Loading...

Table of Content

    10 October 2025, Volume 46 Issue 10
    Content
    Cover and Content of Chemical Journal of Chinese Universities Vol.46 No.10(2025)
    2025, 46(10):  1-4. 
    Asbtract ( )   PDF (15752KB) ( )  
    Related Articles | Metrics
    Articles: Inorganic Chemistry
    Preparation of SrAl2O4@SiO2 Core@shell Structure Composites and Their Luminescence and Anti-hydrolysis Property
    FU Jialin, ZHU Yufeng, YANG Kaiyuan, GUO Yongmei, LU Yan, YAO Tongjie
    2025, 46(10):  20250214.  doi:10.7503/cjcu20250214
    Asbtract ( )   HTML ( )   PDF (5046KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Hydrolysis in alkaline condition and inferior temperature resistance property were two disadvantages of SrAl2O4∶Eu2+,Dy3+(SrAl2O4) long persistence phosphors. To address these two issues, this study employed ethylene glycol as a non-aqueous reaction medium to cover a SiO2 layer on the SrAl2O4 surface. This strategy effectively isolated the SrAl2O4 matrix from water molecules, hence avoiding the side hydrolysis reactions during the coating process. After careful study, the optimized coating process was determined as follows: solution pH value was 11.0, reaction temperature was 80.0 ℃, reaction time was 2.0 h, Na2SiO3 dosage(mass) was 6.0% of SrAl2O4 powders. Under the optimized condition, a dense SiO2 layer with the thickness of 60 nm was seamlessly coated on SrAl2O4 surface, leading to a SrAl2O4@SiO2 core@shell composite. According to X-ray diffraction pattern, the crystal phase of the SrAl2O4 was not changed during the coating process. Compared to the pristine SrAl2O4, the luminescence intensity of composites was only reduced 11.2%, while the anti-hydrolysis property was largely improved. In practical application, the bright green color could be easily observed by naked eyes after the composite was washed for 6 h in the presence of detergent. The thermogravimetric analysis indicated the remained weight of SrAl2O4@SiO2 composites was 93.7%(mass fraction) after calcinated at 800 ℃. This study provided a novel way to improve the anti-hydrolysis property and high-temperature resistance property of SrAl2O4 without remarkably sacrificing their luminescence property, and this is beneficial for their real application in fire protection.

    Organic Chemistry
    Visible-light Photocatalytic Silylacylation of Alkenes
    JI Baobao, WANG Zhixiang, LIU Yan, CAO Jia
    2025, 46(10):  20250202.  doi:10.7503/cjcu20250202
    Asbtract ( )   HTML ( )   PDF (4119KB) ( )  
    Figures and Tables | References | Supplementary Material | Related Articles | Metrics

    Carbonyl compounds are prevalent in bioactive molecules and organic functional materials, with ketones being particularly important structural motifs. This work focuses on the development of a visible-light photocatalytic three-component difunctionalization of alkenes using silylborates and acyl ammonium salts to access ketone derivatives. Control experiments and DFT calculations revealed that reaction proceeds via a single-electron transfer cascade process between a base/silylboronate complex and an acyl ammonium salt, triggered by a photocatalyst, generating silyl radicals and acyl radical anions. Subsequent sequential coupling with alkenes affords β-silyl ketones. This method features excellent functional group tolerance, mild reaction conditions, and broad substrate scope.

    Design, Synthesis and Biological Evaluation of ERK Inhibitors with Isoindolin-1-one Structure
    ZHANG Lingzhi, JU Qiurong, GUAN Zhe, ZHU Qihua, ZHANG Tingting, YANG Shiqin, XU Yungen
    2025, 46(10):  20250123.  doi:10.7503/cjcu20250123
    Asbtract ( )   HTML ( )   PDF (2424KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Using the ERK inhibitor EK-I-22 and MK-8353 as the lead compounds, 14 compounds were designed and synthesized by pharmacophore fusion strategy. Preliminary pharmacological activity assessments revealed that compounds 19a(IC50=16 nmol/L), 19b(IC50=15 nmol/L), 19e(IC50=20 nmol/L), 27a(IC50=19 nmol/L) and 27b(IC50=56 nmol/L) exhibited significant inhibitory activity against ERK2 kinase. Notably, compound 27b demonstrated moderate inhibitory effects against four human tumor cell lines(Colo-205, A375, A2058 and HT-29).

