APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING
·
2025
·Vol. 131
·期 10
·1-14
·
IF 2.8
Ning Qiyun,Li Bingwei,Zhou Wang,Xu Xiaoting,Li Jun
In this study, Bi₂O₂Se nanosheets were synthesized via a hydrothermal method, and a Bi₂O₂Se/WSe₂ heterostructure was subsequently constructed using a mechanical compounding approach to develop a photoelectrochemical photodetector. By optimizing the mass ratio and KOH electrolyte concentration, the Bi₂O₂Se/WSe₂ heterostructure exhibited optimal performance at a 7:1 ratio in 0.1 M KOH. Benefiting from the interfacial heterojunction between the two materials, the Bi₂O₂Se/WSe₂ heterostructure achieved a photocurrent density of -2.74 µA/cm² under zero external bias, representing an order-of-magnitude enhancement compared to pristine Bi₂O₂Se nanosheets. Concurrently, the rise time was significantly reduced from 0.86 s to 0.28 s, And the decay time decreased from 4.85 s to 0.32 s, demonstrating superior self-powered characteristics. Furthermore, the Bi₂O₂Se/WSe₂ heterostructure exhibited a maximum photoresponsivity of 61 µA/W. The optimized Bi₂O₂Se/WSe₂ photodetector showed no notable performance degradation during a 10,000 s cyclic on/off illumination test. This work highlights the immense potential of the Bi₂O₂Se/WSe₂ heterostructure-based self-powered photodetector in delivering exceptional self-driven functionality, outstanding optoelectronic properties, and robust stability for practical applications.
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Advanced Energy Materials
·
2023
·Vol. 13
·期 27
·2300746
·
IF 27.8
Yaoshen Niu,Zilin Hu,Bo Zhang,Dongdong Xiao,Huican Mao,Lin Zhou,Feixiang Ding,Yuan Liu,Yang Yang,Juping Xu,Wen Yin,Nian Zhang,Zhiwei Li,Xiqian Yu,Hao Hu,Yaxiang Lu,Xiaohui Rong,Ju Li,Yong-Sheng Hu
Na-ion batteries (NIBs) are promising for grid-scale energy storage applications. However, the lack of Co, Ni-free cathode materials has made them less cost-effective. In this work, Mg 2+ is successfully utilized to activate the oxygen redox reaction in earth-abundant Fe/Mn-based layered cathodes to achieve reversible hybrid anionic and cationic redox capacities. A high first charge capacity of ≈210 mAh g −1 with balanced charge–discharge efficiency is achieved without O-loss, showing a promising energy cost of $2.02 kWh −1 . Full cell against hard carbon anode without pre-sodiation shows energy density exceeding ≈280 Wh kg −1 with a decent capacity retention of 85.6% after 100 cycles. A comprehensive analysis of the charge compensation mechanisms and structural evolution is conducted. Voltage and capacity loss resulting from partially reversible Fe 3+ migration to the Na layer is confirmed, shedding light on further improvements for low-cost NIB cathodes in application scenarios.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2025
·
IF 21.1
Ye Chen,Xiaokang Sha,Junpo Guo,Xupo Liu,Meinan Chang,Jiayao Qiu,Jingru Zhang,Bowen Cai,Jiashu Tang,Yi Liu,Huaiyu Shao,Deli Wang
Rational design of heteroatom-doped catalysts with prominent reaction kinetics holds immense potential for enhancing biomass electrooxidation processes. Here, we introduce a F-doped NiO nanosheet architecture enriched with F-Ni δ+ -O coordination motifs as an advanced electrocatalyst for the oxidation of 5-hydroxymethylfurfural (HMF). XPS depth profiling and differential charge density calculations reveal that the distinctive F-Ni δ+ -O configuration induces asymmetric charge redistribution at Ni sites, effectively reducing the activation energy for Ni 3+ OOH species and their subsequent interaction with HMF. Meanwhile, pH-dependent and in-situ Raman measurements demonstrate that F sites function as proton relays, facilitating proton transfer and enabling efficient proton-coupled electron transfer kinetics. The synergistic electronic and proton effects endow excellent catalytic performance, with an oxidation current density of 66.45 mA cm −2 and a reaction rate of 5.23 × 10 −4 s −1 , far higher than that of the original NiO. Notably, the catalyst retains over 95 % Faradaic efficiency and yield of 2,5-furandicarboxylic acid (FDCA) after twenty consecutive cycles. This work establishes a dual regulation strategy via heteroatom doping to simultaneously modulate electronic configuration and proton transfer dynamics, offering novel insights into the design of high-performance electrocatalysts for biomass valorization.
