Journal of Colloid and Interface Science最新文献

{"title":"Encapsulation of FeCoNiCrMn high-entropy alloy in N-doped carbon fiber as a robust catalyst for boosting sulfur redox kinetics","authors":"YuFei Zhang,&nbsp;LiRong Zhang,&nbsp;FengFeng Han,&nbsp;Yang Zhao,&nbsp;HongXu Su,&nbsp;Lu Li,&nbsp;LiLi Wu,&nbsp;XiTian Zhang,&nbsp;Qi Jin","doi":"10.1016/j.jcis.2026.139999","DOIUrl":"10.1016/j.jcis.2026.139999","url":null,"abstract":"<div><div>Lithium‑sulfur batteries (LSBs) suffer from lithium polysulfide (LiPS) shuttling and slow redox kinetics. To mitigate these issues, we report an efficient electrocatalytic interlayer based on a FeCoNiCrMn high-entropy alloy embedded in N-doped carbon nanofibers (HEA@NCNF). The multi-metallic HEA offers abundant active sites, while the N-doped carbon shell not only prevents HEA particle agglomeration and metal leaching, but also establishes a three-dimensional conductive network. Combined X-ray photoelectron spectroscopy and density functional theory calculations elucidate the underlying mechanism: electron modulation from the N-doped carbon layer raises the d-band center of the HEA, thereby strengthening LiPS adsorption and promoting its electrocatalytic conversion. Consequently, the HEA@NCNF interlayer functions as an efficient “trap-and-convert” reactor for LiPSs, which simultaneously suppresses shuttle effects and accelerates redox kinetics. The cells with HEA@NCNF demonstrate exceptional cycling and rate performance, with a capacity decay of only 0.023% per cycle over 1500 cycles at 1C. Remarkably, this superior performance extends to challenging conditions, including high sulfur loading (≥ 7 mg cm⁻²), lean electrolyte, and high-rate operation. This work demonstrates a strategy of integrating HEAs with conductive N-doped carbon matrices to create a synergistic trap-convert mediator for LiPSs.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 139999"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146111738","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":"Photoluminescence of silicon nanorods via plasmonic gold nanopore arrays","authors":"Yizhi Wu ,&nbsp;Yankai Rong ,&nbsp;Mingchao Ren ,&nbsp;Xiaoliang Xu","doi":"10.1016/j.jcis.2026.140000","DOIUrl":"10.1016/j.jcis.2026.140000","url":null,"abstract":"<div><div>Silicon luminescence remains a significant challenge, and its origin is intense debate ever since. Here we show, for the first time, a luminescent strategy involving silicon nanorods coupled with plasmonic gold nanopore arrays. It is demonstrated that the luminescence intensity of silicon nanorods induced by plasmonic gold nanopore arrays is nine times higher than that of pure silicon nanorod samples. Despite the absence of an insulating spacer between the gold nanopore arrays and silicon nanorods, no luminescence quenching is observed. Furthermore, we employ finite difference time domain simulations to map the electric field distribution and estimate a Purcell factor of 5, which is lower than the experimentally measured luminescence enhancement. This indicates that the observed luminescence enhancement is only partially attributable to the Purcell effect. Importantly, the Purcell effect would not cause a shift in the luminescence peak, whereas a significant peak shift is observed in our experiments. Based on these facts, a novel luminescence mechanism is proposed to complementally account for the remarkable luminescence enhancement observed in our experiments. Plasmonic gold nanopore arrays-induced energy level splitting may appear in silicon nanorods, which generates a localized direct bandgap, thereby yielding enhanced visible light emission.