    Chemical Biology
    Design Strategies for DNA Strand Displacement Reactions via Secondary Structure Modulation of DNA Strands
    LI Zimu, TANG Yuqing, CHENG Jianing, SUN Chenyun, LYU Hui, ZUO Xiaolei
    2025, 46(10):  20250174.  doi:10.7503/cjcu20250174
    Asbtract ( )   HTML ( )   PDF (3095KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    In this study, various types of self-complementary secondary structures were introduced into the input single-strand DNA of strand displacement reactions to change their free energy and conformations, aiming to investigate the influence of different structures on the rate of the strand displacement reaction. We found that the reaction rate decreased as the length of the self-complementary structure increased. This effect was more pronounced when the self-complementary structure was designed in the toehold domain than when it formed in the non-toehold region. The incorporation of secondary structures into the input strands led to varying degrees of reduction in strand displacement reaction rates, and in some cases, completely inhibited the reaction. Finally, we elucidate the mechanism by which secondary structures influence the kinetics of strand displacement reactions, offering new insights into expanding the temporal regulation capabilities of DNA strand displacement and advancing its applications in DNA molecular computing and biosensing.

    Chemical Enzymatic Analysis of Temporal Alterations in Mitochondrial Protein O-GlcNAc Modification during the Therapeutic Senescence Process of Breast Cancer Cells
    JIANG Xinya, MA Qile, CHENG Hongying, LIU Yin, HUANG Huang, ZHAO Ran, LIU Yubo, ZHONG Xiaomin
    2025, 46(10):  20250121.  doi:10.7503/cjcu20250121
    Asbtract ( )   HTML ( )   PDF (8934KB) ( )  
    Figures and Tables | References | Supplementary Material | Related Articles | Metrics

    Cellular premature senescence is closely related to mitochondrial dysfunction. In this study, doxorubicin was used to induce breast cancer cells MCF-7 to establish a model of therapeutic premature senescence cells. The chemical enzymatic method based on GalT1 enzyme(Y289L) was employed to label the mitochondrial O-GlcNAc glycoproteome of MCF-7 cells at multiple time points during the premature senescence process. Click chemistry reaction was utilized to orthogonally capture mitochondrial glycoproteins. Label-free quantitative proteomics analysis was carried out through LC-MS/MS to investigate the temporal quantitative changes of mitochondrial O-GlcNAc glycoproteins during the cellular premature senescence process. Moreover, the biological function enrichment analysis was conducted to identify mitochondrial O-GlcNAc modified proteins involved in the regulation of premature senescence of breast cancer cells, and to elucidate the mechanism by which mitochondrial O-GlcNAc glycosylation regulates cellular premature senescence.

    Physical Chemistry
    Thiadiazole-based Rare Earth Metal-organic Frameworks for Efficient Catalysis of CO2 Cycloaddition Reactions
    GUO Jingpeng, ZHANG Hangchuan, WEI Na, WANG Shu, JIANG Hongbo, ZHAO Zhen
    2025, 46(10):  20250196.  doi:10.7503/cjcu20250196
    Asbtract ( )   HTML ( )   PDF (3599KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    A series of novel isostructural three-dimensional rare earth metal-organic frameworks(MOFs), [RE4(BTDI)3(DMF)4]·solv(RE-BTDI, RE=Er, Dy, Y), was synthesized by solvothermal method using tetracarboxylic acid ligand containing thiadiazole groups, 5,5′-(benzothiadiazole-4,7-diyl)diisophthalic acid(H4BTDI), and rare earth metal nitrates. The rare earth metal nodes on the frameworks of RE-BTDI are Lewis acidic sites which was confirmed qualitatively and quantitatively by Py-IR and NH3-TPD. Meanwhile, the thiadiazole groups introduced by ligands can be used as polar sites to enhance the CO2 adsorption performance of these materials. Under the synergy of the Lewis acidic sites and thiadiazole groups, RE-BTDI showed good catalytic activity for the cycloaddition reaction of CO2 and a series of epoxides. Under the conditions of 80 ℃, 1 MPa CO2, 0.1%(molar fraction) RE-BTDI catalyzed the cycloaddition reaction of CO2 and styrene oxide for 5 h, the yield of styrene cyclic carbonate can reach 90%, and after 5 rounds of cyclic catalysis, the catalytic activity and catalyst structure maintained well. In addition, for other epoxides, the yields of the corresponding cyclic carbonate products can reach 92.5% to 99.0% catalyzed by RE-BTDI under relatively mild conditions.

