Nanoscale Advances最新文献

{"title":"A review of interface optimization strategies for solid electrolytes and anode materials.","authors":"Dandan Wang, Xinyang Wu, Yongpeng Ren, Yaru Li, Xiaolin Xie, Xiqiang Ma, Ihar Razanau, Xuemin Chen, Junhao Lu, Kunming Pan","doi":"10.1039/d5na00286a","DOIUrl":"10.1039/d5na00286a","url":null,"abstract":"<p><p>With the increasing demand for high-performance power batteries in electric vehicles, low-altitude economy, military applications, and other fields, existing liquid electrolyte-based battery technologies are gradually becoming incapable of meeting the energy density and safety requirements. New battery systems based on solid electrolytes are the main candidate materials for future power batteries owing to their high safety and energy density. Thus far, researchers have conducted extensive studies on the ionic/electronic transfer mechanisms of solid electrolytes and electrode materials, as well as the cooperative effects and interface issues between them. Although much progress has been made, the practical application of solid-state batteries is still severely limited by the high interface impedance between the solid electrolyte and the anode. This impedance stems from incompatible physical and chemical properties and dynamic interface evolution. This paper focuses on the latest progress in the interface engineering strategies of solid electrolytes and anodes and systematically analyzes the cooperative coupling effect between charge transfer dynamics and mechanical stability at the interface. This review provides insights into the future research in this field, aiming to offer a new perspective to enhance our understanding of solid-state lithium batteries, thereby facilitating their more optimal design and promoting their practical applications.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" ","pages":""},"PeriodicalIF":4.6,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12203239/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144528885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"First principles exploring the tunable electronic and optical features of silicane/γ-GeSe heterostructures for advanced electronic devices","authors":"Nguyen P. Q. Anh, Ho V. Cuu, Truong Tan, Chuong V. Nguyen and Nguyen N. Hieu","doi":"10.1039/D5NA00181A","DOIUrl":"10.1039/D5NA00181A","url":null,"abstract":"<p >In this work, we explore the electronic and optical properties of the SiH/γ-GeSe heterostructure using first-principles calculations, emphasizing its remarkable tunability under applied electric fields. Our findings demonstrate that the SiH/γ-GeSe heterostructure exhibits stability, indicating its feasibility for future synthesis. The SiH/γ-GeSe exhibits type-I band alignment and an indirect band gap, with optical absorption characteristics revealing enhanced absorption in specific energy regions, highlighting its potential for advanced optoelectronic applications. Under the influence of electric fields, the SiH/γ-GeSe heterostructure transitions to type-II band alignment and switches to a direct band gap, which significantly improves charge separation and light absorption efficiency. These findings underscore the versatility of the SiH/γ-GeSe heterostructure, positioning it as a promising candidate for a wide range of electronic and optoelectronic applications.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 12","pages":" 3784-3791"},"PeriodicalIF":4.6,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12079118/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144094337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"TiN/SiO2 core–shell refractory plasmonic nanostructures unlock unprecedented 26.7% power conversion efficiency in Pb-free perovskite solar cells","authors":"Ahmed A. Mohsen, Mohamed Zahran, S. E. D. Habib and Nageh K. Allam","doi":"10.1039/D5NA00210A","DOIUrl":"10.1039/D5NA00210A","url":null,"abstract":"<p >TiN/SiO<small>₂</small> core–shell refractory plasmonic nanoparticles have been utilized as highly efficient nanoantennas to enhance the performance of lead-free perovskite solar cells (PSCs). The SiO<small>₂</small> shell, selected for its high refractive index and low extinction coefficient, enables precise light control while minimizing optical losses. A 3D finite element method (FEM)-based optoelectronic model was developed to analyze the optical and electrical characteristics of both unmodified and TiN/SiO<small>₂</small>-integrated PSCs. The results demonstrate a strong correlation between power conversion efficiency (PCE) and nanoparticle size. Incorporating 90 nm nanoparticles increases the PCE from 12.9% to 17.3%, while 115 nm nanoparticles achieve an impressive 26.7%, marking a 97.3% improvement. These findings highlight the pivotal role of tailored plasmonic nanostructures in maximizing light absorption and energy conversion. This study advances the understanding of plasmonic nanomaterials in photovoltaics and offers a viable strategy for enhancing the efficiency of lead-free PSCs. The integration of TiN/SiO<small>₂</small> nanoparticles presents a promising pathway for developing high-performance, sustainable solar technologies.