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 140000"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146111745","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":"Dual-redox cycling driven charge transfer in CuxO/CeO2 heterojunction for photocatalytic activation of peroxymonosulfate toward tetracycline degradation","authors":"Huijie Wang ,&nbsp;Jiaxin Li ,&nbsp;Zixiang Jiao ,&nbsp;Xiaodan Zheng ,&nbsp;Wei Ma ,&nbsp;Kesheng Cao ,&nbsp;Lingwei Xue ,&nbsp;Fu Xu ,&nbsp;Yang Wan ,&nbsp;Yangyang Yang ,&nbsp;Binrong Li ,&nbsp;Pengwei Huo","doi":"10.1016/j.jcis.2026.139996","DOIUrl":"10.1016/j.jcis.2026.139996","url":null,"abstract":"<div><div>The efficient removal of antibiotic residues such as tetracycline (TC) from water remains challenging. Research has demonstrated that heterogeneous systems utilizing photocatalysis to activate peroxymonosulfate (PMS) exhibit exceptional performance. However, preparing materials with strong charge transfer capabilities and stability still poses certain challenges. This study developed a Cu_xO/CeO₂ heterojunction composite with abundant oxygen vacancies (O_V) for visible-light-driven activation of peroxymonosulfate (PMS). The hierarchical flower-sphere structure of CeO₂ provides ample adsorption sites and mass transfer channels, while the synergy between the heterojunction interface and the dual redox cycles of Cu⁺/Cu²⁺ and Ce³⁺/Ce⁴⁺ significantly enhances visible-light absorption and accelerates the separation and transfer of photogenerated carriers. Femtosecond transient absorption (fs-TA) spectroscopy further confirms that the formation of the heterojunction effectively regulates the direction of carrier transfer and prolongs the charge lifetime. Density functional theory (DFT) calculations reveal that O_V markedly promote the adsorption and activation of PMS. Under visible light irradiation, the system achieves a TC degradation efficiency of 99.2% within 60 min, primarily driven by sulfate radicals (SO₄^•−) and hydroxyl radicals (•OH), with the intermediates exhibiting generally low toxicity. In addition, in-situ infrared spectroscopy (in-situ FT-IR) further confirmed the outstanding TC adsorption capacity and degradation activity of the Cu_xO/CeO₂ heterojunction composite. This work provides insightful perspectives for designing efficient and stable heterojunction catalysts through defect and interface engineering for water purification.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 139996"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077049","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":"Macropore engineering of MOF-derived carbon for superior microwave absorption","authors":"Zi Wang ,&nbsp;Junru Yao ,&nbsp;Jinlong Lv ,&nbsp;Yang Cao ,&nbsp;Biao Lv ,&nbsp;MinJie Liang ,&nbsp;Honghong Zhao ,&nbsp;Youyi Sun","doi":"10.1016/j.jcis.2026.139993","DOIUrl":"10.1016/j.jcis.2026.139993","url":null,"abstract":"<div><div>Regulating electromagnetic pollution has become significance as 5G communication and radar technologies rapidly progress. This study proposes a macroporous engineering method utilizing polystyrene microsphere templates to address the limitations of single pore size structure and the difficulties in achieving impedance matching and loss capability in traditional carbon materials derived from metal-organic frameworks (MOFs). Co-Zn-C/C composite materials with a multi-level pore structure have been successfully synthesized. Through meticulous regulation of the PS template's dimensions via PVP dosage modifications, Metal-organic framework-on-Metal-organic framework (MOF-on-MOF) epitaxial growth, and a high-temperature carbonization of ZIF-8/ZIF-67, a composite material featuring a multi-level pore architecture (macropore mesoporous carbon nanotube network) and tunable pore size was synthesized. The results indicate that the material contains uniformly dispersed Co nanoparticles, a substantial specific surface area, and many nitrogen-doped defects. The optimized CZCC-2 sample demonstrates superior impedance matching and multi-mechanism synergistic attenuation, achieving an effective absorption bandwidth of 6.59 GHz at a thickness of 2.1 mm and a minimum reflection loss of −59.48 dB at 9 GHz at 3.0 mm, as per electromagnetic performance testing. The exceptional capability for suppressing electromagnetic wave scattering in practical applications is further validated by finite element modeling and radar cross-section (RCS) analysis. This paper presents innovative methods for developing absorbent materials that are thin, lightweight, broadband, high-intensity.