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    10 October 2026, Volume 47 Issue 10
    Contents
    Cover and Content of Chemical Journal of Chinese Universities Vol.47 No.10(2026)
    2026, 47(10):  1-6. 
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    Letter
    Bismuth/Mesoporous Carbon Material for High Performance Near-neutral Zinc-air Batteries
    CHU Yenpin, LI Yuxuan, LI Kailin, CHU Juan, LI Wei
    2026, 47(10):  20260298.  doi:10.7503/cjcu20260298
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    Near-neutral zinc-air batteries have attracted considerable attention owing to their high theoretical energy density, enhanced electrochemical reversibility and improved compatibility with practical operating environments. However, their performance remains severely constrained by sluggish oxygen-related reaction kinetics and the accumulation of insoluble discharge products, which pronounced electrochemical polarization, inefficient charge- discharge processes and unsatisfactory energy efficiency, thereby impeding their further development. Here we report a multifunctional mesoporous carbon catalyst incorporating monodisperse bismuth single atoms and bismuth clusters as an efficient air cathode for near-neutral zinc-air batteries. The atomically dispersed Bi species synergistically promote the deposition and decomposition of discharge products during cycling, thereby improving the reversibility of the cathodic processes. Moreover, the homogeneous distribution of Bi species across the catalyst surface guides the spatially uniform deposition of discharge products within the mesoporous channels, effectively mitigating pore blockage, reducing concentration gradients and suppressing electrochemical polarization. Benefiting from this rational structural and compositional design, the assembled batteries deliver a high discharge voltage of 1.28 V and an excellent energy efficiency of 84.82% at 0.1 mA·cm-2, achieve a long cycle life up to 400 h at current densities of 0.5 mA·cm-2. This rationally designed multifunctional mesoporous catalyst provides a promising strategy for regulating discharge-product chemistry and advancing high-efficiency near-neutral zinc-air batteries.

    Review
    Synergistic Regulation of Size and Structure on the Metallicity Evolution of Gold Nanoclusters
    FENG Jingqi, FAN Chunhai, CHEN Jing
    2026, 47(10):  20260067.  doi:10.7503/cjcu20260067
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    Gold nanoclusters(Au NCs) feature atomically precise structures with core sizes ranging from 1 to 3 nm, serving as a unique system that bridges organometallic molecules and conventional gold nanoparticles; combining molecular-like properties with the advantages of nanomaterials, their transition from a molecular state to a metallic state is one of the core issues in the field of nanoscience. As large-sized gold nanoclusters(containing >100 gold atoms) increase in size, their energy levels gradually shift from discrete to continuous, exhibiting metallic properties. However, this transition is not solely determined by size, and a critical size regime exists. Within this critical size regime, the clusters exhibit dual molecular and metallic properties, which are synergistically regulated by multiple factors including crystal structure and geometric morphology, and this phenomenon has been extensively and intensively investigated. This review summarizes the research progress on the metallicity evolution of large-sized gold nanoclusters, outlines the structure-activity relationships among size, structure, and metallicity for non-metallic, metallic, and critical-regime clusters, and clarifies the determination criteria and key research techniques for metallicity. Finally, the future challenges and development directions in this field are discussed.

    Articles: Inorganic Chemistry
    One-pot Preparation of Hesperetin-loaded ZIF-8 for Tumor Acidic Microenvironment-responsive Drug Release
    ZHAO Yang, ZHU Zhen, YANG Liuqing, CAO Zhanhua, ZHONG Bingwen, ZHUANG Yuan, LIU Zhihui
    2026, 47(10):  20260133.  doi:10.7503/cjcu20260133
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    Hesperetin(HES) was incorporated into the zeolitic imidazolate framework-8(ZIF-8) via a one-pot method to construct HES@ZIF-8 nanocomposites. The morphology, crystal structure, pore structure, and thermal stability were systematically characterized using scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, nitrogen adsorption-desorption, and thermogravimetric analysis. Furthermore, the drug-loading capacity and in vitro release behavior under different pH values were evaluated. The results demonstrate the construction of HES@ZIF-8, which retained the regular polyhedral morphology and characteristic crystal framework of ZIF-8 after HES loading, indicating that the introduction of HES did not disrupt the host framework structure. Changes in pore structure parameters and thermal mass loss behavior further confirmed the effective integration of HES into the ZIF-8 system, achieving a drug-loading capacity of 72.0%. In vitro drug release studies revealed that HES@ZIF-8 exhibited a pronounced pH value-dependent release profile, with cumulative release rates of 42.9%, 72.6%, and 92.9% at pH value of 7.4, 6.5, and 5.5, respectively. The significant dissociation of the particle framework under acidic conditions indicates that the accelerated release is closely related to the acid- induced structural disruption of ZIF-8. In vitro cellular experiments showed that HES@ZIF-8 possessed good biocompatibility with normal fibroblasts(L929) within a working concentration range of 0—40 μg/mL. Concurrently, the material decreased the viability of oral squamous cell carcinoma(OSCC, CAL-27) and salivary adenoid cystic carcinoma(SACC), inhibited cell migration, and promoted apoptosis, with a more pronounced effect observed in SACC cells. These in vitro findings preliminarily suggest that HES@ZIF-8 features structure-retaining loading and tumor microacidic environment-responsive release, providing an experimental basis for further research on natural small molecule/metal-organic framework composite drug delivery systems.