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 12","pages":" 3859-3866"},"PeriodicalIF":4.6,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12091242/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144120310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"An AlFe2O4@SiO2–SO3H innovative nanocatalyst: a sustainable approach for the A3 coupling reaction in a DES for 2-thioarylbenzoazoles†","authors":"Ahmad Sajjadi, Suranjana V. Mayani, Suhas Ballal, Shaker Al-Hasnaawei, Abhayveer Singh, Kattela Chennakesavulu and Kamal Kant Joshi","doi":"10.1039/D5NA00247H","DOIUrl":"10.1039/D5NA00247H","url":null,"abstract":"<p >The A3 coupling reaction, which facilitates the synthesis of 2-thioarylbenzoazoles, represents a significant transformation in organic chemistry with implications in drug discovery and materials science. In this study, we introduce a novel nanocatalyst, AlFe<small>₂</small>O<small>₄</small>@SiO<small>₂</small>–SO<small>₃</small>H, designed to enhance the efficiency and sustainability of this reaction. The catalyst is synthesized by functionalizing aluminum ferrite (AlFe<small>₂</small>O<small>₄</small>) with chlorosulfonic acid (Cl–SO<small>₃</small>H), promoting its role as an effective acid catalyst. Utilizing deep eutectic solvents (DESs) as a green reaction medium further contributes to the sustainability of the process by providing a biodegradable and non-toxic environment. Optimization studies were conducted to determine the optimal reaction conditions, including catalyst loading, temperature, and solvent composition. Characterization of the nanocatalyst was performed using techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FTIR) to confirm successful synthesis and functionalization. The AlFe<small>₂</small>O<small>₄</small>@SiO<small>₂</small>–SO<small>₃</small>H nanocatalyst exhibited excellent catalytic activity, resulting in high yields of 2-thioarylbenzoazoles under mild conditions while allowing for easy recovery and reuse without significant loss of activity. This work demonstrates the potential of AlFe<small>₂</small>O<small>₄</small>@SiO<small>₂</small>–SO<small>₃</small>H as a sustainable catalytic system for A3 coupling reactions, contributing to the development of environmentally friendly methodologies in organic synthesis.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 13","pages":" 4039-4055"},"PeriodicalIF":4.6,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12101128/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144142507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Enhanced photocatalytic degradation of methylene blue dye via valorization of a polyethylene terephthalate plastic waste-derived metal–organic framework-based ZnO@Co-BDC composite catalyst†","authors":"Biniyam Abdu Berehe, Ali Ahmed Desalew, Getahun Worku Derbe, Derese Moges Misganaw, Kedir Seid Mohammed, Jia-Yaw Chang and Wubshet Mekonnen Girma","doi":"10.1039/D4NA01071J","DOIUrl":"10.1039/D4NA01071J","url":null,"abstract":"<p >The growth of industrialization contributes to the pollution of natural water bodies. Among these pollutants, organic dyes and plastic waste materials account for the majority of contaminants and are associated with health risks. This research explores a metal–organic framework (MOF)-based composite catalyst, ZnO@Co-BDC, for the degradation of methylene blue (MB). We developed a Co-BDC MOF synthesized through a solvothermal route using terephthalic acid (BDC) as a linker, which was extracted from polyethylene terephthalate plastic waste <em>via</em> alkaline hydrolysis, and using cobalt nitrate hexahydrate as a cobalt source. The ZnO@Co-BDC composite catalyst was synthesized through a solvothermal route using cobalt, BDC and zinc precursors. The obtained products were characterized using powder X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and ultraviolet diffuse reflectance spectroscopy (UV-DRS). The performance of ZnO@Co-BDC was assessed for the degradation of MB and showed 87.5% under visible light irradiation for 80 min, surpassing pristine ZnO (74%) and Co-BDC MOF (39%) under the same conditions. The kinetic study indicated that the degradation followed first-order kinetics with a rate constant of 2.501 × 10<small>⁻²</small> min<small>⁻¹</small>. Furthermore, the effects of catalyst dose, irradiation time, pH, and MB concentration were optimized for the efficient composite catalyst ZnO@Co-BDC. The photodegradation mechanism was also investigated through UV-DRS and quenching experiments in the presence of different scavengers. Meanwhile, the developed composite demonstrated excellent recovery and reuse capabilities for up to six cycles under optimal conditions. The developed MOF-based composite catalyst enabled the simultaneous valorization of plastic waste and remediation of environmental pollutants by converting waste to wealth.