Journal of Colloid and Interface Science最新文献

{"title":"Expression of concern to \"Probing the relevance of synergistic lipid membrane disruption to the eye irritation of binary mixed nonionic surfactants\" [J. Colloid Interface Sci. 678(Part C) (2025) 854-863].","authors":"Feng Wei, Hao Qi, Bin Li, Rongsheng Cai, Mingrui Liao, Peixun Li, Xiaozhi Zhan, Tao Zhu, Hai Xu, Xuzhi Hu, Jian Ren Lu, Feng Zhou","doi":"10.1016/j.jcis.2025.02.185","DOIUrl":"https://doi.org/10.1016/j.jcis.2025.02.185","url":null,"abstract":"","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"689 ","pages":"137177"},"PeriodicalIF":9.4,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143699217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Magnetic graphene vacancies: atomic-scale O2 scissors mediated by antiferromagnetic exchange interaction–spin-orbit selective coupling effects","authors":"Gu Gaoyuan ,&nbsp;Ge Ruijie ,&nbsp;Zhou Yan ,&nbsp;Zhang Jianing ,&nbsp;Li Wenhui ,&nbsp;Peng Chong ,&nbsp;Bi Changlong ,&nbsp;Yang Shuyi ,&nbsp;E Tao","doi":"10.1016/j.jcis.2025.137998","DOIUrl":"10.1016/j.jcis.2025.137998","url":null,"abstract":"<div><div>The serious corrosion of electrode caused by hydrogen peroxide (H₂O₂) generated by noble metal catalyst through two-electron path is the key bottleneck of large-scale application of fuel cell. Based on the study of the structure–activity relationship between defect size and oxygen reduction reaction (ORR) activity of graphene, a strategy is proposed to use the single-atom vacancy (SAV) of graphene to induce electrons to preferentially fill the antibonding orbital (π*<em>_p</em>) of oxygen (O₂) and achieve four-electron path selectivity far exceeding conventional carbon defects via Yeager-type adsorption. Among them, a new mechanism of electron transfer induced by the magnetic properties of SAV and O₂ (spin inversion induced by antiferromagnetic exchange and selective injection of the same spin orbitals (<em>p</em>_z-π*<em>_p</em>)) is the key to realize the strong electron transfer and shear of O₂. In thermodynamic analysis, the magnetic SAV has the lowest ORR overpotential (0.26 V) and the highest *OOH desorption barrier, showing a unique four-electron path selectivity. The above results will provide new insights into the electron transfer mechanism of magnetic materials and fill the theoretical gap of magnetism in the development of atomic scale construction of graphene defects, non-metallic catalysts for fuel cells, and corrosion resistance technology.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"698 ","pages":"Article 137998"},"PeriodicalIF":9.4,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Photovoltaic charge lithography for droplet transport and electrowetting on passive dielectric substrates","authors":"Riccardo Zamboni ,&nbsp;Carlos Sebastián-Vicente ,&nbsp;Athira Sadasivan ,&nbsp;Angel García-Cabañes ,&nbsp;Mercedes Carrascosa ,&nbsp;Jörg Imbrock","doi":"10.1016/j.jcis.2025.137976","DOIUrl":"10.1016/j.jcis.2025.137976","url":null,"abstract":"<div><h3>Hypothesis</h3><div>Photovoltaic charge lithography is an innovative method for printing surface charges from an illuminated iron-doped lithium niobate crystal stamp onto passive dielectric substrates. We hypothesize that this approach can be effectively utilized for droplet manipulation, including electrowetting and droplet transport, offering high reconfigurability similar to optical techniques and avoiding the need for the presence of photosensitive materials in the main platform, simplifying the design of the system and expanding its practical applicability.</div></div><div><h3>Experiments</h3><div>We tested photovoltaic charge lithography on a variety of dielectric substrates with different wetting properties. Using incoherent illumination in an air atmosphere, we examined the method's versatility by exploring the effects of varying light exposure on electrowetting and dielectrophoretic droplet attraction. Numerical simulations were also conducted to investigate the interactions between the printed surface charges and the droplets, providing a deeper understanding of the underlying mechanisms.