    Analytical Chemistry
    Quantitative Analysis of Boron Isotopes in Solution by Microwave Plasma Torch Molecular Isotopic Spectroscopy
    JIA Chenyang, LIN Genxian, JIN Wei, YU Bingwen
    2026, 47(10):  20260205.  doi:10.7503/cjcu20260205
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    To meet the demand for rapid analysis of boron isotope ratios in solution systems, this study established a microwave plasma torch molecular isotopic spectrometry(MPT-MIS) method for the quantitative determination of boron isotope ratios in solutions. The method employs a microwave plasma torch(MPT) to excite the emission spectrum of BO2 molecules and combines partial least squares regression(PLSR) to extract boron isotopic abundance from full-spectral shape, enabling rapid measurement of boron isotope ratios. The memory effect of boron was effectively reduced by using a quartz inner tube, and the spectral preprocessing methods as well as the wavelength range were systematically optimized based on leave-one-out cross-validation(LOOCV). Under the optimal preprocessing combination(first derivative+area normalization+25-point smoothing) and the optimal wavelength range(464—589 nm), only two latent variables(LVs) were needed to sufficiently extract the spectral information related to isotope abundance. On the three samples in the validation set, the maximum relative bias of the model-predicted 11B/10B ratio was 2.04%, and the prediction precision was 1%—2%(2σ). Furthermore, it was found experimentally that the BO2 molecular spectral intensity exhibited a good linear relationship with total boron concentration in the range of 5—3000 μg/mL(R²>0.999), indicating the potential of this method for simultaneous determination of total boron concentration. This provides a simple and low-cost new approach for the online simultaneous analysis of boron isotope ratios and total boron concentration in scenarios such as the nuclear industry.

    Organic Chemistry
    Design, Synthesis and Antibacterial Activities of 3-Methylcarbazole Derivatives Containing Isoxzole
    YAN Yu, LU Zicong, WANG Qing, YANG Jiaqiang
    2026, 47(10):  20260151.  doi:10.7503/cjcu20260151
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    In order to obtain antibacterial candidate compounds, natural product 3-methylcarbazole was used as a hit compound for structural modification and optimization. A series of 3-methylcarbazole derivatives containing isoxazole moieties was designed and synthesized in this study, and their structures were confirmed by means of ¹H NMR, ¹³C NMR and elemental analysis. Antibacterial activity tests showed that these compounds exhibited significant activity against S. aureus, S. epidermidis and methicillin-resistant S. aureus(MRSA), with most derivatives demonstrating superior antibacterial activity compared to 3-methylcarbazole. Among them, compound 3q was the most prominent, with minimum inhibitory concentration(MIC) values of 0.5, 1 and 2 μg/mL against the three strains, respectively. Its anti-S. aureus and anti-S. epidermidis activities were comparable to those of the control drugs, while its anti-MRSA effect was significantly superior to that of the control drugs. The time-kill curve showed that compound 3q exerted rapid bactericidal activity against S. aureus throughout its entire growth cycle at 4×MIC. Molecular docking results revealed that compound 3q exhibited favorable binding interactions with the target protein GyrB. Additionally, compound 3q showed no toxicity toward mouse mononuclear macrophages. The introduction of the isoxazole moiety can enhance the antibacterial activity of 3-methylcarbazole.