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 12","pages":" 3834-3845"},"PeriodicalIF":4.6,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12091243/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144120306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Thermal conductivity of graphene coated copper under uniaxial tensile mechanical strain†","authors":"Micah P. Vallin, Hisato Yamaguchi, Rijan Karkee, Chanho Lee, Ramon M. Martinez, Saryu J. Fensin, Jun Beom Park, Hi Tin Vo, Richard Z. Zhang and Michael T. Pettes","doi":"10.1039/D5NA00088B","DOIUrl":"10.1039/D5NA00088B","url":null,"abstract":"<p >Graphene continues to demonstrate promise as a highly effective barrier coating, even at only one atom thick. The thermal properties of this coating are also promising to allow diffusion of heat across the surface, as the isolated graphene is an intrinsically good thermal conductor. However, this and its behavior under mechanical deformation have been less extensively studied. This report demonstrates that the in-plane thermal conductivity and interfacial thermal conductance of graphene coatings on copper are affected by mechanical strain. By inducing strain in the copper substrate, the Raman-active 2D peak exhibits a change in position and a change in laser power dependence as the copper substrate is uniaxially elongated to a maximum of 0.5%. Non-linear trends in thermal conductivity are observed with tensile strain in samples with differing strain transfer rates from the substrate, indicating the close correlation between intrinsic thermal conduction and interfacial properties in atomically thin coatings transferred onto metals.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 12","pages":" 3655-3663"},"PeriodicalIF":4.6,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12097146/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144142940","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Carbon quantum dots for sustainable energy: enhancing electrocatalytic reactions through structural innovation","authors":"Fadhel F. Sead, Yashwantsinh Jadeja, Anjan Kumar, Rekha M. M., Mayank Kundlas, Suman Saini, Kamal Kant Joshi and Hadi Noorizadeh","doi":"10.1039/D5NA00205B","DOIUrl":"10.1039/D5NA00205B","url":null,"abstract":"<p >Carbon quantum dots (CQDs) have emerged as a promising class of nanomaterials due to their unique optical, electrical, and catalytic properties, positioning them as key players in electrocatalytic applications. This review provides a comprehensive and up-to-date analysis of CQDs, focusing on their electrocatalytic behavior in critical reactions such as the oxygen evolution reaction (OER), hydrogen evolution reaction (HER), oxygen reduction reaction (ORR), carbon dioxide reduction reaction (CO<small>₂</small>RR), bifunctional catalysis and liquid fuel electrooxidation. Distinct from prior studies, this study highlights recent innovations in CQD synthesis, including heteroatom doping and defect engineering, and explores their structural properties—like absorbance, photoluminescence, and electroluminescence—that enhance catalytic performance. We elucidate the electrocatalytic mechanisms (<em>e.g.</em>, reactant adsorption, electron transfer, and intermediate stabilization) and address challenges such as low conductivity and scalability, proposing advanced strategies like hybridization with transition metals. Additionally, this review uniquely emphasizes the potential of CQDs in bifunctional catalysis and environmental applications, offering fresh insights into their role in advancing sustainable energy technologies.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 13","pages":" 3961-3998"},"PeriodicalIF":4.6,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12118363/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144182769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Polymer/AgPt bimetallic nanoparticle synergy: optimizing plasmonic durability through controlled synthesis and matrix integration†","authors":"Abeer Fahes, Lavinia Balan, Caroline Andreazza-Vignolle, Claudia de Melo, Didier Zanghi and Pascal Andreazza","doi":"10.1039/D5NA00187K","DOIUrl":"10.1039/D5NA00187K","url":null,"abstract":"<p >An innovative approach combining UV-induced polymerization and ultra-high vacuum (UHV) atomic vapor deposition was developed to synthesize and disperse 2–3 nm AgPt bimetallic nanoparticles (BNPs) within a non-porous poly (dipropylene glycol diacrylate) (PDGDA) matrix, surpassing conventional porous polymer strategies. This method offers unprecedented control over the structural properties of BNPs and in general nanoalloys, with the polymer matrix playing a critical role in regulating nanoparticle formation, spatial arrangement, and size uniformity. The PDGDA matrix enhances nanoparticle stability through steric stabilization and controlled diffusion, effectively maintaining small nanoparticle sizes (∼2.4–2.8 nm) and low dispersity (<em>σ</em><small>_D</small>/<em>D</em> = 0.16) during extended high-temperature annealing. Confinement of nanoparticles (NPs) was significantly accelerated by successive thermal annealing to 320 °C, which increased polymer chain mobility and reduced viscosity, enabling rapid diffusion while preserving the structural integrity of the polymer matrix. This process dramatically reduced the embedding time from 12 days at room temperature to near-instantaneous incorporation upon heating. Successful confinement is attributed to key thermodynamic factors that promote interfacial interactions and particle mobility within the polymer network. Experimental results reveal distinctive UV plasmonic properties of the embedded AgPt BNPs with long-term stability. The produced AgPt BNPs exhibit significantly stronger localized surface plasmon resonances (LSPRs) than pure platinum nanoparticles, attributed to synergistic effects between the two metals. Factors contributing to this enhancement include silver's high electrical conductivity and relatively low optical losses, electromagnetic coupling, and localized electric field enhancement, highlighting the potential of these BNPs for advanced plasmonics. This research addresses the growing demand for surface-enhanced Raman scattering (SERS) detection of UV-absorbing biospecies and the development of more efficient broad-spectrum solar cells.