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ADVANCED FUNCTIONAL MATERIALS
·
2022
·Vol. 32
·期 30
·2202245
·
IF 19.924
Tingting Liang,Xiaqing Zhang,Lijun Su,Ruilin Hou,Bingjun Yang,Junwei Lang,Shengrong Yang,Xingbin Yan
Perovskite materials can store charge through rapid oxygen anions intercalation. Although numerous perovskite materials owing to rich selections of A and B-site elements are reported as electrodes of supercapatteries, the effect of the crystal structure of perovskite materials on their electrochemical performance has never been studied so far. Herein, using SrCo 0.9 Mo 0.1 O 3− δ , SrFeO 3− δ , Ba 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3− δ , and LaMnO 3− δ as research targets, it is proved that their corresponding cubic structure materials display the best electrochemical performance. And then, the origin of such superiority of cubic structure for SrCo 0.9 Mo 0.1 O 3− δ is explored through experimental investigations and theoretical calculations. The results show that the increase in the content of oxygen vacancies and the enhancement of B-O hybridization of cubic structure can optimize the electronic structure of the perovskite materials, thereby improving its conductivity and accelerating the reaction kinetics. The filtering strategy based on crystal structure proposed by this report will provide a new perspective to faster and more efficient choice of perovskite materials for supercapatteries.
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JOURNAL OF THE ENERGY INSTITUTE
·
2024
·
IF 5.6
Ruotong Cui,Wenlong Xu,Feng Liu,Lei Yu,Jiming Liu,Xi Chen,Yingyun Qiao,Yuanyu Tian
The structure and reactivity of coal is the core problem of coal chemistry, and solving it at the molecular level has been an international unsolved problem. The chemical similarity-based coal chemistry group elevates the study from the macroscopic to the molecular level. However, the previous free radical mechanism lacks experimental confirmation and theoretical computational support. Here, the pyrolysis products of model compounds are first utilized to predict pyrolysis. The hydrogen-donating solvent is then used as a radical trap to confirm the reaction. Subsequently, density functional theory calculations are utilized to aid in the validation. Finally, family components are utilized to demonstrate the universality of the free radical mechanism of coal pyrolysis. This work combines radical trapping with quantum chemical calculations to analyze the radical reaction mechanism of coal pyrolysis in depth at the molecular level. This will provide a theoretical basis for coal pyrolysis and clean and efficient utilization.
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Journal of Environmental Chemical Engineering
·
2024
·
IF 7.4
Haimei Zhong,Yiwen Wang,Qinliang Jiang,Huali Tian,Cheng Jiang,Pei Han,Yingying Qin,Lixiang Li,Shuanglin Gui
The trade-off between permeability and selectivity, along with the issue of membrane fouling, has constrained the widespread application of ultrafiltration (UF) membranes in recycling rare earth wastewater. Here, we present the incorporation of tannic acid (TA) modified molybdenum disulfide oxide (O-MoS 2 ) as a functional enhancer to fabricate polyethersulfone (PES) based mixed matrix membranes through a nonsolvent induced phase separation (NIPS) approach. Compared to the unmodified PES membrane, the integration of TA-O-MoS 2 significantly improves the hydrophilicity, porosity in the mixed matrix membrane. By altering the concentration of TA-O-MoS 2 , the TA-O-MoS 2 /PES UF membrane achieves enhanced hydrophilicity and charge properties, resulting in a remarkable improvement in separation performance. Specifically, the optimized membrane M2 (TA-O-MoS 2 addition of 0.1 wt%) exhibits a water flux of 140.98 Lm −2 h −1 bar −1 and a PEG 20000 rejection rate of 91.00 %, representing increases of 180 % and 120 % over the control PES membrane, respectively. Notably, membrane M2 effectively retains 91.31 % of macromolecular organic compounds in rare earth wastewater, while permitting nearly complete passage of inorganic salts, for instance CaCl 2 (3.26 %) and MgSO 4 (4.84 %). Moreover, the TA-O-MoS 2 /PES membrane demonstrates robust antifouling properties and exceptional durability, indicating its significant potential for efficient treatment and resource recovery in rare earth wastewater.
