SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2026
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IF 4.8
Jiawei Wu,Silin Yang,Yongping Li,Liwei Liu,Junle Qu,Jun Song,Jiaqing Guo
NSCDs show a 180-fold intensity change and an 80 nm polarity-induced red shift. • NSCDs target LDs and enable sustained imaging of individual LDs. • Live-cell imaging captured individual LD metabolic responses and fusion-like remodeling. Lipid droplets (LDs) undergo remodeling of their polarity microenvironment during abnormalities in lipid metabolism, accompanied by changes in LD abundance and size. However, the narrow ranges of polarity response, insufficient targeting specificity, and limited stability of existing probes hinder the dynamic and accurate monitoring of individual LDs. Here, we developed nitrogen and sulfur codoped carbon dots (NSCDs) for monitoring polarity-related microenvironmental responses of individual LDs under metabolic perturbations. NSCDs exhibited a solvent-dependent decrease in fluorescence intensity and an approximately 80 nm red shift in emission. NSCDs were rapidly internalized and preferentially localized in LDs. Nutrient deprivation and inhibition of triacylglycerol synthesis decreased area-normalized NSCDs fluorescence, whereas OA-induced lipid accumulation increased it, reflecting distinct polarity-related microenvironmental responses. Furthermore, time-lapse imaging captured local events resembling LD fusion during SR59230A treatment, accompanied by enhanced local fluorescence during these remodeling events. These results support the use of NSCDs for dynamically monitoring polarity-related microenvironmental responses of individual LDs under metabolic perturbations Download: Download high-res image (127KB) Download: Download full-size image
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高影响因子
Journal of Environmental Chemical Engineering
·
2025
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IF 7.2
Rui Li,Jingjing Peng,Fangxia Xie,Qing Xi,Jilong Qin,Houfen Li,Yawen Wang,Jianxin Liu,Xiaoli Ma,Xiuping Yue
Semiconductor photocatalytic oxygen evolution via water splitting is one of the most effective ways to address energy and environmental challenges. However, rapid recombination of photogenerated electrons and holes limits the performance of single photocatalysts. Herein, we employed a facile alcoholysis-calcination method to synthesize BiOBr/BiVO 4 S-scheme heterojunction photocatalysts through the in situ conversion of BiOBr. This preparation method ensures intimate contact between BiOBr and BiVO 4 , establishing an electronic transfer channel that reduces the charge transfer distance and enhances charge transfer capabilities. Simultaneously, we used density functional theory (DFT) calculations and in situ X-ray photoelectron spectroscopy (XPS) to analyze charge transfer behavior. The results show that the S-scheme heterojunction promotes photogenerated electrons to transfer from the conduction band (CB) of BiVO 4 to the valence band (VB) of BiOBr. This transfer process facilitates efficient charge separation and enhances the system’s redox capabilities. Under simulated sunlight irradiation, the BiOBr/BiVO 4 photocatalyst exhibits excellent photocatalytic oxygen evolution activity, with a rate of 266.38 μmol·g -1 ·h -1 and a photocurrent density of 1.8 μA·cm⁻². This corresponds to a 1.60-fold enhancement over pristine BiOBr and a 2.20-fold increase relative to BiVO 4 . Finally, the possible reaction mechanism has also been discussed. This work has provided valuable insights for the effective design of Bi-based S-scheme catalysts, which play a critical role in facilitating efficient directional transfer of photogenerated charges.
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CHEMICAL ENGINEERING JOURNAL
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2020
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IF 10.652
Yang Bai,Yanbiao Zhao,Weidong Li,Linghui Meng,Yongping Bai,Guorong Chen
The developing sulfide solid electrolyte is a promising way to overcome shuttle effect of polysulfide in the traditional liquid Li-S battery. However, an air stable sulfide solid electrolyte and competitive solid–solid interface structure must be constructed firstly. Herein, we have designed an organic–inorganic multi-scale composite electrolytes to overcome the interfacial issues of solid state Li-S batteries (SSLSBs). The organic–inorganic composite electrolyte consists of a gel polymer electrolyte (GPE) and an oxygen doped inorganic sulfide solid electrolyte. The O doped sulfide solid electrolyte improves its chemical stability and suppresses the lithium dendrites. A thin GPE film protects the crystal structural stability during cycles and greatly enhances the performance of O doped sulfide solid electrolyte due to the GPE not only constructs soft interface contact between S cathode and solid electrolyte, but also builds lithium ion transport paths by ionic liquid between them. Those SSLSBs display a very good cycling performance with the specific capacity of 1023 mAh/g after 50 cycles at 60 °C and 541 mAh/g after 150 cycles at 30 °C under same rate of 0.1 C. This study demonstrates that the development of advanced solid-state Li-S battery needs to fully integrate a number of technical advantages.
