INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY
·
2026
·
IF 5.7
Gaolei Bai,Jing Gao,Shizi Zhang,Liumi Meng,Ren Chu,Jichang Zhang,Lijuan Luo,Lingyan Jiang
The search for natural and safe alternatives to synthetic fungicides is crucial for controlling postharvest anthracnose in papaya, a disease primarily caused by Colletotrichum species. This study identifies Bacillus cereus ZW21 as a potent biocontrol agent and delineates the mechanism of its volatile organic compounds (VOCs) directly in a fruit system. In vivo assays on papaya fruit demonstrated that ZW21 VOCs significantly reduced lesion area and disease incidence by up to 80.95% and 70.46%, respectively. Bioactivity-guided identification revealed hydroxyacetone (HA) and 3-methyl-3-buten-1-ol (ME) as the key antifungal VOCs. These compounds exhibited direct antifungal activity by disrupting fungal membrane integrity, inducing mitochondrial dysfunction, and elevating reactive oxygen species. Beyond direct inhibition, transcriptomic analysis of treated fruit revealed that HA and ME activated host defense pathways, including phenylpropanoid biosynthesis and hormone signaling, while suppressing ripening-related metabolism. A critical distinction was observed: ME enhanced glycolysis and pyruvate metabolism, providing a mechanistic explanation for potential phenolic overflow and fruit blackening, whereas HA avoided this metabolic overdrive. Our findings not only validate the efficacy of a novel biocontrol strain and its defined VOCs but also provide a comprehensive mechanistic framework supporting their application for sustainable postharvest protection.
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高影响因子
MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Shimeles Addisu Kitte,Fuad Abduro Bushira,Tesfaye Refera Soreta
Efficient coreactants are of high importance in electrochemiluminescence sensing. Herein, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide was demonstrated as an effective coreactant for tris(2,2′-bipyridine)ruthenium(II) electrochemiluminescence system for the first time. The new electrochemiluminescence system showed a good sensing performance for H 2 O 2 on the basis of quenching of the electrochemiluminescence intensity. It allows the detection of H 2 O 2 in the dynamic range of 0.5–200 µM. The limit of detections for H 2 O 2 was 0.33 µM ( 3σ/m ). In addition, the developed ECL system exhibited satisfactory recoveries for H 2 O 2 sensing in real samples.
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CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Le Gao,Yawen Li,Guifang Li,Jiaqi Huo,Lishan Jia
Interface engineering as an effective material modification method can regulate local corresponding interfacial geometry and electronic structures, thus enabling a higher intrinsic activity for the oxygen evolution reaction (OER). Herein, we carefully designed p-p heterojunction precursor Co4-MOF@La(HCO 2 ) 3 with internal electric field through electrostatic adherence, which then in-situ transformed into p-p type heterojunction electrocatalyst (Co(OH) 2 )4@La(OH) 3 under KOH activation strategy. The one-step in-situ conversion of (Co(OH) 2 )4@La(OH) 3 generated the interface with significant difference in metal atomic radius and exhibits fascinating nanostructures, which enhances the specific surface area and increases the number of active sites compared with the parent material. Impressively, the obtained material (Co(OH) 2 )4@La(OH) 3 demonstrates satisfying electrocatalytic activity in OER with a low overpotential of only 233 mV to reach a current density of 20 mA cm −2 , and excellent stability for 50 h at 10 mA cm −2 in alkaline medium. In-situ Raman technique indicates that multivalent Co centers are the true active sites during the OER process. Based on density functional theory (DFT) calculation results, La atoms possess empty d orbitals, which are beneficial to facilitate charge transfer from Co to La at the heterojunction interface. Meanwhile, the introduction of La atoms changes the coordinated environment around the adjacent atoms at the interface, which induces the upshift of the d-band center for Co atoms and increases the binding strength of the adsorbed oxygen intermediate.
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Qiu-feng Lan,Wen-chang Wang,Xiao-hui Chen,Zhi-dong Chen
The poly(3-amino-4-hydroxybenzenesulfonic acid)/Ru(bpy) 3 2+ modified glassy carbon electrode (PAHBS/Ru(bpy) 3 2+ /GCE) is a novel solid-state electrochemiluminescence (ECL) sensor. It was prepared by electropolymerization of 3-amino-4-hydroxybenzenesulfonicacid (AHBS) followed by soaking into Ru(bpy) 3 2+ solution. Ru(bpy) 3 2+ was entrapped on the electrode via the electrostatic interactions between sulfonic acid groups and Ru(bpy) 3 2+ cation. The morphology and composition of the modified electrodes were analysed using scanning electron microscope and energy-dispersed spectrum. Cyclic voltammetry and electrochemical impedance spectroscopy were used to compare the electrochemical behavior of the electrodes before and after modification. Under the optimal conditions, the ECL intensity of the quenching value (ΔECL) versus the logarithm of the concentration of malachite green (MG) was linear over a concentration range from 5.0 × 10 -8 to 1.0 × 10 -5 mol L -1 ( r = 0.9931) and the limit of detection (LOD) was 2.5 × 10 -8 mol L -1 . This method has been successfully applied to the determination of MG in pond water.