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 139993"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077109","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":"Guided electron flow in anthraquinone-methoxy donor-acceptor1-acceptor2 covalent triazine frameworks enabling superior selective uranium capture","authors":"Ruoxuan Guo,&nbsp;Liping Song,&nbsp;Wencheng Yao,&nbsp;Yingzhong Huo,&nbsp;Lu Wang,&nbsp;Yang Liu,&nbsp;Yuejie Ai,&nbsp;Xiangke Wang","doi":"10.1016/j.jcis.2026.140012","DOIUrl":"10.1016/j.jcis.2026.140012","url":null,"abstract":"<div><div>Rational design and synthesis of stable and efficient photocatalysts for selective U(VI) capture in water remains a great challenge due to the complicated water environment. Herein, considering the synergistic interaction between anthraquinone (−AQ, electron acceptor) and methoxy (–OCH₃, electron donor), a series of ternary donor-acceptor-acceptor (D-A1-A2) covalent triazine frameworks named as OCH₃(x)-AQ(y) (x and y represent different content ratios) were rationally designed and synthesized via molecular regulation. This work not only constructed a directional charge-transfer pathway, but also greatly improved the utilization efficiency of photogenerated electrons in OCH₃(x)-AQ(y) framework, which was also further verified by density functional theory (DFT) calculations. Finally, OCH₃(2)-AQ(3) could reach nearly 100% removal efficiency of U(VI) within 240 min under visible light irradiation in air. Meanwhile, OCH₃(2)-AQ(3) showed an extremely high distribution coefficient (K_d, 1.07 × 10⁶ mL·g⁻¹) for U(VI) under multicomponent ion competition and further performed high removal efficiencies (&gt;98%) in real water environments, such as seawater and groundwater. Importantly, the machine learning results also demonstrated that the structural characteristics would greatly influence the catalytic performance of CTF catalysts. The component tuning of donor-acceptor groups achieved synergistic effects in stepwise charge transport and target-selective site accessibility, which offered an effective photocatalytic strategy for U(VI) extraction in complex water environment.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 140012"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146117375","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":"Engineered hollow cubic structures CoS/NiS heterojunctions enable high-performance magnesium-ion batteries","authors":"Runjing Xu ,&nbsp;Han Xiao ,&nbsp;Yuan Fang ,&nbsp;Ya Chen ,&nbsp;Pengfei Zhang ,&nbsp;Kailin Li ,&nbsp;Yuxuan Li ,&nbsp;Huinan Yu ,&nbsp;Jiayun Zhang ,&nbsp;Chaoxin Wu ,&nbsp;Xin Gao ,&nbsp;Tao Meng ,&nbsp;Xiaodong Chen ,&nbsp;Lifeng Cui","doi":"10.1016/j.jcis.2026.139992","DOIUrl":"10.1016/j.jcis.2026.139992","url":null,"abstract":"<div><div>Rechargeable magnesium-ion batteries (RMBs) demonstrate notable benefits, including higher theoretical energy density, cost-effectiveness, and improved safety characteristics, positioning them as a viable substitute for conventional energy storage solutions. Nevertheless, the ongoing development of high-performance RMBs continues to face inevitable challenges, such as unsatisfactory practical capacity, inadequate cycle durability, swift energy degradation, and a comparatively limited-service life. Herein, CoS/NiS nanomaterials with cubic-shaped morphology were prepared by a two-step metal sulfide template-free solvothermal synthesis method. The material with internal cavity structure effectively mitigates the large expansion of magnesium-ion battery cathode material due to Mg²⁺ embedding during the charging and discharging process, and provides a robustness electrode-electrolyte interface, thus greatly improving the cycle life. Besides, the introduction of Ni elements into CoS materials may form heterojunctions thereby lowering the potential barrier of the conversion reaction and improving the reaction kinetics and redox