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Journal of Energy Storage
·
2024
·
IF 8.9
Qing Xu,Pengcheng Cai,Xuanyuan Ni,Yunxing Zhao,Denian Li,Yong Chen,Haoran Yuan
Electronic-double-layer supercapacitors (EDLC) usually use activated carbon with large specific surface area and abundant pore structure as the electrode active material for adsorption/desorption of electrolyte ions. Featuring huge yield, low price, multi-level structure, and inherent heteroatoms/functional groups, biomass-derived activated carbon has been demonstrating excellent specific capacitance, low electrochemical impedance, and long-term durability in supercapacitor applications. Loofah sponge is an ideal precursor for activated carbon because of its unique cross-linked parallel channel structure that facilitates ion transfer and storage in supercapacitor. Upon pre‑carbonization combined with KHCO 3 -incorporated activation pyrolysis in this study, the loofah sponge is transformed into a three-dimensional hierarchical porous structured carbon (LC-K1–800), while retaining the primary skeleton and heteroatoms (oxygen and nitrogen) of the biomass. The specific capacitance of LC-K1–800 at a current density of 0.2 A g −1 is measured to be 344 F g −1 , and that at a current density of 1 A g −1 is 296 F g −1 . Moreover, the symmetric two-electrode device assembled by the LC-K1–800 has a specific capacitance of 216 F g −1 at the current density of 0.2 A g −1 and a capacitance retention rate of 103.4 % after 10,000 charge/discharge cycles at the current density of 10 A g −1 , showcasing exceptional cycling stability. Additionally, the symmetric supercapacitor assembled with 1 M Na 2 SO 4 electrolyte has achieved an energy density of 18 Wh kg −1 in a 1.6 V voltage window. The impressive performance of the LC-K1–800 assembled EDLC is derived from the well-developed hierarchical porous structure, robust carbon skeleton, high specific surface area, as well as the superior hydrophilicity of loofah sponge-derived activated carbon. This work provides an outstanding option for high-performance and cost-effective carbon-based EDLC.
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ChemistrySelect
·
2025
·Vol. 10
·期 37
·e02789
·
IF 2
Li Zhong,Yuxin Duan,Meiying Wang,Xiao Xu,Minghuan Qian,Xu Jia
The polymers of N , N -diethylacrylamide (DEA) exhibit temperature-dependent sensitivity attributable to the presence of both hydrophilic and hydrophobic groups. However, their lower critical solution temperature (LCST) is only 25 °C, a limitation that restricts their practical applications. Previous studies have shown that the incorporation of cationic monomers for copolymerization can enhance the LCST of polymers. In this study, dimethyldiallylammonium chloride (DMDAAC) and DEA were selected for copolymerization to obtain a series of thermosensitive water-soluble polymers, poly(DMDAAC- co -DEA). Structure and properties were characterized using FT-IR, 1 H NMR, TG-DSC, and surface tension test. Combined with the critical phase transition mechanism, it was determined that the hydrophilicity of the polymer underwent a gradual increase in proportion with the increase of DMDAAC blocks in polymers, and the LCST exhibited an increase of up to 36.8 °C. The relationship between polymer structure and demulsification performance was also explored, as represented by the application of O/W emulsion. The experimental findings demonstrated that all poly(DMDAAC- co -DEA) products exhibited effective demulsification performance. The demulsification rate of the polymers with 30%, 50%, and 70% of DMDAAC could reach 97.03%, 98.20%, and 98.40% respectively, which shows great potential for the petroleum demulsification application. Graphical Water-soluble polymer Poly(DMDAAC- co -DEA) are synthesized using a three-step heating method. A comprehensive investigation is conducted into the relationship between its LCST and copolymerization ratio, resulting in the elucidation of the underlying mechanism. Furthermore, the demulsifying properties of the copolymer are investigated.
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ACS Applied Energy Materials
·
2025
·
IF 5.5
Zhen Wang,Yunhao Wu,Jianjian Zhong,Jianling Li
Two-dimensional transition metal carbide/nitride MXenes have become a hot topic in the field of lithium-ion energy storage due to their unique surface chemistry and excellent electronic conductivity. However, electrodes made of multilayer MXenes suffer from low capacity, poor cycling performance, and slow lithiation kinetics. In this paper, the MoP2@Ti3C2Tx composite was prepared by adsorbing Mo cations on the surface of Ti3C2Tx followed by phosphatization. The uniformly distributed MoP2 nanostructure effectively increases the layer spacing, enlarges the specific surface area, and improves the structural stability of the material. At the same time, MoP2 and Ti3C2Tx are connected by a P−O bond, which accelerates the diffusion and migration of lithium ions and the charge transfer, and the strong covalent Ti−O−P bond can cause rapid charge transfer and stabilize the structure of the material. The electrochemical activity of MoP2 nanostructures also provides more active sites for lithium ions. The presence of the lamellar structure of Ti3C2Tx also inhibits to some extent the expansion of the transition metal phosphide volume with the cycling process, thus realizing more excellent lithium storage capacity. 1/2 MoP2@Ti3C2Tx material has a high reversible capacity of 165.7 mAh g−1 (172% improvement over the original material) at a current density of 3000 mA g−1. The assembled 1/2 MoP2@Ti3C2Tx//AC Li-ion hybrid capacitor LIC has 85.5% capacity retention after cycling at a current density of 1500 mA g−1. The ability of the assembled full battery to illuminate light-emitting diode (LED) light bulbs further confirms that the electrochemical reliability of the device meets the requirements of real-world applications. The results demonstrate that the strategy of constructing in situ-grown MoP2 nanostructures can effectively improve MXene high-energy-density applications in lithium-ion energy storage.