</div></div><div><h3>Findings</h3><div>Our results confirmed the effectiveness of photovoltaic charge lithography for manipulating droplets on diverse dielectric substrates. The method enabled complex functionalities, including light-exposure-tailored electrowetting, droplet transport of single and multiple consecutive droplets (even uphill), and controlled coalescence. Furthermore, the technique proved to be capable of printing surface charges on flexible polymeric substrates, demonstrating its broad applicability. Numerical simulations supported the experimental observations by offering valuable insights into the interactions between the printed charges and the droplets.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"698 ","pages":"Article 137976"},"PeriodicalIF":9.4,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167049","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"High-performance supercapacitor based on 3D Ti3C2Tx electrodes and sulfonated lignin gel electrolyte","authors":"Jiabei Li ,&nbsp;Tursun Abdiryim ,&nbsp;Ruxangul Jamal ,&nbsp;Kai Song ,&nbsp;Hongtao Yang ,&nbsp;Jiachang Liu ,&nbsp;Yanqiang Zhou ,&nbsp;Guoliang Zhang ,&nbsp;Wenjing Zhang ,&nbsp;Jinglei Chen","doi":"10.1016/j.jcis.2025.137948","DOIUrl":"10.1016/j.jcis.2025.137948","url":null,"abstract":"<div><div>Supercapacitors are highly efficient energy storage systems. The electrode substances and electrolytes, which form their primary components, are key areas of research for scientists. In this study, the transition metal material Ti₃C₂T_x and Poly(3,4-ethylenedioxythiophene) (PEDOT)-based polyacrylamide dual-crosslinked network polymers with good conductivity are selected as the cathode material and gel electrolyte, respectively. To address issues such as self-aggregation of Ti₃C₂T_x during use, insufficient energy density, and poor dispersibility of 3,4-Ethylenedioxythiophene (EDOT) during the preparation of the hydrogel, polystyrene nanospheres are first used as templates to convert Ti₃C₂T_x from a two-dimensional sheet to a three-dimensional spherical structure, followed by the introduction of bimetallic cobalt–nickel hydroxide (CoNi-OH) to effectively enhance its performance. In addition, sulfonated lignin (SL) is incorporated into the hydrogel to improve the dispersibility of PEDOT in water-based solvents, promoting the development of a uniform hydrogel. The results show that the fabricated composite CoNi-OH/3D Ti₃C₂T_x exhibits a specific capacitance of up to 2020 ± 50<!--> <!-->F g⁻¹ at a current density of 1 A g⁻¹. The assembled asymmetric supercapacitor demonstrates a specific capacitance of 278.3 ± 30<!--> <!-->F g⁻¹. At a power density of 750 W kg⁻¹, it exhibits an energy density of 87 Wh kg⁻¹. After 7,000 cycles of testing, the device shows a Coulombic efficiency of 99.4 % ± 0.1 % and maintains 83.7 % ± 0.2 % of its initial capacitance at a current density of 3 A g⁻¹. These findings indicate that the CoNi-OH/3D Ti₃C₂T_x electrodes and PEDOT/SL gel electrolytes have significant potential for development in the energy storage field.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"698 ","pages":"Article 137948"},"PeriodicalIF":9.4,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Imprinted probes achieve highly specific recognition of L-phenylalanine","authors":"Ziwei Wang,&nbsp;Jiawei Li,&nbsp;Zhaoxuanxuan Chen,&nbsp;Zhanfang Ma,&nbsp;Hongliang Han","doi":"10.1016/j.jcis.2025.137987","DOIUrl":"10.1016/j.jcis.2025.137987","url":null,"abstract":"<div><div>Molecularly imprinted polymers (MIPs) for amphiphilic small molecules are typically synthesized using a “monolithic imprinting” approach and enable target monolithic recognition, but suffer from non-specific adsorption in complex samples, thereby limiting specificity. To address these limitations, a