Two-dimensional layered metal oxides (2D LMOs) have emerged as a rapidly growing class of materials that combine the advantages of reduced dimensionality with the functional diversity of transition metal oxides. Their high surface-to-volume ratio, structural anisotropy, tunable bandgap, and variable oxidation states endow them with unique electrical, optical, and catalytic properties. Recent advances in atomic layer deposition, vapor-phase synthesis, and liquid-phase exfoliation have enabled the scalable fabrication of high-quality 2D LMOs with controlled stoichiometry and thickness. This review provides a comprehensive overview of their structure–property relationships, charge transport mechanisms, and interfacial phenomena, emphasizing how defect engineering, quantum confinement, and interlayer coupling can be exploited to tailor their performance. The integration of 2D LMOs into van der Waals heterostructures further enhances band alignment, charge transfer, and excitonic control, unlocking new opportunities for transistors, sensors, and spintronic and optoelectronic devices. Current challenges such as environmental stability, phase control, and large-scale processability are critically assessed. Finally, emerging computational and machine learning-guided approaches are discussed as pathways to accelerate the rational design of 2D LMOs for flexible, energy-efficient, and multifunctional electronic applications.
{"title":"Two-dimensional layered metal oxides (2D LMOs) for next-generation electronic devices","authors":"Arpit Verma, Alka Rani and Bal Chandra Yadav","doi":"10.1039/D5NA00895F","DOIUrl":"10.1039/D5NA00895F","url":null,"abstract":"<p >Two-dimensional layered metal oxides (2D LMOs) have emerged as a rapidly growing class of materials that combine the advantages of reduced dimensionality with the functional diversity of transition metal oxides. Their high surface-to-volume ratio, structural anisotropy, tunable bandgap, and variable oxidation states endow them with unique electrical, optical, and catalytic properties. Recent advances in atomic layer deposition, vapor-phase synthesis, and liquid-phase exfoliation have enabled the scalable fabrication of high-quality 2D LMOs with controlled stoichiometry and thickness. This review provides a comprehensive overview of their structure–property relationships, charge transport mechanisms, and interfacial phenomena, emphasizing how defect engineering, quantum confinement, and interlayer coupling can be exploited to tailor their performance. The integration of 2D LMOs into van der Waals heterostructures further enhances band alignment, charge transfer, and excitonic control, unlocking new opportunities for transistors, sensors, and spintronic and optoelectronic devices. Current challenges such as environmental stability, phase control, and large-scale processability are critically assessed. Finally, emerging computational and machine learning-guided approaches are discussed as pathways to accelerate the rational design of 2D LMOs for flexible, energy-efficient, and multifunctional electronic applications.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 1","pages":" 13-52"},"PeriodicalIF":4.6,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12690833/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145743382","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}
Subham Preetam, Muhammad Fazle Rabbee, Richa Mishra, Shailendra Thapliyal, Ravi Deshwal, Sarvesh Rustagi, Archana Dashmana, Rasiravathanahalli K. Govindarajan and Sumira Malik
Brain cancer remains one of the most challenging malignancies due to the blood–brain barrier (BBB), limited drug penetration, and resistance to conventional therapies. Recent advancements in magnetic nanoparticles (MNPs) have opened new avenues for targeted and efficient brain cancer treatment. MNPs offer multifunctionality, including magnetic hyperthermia therapy, targeted drug delivery, and enhanced imaging via magnetic resonance imaging (MRI). This review explores the latest progress in MNP-based theranostics, highlighting their physicochemical properties, functionalization strategies, and mechanisms of action in brain cancer therapy. Additionally, we discuss novel approaches such as stimuli-responsive nanocarriers, BBB penetration techniques, and multifunctional hybrid nanoparticles. Furthermore, preclinical and clinical studies are reviewed to assess the current status and translational challenges. Despite promising outcomes, toxicity, biodistribution, and long-term biocompatibility remain key hurdles in clinical applications. Addressing these limitations will pave the way for personalized nanomedicine-based brain cancer treatment, optimizing therapeutic efficacy and patient outcomes.