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高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2025
·Vol. 36
·期 18
·1-16
·
IF 2.8
Yang Zaizhi,Shen Yalong,Zhu Yuan,Jiang Xiaoming,Liu Rui,Yang Zhen,Wang Shouliang,Xu Dong
Flash sintering has revolutionized the field of advanced ceramic preparation with the low heating temperature and extremely short sintering time. The difference of doped ions radius can influence the defect structure and resistivity of the sample through lattice distortion, subsequently altering the parameters and dielectric properties of flash sintering samples. By flash sintering technology, co-doped TiO 2 ceramics with the acceptor ions (Mg 2+ , Ca 2+ , Sr 2+ , Ba 2+ ) and donor ions (Nb 5+ ) were successfully prepared at 1100 °C for 24 min. According to the blackbody radiation model, Mg 2+ and Nb 5+ co-doped TiO 2 ceramics exhibit the highest surface temperature at the moment of flash sintering, approximately 1852 °C. Additionally, the co-doped TiO 2 ceramics with Ba 2+ and Nb 5+ ions exhibit the strongest polarization effect, with a dielectric constant above 10 5 . The acceptor ions with larger ions increase oxygen vacancies by enhancing the stability of defect complexes. The excellent giant dielectric properties are attributed to the combined action of the electron-pinned defect dipole effect and the internal barrier layer capacitor effect.
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JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2018
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IF 2.196
Bing Jia,Liping Wang,Mengmeng Yan,Hai Liu,Yingmin Yu,Qingsong Li
Liquid–liquid equilibrium (LLE) data for ternary systems of water + 2,2,3,3-tetrafluoro-1-propanol + anisole/1-octanol were determined at temperatures of 298.2, 308.2, and 318.2 K under 101.3 kPa. The distribution coefficients and separation factors were calculated from experimental LLE data, which indicated that anisole/1-octanol extracted 2,2,3,3-tetrafluoro-1-propanol from aqueous solution with high efficiency. The consistency of the experimental LLE data was assessed by the Othmer–Tobias and Hand equations. Meanwhile, the NRTL and UNIQUAC models were successfully applied to regress and correlate the experimental data, presenting the root-mean-square deviations (RMSD) less than 1.0%. The relevant binary interaction parameters of these two models were also regressed.
研究领域:
化学工程
·
物理化学
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INORGANIC CHEMISTRY
·
2025
·
IF 4.7
Cheng Ye,Xinyu Zheng,Lingmiao Fang,Zhanpeng Fu,Di Li,Jianjun Zhu,Deli Jiang
Designing cost-effective and efficient bifunctional electrocatalysts for overall water splitting is crucial for the production of renewable energy, yet still remains challenging. Herein, we report a bifunctional electrocatalyst assembled from CoMoP nanosheets and Cr(OH)3 nanoblocks via hydrothermal and electrodeposition methods. The strong coupling interface formed between CoMoP and Cr(OH)3 not only induces the formation of d–d orbital hybridization, exposing abundant active sites and improving charge transfer efficiency, but also accelerates the reaction kinetics, forming a stable heterostructure, thereby improving the catalytic activity and stability. Meanwhile, the prepared CoMoP/Cr(OH)3/NF electrode demonstrates overpotentials of 88 mV for the hydrogen evolution reaction (HER) and 207 mV for the oxygen evolution reaction (OER) at 10 mA cm–2. Remarkably, assembled CoMoP/Cr(OH)3||CoMoP/Cr(OH)3 requires only 1.52 V at 10 mA cm–2, outperforming most reported advanced bifunctional catalysts. This study proposes a rapid and rational strategy for constructing novel bimetallic phosphide/hydroxide heterostructured electrocatalysts.
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高影响因子
JOURNAL OF CRANIOFACIAL SURGERY
·
2023
·
IF 0.9
Li Zeyu,Jiang Dongbo,Yao Yusheng
Distraction osteogenesis devices are complicated. To simplify these devices, we used 3 simple screws and 1 rubber band to realize the idea and analyzed histologic changes induced by mechanical forces. Ten female New Zealand white rabbits were studied. A left or right side of the mandible was randomly selected as the experimental side (ES). The unilateral mandible was distracted, and 2 fixation screws and 1 traction screw were implanted. When the traction screw was rotated downward, the opposite force made the osteotomy block move in opposite directions to increase the bone height. The control side (CS) was not processed. The results were assessed after 20 days of traction. Bone height in the ES increased by 5 mm. Toluidine blue staining showed that the number of osteoblasts per unit area on the ES was higher than that of the CS ( P <0.01). PerkinElmer showed that the expressions of proliferating cell nuclear antigen ( P =0.016) and collagen-I ( P =0.000) on the ES were higher than those on the CS. Transmission electron microscopy showed that the number of mitochondria, endoplasmic reticulum, and Golgi apparatus on the ES was significantly greater than the CS. The results confirmed that the 3 screws vertically increase the bone height. Mechanical force signals stimulate tissue activity and lead to significant cell proliferation and differentiation in the traction zone. Collagen-I may induce osteogenesis in the early stage of traction.