    Extending the Polarizable Bond-dipole Model to Enable the Rapid Prediction of the Conformational Stability of Cyclic Peptides
    ZHENG Xiaohan, ZHU Jiayi, LI Xiaolei, HAO Qiang, WANG Changsheng
    2025, 46(10):  20250173.  doi:10.7503/cjcu20250173
    Asbtract ( )   HTML ( )   PDF (2901KB) ( )  
    Figures and Tables | References | Supplementary Material | Related Articles | Metrics

    Cyclic peptides possess unique conformational stability, diverse biological activities, and favorable target specificity, making them important lead compounds in drug development. Rapid and accurate prediction of their conformational stability not only aids in uncovering the molecular mechanisms of protein misfolding, but also provides a theoretical basis for target identification and intervention. This is of great significance for the rational design of structurally stable and highly active cyclic peptide-based drugs. In this paper, the polar chemical bonds C=O, N—H, C α —H and C—O, O—H in cyclic peptides are regarded as bond dipoles. The permanent dipole- permanent dipole interaction is used to describe the electrostatic interaction in the system, and the permanent dipole-induce dipole interaction and induce dipole-induced dipole interaction are used to describe the polarization. The bonded terms, including the bond-stretching, angle-bending, and dihedral torsion, are also introduced. The polarizable dipole-dipole interaction model is thus developed into a potential function that can be used to rapidly calculate the relative energies of different conformations of cyclic peptides. The potential function is applied to 9 cyclic peptides, total 33 different conformations to rapidly predict the conformational energies of these conformations. The conformational energies of these conformations are also calculated using the AMOEBA and DLPNO-MP2/aug-cc-pVTZ methods. The calculation results show that, compared with the DLPNO-MP2/aug- cc-pVTZ conformational energies, the linear correlation coefficient R2 of our model is 0.9784, and the root mean square deviation is 13.43 kJ/mol, slightly better than the linear correlation coefficient 0.9682 and root mean square deviation 16.28 kJ/mol of the AMOEBA method. The results of structural optimization and frequency calculation further suggest the rationality of our model. Furthermore, compared with the AMOEBA polarizable force field, our polarizable model significantly reduces the number of electrostatic terms. The model proposed in this paper may provide a new tool for the research and development of novel cyclic peptides as drug candidate molecules.

    Synergistic Catalysis of Cu/TS-1 for Low-temperature Methanol Steam Reforming Reaction
    LU Qing, CHEN Xue, LIU Yuanyuan, WANG Fei, TUO Yongxiao, ZHAO Haoyang, YI Chenxue, MU Taoyang, XU Shaofei, QIN Haotian, FENG Xiang, CHEN De
    2025, 46(10):  20250167.  doi:10.7503/cjcu20250167
    Asbtract ( )   HTML ( )   PDF (4342KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Low-temperature methanol steam reforming(L-MSR) for hydrogen production is a promising approach to addressing the challenges of hydrogen energy sustainability and uneven hydrogen sources distribution. This research focuses on investigating the performance of copper-loaded titanium silicate molecular sieves(Cu/TS-1) with varying Ti coordination configurations in hydrogen production via L-MSR. Through comprehensive characterization employing X-ray diffraction(XRD), transmission electron microscope(TEM), NH3-temperature programmed desorption(TPD) and CO2-TPD, we demonstrate that the synergistic adsorption interaction between Cu and framework Ti significantly enhances both the low-temperature catalytic activity and stability. The results indicate that under atmospheric pressure at 240 ℃ with a water/methanol ratio of 2, the Cu/TS-1 catalyst exhibits a hydrogen production rate of 148.4 mmol·g-1·h-1 and its copper mass-specific activity reaches 891 mmol·g-1·h-1, representing a 1.4-fold enhancement compared to the ca. 621 mmol·g-1·h-1 of the co-precipitation synthesized Cu/ZnO catalyst reported in literature. Structural-activity relationship analysis reveals that the framework Ti in TS-1 increases the weak acidic sites, improves the Cu nanoparticles dispersion, and strengthens the interaction between Cu and TS-1 surface. Additionally, the interaction between framework Ti and Cu nanoparticles facilitates the formation of bidentate CO2 adsorption sites, optimizing the adsorption of formic acid intermediates and accelerating their decomposition, which significantly boosts low-temperature hydrogen production.