    A Schiff-base Covalent Organic Framework Fluorescent Probe for Selective Recognition of HS- and Its Application
    GE Yueqin, WANG Di, TANG Lijun, HOU Shuhua, LI Yulong
    2026, 47(10):  20260185.  doi:10.7503/cjcu20260185
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    A functionalized covalent organic framework probe, COF-TPA, was designed and synthesized for the specific recognition of HS-. The small-molecule triphenylamine derivative fluorescent probe was grafted onto a carboxyl-containing covalent organic framework(Tp-COOH COF) via EDC/NHS activation, yielding the novel probe COF-TPA. By virtue of the preorganized rigid aggregate structure of the COF framework and the extremely small ionic radius of HS-, the probe exhibited a marked fluorescence enhancement response toward HS⁻ in pure water, thereby obviating the need for organic solvents and concentration adjustment that conventional AIE probes typically require. The probe was able to effectively eliminate interference from biothiols and other anions present in food matrices, featured a wide applicable pH range(5—13), and achieved a detection limit as low as 2.62×10-7 mol/L. The results demonstrate that the probe possesses a wide linear range, a low detection limit, and high sensitivity. Satisfactory accuracy and reliability were obtained for the determination of HS- in environmental water samples and alcoholic beverage matrices, indicating its promising potential for application in food safety detection.

    Integrated Tag-assisted Continuous-flow Peptide Synthesis in Green Solvents: Circumventing Solubility Bottlenecks and Minimizing Process Mass Intensity
    YAN Yangli, LI Jinyu, QIN Shicheng, SU Xianbin
    2026, 47(10):  20260117.  doi:10.7503/cjcu20260117
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    This study reports an integrated tag-assisted continuous-flow liquid-phase peptide synthesis(CF-TAPS) platform based on a green solvent system, achieving a 3.7-fold reduction in process mass intensity(PMI) relative to the solid-phase peptide synthesis(SPPS) benchmark. The core innovation lies in a "dual-flow intensification" framework: first, a fixed-bed reactor was utilized for the efficient continuous-flow hydrogenation of the hydrophobic amino-tag carrier(BTPM), establishing the material foundation for end-to-end automation; second, a tunable binary solvent system(EA/DMSO) was synergized with a static-mixer-incorporated tubular reactor(SMTR) to ensure robust solvation and ultrafast reaction kinetics. This modular architecture integrated automated in-line membrane separation, transforming emulsion-prone washing into a high-throughput workflow and significantly compressing cycle time for coupling(52 s) and deprotection(38 s). The utility of this tag-based flow strategy was validated through the total synthesis of cell-penetrating peptide 5R, requiring only 1.05~1.2 mol of amino acids. Notably, the platform achieved a transformative 4-fold reduction in organic solvent consumption(OSC), providing a sustainable paradigm for green peptide manufacturing that effectively integrates the high atom economy of liquid-phase strategies with the automated industrial scalability of continuous processes.

    Physical Chemistry
    Cobalt Single-atom Sites for Kinetically Enhanced Rate Performance of Carbon-based Supercapacitor Electrodes
    YANG Shaoqing, ZHANG Hao, ZHANG Hanming, ZHANG Wangzhi, ZHANG Haitao, LUO Jun
    2026, 47(10):  20260201.  doi:10.7503/cjcu20260201
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    To elucidate the influence of adjacent transition-metal single-atom sites on the energy-storage kinetics of carbon-based supercapacitor electrodes, Fe and Co single-atom-modified nitrogen-doped carbon materials, denoted as Fe@NC and Co@NC, were prepared using activated carbon as the carbon substrate via a metal-ligand coordination and carbonization strategy. Nitrogen-doped carbon without metal single-atom sites was used as the control sample. Structural characterizations reveal that NC, Fe@NC, and Co@NC possess similar carbon frameworks and porous structures, while Fe and Co species are highly dispersed and anchored in the nitrogen-doped carbon matrix, forming M-N4 coordination configurations. Electrochemical measurements show that Fe@NC and Co@NC deliver higher specific capacitances than NC, indicating that the introduction of metal single-atom sites can improve the charge-storage capability of carbon-based electrodes. Fe@NC and Co@NC exhibit comparable specific capacitances at current density of 1 A/g, with values of 106 and 109 F/g, respectively. When the current density increases to 20 A/g, Co@NC retains 55% of its capacitance, markedly higher than Fe@NC(38%), suggesting that Co single-atom sites are more favorable for improving high-rate capacitance retention. Further kinetic analyses demonstrate that Co@NC possesses a higher capacitive-controlled contribution, lower charge-transfer resistance, and more favorable ion-diffusion behavior, indicating that Co single-atom sites are more effective in facilitating rapid charge/ion transport. These results reveal that the rate-performance enhancement of carbon-based supercapacitor electrodes induced by metal single-atom sites mainly originates from optimized electrochemical kinetics, with Co single-atom sites showing greater advantages in promoting fast energy storage. This study provides mechanistic insight into the regulation of rate performance in carbon-based supercapacitor electrodes through single-atom site engineering.