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 13","pages":" 4087-4103"},"PeriodicalIF":4.6,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12108967/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144174240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Monodisperse spherical Ag+ doped Cs2KBiCl6 nanocrystals: utilizing steric hindrance engineering for inkjet printing of anti-counterfeiting patterns†","authors":"Shaoli Song, Youlun Zhu, Hanmei Jiang, Huichao He, Qian Yang, Jianbei Qiu and Tao Han","doi":"10.1039/D4NA00988F","DOIUrl":"10.1039/D4NA00988F","url":null,"abstract":"<p >Anti-counterfeiting is one of the critical application fields of luminescent materials. Nanocrystal luminescent materials are more suitable for anti-counterfeiting applications because they are tiny and more conducive to patterning. The preparation of monodisperse and spherical lead-free perovskite nanocrystals by a propagable method is a hot topic in anti-counterfeiting materials. In this work, monodisperse spherical Ag<small>⁺</small> doped Cs<small>₂</small>KBiCl<small>₆</small> nanocrystals with an average diameter of 3.51 nm were prepared by using the propagable ligand-assisted reprecipitation method at room temperature, attributed to steric hindrance engineering by increasing the ligand size. Due to relaxation of the transition barrier due to doping, excited with 365 nm ultraviolet light, the nanocrystals exhibit orange emission peaking at 600 nm, which is related to the transition recombination of Bi<small>³⁺</small> (<small>¹</small>S<small>₀</small> → <small>³</small>P<small>₁</small>), and the maximum photoluminescence quantum yield is 3.80%. A printable ink is prepared by combining the nanocrystals with PDMS adhesive and its curing agent, which can be used for inkjet printing of anti-counterfeiting patterns.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 12","pages":" 3828-3833"},"PeriodicalIF":4.6,"publicationDate":"2025-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12086864/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144111028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Synthesis of CsPbBr3 decorated ZIF-8 nanocomposite for enhanced photocatalytic performance†","authors":"Alen Sam Thomas, Philip Nathaniel Immanuel, Neena Prasad, Achiad Goldreich, Jonathan Prilusky, Raanan Carmieli and Lena Yadgarov","doi":"10.1039/D5NA00217F","DOIUrl":"10.1039/D5NA00217F","url":null,"abstract":"<p >CsPbBr<small>₃</small> (CPB) perovskite nanocrystals (NCs) have attracted considerable interest due to their outstanding charge carrier mobility, long diffusion lengths, and efficient visible light absorption, making them ideal candidates for photocatalysis, light-emitting diodes (LEDs), solar cells, and photodetectors. However, their practical applications are limited by poor environmental stability. To address this challenge, we employ a zeolitic imidazolate framework (ZIF), specifically ZIF-8, as a stabilizing matrix for its exceptional thermal and chemical stability, high surface area, and versatile synthesis routes. The CPB/ZIF-8 nanocomposite was synthesized by integrating hot-injection-produced CPB NCs with ZIF-8 using an optimized mixing approach, ensuring a uniform NCs distribution. Electron microscopy (EM) analysis confirmed the well-controlled and uniform distribution of the NCs on the surface of the ZIF-8. Moreover, the Fourier-transform infrared spectroscopy (FTIR) revealed ligand exchange, where the imidazole linkers of the ZIF-8 structure replace the NCs ligands. The process advances almost epitaxial attachment of the latter, thus promoting effective charge interactions in the integration process. Indeed, we observe that upon formation of the composite, there is a 92% quenching in the photoluminescence (PL) of the NCs. This finding further indicates efficient charge separation and reduced electron–hole recombination. To gain deeper insight into the charge transfer mechanisms, we conducted electron paramagnetic resonance (EPR) measurements to compare the radical generation capabilities of CPB and ZIF with those of the CPB/ZIF composite. The composite exhibited superior radical generation capabilities, particularly hydroxyl radicals (˙OH), indicating enhanced charge transfer. These findings suggest that the composite is a highly promising candidate for photocatalysis. Building on these findings, we explored the photocatalytic abilities of the composite through dye degradation experiments, using methyl orange (MO) and bromocresol green (BCG) as model dyes. The CPB/ZIF nanocomposite demonstrated significantly enhanced photocatalytic performance compared to pristine ZIF and CPB NCs. Specifically, its degradation rates were 1.48× and 1.75× higher for MO and BCG, respectively, than those of CPB NCs. This improvement highlights the effective interaction between CPB NCs and ZIF, establishing the CPB/ZIF nanocomposite as a promising material for photocatalysis and optoelectronic applications.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 12","pages":" 3764-3777"},"PeriodicalIF":4.6,"publicationDate":"2025-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12076080/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144078661","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}