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FOOD CHEMISTRY
·
2025
·
IF 9.8
Tao Chen,Changdong Lin,Weihang Lu,Shuo Wang,Cheng Shen,Juyuan Luo,Yulin Li
In the present study, six 7- O -glycosyl acylation of flavonoids derived from lutonarin and saponarin were obtained from barley seedlings by medium-pressure LC, high-speed counter-current chromatography and preparative HPLC guided by UPLC-QTOF-MS/MS. Their inhibitory effects on α-glucosidase were investigated. Structure–activity relationship showed 7- O -glycosyl acylation enhanced inhibitory effect on α-glucosidase with coumaroyl > feruloyl > hydroxybenzoyl > sinapoyl. The IC₅₀ values for saponarin and its four acylated products were 802.4 ± 0.48 μg/mL, 374.6 ± 0.16 μg/mL, 461.6 ± 0.27 μg/mL, 523.8 ± 0.24 μg/mL and 585.8 ± 0.42 μg/mL, respectively. Steady-state fluorescence spectroscopy revealed 7- O -glycosyl acylation enhanced the fluorescence quenching rate of α-glucosidase. Molecular docking revealed 7- O -glycosyl acylation formed more hydrogen bonds and hydrophobic interactions with α-glucosidase. Synchronous fluorescence spectroscopy showed all compounds altered the hydrophobic microenvironment surrounding the tryptophan residues in α-glucosidase. Circular dichroism spectroscopy indicated 7- O -glycosyl acylation modified the conformation and secondary structure of α-glucosidase.
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高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2019
·
IF 3.571
Yu Lu,Jie Liu,Yue Jia,Yuerong Yang,Qinghui Chen,Lujia Sun,Shuang Song,Linjuan Huang,Zhongfu Wang
Human milk oligosaccharides are complex carbohydrates with multibiofunctional health benefits to newborns. Human milk free oligosaccharides (HMOs) are well characterized. However, changes in the N/O-glycome during lactation are poorly reported. Herein, we qualitatively and quantitatively investigated N/O-glycome profiles and their alteration in human milk at different lactation stages. N-Glycans were mainly fucosylated and nonsialylated, nonfucosylated throughout lactation. O-Glycans mainly consisted of sialylated and nonsialylated, nonfucosylated in colostrum and transitional milk, and fucosylated and nonfucosylated, nonsialylated in mature milk. Fucosylated and sialylated N-glycans gradually decreased and increased, respectively, as lactation progressed; O-glycans showed the reverse. Interestingly, changes in HMO abundance decreased during lactation, complementing HMG N/O-glycome changes. In conclusion, temporal HMG glycosylation changes provide the groundwork for developing infant formula that is closer to breast milk at different lactation stages.
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高影响因子
MICROCHIMICA ACTA
·
2024
·Vol. 191
·期 11
·1-11
·
IF 5.3
Zhu Guancheng,Zou Jiahui,Lin Xueer,Zhong Huimin,Jiang Cong,Huang Yanyan
By self-assembly of MnCl 2 and arginine under alkaline conditions, ultra-small MnArg nanoparticles were successfully constructed as oxidase (OXD) mimics for intelligent detection of the Ginkgo toxin 4′- O -methylpyridoxal (MPN). The obtained MnArg nanozymes possessed excellent OXD-like activity and thermal stability. Based on the inhibitory effect of MPN for the catalytic activity of MnArg, this system was utilized for the colorimetric sensing of MPN with a low limit of detection (LOD) of 2.16 µg mL −1 . The detection system exhibited good selectivity against other potential interferents. FTIR data showed that the presence of MPN binds with MnArg and shields the active sites, thereby interfering with the oxidase-like activity. Combined with a smartphone and the ColorMax software, this nanozyme-based intelligent detection platform could effectively detect MPN with a LOD of 2.1 µg mL −1 . Our MnArg nanozyme–based system was applied to detect real ginkgo nut samples with recoveries of 92.4–108.7%, and the relative standard deviations were less than 0.7%. This work may promote the development of novel nanozymes and expand their applications in the field of food safety detection. Graphical Abstract
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高影响因子
危险品化学品经营许可证（带存储）