    Theoretical Study of the Influence of H-SAPO-34 Modified with Zn2+ on Olefin-based Cycles During Methanol-to-olefins Reaction
    GAO Fen’e, WANG Ruiying, GUO Junlan, ZHANG Xi, CHENG Shangyuan, YUAN Zhiguo, LIU Jingyao
    2026, 47(10):  20260245.  doi:10.7503/cjcu20260245
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    The reaction mechanisms of the olefin‑based cycles for ethene and propene formation at Brønsted acid sites(BAS) in H‑SAPO‑34 and at BAS and Lewis acid sites(LAS) in Zn@H‑SAPO‑34 were systematically investigated by means of density functional theory(DFT) calculations combined with microkinetic simulations, with the aim of elucidating the influence of Zn2+ modification on the catalytic performance of the methanol‑to‑olefins(MTO) reaction. The results demonstrate that the selectivity to propene based on the olefin-based cycle catalyzed by H-SAPO-34 is higher than that to ethene(consistent with the previous reports). The Zn2+ modification enhances the acidic strength of neighbouring BAS, significantly reducing the overall free energy barriers for both the ethene and propene formation pathways and improving activity. It also decreases the difference in their barriers. At LAS, the overall free energy barrier for ethene formation has been found to be slightly lower than that for propene, indicating a relative selectivity advantage toward ethene; however, both barriers are significantly higher than those at BAS, suggesting that LAS are not the dominant active sites. Further microkinetic simulations show that BAS remain the main active sites after Zn2+ modification, with total turnover frequencies(TOF) increased by 2—3 orders of magnitude compared to unmodified H‑SAPO‑34. The propene selectivity advantage is kept and the relative selectivity towards ethene increases with rising temperature. In summary, the enhancement of B-acid strength and the introduction of LAS by Zn2+ modification improve the overall catalytic activity while maintaining the propene selectivity advantage and reducing the selectivity difference between ethene and propene. This work provides theoretical guidance for the rational design of high‑performance MTO catalysts.

    Synthesis of Pure Silica ZSM-12 Zeolite and ZSM-12-supported Co Catalyst for Propane Dehydrogenation
    SHI Dao, GUO Liwen, SUN Qiming
    2026, 47(10):  20260183.  doi:10.7503/cjcu20260183
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    Propane dehydrogenation(PDH) is regarded as one of the most promising routes for propylene production owing to its advantages of high product purity and low separation energy consumption. Developing efficient and stable catalytic materials is crucial for improving PDH performance. In this work, the controllable synthesis and thermal stability of pure-silica ZSM-12 zeolite with a twelve-membered-ring pore structure were systematically investigated. By tuning the gel composition and crystallization conditions, the optimized synthetic parameters for ZSM-12 zeolite were established. In addition, the NH4+-exchanged ZSM-12 zeolite retains high crystallinity even after calcination at 1100 ℃, demonstrating excellent thermal stability. On this basis, highly dispersed Co catalyst encapsulated in ZSM-12 zeolite was successfully constructed via a ligand-protected in situ synthesis strategy. The catalyst exhibited excellent catalytic performance in PDH at 550 ℃, achieving a propylene formation rate of 16.4 mmolC3H6·gcat-1·h-1. Moreover, after a long-term reaction of 1600 min, its activity could be nearly restored to the initial level through regeneration, indicating good structural stability and regenerability. This study provides useful guidance for the design and preparation of pure silica large-pore zeolite and the development of efficient and stable PDH catalysts.