研究领域:
电化学
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材料科学
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固态电池
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能源存储
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界面化学
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纳米材料
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电极材料
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高影响因子
SOLAR ENERGY MATERIALS AND SOLAR CELLS
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2020
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IF 6.984
Xue Yu,Shuying Cheng,Qiong Yan,Junjie Fu,Hongjie Jia,Quanzhen Sun,Zhiyuan Yang,Sixin Wu
Cation substitution has an important impact on the power conversion efficiency (PCE) of Cu 2 ZnSn(S,Se) 4 (CZTSSe) solar cells. Herein, a significant PCE enhancement of flexible indium-doped CZTSSe solar cells has been achieved by partially substituting Sn 4+ with In 3+ . Systematic measurements indicate that In doping in CZTSSe film effectively improves the crystallinity and carrier concentration of the absorber layer . Meanwhile, the treatment reduces interface recombination and band tailing by passivating deep defects and increases the open-circuit voltage ( V oc ) of the solar cells. By physical analysis, the key parameters for the solar cell diode such as A , J 0 , R s and R sh are significantly improved after In-doping, indicating better PN junction quality. Under the optimal In-doping (x = In/(Sn + In) = 9%), the flexible Cu 2 ZnSn 1- x In x (S,Se) 4 solar cell has been successfully obtained with the best efficiency of 7.19% and the V oc enhancement of 62 mV due to reduced V oc deficit and band tailing.
研究领域:
材料科学
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半导体物理
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光伏技术
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无机功能材料
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能源材料
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高影响因子
PEST MANAGEMENT SCIENCE
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2023
·Vol. 79
·期 8
·2713-2724
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IF 4.1
Lang Ming,Yuan-Wen Du,Ge-Ge Yuan,Qi Su,Xiao-Bing Shi,Huan Yu,Gong Chen
Background Herbivore-induced plant volatiles (HIPVs) are important self-defense outputs of pepper plants to resist insect pests. Ascoviruses are pathogenic to the larvae of most lepidopteran vegetable pests. However, whether Heliothis virescens ascovirus 3h (HvAV-3h)-infected Spodoptera litura larvae can change pepper leaf HIPVs is not well understood. RESULTS Spodoptera litura larvae preferred S. litura -infested leaves, and this preference was stronger with longer duration of S. litura infestation. In addition, S. litura larvae significantly chose pepper leaves damaged by HvAV-3h-infected S. litura over the healthy pepper leaves. Results also showed that S. litura larvae preferred leaves mechanically damaged and treated with oral secretions from HvAV-3h infected- S. litura larvae in a simulation test. We captured the volatiles emitted by leaves under six treatments. Results showed that the volatile profile changed with the different treatments. Testing of volatile blends, prepared to the proportion released showed that the blend from simulated HvAV-3h-infected S. litura larvae-damaged plants was the most attractive to S. litura larvae. Further, we also found that some of the compounds significantly attracted S. litura larvae at specific concentrations. CONCLUSION HvAV-3h-infected S. litura can alter the release of HIPVs in pepper plants and thus become more attractive to S. litura larvae. We speculate that this may be due to alterations in the concentration of some compounds (such as geranylacetone and prohydrojasmon) affecting the behavior of S. litura larvae. © 2023 Society of Chemical Industry.
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高影响因子
Food Science and Human Wellness
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2023
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IF 7
Linglin Fu,Rongrong Wang,Jinru Zhou,Chong Wang,Yanbo Wang
N -glycans in many proteins are of great concern because of their strong association with food allergies. Triticum aestivum (bread wheat), a major food crop, is known as one of the “Big Eight” allergenic groups. However, little research has been done about N -glycans in wheat glycoproteins. In this study, a soluble wheat glycoprotein was purified from wheat and further identified as globulin-1 S allele (GSA). The wheat GSA displayed significant IgE-binding activity. Moreover, one N -glycosylation site and 6 kinds of N -glycans were identified by mass spectrometry, including 3 high mannose types and 3 complex types. Furthermore, the IgE-binding activity of wheat GSA is proved to be reduced by the removal of N -glycan, thermal treatment (temperatures > 80 °C), and strong acidic treatment (pH 3.0). These findings would provide a better understanding of the effects of N -glycosylation, thermal treatment, and acidic treatment on the molecular characteristics of GSA, and further provide new insights into the development of hypoallergenic wheat products.