reversibility. In addition, the abundance of highly electronegative S<img>S bonds in the CoS/NiS material, which also provides many electrochemically active sites and smooth transport paths for the embedding of Mg²⁺, leads to the reduction of its polarization and the improvement of its reaction kinetics, which makes the CoS/NiS as a RMBs cathode material with a high specific capacity and a long cycling life. Thus, this research presents a feasible and effective strategy for enhancing the Mg²⁺ storage capability of engineered CoS nanomaterials, with potential applicability and adaptability to other electrode materials.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 139992"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146117436","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":"Light-driven host-guest supramolecular transport engineering an antibacterial trap switch","authors":"Xuejiao Wang ,&nbsp;Zhi Su ,&nbsp;Lan Zheng ,&nbsp;Kaifa Zhao ,&nbsp;Qiyang Cai ,&nbsp;Xiangyu Wei ,&nbsp;Yaqing Zhao ,&nbsp;Yan Ke ,&nbsp;Yuelu Fan ,&nbsp;Hu Zhu","doi":"10.1016/j.jcis.2026.139982","DOIUrl":"10.1016/j.jcis.2026.139982","url":null,"abstract":"<div><div>Inspired by nature's sophisticated use of light energy, we report a bioinspired antibacterial trap switch operating without exogenous competitors. This work engineers a light-gated supramolecular system where host-guest conformational reorganization between cucurbit[8]uril (CB[8]) and dicationic symmetric azobenzene derivative (Azo-<em>E</em>) enables precise control over antimicrobial agent release. Upon ultraviolet (UV) irradiation triggers <em>E</em>-<em>Z</em> isomerization, enhancing its binding affinity to CB[8] and resulting in steric displacement of the encapsulated antibacterial agent through conformational reorganization. This system achieves &gt;99.9% bacterial eradication, supports reversible switching across four conventional antibacterial agents, and reduces mammalian cell cytotoxicity. Spray-coatable on different biomaterial surfaces, it demonstrates spatial precision for localized disinfection. This molecular engineering establishes a general platform for spatiotemporally precise regulation of bioactive cargoes, enabling adaptive supramolecular systems with infection control.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 139982"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146123299","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":"Halloysite nanotubes interacting with lipid vesicle membranes","authors":"Chiara Ferlito ,&nbsp;Lorenzo Lisuzzo ,&nbsp;Giuseppe Lazzara ,&nbsp;Marc Schmutz ,&nbsp;Antonio Stocco","doi":"10.1016/j.jcis.2026.140013","DOIUrl":"10.1016/j.jcis.2026.140013","url":null,"abstract":"<div><div>Halloysite nanotubes (HNTs), naturally occurring aluminosilicates with a tubular structure, are promising nanocarriers for drug delivery due to their biocompatibility and unique morphology. However, their interaction with lipid membranes remains not fully explored. In this work, we aim at elucidating on the adhesion of HNTs on unilamellar vesicles made of phospholipids used as model of biological membranes. The adhesion was modulated by varying the lipid composition, ionic strength, and the size ratio between HNTs and vesicles. The adhesion mechanism was also studied by trapping a single HNT with optical tweezers and let it interact with a single vesicle. These findings show a preferential adhesion of the HNT tip on the lipid bilayer, which represents an important step toward directional membrane targeting in biomedical applications.