    In situ Construction of a Stable N-doped Graphene/Carbon Nanotubes Three-dimensional Host for Dendrite-free and Long-life Lithium Metal Anodes
    SHE Suhui, XIN Guoxiang, BAO Jinxiao, SUN Guangshu, WANG Haitao, SONG Jinling, WANG Qingchun, BULIN Chaoke, ZHANG Jinhui
    2026, 47(10):  20260160.  doi:10.7503/cjcu20260160
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    To suppress the growth of lithium dendrites on lithium metal anodes, this study constructs a stable three-dimensional(3D) host structure of N-doped graphene/carbon nanotubes(N-G/CNTs) designed to suppress dendrite growth and facilitate long cycle life in lithium metal batteries. The N-G/CNTs composite was prepared via chemical vapor deposition(CVD) and pyrolysis, and subsequently mechanically calendered onto a lithium foil to obtain the N-G/CNTs-Li anode. Morphological characterization reveals that slender, curved CNTs are in situ grafted onto the graphene substrate. First-principles calculations indicate that lithium preferentially nucleates and deposits on pyrrolic and pyridinic nitrogen sites. The N-G/CNTs half-cell exhibits a low nucleation overpotential of merely 21.3 mV. Furthermore, the N-G/CNTs-Li symmetric cell demonstrates stable cycling for up to 1000 h at a current density of 1 mA/cm², maintaining minimal voltage polarization throughout. Post-cycling morphology after 100 h shows a smooth and compact electrode surface, completely free of lithium dendrites. The full cell delivers a high capacity of 129.3 mA·h/g and a capacity retention of 91.5% at a 1C rate. These results collectively demonstrate that the N-G/CNTs host effectively mitigates electrode volume fluctuations and suppresses lithium dendrite growth during cycling. The excellent performance of the N-G/CNTs is attributed to the synergistic effect of the stability of the G/CNTs three-dimensional framework structure and the high content of the lithiophilic nitrogen species. Consequently, the N-G/CNTs-Li electrode holds great promise for applications in high-performance lithium metal batteries.

    Preparation of Prussian Blue Analogue-derived FeSe2/CoSe2 Composites and Their Efficient Alkaline Electrocatalytic Hydrogen Evolution Performance
    LU Ting, LIU Lu, WANG Leifei, YANG Yang, LIU Zechang, WANG Juntao, YUN Sining
    2026, 47(10):  20260141.  doi:10.7503/cjcu20260141
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    Using a coprecipitation method combined with a selenization strategy, Prussian blue analogue(PBA) derived transition metal selenides-based(FeSe2, CoSe2 and FeSe2/CoSe2) composites were synthesized, and the catalytic activity and stability of these three catalysts as cathodes for the hydrogen evolution reaction(HER) in alkaline electrolytes were systematically evaluated. The synthesized catalysts were characterized by XRD, SEM, and XPS to determine their phase composition, morphology, and surface chemistry. The results indicate that the FeSe2/CoSe2 composite exhibits the most outstanding electrocatalytic hydrogen evolution performance, with an overpotential of only 118 mV at 10 mA/cm2 and a Tafel slope of only 86 mV/dec. FeSe2/CoSe2 catalytic performance surpasses that of the single-phase FeSe2 and CoSe2, owing to the strong electronic coupling at the FeSe2/CoSe2 interface, which optimizes the electronic structure of FeSe2/CoSe2. After an 8 h chronopotentiometry test, the FeSe2/CoSe2 catalyst exhibited an overpotential retention rate of 91.74%, and the linear sweep voltammetry curves of all three catalysts remained nearly unchanged after 1000 cyclic voltammetry cycles.