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高影响因子
JOURNAL OF POWER SOURCES
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2023
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IF 9.2
Hongjiao Wang,Wenzhi Li,Lilin Wu,Bai Xue,Fang Wang,Zhongkuan Luo,Xianghua Zhang,Ping Fan,Laurent Calvez,Bo Fan
The solid/liquid Li-S battery shows promise in solving both the polysulfide “shuttle effect” in liquid batteries and the interfacial contact in all-solid-state batteries. However, increasing the interfacial stability of the electrolyte and the solid electrolyte remains a challenge in the solid/liquid batteries. In this work, a high ionic conductivity Li 3 PS 4 solution is synthesized using a nano-Li 2 S precursor, which is then utilized to form a solid electrolyte Li 3 PS 4 @Li 7 P 3 S 11 via dip-coating. The Li 3 PS 4 @Li 7 P 3 S 11 can form a dense protective interface Li 3 PS 4 -DME with the DOL/DME and DME electrolyte. This interface can prevent direct contact between the solid electrolyte and the electrolytes, efficiently inhibiting further solid electrolyte decomposition. The lithium symmetric battery with the solid electrolyte Li 3 PS 4 @Li 7 P 3 S 11 is cycled stably for 1000 h, at a current density of 0.38 mA cm −2 and a capacity of 1.51 mA h cm −2 . The Li-S battery with the solid electrolyte Li 3 PS 4 @Li 7 P 3 S 11 can cycle stably for 300 cycles at 0.2C with a capacity of 600 mA h g −1 remaining.
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高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
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2023
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IF 22.1
Yi Yang,Jingjing Liu,Miaoli Gu,Bei Cheng,Linxi Wang,Jiaguo Yu
Coupling photocatalytic H 2 O 2 evolution with simultaneous furfuryl alcohol oxidation can avoid the slow water oxidation reaction and fully utilize photogenerated carriers to produce valuable chemicals. Herein, a COF (denoted as BTTA) was synthesized by the Schiff-base condensation and in-situ grown on the surface of TiO 2 nanofibers. The resultant TiO 2 /BTTA composite has a large interface and a short carrier migration distance. Furthermore, the porous and ultrathin BTTA layers endow the composites abundant active sites and excellent light absorption ability. Remarkably, a H 2 O 2 -evolution rate of 740 μmol L −1 h −1 and a furoic alcohol conversion of 96 % are achieved. In-situ irradiated X-ray photoelectron spectroscopy and electron spin resonance confirm the S-scheme carrier transfer mechanism, which spatially separates photogenerated carriers with strong redox power. This work opens a new door to the rational design of S-scheme photocatalysts for economic and green photosynthesis of H 2 O 2 and organic compounds.
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高影响因子
Journal of Water Process Engineering
·
2023
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IF 7
Junhui Yi,Runkun Xie,Ruilong Liu,Minghao Li,Haoxian Zeng,Qingqing Chen,Linxuan Cai,Ning Li,Changlin Yu,Zhenghui Liu,Dehao Li
The problem of environmental pollution caused by the frequent use of antibiotics has attracted extensive attention. The heterojunction composed of various bismuth oxyiodide (such as BiOI, Bi 4 O 5 I 2 , Bi 5 O 7 I, etc.) were widely used in the treatment of antibiotic wastewater. Herein, a hollow BiOI/Bi 5 O 7 I hierarchical microsphere was constructed in-situ by annealing BiOI precursors synthesized by the solvothermal method. The phase transition temperature for the formation of heterojunctions has been investigated in detail. The obtained products were characterized by various technologies including transmission electron microscope (TEM), X-ray photon-electron spectroscopy (XPS), and so on. Experimental results suggested that 390-BiOI/Bi 5 O 7 I microsphere with hollow structure exhibits the optimal performance and maximum photocurrent response under visible light irradiation. The efficiency for degradation of tetracycline hydrochloride (TH) was up to 83 % in 100 min. The value still maintained at 95 % after the catalyst has been reused for four times. The capture experiment indicates that produced ·O 2 − played the most important role. But formed h + and ·OH played a secondary role. The degradation intermediates were analyzed by Liquid Chromatography-Mass Spectrometry (LC-MS). Accordingly, the possible degradation pathways are proposed. An S-scheme based heterostructure photocatalytic mechanism is proposed aiming to explain the enhanced catalytic performance. The BiOI/Bi 5 O 7 I heterojunction with exceptional activity and stability is bound to expand applications in the field of water treatment .