novel “imprinted probe recognition” mode was proposed for the first time. According to the hydrophilic and hydrophobic structures of molecules as templates respectively, two kinds of MIPs were fabricated, and the “imprinted substrate–target analyte–imprinted probe (with electrochemical signals)” recognition mode was constructed. As a proof of concept, L-phenylalanine was selected as a model analyte for verification. The imprinting factor (evaluating specificity) of “imprinted probe recognition” is increased from 3.63 to 5.47 compared with “monolithic recognition”, and the specificity is improved by more than 50 %. This technology enables effective labeling of amphiphilic small molecules with substantially improved specificity in various environments, providing a general and feasible concept for the accurate recognition of small molecules.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"697 ","pages":"Article 137987"},"PeriodicalIF":9.4,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167971","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Encapsulation of cobalt-iron Prussian blue analog nanocubes using a redox polymer for advanced supercapacitor cathode materials","authors":"Yan Bao,&nbsp;Guangchun Chen,&nbsp;Xinglin Zhu,&nbsp;Pingfan Zou,&nbsp;Quanwei Yang,&nbsp;Saisai Yuan,&nbsp;Chuanxiang Chen","doi":"10.1016/j.jcis.2025.137975","DOIUrl":"10.1016/j.jcis.2025.137975","url":null,"abstract":"<div><div>Prussian blue analogs (PBAs) are promising cathode materials for aqueous supercapacitors because of their open 3D framework, low cost, and large theoretical capacitance. Nevertheless, their poor electrical conductivity and unavoidable dissolution during cycling result in a low rate capability and cycle life. Herein, a facile <em>in situ</em> polymerization encapsulation strategy, which can increase the energy storage performance of cobalt-iron PBA nanocubes <em>via</em> the use of a redox polymer nanoskin (CFP@PTMT), is demonstrated for aqueous supercapacitors. The poly(trimethyl thionine) (PTMT) nanoskin serves a triple-functional role as a conductive skeleton, electroactive protection layer, and structural stabilizer to increase the electrical conductivity, pseudocapacitance contribution, and structural stability of CFP. Interestingly, CFP@PTMT delivers a high capacitance of 984 F g⁻¹ at 1 A g⁻¹ and a superior rate capability of 87.19 % capacitance retention at 10 A g⁻¹, with a 99.34 % capacitance retention over 5,000 cycles. Notably, an asymmetric supercapacitor is assembled using a CFP@PTMT cathode and an activated carbon anode, which results in a high capacitance of 287 F g⁻¹, a large energy density of 45.26 Wh kg⁻¹, and an excellent power density of up to 8,000 W kg⁻¹ with 99.00 % capacitance retention after 5,000 cycles. This work establishes that redox polymer nanoskin encapsulation not only addresses the intrinsic drawbacks of PBAs but also creates a new design paradigm for integrating conductivity, pseudocapacitance, and structural stability at a single nanoscale interface. This strategy paves the way for next-generation aqueous energy storage devices with balanced high performance and durability.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"697 ","pages":"Article 137975"},"PeriodicalIF":9.4,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144168369","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Constructing heterojunction interface between Co-Fe layered double hydroxide and Ni-Fe metal–organic framework as efficient oxygen evolution electrocatalyst: Mechanism insights into CoOOH-FeOOH-NiOOH ternary system","authors":"Kuo Yang ,&nbsp;Wenjie Ren ,&nbsp;Luowei Li ,&nbsp;Bingjie Ye ,&nbsp;Wei Li ,&nbsp;Wenhao Fang ,&nbsp;Shixi Liu","doi":"10.1016/j.jcis.2025.137991","DOIUrl":"10.1016/j.jcis.2025.137991","url":null,"abstract":"<div><div>The creation of available and cost-effective non-noble-metal electrocatalysts for oxygen evolution was of considerable practical significance. In