{"title":"Targeting brain tumours with precision: advances in magnetic nanoparticle therapy","authors":"Subham Preetam, Muhammad Fazle Rabbee, Richa Mishra, Shailendra Thapliyal, Ravi Deshwal, Sarvesh Rustagi, Archana Dashmana, Rasiravathanahalli K. Govindarajan and Sumira Malik","doi":"10.1039/D5NA01046B","DOIUrl":"10.1039/D5NA01046B","url":null,"abstract":"<p >Brain cancer remains one of the most challenging malignancies due to the blood–brain barrier (BBB), limited drug penetration, and resistance to conventional therapies. Recent advancements in magnetic nanoparticles (MNPs) have opened new avenues for targeted and efficient brain cancer treatment. MNPs offer multifunctionality, including magnetic hyperthermia therapy, targeted drug delivery, and enhanced imaging <em>via</em> magnetic resonance imaging (MRI). This review explores the latest progress in MNP-based theranostics, highlighting their physicochemical properties, functionalization strategies, and mechanisms of action in brain cancer therapy. Additionally, we discuss novel approaches such as stimuli-responsive nanocarriers, BBB penetration techniques, and multifunctional hybrid nanoparticles. Furthermore, preclinical and clinical studies are reviewed to assess the current status and translational challenges. Despite promising outcomes, toxicity, biodistribution, and long-term biocompatibility remain key hurdles in clinical applications. Addressing these limitations will pave the way for personalized nanomedicine-based brain cancer treatment, optimizing therapeutic efficacy and patient outcomes.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 2","pages":" 458-478"},"PeriodicalIF":4.6,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12704653/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145768459","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}
Asif Al Suny, Tazrian Noor, Md. Hasibul Hossain, A. F. M. Afnan Uzzaman Sheikh and Mustafa Habib Chowdhury
Composite light-trapping structures offer a promising approach to achieving broadband absorption and high efficiency in thin-film solar cells (TFSCs) in order to accelerate sustainable energy solutions. As the leading material in thin-film solar technology, cadmium telluride (CdTe) faces challenges from surface reflective losses across the solar spectrum and weak absorption in the near-infrared (NIR) range. This computational study addresses these limitations by employing a dual light trapping technique: the top surfaces of both the cadmium sulfide (CdS) and CdTe layers are tapered as nanocones (NCs), while germanium (Ge) spherical nanoparticles (NPs) are embedded within the CdTe absorber layer to enhance broadband absorption. Numerical simulations using Finite-Difference Time-Domain (FDTD) and other methods are used to optimize the parameters and configurations of both nanostructures, aiming to achieve peak optoelectronic performance. The results show that a short-circuit current density (Jsc) of 35.38 mA cm−2 and a power conversion efficiency (PCE) of 27.76% can be achieved with optimal nanocone (NC) texturing and spherical Ge NP configurations, an approximately 45% and 81% increase in Jsc and PCE, respectively. To understand the enhancement mechanisms, the study includes analyses using diffraction grating theory and Mie theory. Fabricability of these structures is also evaluated. Furthermore, an additional study on the effects of incident angle variation and polarization change demonstrates that the optimal structure is robust under practical conditions, maintaining consistent performance.
复合光捕获结构为实现薄膜太阳能电池(TFSCs)的宽带吸收和高效率提供了一种有前途的方法,以加速可持续能源解决方案的发展。作为薄膜太阳能技术的主要材料,碲化镉(CdTe)面临着横跨太阳光谱的表面反射损失和近红外(NIR)范围的弱吸收的挑战。本计算研究通过采用双光捕获技术解决了这些限制:硫化镉(CdS)和碲化镉层的顶表面都被锥形为纳米锥(nc),而锗(Ge)球形纳米颗粒(NPs)被嵌入碲化镉吸收层中,以增强宽带吸收。利用时域有限差分(FDTD)等方法进行数值模拟,优化两种纳米结构的参数和结构,以达到峰值光电性能。结果表明,优化纳米锥(NC)织构和球形Ge NP结构可实现35.38 mA cm-2的短路电流密度(jsc)和27.76%的功率转换效率(PCE), jsc和PCE分别提高了约45%和81%。为了理解增强机理,研究包括衍射光栅理论和米氏理论的分析。这些结构的可制造性也进行了评估。此外,对入射角变化和偏振变化的影响进行了研究,结果表明该优化结构在实际条件下具有较强的鲁棒性,并保持了稳定的性能。
{"title":"Broadband light absorption in cadmium telluride thin-film solar cells via composite light trapping techniques","authors":"Asif Al Suny, Tazrian Noor, Md. Hasibul Hossain, A. F. M. Afnan Uzzaman Sheikh and Mustafa Habib Chowdhury","doi":"10.1039/D5NA00325C","DOIUrl":"10.1039/D5NA00325C","url":null,"abstract":"<p >Composite light-trapping structures offer a promising approach to achieving broadband absorption and high efficiency in thin-film solar cells (TFSCs) in order to accelerate sustainable energy solutions. As the leading material in thin-film solar technology, cadmium telluride (CdTe) faces challenges from surface reflective losses across the solar spectrum and weak absorption in the near-infrared (NIR) range. This computational study addresses these limitations by employing a dual light trapping technique: the top surfaces of both the cadmium sulfide (CdS) and CdTe layers are tapered as nanocones (NCs), while germanium (Ge) spherical nanoparticles (NPs) are embedded within the CdTe absorber layer to enhance broadband absorption. Numerical simulations using Finite-Difference Time-Domain (FDTD) and other methods are used to optimize the parameters and configurations of both nanostructures, aiming to achieve peak optoelectronic performance. The results show that a short-circuit current density (<em>J</em><small><sub>sc</sub></small>) of 35.38 mA cm<small><sup>−2</sup></small> and a power conversion efficiency (PCE) of 27.76% can be achieved with optimal nanocone (NC) texturing and spherical Ge NP configurations, an approximately 45% and 81% increase in <em>J</em><small><sub>sc</sub></small> and PCE, respectively. To understand the enhancement mechanisms, the study includes analyses using diffraction grating theory and Mie theory. Fabricability of these structures is also evaluated. Furthermore, an additional study on the effects of incident angle variation and polarization change demonstrates that the optimal structure is robust under practical conditions, maintaining consistent performance.