    Fluorinated Co-solvent Enabled Localized High-concentration Electrolyte for High-voltage Lithium Metal Batteries
    HUANG Dequan, YANG Fujian, CHEN Yuanhua, ZHANG Man, YIN Guangda, WEI Tao, MO Haoyue, MO Xiaomin, LIANG Yi
    2026, 47(10):  20260132.  doi:10.7503/cjcu20260132
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    Lithium metal is regarded as one of the most promising anode materials for next- generation high-energy-density batteries because of its ultrahigh theoretical specific capacity and low electrochemical potential. However, the practical application of high-voltage lithium metal batteries(LMBs) is still severely hindered by uncontrolled lithium dendrite growth, unstable solid electrolyte interphase(SEI), and the poor oxidative stability of conventional ether-based electrolytes. Herein, a localized high-concentration electrolyte(LHCE) is constructed by introducing the fluorinated co-solvent 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether(TTE). Combined molecular dynamics simulations and in-situ optical microscopy reveal that the strong electronegativity of fluorine atoms in TTE effectively regulates the anion coordination structure, promotes the formation of an inorganic-rich SEI, markedly improves Li+ transport kinetics, and suppresses lithium dendrite growth. Electrochemical measurements show that the Li||Cu half-cell with LHCE delivers an average Coulombic efficiency of 98.5% after 670 cycles at 0.5 mA/cm2. The full cells based on LHCE also exhibit excellent electrochemical performance: the Li||LFP cell retains 97.4% of its capacity after 400 cycles at 1.0C, while the Li||NCM811 cell maintains 68.8% capacity retention after 500 cycles at 1.0C. This work provides an effective strategy for electrolyte design and interfacial regulation in high-voltage LMBs.

    Controllable Preparation and Capacitance Performance of Fabric-based Polyaniline Interdigitated Electrodes
    CHANG Jinhui, MOU Wenbin, WANG Pengwei, DONG Xufeng, WU Yuchen
    2026, 47(10):  20260131.  doi:10.7503/cjcu20260131
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    A synergistic strategy of “polymer-assisted metal deposition-intra-fabric lithography-controllable electropolymerization” was adopted to realize the controllable preparation of fabric-based polyaniline interdigitated electrodes. Polyester fiber fabric was used as the substrate: the fabric was metallized via the polymer-assisted metal deposition method, then high-resolution metal interdigitated current collectors were fabricated through intra-fabric lithography, and finally polyaniline was electropolymerized on the surface of metal current collectors by the potentiostatic method. The controllable loading of active materials was achieved by adjusting the polymerization time in the range of 5—15 min. The results showed that the optimal polymerization time was 12.5 min, and the areal specific capacitance of the electrode prepared under this condition reached 16.4 mF/cm². After 1000 charge-discharge cycles at a current density of 0.15 mA/cm², the capacitance retention rate reached 91.6%, and the electrode exhibited excellent rate performance at different scan rates and current densities. Flexibility tests indicated that the electrode had stable resistance at different bending angles, with its resistance only increasing by 0.15 Ω after 1000 cycles of 180° bending, showing good mechanical flexibility. The electrode prepared by this method fully retains the inherent three-dimensional network structure of the fabric and achieves a synergistic combination of high capacitive performance and excellent flexibility, which provides a new approach for the preparation of fabric-based planar interdigitated supercapacitors.

    Synergistic Effect of Carbon Nanotubes and High-entropy Perovskite Fluorides for Enhanced Alkaline Oxygen Evolution Performance and Mechanism
    CAO Yuming, GUO Xindan, HAO Zeyu, YU Shansheng, TIAN Hongwei
    2026, 47(10):  20260096.  doi:10.7503/cjcu20260096
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    In this work, a HEPF-PVP/CNT composite electrocatalyst with a three-dimensional interwoven network was successfully constructed by anchoring polyvinylpyrrolidone(PVP)-modified high-entropy perovskite fluoride(HEPF) nanoparticles onto pre-dispersed multi-walled carbon nanotubes(CNTs) via an in-situ nucleation and growth process during a one-pot solvothermal reaction. Serving as heterogeneous nucleation scaffolds, CNTs achieved uniform anchoring and high dispersion of HEPF nanoparticles, effectively overcoming the inherent defects of severe agglomeration and poor conductivity in pristine high-entropy fluorides. Microscopic characterizations revealed that the introduction of an optimal carbon skeleton(CNT-20) exerted a spatial confinement effect, significantly increasing the specific surface area and the exposure degree of active sites. Meanwhile, strong electronic coupling effects emerged at the hetero-interface, inducing the redistribution of electron clouds at metal centers, which increased the proportion of high-valence active sites such as Co3+ and Fe3+, and suppressed the generation of easily leachable Cr6+. Electrochemical tests demonstrated that the optimal HEPF-PVP/CNT-20 catalyst delivered a low overpotential of only 258 mV at a current density of 10 mA/cm2, with a Tafel slope of 85 mV/dec, and showed only a 10.7 mV increase in overpotential after 120 h of continuous operation. This work provides a reliable structural engineering strategy for designing multi-metal synergistic electrocatalytic networks with high activity and long lifespan.