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MATERIALS LETTERS
·
2012
·
IF 2.307
Hanning Duan,Xianfeng Zheng,Songliu Yuan,Yu Li,Zhaoming Tian,Zhao Deng,Baolian Su
Organic solution-phase reaction under oxygen atmosphere for synthesis of single crystalline and uniform sub-3 nm NiO nanoparticles has been developed. Larger NiO nanoparticles with diameter about 26 nm can be also prepared by seed-mediated growth method. Optical property of the NiO nanoparticles was conducted by means of UV–vis spectrum, exhibiting obviously blue shift compared with the bulk counterpart due to the quantum confinement effect . The photocatalytic activity in degradation of rhodamine B was also investigated. The results showed that the sub-3 nm NiO nanoparticles exhibit much higher activity for UV-photodegradation than the as-synthesized larger NiO particles and commercial 30 nm nanopowder .
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ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Xiaoyi Li,Yongjian Zhou,Jiawen Tang,Siliang Zhao,Jingyong Zhang,Xiao Huang,Bingbing Tian
NASICON-type Li1.3Al0.3Ti1.7(PO4)3 (LATP) has attracted a lot of attention because of its high ionic conductivity and stability to air and moisture. However, the size effect of LATP primary particles on ionic conductivity is ignored. In this study, different sizes of LATP particles are prepared to investigate the morphology, relative density, and ionic conductivity of the LATP solid electrolyte. The influences of particle size and sintering temperature on the microstructure, phase composition, and electrical properties of LATP ceramics were systematically studied. The medium-sized LATP particle (2 μm) presents a great microstructure with a high relative density of over 97%, the highest ionic conductivity of 6.7 × 10–4 S cm–1, and an activation energy of 0.418 eV. The Li–Li symmetric cells and Li–LFP batteries delivering good electrochemical performance were fabricated with highly conductive LATP ceramics. These results make significant strides in elucidating the relationship between the particle sizes of LATP and its electrochemical performance.
研究领域:
材料科学
·
固体离子学
·
储能
·
陶瓷材料
·
电化学
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高影响因子
ACTA MATERIALIA
·
2024
·
IF 8.3
Qingjie Wang,Yongqiang Qiao,Kaiyue Zhao,Peixian Zhang,Huan Zhao,Juan Guo,Xinwei Shi,Erjun Liang,Qilong Gao
Zero thermal expansion (ZTE) materials can solve problems such as device failure and cracking caused by mismatched coefficient of thermal expansion . However, ZTE material is rare in nature. NaZr 2 (PO 4 ) 3 is a framework compound with near-zero thermal expansion due to coupled rotations of rigid ZrO 6 and PO 4 polyhedra in the structure, and several studies have been devoted to obtaining more ZTE compounds by chemical substitution of Na or Zr. Inspired by the AAV concept we proposed, in this work, the PO 4 tetrahedra with a small volume has been replaced by the large volume MoO 4 tetrahedra in K x Mn x In 2- x (MoO 4 ) 3 ( x = 0.4, 0.6, 0.8, and 1.0) compounds to provide more space for the coupling rotation of the polyhedron, and reduce the coefficient of thermal expansion. On the other hand, the flexibility of the framework structure has been modulated by the content of K + to achieve new ZTE materials, and the effects of K + content on crystal structure and thermal expansion have been analyzed in detail by combining variable temperature XRD and Raman. These findings not only provide more ZTE materials, but also suggest a promising design method for ZTE materials.
研究领域:
材料科学
·
固体化学
·
热功能材料
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高影响因子
Materials Reports: Energy
·
2022
·
IF 0
Zhanyou Xu,Yi Xie,Ying Wang
Electrochemical CO 2 reduction reaction (CO 2 RR) exhibits remarkable potential in producing valuable chemicals with renewable energy. Operating CO 2 RR in acidic media is beneficial to solve the issue of low carbon utilization brought by (bi)carbonate formation at the cathode. Suppressing the competing hydrogen evolution reaction and achieving stable CO 2 RR performance remains challenging. Herein, we constructed a 3-dimensional Cu (3D-Cu) gas diffusion electrode (GDE) to achieve efficient C 2 H 4 production with a partial current density ( j C2H4 ) of over 470 mA cm −2 and a Faradaic efficiency (FE C2H4 ) of 40%. With pause electrolysis, the decay rate of the j C2H4 is only half that of the traditional constant electrolysis. The GDE after constant electrolysis was found to suffer from severe salt formation, leading to the decreased activity and poor stability.
研究领域:
电化学
·
材料科学
·
能源化学
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