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高影响因子
ELECTROCHIMICA ACTA
·
2023
·
IF 6.6
Chunyan Fan,Zehao Zang,Xiang Li,Junfang Zhang,Ping Yang,Lanlan Li,Xiaofei Yu,Xiaojing Yang,Zunming Lu,Xinghua Zhang
Transition metal hydroxides have superior oxygen evolution reaction (OER) activity but poor hydrogen evolution reaction (HER) performance, which greatly limits the water splitting for hydrogen production. Herein, copper modification of sulfur doped Co(OH) 2 hybrid catalyst (Cu@S-Co(OH) 2 ) was prepared by one-step of electrodeposition method which can serve as efficient hydrogen evolution reaction catalyst. In the presence of sulfur and copper, Cu@S-Co(OH) 2 hybrid catalyst exhibits the best catalytic activity, showing ultralow overpotential of 42 mV at a current density of 10 mA cm −2 . Compared with Co(OH) 2 , the overpotential is improved by nearly 100 mV as well as enhanced stability. In addition, the active site poison experiments proved that the active center is cobalt metal. Combined with the adsorption strength of the catalyst for OH and H species, it is considered that both S and Cu can enhance the adsorption of OH for Co(OH) 2 , while S is contributed to the adsorption of H, and Cu can promote the desorption of H. This work provides a facile method and new insight to enhance the HER activity for transitional metal hydroxides via metal and non-metallic elements co-modulation.
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高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2023
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IF 6.1
Chao Hu,Yu-Xi Liu,Shi-Pang Zhang,Ya-Qi Wang,Ping Gao,Yu-Ting Li,Xue-Qing Yang
Aryl hydrocarbon receptor (AhR) enhances insect resistance to insecticides by regulating the detoxification network. Our previous studies have confirmed that overexpressions of cytochrome P450 monooxygenases (P450s) and glutathione S-transferases (GSTs) are involved in lambda-cyhalothrin resistance in Cydia pomonella. Here, we report that CpAhR regulates the expression of GST and P450 genes, thus conferring resistance. Expression patterns indicated that the expression of CpAhR was highly induced by lambda-cyhalothrin exposure and upregulated in a lambda-cyhalothrin-resistant population. RNA interference (RNAi) of CpAhR decreases the expression of key resistance-related genes (CpGSTe3, CpCYP9A121, and CpCYP9A122) and the activity of the GST enzyme, reducing the tolerance to lambda-cyhalothrin. Furthermore, β-naphthoflavone, a novel agonist of AhR, was first proven to be effective in increasing CpAhR expression and larval tolerance to lambda-cyhalothrin. These results demonstrate that CpAhR regulates the expression of key detoxifying genes and GST activity, resulting in the development of resistance to lambda-cyhalothrin in C. pomonella.
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高影响因子
Journal of Materials Chemistry C
·
2022
·Vol. 10
·期 48
·18164-18173
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IF 8.067
Weifeng Kong,Zipeng Xing,Hang Zhang,Bin Fang,Yongqian Cui,Zhenzi Li,Peng Chen,Wei Zhou
A hollow polyhedral structure can effectively capture light and facilitate carrier separation, thus enhancing photocatalytic performance. Herein, hollow cubic CdS@CoS/WS2 dual S-scheme heterojunction superstructure photocatalysts are fabricated using a simple sulfidation and hydrothermal method. CdS@CoS/WS2 with a band gap of 1.59 eV and a relatively narrow band gap broadens the photoreaction to the near-infrared region and shows a good photothermal effect, which can promote photocatalytic reactions. It shows a relative specific surface area of 91.58 m2 g−1, which provides abundant surface-active sites to enhance the photocatalytic reaction. Under light conditions, the photocatalytic degradation ratios of CdS@CoS/WS2 for tetracycline and bisphenol A are up to 98.9 and 99.1%, and the hydrogen evolution efficiency is also up to 10.62 mmol h−1 g−1. The enhanced photothermal–photocatalytic performance could be due to the formation of a dual S-scheme heterojunction superstructure that facilitates space charge separation, a narrow band gap and a mesoporous hollow structure promoting solar light utilization, providing abundant surface-active sites and enhanced mass transfer. This simple strategy provides a new idea for the construction of high-performance hollow superstructure photocatalysts.
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