integrated materials that simultaneously deliver mechanical loading and broadband electromagnetic wave (EMW) absorption performance are critical for next generation stealth aircraft. Although conventional carbon fiber reinforced ceramic matrix composites (C f /CMCs) exhibit outstanding load-bearing capacity, their inherent EMW reflection characteristics often fail to meet stealth requirements. This work proposes a multiscale design strategy synergizing microscopic defect engineering with macroscopic gradient permittivity modulation. Accordingly, (SiO 2 –C) f /(CrZrHfNbTa)C–Si 3 N 4 –SiBCN composite featuring self-adaptive impedance matching and multi-mechanism EMW absorption were successfully constructed. The material demonstrates acceptable load-bearing capacity (101 ± 5 MPa) while achieving a remarkably high effective absorption bandwidth (EAB) per unit thickness (2.68 GHz mm −1 ). More importantly, radar cross section (RCS) simulations reveal that the sample achieves a remarkable RCS reduction of 35.52 dB m 2 . This surpasses most reported materials system, demonstrating high practical application potential. Density functional theory calculations reveals that defect engineering (lattice distortion and point defects) in the sample constructs new polarization centers at the microscopic level, which significantly enhances polarization relaxation loss for improved EMW absorption. On the other hand, macroscopic structural design (SiO 2f -C f -SiO 2f ) significantly optimizes the impedance matching, which effectively broadens EAB. The multiscale design strategy overcomes the inherent conflict between strong EMW reflection and attenuation in carbon fibers, which provides a novel material solution for stealth aircraft.

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CHEMOSPHERE · 2017 · IF 4.208

Spectroscopic and molecular modeling approaches to investigate the interaction of bisphenol A, bisphenol F and their diglycidyl ethers with PPARα

Jie Zhang,Tiehua Zhang,Tianzhu Guan,Ping Ruan,Dayong Ren,Weichang Dai,Hansong Yu,Tiezhu Li

A fluorescence polarization (FP) assay for the simultaneous determination of bisphenol A (BPA), bisphenol F (BPF), bisphenol A diglycidyl ether (BADGE) and bisphenol F diglycidyl ether (BFDGE) was developed. The method was based on the competition between bisphenols (BPs) and fluorescein-labeled dexamethasone derivative (Dex-fl) for mouse peroxisome proliferator-activated receptor α ligand binding domain (mPPARα-LBD). A recombinant soluble protein derivative mPPARα-LBD* was prepared, then in vitro binding of 4 BPs to mPPARα-LBD* was investigated. Fluorescence polarization assay showed that these compounds exhibited different binding potencies with mPPARα-LBD*. Additionally, molecular dynamics simulations were performed to further understand the mechanism of BPs binding affinity for mPPARα-LBD*. Docking results elucidated that the driving forces for the binding of BPs to mPPARα-LBD* were predominantly dependent on hydrophobic and hydrogen-bonding interactions. Comparison of the calculated binding energies vs. experimental binding affinities yielded a good correlation (R 2  = 0.7258). The proposed method has potential for multi-residue detection of BPA, BPF, BADGE, and BFDGE.

✓ 已验证 DOI PubMed 高影响因子
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