    Excited-state Relaxation in Thermally Activated Delayed Fluorescence-sensitized Fluorescence Films: The Critical Role of Acceptor Transition Dipole Moment
    DU Min, GUO Zilong, MA Xiaonan, YANG Wensheng
    2025, 46(10):  20250161.  doi:10.7503/cjcu20250161
    Asbtract ( )   HTML ( )   PDF (4320KB) ( )  
    Figures and Tables | References | Supplementary Material | Related Articles | Metrics

    In thermally activated delayed fluorescence(TADF)-sensitized fluorescence(TSF) systems, the role of acceptor transition dipole moment(TDM) in governing excited-state energy relaxation pathways remains insufficiently understood. To elucidate this mechanism, we constructed TSF films with distinct acceptor TDMs: bis[4-(9,9- dimethyl-9,10-dihydroacridine)phenyl]-solfone/1,3,5,7-tetramethyl-8-phenyl-BODIPY(DMAC-DPS/TMePh-BDP) and 2,6-bis[4-(diphenylamino)phenyl]-9,10-anthraquinone/2,4-bis(4-diethylamino-2-hydroxyphenyl)-squaraine [AQ(PhDPA)2/DiEA-SQ]. The excited state relaxation dynamics in these TSF systems was systematically investigated using steady-state and time-resolved fluorescence spectroscopy. The experimental results show that DiEA-SQ with larger TDM effectively suppresses Dexter energy transfer(DET) by enhancing the spectral overlap integral to extend the Förster radius(R0). Notably, while high-TDM acceptors can inhibit non-radiative relaxation caused by DET, their photoluminescence quantum yield significantly decreases due to the self-absorption(SA) effect. Our findings suggest that increasing acceptor TDM is an effective strategy to enhance Förster resonance energy transfer(FRET) efficiency and suppress DET, but designing acceptor molecules with large Stokes shifts or targeted optical engineering is essential to mitigate SA effects. This mechanistic understanding provides critical insights for developing TSF optoelectronic devices.

    Fabrication of Highly Efficient 1D Pod-like NiFe2O4-Ni x Fe1-x S Heterogeneous Electrocatalysts for Enhanced Oxygen Evolution
    CHEN Hong, ZHANG Hang, FU Siyu, ZHANG Xin, MU Jiajia
    2025, 46(10):  20250156.  doi:10.7503/cjcu20250156
    Asbtract ( )   HTML ( )   PDF (6287KB) ( )  
    Figures and Tables | References | Supplementary Material | Related Articles | Metrics

    To address the challenges of insufficient activity and sluggish kinetics in oxygen evolution reaction(OER) catalysts, this study innovatively designed and synthesized a one-dimensional pod-like NiFe2O4-Ni x Fe1-x S heterojunction material via a two-step method combining electrospinning and sulfurization calcination. By regulating the sulfurization temperature(350—550 ℃), the interfacial heterostructure and component synergy were optimized. Characterization results revealed that the sample sulfurized at 450 ℃(NiFe2O4-Ni x Fe1-x S-450) exhibited that Ni x Fe1-x S nanosheets uniformly anchored on NiFe2O4 nanorods, forming a stable heterointerface with coexisting Fe²+/Fe³⁺ and Ni²+/Ni³⁺ multivalent states, along with enriched oxygen vacancies. Electrochemical tests demonstrated outstanding OER performance in 1 mol/L KOH, achieving low overpotentials of 344 and 396 mV at current densities of 10 and 50 mA/cm², respectively, and a Tafel slope of 40.7 mV/dec. The Electronic redistribution at the heterointerface enhanced exposed active sites and oxygen vacancies accelerated charge transfer. The one-dimensional pod-like structure improved mass transport efficiency and structural stability. This work provides a new paradigm for the rational design of transition metal-based heterojunction catalysts through structure-performance synergy, offering valuable insights for advancing efficient water-splitting technologies.