this study, we introduced a CoFe-layered double hydroxide (LDH) and NiFe metal–organic framework (MOF) electrocatalyst that was supported on nickel foam (NF) for oxygen evolution reaction (OER). The coordination structure between Co/Ni and Fe was modulated by varying the Fe content, which enhances the electron tunneling ability between CoFe-LDH and NiFe-MOF. Additionally, characterization techniques confirmed the synergistic interactions of the active sites Co²⁺/Co³⁺, Ni²⁺/Ni³⁺ and Fe²⁺/Fe³⁺ in the OER process. Calculations using density-functional theory (DFT) substantiated the swift electron transfer that occurs among the ternary active substances CoOOH, FeOOH, and NiOOH during the generation of OER in strong alkaline environments, which was enhanced by synergistic effects and the efficient adjustment of electronic interactions. CoFe-LDH@NiFe-MOF fully exposes the active centers within its nanosheet structure, featuring a hierarchical porous architecture that promotes rapid charge and mass transfer. The measured overpotential was found to be 225 mV with an current density of 10 mA cm⁻², and Tafel slope was recorded at 28.10 mV dec⁻¹. The results presented show that the as-prepared electrocatalysts exhibited superior activity in OER compared with commercial RuO₂ catalysts. Furthermore, this self-supported electrocatalyst displays impressive durability, as there was no observed degradation in its activity over a continuous 60h operation period. This research illustrates a straightforward and practical approach to developing effective catalysts for water oxidation, achieving both highly catalytic competence and long-term fixity.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"698 ","pages":"Article 137991"},"PeriodicalIF":9.4,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167053","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"In-situ amorphous transformation of V2O5 in V2O5/V6O13 for aqueous zinc ion batteries with high capacity and long cycles","authors":"Li Chen ,&nbsp;Hui Zhou ,&nbsp;Zhi Chen ,&nbsp;Zhaohui Wu ,&nbsp;Yabing Chen ,&nbsp;Haijun Zeng ,&nbsp;Juntong Huang ,&nbsp;Huiyong Yang ,&nbsp;Di Guo","doi":"10.1016/j.jcis.2025.137999","DOIUrl":"10.1016/j.jcis.2025.137999","url":null,"abstract":"<div><div>Rechargeable aqueous zinc-ion batteries (AZIBs) are attractive due to their superior safety, rich zinc resources, and cost-efficient. Vanadium-based oxides, as popular cathode materials, are inevitably subject to dissolution in aqueous solutions, and inherent low electrical conductivity and sluggish reaction kinetics, significantly impeding the performances in Zn²⁺ storage. In this study, V₂O₅/V₆O₁₃ composites are successfully prepared by a novel three-roll milling technique combined with high-temperature treatment to improve these shortcomings. The results demonstrate that the V₂O₅/V₆O₁₃ electrode sustains excellent cycling (316.0 mAh g⁻¹ at 5 A g⁻¹ after 4000 cycles) and superior rate performance (186.69 mAh g⁻¹ at 20 A g⁻¹). Ex-situ characterization reveals that the mechanism involves the co-intercalation of H₂O with Zn²⁺. It is found by testing in different electrolytes that V₂O₅ is gradually amorphous in aqueous electrolyte during cycling, which greatly improves the structural stability and enhances the ability for capturing Zn²⁺. Moreover, it is demonstrated by calculations that a higher degree of amorphization promotes the adsorption of Zn²⁺. The present work provides a new idea for the development and mechanism explanation of high-performance AZIB materials.