    Polymer Chemistry
    Preparation of Porous Poly Ether Ether Ketone Composite Scaffolds with Osteogenic and Anti-tumor Functionalization
    MEI Xiaohan, LIANG Liubo, JIAO Jianpeng, BAI Yu, WANG Guibin, ZHANG Shuling
    2026, 47(10):  20260119.  doi:10.7503/cjcu20260119
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    Hydroxyapatite nanorods(nHAp) were synthesized using a solution precipitation method to mimic the inorganic composition of natural bone matrix, enhancing the osteoconductivity of the material. Concurrently, cobalt molybdenum phosphate microrods(CPMmr) were synthesized through a hydrothermal method. Their mediated Fenton-like reaction can catalyze the conversion of hydrogen peroxide into hydroxyl radicals, achieving effective tumor cell killing. A porous polyether ether ketone(PEEK) scaffold with continuous interconnected finger-like macropores and micropores was prepared using phase inversion to promote cell migration, nutrient exchange, and tissue ingrowth. CPMmr and nHAp were uniformly dispersed in a composite hydrogel precursor solution of methylacrylated oxidized hyaluronic acid(AHAMA) and polyethylene glycol methacrylate(PEGMA), then they were grafted onto the porous PEEK scaffold surface through UV-initiated polymerization, synthesizing a porous PEEK composite scaffold with osteogenic activity and anti-tumor properties. In vitro cell experiments demonstrated that the porous PEEK composite scaffold exhibits excellent biocompatibility with mouse embryonic osteoblast precursor cells(MC3T3-E1) and significantly enhances the expression levels of osteogenesis-related genes. Furthermore, the presence of CPMmr mediates a Fenton-like reaction within the tumor microenvironment, significantly elevating oxidative stress levels in human osteosarcoma cells(MG-63). This leads to reactive oxygen species accumulation and induces tumor cell apoptosis, demonstrating potent anti-tumor effect.

    Chemical Biology
    Selenazole Carboxamide Src Kinase Inhibitor Against A β -induced Toxicity in Alzheimer’s Disease
    WU Hao, WANG Lei, LIU Yang, ZHANG Xinwei, PAN Xinliang, ZHANG Mingjie, JIANG Fengyu, XIAO Junhai, LIN Feng
    2026, 47(10):  20260241.  doi:10.7503/cjcu20260241
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    The study was designed to investigate the effects of Src tyrosine protein kinase inhibitor(SAFA320) on transgenic Caenorhabditis elegans strainCL4176, along with its underlying mechanism. In the study, C. elegans CL4176 adminstrated with SAFA320 could reduce the deposition of Aβ oligomer to alleviate nematode paralysis, and decrease ROS production. Results of tissue Src kinase activity spectrophotometry analysis showed that SAFA320 could reduce the activities of Src in C. elegans. Meanwhile, the gene expression of skn-1 and its downstream target gene gst-4 were significantly increased, suggesting that compound inhibited Aβ toxicity may involve in SKN-1 signaling pathway in CL4176. In conclusion, SAFA320 is effective in alleviating Aβ toxicity and improving cognitive functions in C. elegans CL4176, and it is a potent candidate agent against Alzheimer’s Disease(AD).

    Chemical Education
    Cross-university Collaboration and Continuous Optimization: Practice in Constructing the High-quality Textbook—— Inorganic Chemistry
    WANG Li, ZHANG Lirong, XU Jianing, SONG Tianyou
    2026, 47(10):  20260206.  doi:10.7503/cjcu20260206
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    This paper presents the development of the textbook Inorganic Chemistry from the 1st to the 5th edition, which had received the national textbook awards two times. The textbook is the achievement of cross-university colla-boration of Jilin University, Wuhan University and Nankai University, and of continuous improvement by the teaching teams from these universities over two decades. It systematically summarizes the developmental trajectory of the book as it has evolved and been upgraded from a traditional print textbook to a new-form textbook with continuing advancement in digital construction. The paper conducts an in-depth analysis of its construction pathways and key revising measures, and summarizes its educational effectiveness in teaching practice. It further extracts universal and replicable experiences for the construction of basic discipline textbooks in high education, aiming to provide a practical guidance for the cultivation of high-quality textbook and the construction of excellent class in domestic universities.