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 140013"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146103083","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":"Tailoring anion-enriched and fluoroethylene carbonate coordinated weak solvation structure for interfacial-stable lithium metal batteries","authors":"Maolin Zhang ,&nbsp;Rui Hao ,&nbsp;Xiaoping Yang ,&nbsp;Fan Yang ,&nbsp;Zhaoxia Xu ,&nbsp;Shixi Liu ,&nbsp;Shouyi Yuan ,&nbsp;Yubo Xing ,&nbsp;Hao Wu ,&nbsp;Yannan Zhang ,&nbsp;Yiyong Zhang ,&nbsp;Wen Lu ,&nbsp;Peng Dong ,&nbsp;Yingjie Zhang ,&nbsp;Fang Cheng","doi":"10.1016/j.jcis.2026.140027","DOIUrl":"10.1016/j.jcis.2026.140027","url":null,"abstract":"<div><div>The development of practical lithium (Li) metal battery (LMB) is severely restricted by the poor stability of electrode-electrolyte interfaces (EEIs) and sluggish interfacial kinetics. Modulating Li-ion solvation structure is critical for addressing this issue, but remains challenging. Herein, we propose a novel strategy of incorporating multiple anions and functional solvent to tailor a unique anion-enriched and fluoroethylene carbonate (FEC) coordinated weak solvation structure for interfacial-stable high-performance LMBs. Theoretical calculations and experimental results indicate that the first Li-ion solvation sheath is dominated by multiple anions and FEC molecules, leading to a largely diminished coordination of Li⁺-solvents and an accelerated interfacial dynamics. Simultaneously, inorganic-rich robust EEIs are further constructed via the preferential redox decomposition of the solvated anions and FEC molecules, achieving a remarkable interfacial stability and dendrite-free Li plating/stripping behavior. Consequently, the symmetric Li||Li cells realize an ultra-long stable cycle of 5400 h at 2 mAh cm⁻², and the Li||LiFePO₄ (LFP) full cells demonstrate an excellent rate and cycling performance even under high LFP-loading, relatively low negative/positive capacity ratio (N/P) and less electrolyte usage. Our findings reveal a facile proposal to precisely tailor weak Li-ion solvation structure by integrating anion chemistry and functional solvent, paving the way for advanced electrolyte design and high-performance LMBs development.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 140027"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146137115","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":"A photothermal antibacterial hydrogel based on a “nano-bridge” strategy with high toughness and self-healing capacity","authors":"Junyan Wang ,&nbsp;Jianhui Wang ,&nbsp;Laixiang Zhu ,&nbsp;Na Zhang ,&nbsp;Nannan Xu ,&nbsp;Fuhao Liu ,&nbsp;Yanqing Wang ,&nbsp;Chuanhui Gao","doi":"10.1016/j.jcis.2026.139995","DOIUrl":"10.1016/j.jcis.2026.139995","url":null,"abstract":"<div><div>Constructing integrated multifunctional hydrogels with both high toughness and diverse functionalities is beneficial for the development of flexible antibacterial materials and wearable sensors. However, current hydrogels often fail to achieve a synergistic balance among toughness, antibacterial activity, and sensing responsiveness, limiting their practical applications. Herein, a “nano-bridge” strategy is proposed to fabricate a double-network hydrogel system (PHS-CT) composed of a covalent polyacrylamide network and a dynamic borate-crosslinked hydroxypropyl guar gum/sodium alginate network. The incorporated Cu-TA nanosheets serve not only as “structural bridges” to enhance the crosslinking density and mechanical performance (strain up to 1997.7%, toughness up to 1.53 MJ/m³), but also as “functional bridges” to enable photothermal conversion and improved antibacterial activity (bacterial killing rate of 99.0% against <em>E. coli</em> under NIR irradiation). In addition, benefiting from the dynamic reversibility of borate ester bonds as well as the re-forming capability of hydrogen bonds at the fracture interface, the hydrogel exhibits favorable self-healing ability (self-healing efficiency up to 91.0%), and can function as a flexible strain sensor capable of accurately detecting both large-scale and subtle deformations. This strategy provides a feasible strategy for constructing multifunctional dual-network hydrogels, and may be useful for photothermal antibacterial and flexible sensing applications.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"710 ","pages":"Article 139995"},"PeriodicalIF":9.7,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146117324","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}