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"697 ","pages":"Article 137999"},"PeriodicalIF":9.4,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144155106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Loaded carbon shell encapsulated transition metal and ZnIn2S4 on carbonized paper for enhanced photocatalytic hydrogen production","authors":"Guiyuan Guo,&nbsp;Jiaxin Feng,&nbsp;Heting Wang,&nbsp;Luyao Guo,&nbsp;Xiujie Huang,&nbsp;Xueren Qian","doi":"10.1016/j.jcis.2025.137990","DOIUrl":"10.1016/j.jcis.2025.137990","url":null,"abstract":"<div><div>Solar-driven semiconductor photocatalysis water splitting is considered a green and efficient method for hydrogen production. But the severe recombination of photogenerated carriers limits the efficiency of hydrogen production. The introduction of transition metal co-catalyst can form an internal electric field (IEF) with semiconductor to achieve efficient directional transfer of photogenerated electron-holes. However, the aggregation of transition metal co-catalyst and the formation of metal-hydrogen bonds are still the main problems for limiting hydrogen production efficiency. Here, metal–organic framework (MOF) derived porous carbon encapsulated transition metal Fe (Fe@C) and ZnIn₂S₄ are loaded on carbonized cellulose fibers (CCF) to construct composite paper for photocatalytic water splitting into hydrogen. The MOF-derived carbon skeleton can provide high conductivity and disperse Fe co-catalyst for increasing the active sites. Moreover, the encapsulation of Fe in the 3D carbon skeleton can avoid the formation of metal-hydrogen bonds and improve the hydrogen adsorption and desorption capacity. The CCF as a carrier is beneficial to improve the dispersibility and reusability of Fe@C and ZnIn₂S₄. The hydrogen evolution rate of the composite paper is as high as 63.8 mmol h⁻¹ g⁻¹ under visible light irradiation. After 5 photocatalytic cycles, the hydrogen evolution rate remains at 94.2 % and the loading state of Fe@C and ZnIn₂S₄ on CCF is maintained. This work provides a new idea for fabrication of high-efficient photocatalytic paper, and develops the application potential of MOF derivatives in photocatalysis.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"697 ","pages":"Article 137990"},"PeriodicalIF":9.4,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144155177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Green and efficient fabrication of high-damping porous films for energy harvesting and self-powered sensing","authors":"Yibing Xie ,&nbsp;Yibo Li ,&nbsp;Tingting Shan ,&nbsp;Zhen Yu ,&nbsp;Leyuan Ma ,&nbsp;Pengchao Wang ,&nbsp;Guangye Liu ,&nbsp;Chuntai Liu ,&nbsp;Zhenxiu Zhang","doi":"10.1016/j.jcis.2025.137988","DOIUrl":"10.1016/j.jcis.2025.137988","url":null,"abstract":"<div><div>Finding a sustainable and scalable strategy for the fabrication of triboelectric materials with unique damped capabilities to enhance the stability and durability of triboelectric nanogenerators (TENGs) is a challenging task. Here, the styrene–ethylene–butylene–styrene (SEBS) foam with a high-damping property was prepared via the supercritical nitrogen dioxide (scN₂) foaming process, resulting in an 87.5 % reduction in rebound height, 700 % increase in buffering effect, and nearly zero rebound times. A complementary-shaped TENG (CS-TENG) was fabricated using a convex polydimethylsiloxane and concave porous-surface foamed SEBS films, which can be obtained by slicing SEBS foam. The optimized CS-TENG increased the output voltage by 270 % to 310 V and current by 287.5 % to 1.15 μA, enabling it to charge capacitors and power small devices. Moreover, the flexible and robust friction layers of the CS-TENG ensured durability across 40,000 cycles, allowing it to serve as a self-powered sensor for the detection of forces and deformations. For feasibility testing, a self-powered remote-control system with four CS-TENGs was developed for the intellectual development of children and rehabilitation support of the elderly. This work offers new insights into the green fabrication of high-damping triboelectric materials and the development of surface-engineered TENGs with high output and durability.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"697 ","pages":"Article 137988"},"PeriodicalIF":9.4,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144168367","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}