    Preparation of MIL-101(Cr)-based Membranes for Removing Diclofenac Sodium
    HU Xiaojing, XIE Jingjing, ZHANG Yuxin, ZHANG Yuhan, HUANG Xiaohui
    2025, 46(10):  20250153.  doi:10.7503/cjcu20250153
    Asbtract ( )   HTML ( )   PDF (16260KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    A kind of MOF-based mixed-matrix membrane, MIL-101@PAN, capable of removing diclofenac sodium from aqueous solution by decompression filtration, was prepared based on a stable MOF, MIL-101(Cr), and polyacrylonitrile(PAN). According to our investigations, the obtained MOF-based membranes displayed loose and porous structure with a membrane thickness of about 14 μm, and the performance of the membranes could be significantly improved with the increase of MOF content. Specifically, when the mass ratio of MIL-101(Cr) to PAN reached to 2∶5, the prepared membrane MIL-101@PAN-2 exhibited the best removal performance for diclofenac sodium, particularly achieving a removal efficiency of 95.59% for a diclofenac sodium solution with a concentration of 20 mg/L, and maintaining a removal efficiency above 75% even after 5 cycles. Furthermore, even in a mixed solution containing Na+, K+, and NH4+ at concentrations comparable to those of diclofenac sodium(20 mg/L), the membrane could still maintain a removal efficiency of over 90%.

    Effects of Pd Electronic Density and Particle Size on the Low-temperature Hydrogenation Pathway of Furfural in Pd/Zr-MOFs Catalysts
    WANG Chunhua, HOU Haiyang, LIU Yingya, DING Hai, LIU Tao, HE Shuwen
    2025, 46(10):  20250138.  doi:10.7503/cjcu20250138
    Asbtract ( )   HTML ( )   PDF (5513KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Pd/UiO-66, Pd/UiO-66-NH2 and Pd/UiO-67-bpydc catalysts were prepared by the impregnation method using a series of Zr-based MOFs materials with the same topological structure as supports. The primary focus was to investigate the influence of different nitrogen-containing ligands in the supports on the size of Pd particles, the electron density, and the hydrogenation pathway of furfural. The characterization results of X-ray photoelectron spectroscopy(XPS), carbon monoxide probe in situ Fourier transform infrared spectroscopy(CO-FTIR), and transmission electron microscope(TEM) indicate that there are interactions of varying strengths between different N-containing ligands and Pd particles, and this interaction not only regulates the size of Pd particles but also has a significant impact on the electron density of Pd. Catalytic reaction results show that different N-containing ligands result in significant differences in both the activity of the catalyst and the selectivity of the products. From the perspective of activity, an appropriate metal-support interaction between Pd and the different supports enhances the activity of the Pd/Zr-MOFs catalysts, while excessively strong interactions suppress catalytic activity. Regarding selectivity, the electron density of Pd is a key factor affecting the selectivity of the furfural hydrogenation pathway. Specifically, the amino nitrogen in UiO-66-NH2 and the bipyridine nitrogen in UiO-67-bpydc not only promote the dispersion of Pd particles, but also facilitate the electron transfer between UiO-66-NH2, UiO-67-bpydc and Pd particles. For the Pd/UiO-67-bpydc and Pd/UiO-66-NH2 catalysts with higher electron density, the furfural preferentially undergoes hydrogenation through the aldehyde group(C=O) in the side chain, for the Pd/UiO-66 catalyst with lower electron density, the furfural preferentially undergoes hydrogenation through the furan ring C=C double bond.

    Construction of Lanthanide-based Corrosion-resistant Films for Aqueous Zinc Batteries with Ultra-long Cycle Life
    GOU Lei, SUN Aihong, LIANG Kai, WANG Yanjing, FAN Xiaoyong, LI Donglin
    2025, 46(10):  20250105.  doi:10.7503/cjcu20250105
    Asbtract ( )   HTML ( )   PDF (14646KB) ( )  
    Figures and Tables | References | Supplementary Material | Related Articles | Metrics

    Herein, a lanthanum-based corrosion-resistant film(LaCRF) was grown on the surface of the zinc anode, which effectively reduced the nucleation overpotential of zinc ions and significantly inhibited the formation of zinc dendrites, substrate corrosion, and by-products. Electrochemical performance tests indicate that symmetric cells modified with LaCRF exhibit over 3000 h of cycling stability and minimal polarization at a current density of 2 mA/cm2-1 mA·h/cm2. Furthermore, in Zn@LaCRF||Cu half-cell, the cycle life exceeds 800 cycles; meanwhile, in Zn@LaCRF||MnO2 full cell, the capacity retention rate remains as high as 91.9% after 2000 cycles at a current density of 1.8 A/g. This achievement not only provides a new solution for addressing the corrosion issues of zinc anodes but also paves a new direction for the application of rare earth elements in rechargeable aqueous zinc batteries.

    Polymer Chemistry
    Effects of Surface Modification Strategies of Spherical Silica Particles on Properties of Epoxy Resin Composites for Electronic Packaging
    ZHANG Lili, HU Haijun, LI Houwen, NIE Xingcheng, LI Bin, ZHANG Hailin, HU Qiaoju, ZHENG Dezhou, ZHANG Gouqing, JING Jinfeng, LIU Wenxing, GAO Changyou
    2025, 46(10):  20250145.  doi:10.7503/cjcu20250145
    Asbtract ( )   HTML ( )   PDF (6810KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The effect of silane coupling agent(SCA) interfacial modification on the properties of silica particles/ epoxy composites was systematically investigated to address the performance bottlenecks of epoxy resin-based electronic packaging materials in terms of high thermal conductivity, low dielectric loss, and moisture and thermal stability. The successful grafting of silane coupling agents onto the silica particle surface was verified by surface energy spectroscopy analysis, and epoxy resin-based packaging films with high filler content(50%, mass fraction) were prepared to compare the overall performance of the composites before and after modification. The incorporation of γ-glycidyloxypropyltrimethoxysilane(KH-560) enhanced the interfacial bonding strength of resin through the participation of epoxy groups in the cross-linking reaction. The resultant composites exhibited an optimal glass transition temperature of 170.38 ℃, a thermal conductivity of 0.15 W/mK, and a tensile strength of 102.79 MPa. The resin prepared by using N-phenyl-3-aminopropyltrimethoxysilane(KBM-573)-modified silica particles exhibited a water contact angle of 114.9° and slightly lower mechanical properties due to the hydrophobicity of the benzene ring and conjugation effect. The γ-aminopropyltrimethoxysilane(KH-540)-modified system demonstrated limited improvement in dielectric properties and hydrophobicity due to the amine polarity. The present study elucidated the synergistic effect of modified silica particles on the mechanical, thermal, and electrical properties. This finding provides a theoretical basis for the targeted optimization of electronic packaging materials.

    Preparation and Property of Sponge-like Graphene Oxide/Polyethylene Glycol Composite Phase Change Materials
    CAI Lei, LI Lizhe, LI Hao, CAI Chang, LI Tiehu
    2025, 46(10):  20250035.  doi:10.7503/cjcu20250035
    Asbtract ( )   HTML ( )   PDF (10270KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    To address the challenges of high carrier mass and insufficient thermal conductivity in existing composite phase change materials(CPCMs), this study synthesized graphene oxide(GO) colloidal solutions via an improved Hummers method. A sponge-like graphene oxide(SLGO) with a porous structure was further fabricated through freeze-drying technology. Utilizing SLGO as the carrier and polyethylene glycol(PEG) as the phase change medium, the SLGO/PEG composite phase change material was prepared by combining vacuum impregnation with ultrasonic- assisted processing. The microstructure and thermophysical properties of the composite materials were systematically characterized using ultraviolet-visible(UV-Vis) spectroscopy, scanning electron microscopy(SEM), Fourier-transform infrared(FTIR) spectroscopy, X-ray diffraction(XRD), differential scanning calorimetry(DSC), and laser thermal conductivity analysis. The results demonstrate that PEG effectively fills the pores of SLGO and adsorbs onto its layers, significantly expanding the graphene interlayer space and forming stable hydrogen bonds with oxygen-containing functional groups on the SLGO surface. The composite materials exhibited high latent heat values exceeding 179 J/g and crystallization enthalpies of 172.7 J/g, with relative enthalpy efficiencies over 90%, highlighting their excellent energy storage performance. Most importantly, the addition of SLGO significantly enhanced the thermal conductivity of the material, reaching 0.98 W·m-1·K-1 when the mass fraction of SLGO was increased to 1%. Furthermore, the shape stabilization of the composite material was significantly enhanced with higher SLGO content.