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 2","pages":" 682-700"},"PeriodicalIF":4.6,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12703628/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145768501","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}
Tasmina Khandaker, Ahmed B. M. Ibrahim, Wael S. Al-Rashed, Khalid I. Anojaidi, Waleed A. Al-Suwaylih, Mohammed A. Al-Suwaylih, Mohamed A. Habib and Muhammad Sarwar Hossain
The emergence of effective, durable waste water treatment technology is of paramount importance due to the rising threat of toxic heavy metal pollution of water resources to human health as well as the environment. In order to improve multi-functional adsorption, we present the synthesis and performance of ZePol-4, a novel zeolite–polymer composite made from ETS-4 zeolite, chitosan, polyvinyl alcohol (PVA), and L-cysteine. The crystallinity, porosity, and functional group integrity of the composite were validated by structural and morphological characterization (XRD, SEM, and EDS). Excellent uptake capacities for important heavy metals were shown by batch adsorption experiments, with equilibrium adsorption capacities of 243.5 mg g−1 (Pb2+), 170.1 mg g−1 (Hg2+), 113.5 mg g−1 (Cu2+), 80.3 mg g−1 (Cd2+), and 45.3 mg g−1 (As3+). In accordance with this, ZePol-4 achieved high removal efficiencies in 60 minutes of 98% for Pb2+, 93% for Cd2+, 88% for Hg2+, 75% for As3+, and 70% for Cu2+. The composite required less extensive chemical adjustment because it worked well over a broad pH range, with optimal removal taking place close to neutral pH. The accuracy of the removal data was guaranteed by dual quantification using UV-vis and ICP-MS. Strong binding interactions and quick kinetics were made possible by the complementary contributions of amino, hydroxyl, and thiol groups through surface complexation and ion exchange. With its quick adsorption, high selectivity, and operational compatibility with actual environmental conditions, ZePol-4 shows great promise as a scalable, environmentally friendly, and highly effective material for tertiary wastewater treatment.
{"title":"Sustainable wastewater treatment using novel zeolite–polymer (ZePol) composite materials","authors":"Tasmina Khandaker, Ahmed B. M. Ibrahim, Wael S. Al-Rashed, Khalid I. Anojaidi, Waleed A. Al-Suwaylih, Mohammed A. Al-Suwaylih, Mohamed A. Habib and Muhammad Sarwar Hossain","doi":"10.1039/D5NA00996K","DOIUrl":"10.1039/D5NA00996K","url":null,"abstract":"<p >The emergence of effective, durable waste water treatment technology is of paramount importance due to the rising threat of toxic heavy metal pollution of water resources to human health as well as the environment. In order to improve multi-functional adsorption, we present the synthesis and performance of ZePol-4, a novel zeolite–polymer composite made from ETS-4 zeolite, chitosan, polyvinyl alcohol (PVA), and <small>L</small>-cysteine. The crystallinity, porosity, and functional group integrity of the composite were validated by structural and morphological characterization (XRD, SEM, and EDS). Excellent uptake capacities for important heavy metals were shown by batch adsorption experiments, with equilibrium adsorption capacities of 243.5 mg g<small><sup>−1</sup></small> (Pb<small><sup>2+</sup></small>), 170.1 mg g<small><sup>−1</sup></small> (Hg<small><sup>2+</sup></small>), 113.5 mg g<small><sup>−1</sup></small> (Cu<small><sup>2+</sup></small>), 80.3 mg g<small><sup>−1</sup></small> (Cd<small><sup>2+</sup></small>), and 45.3 mg g<small><sup>−1</sup></small> (As<small><sup>3+</sup></small>). In accordance with this, ZePol-4 achieved high removal efficiencies in 60 minutes of 98% for Pb<small><sup>2+</sup></small>, 93% for Cd<small><sup>2+</sup></small>, 88% for Hg<small><sup>2+</sup></small>, 75% for As<small><sup>3+</sup></small>, and 70% for Cu<small><sup>2+</sup></small>. The composite required less extensive chemical adjustment because it worked well over a broad pH range, with optimal removal taking place close to neutral pH. The accuracy of the removal data was guaranteed by dual quantification using UV-vis and ICP-MS. Strong binding interactions and quick kinetics were made possible by the complementary contributions of amino, hydroxyl, and thiol groups through surface complexation and ion exchange. With its quick adsorption, high selectivity, and operational compatibility with actual environmental conditions, ZePol-4 shows great promise as a scalable, environmentally friendly, and highly effective material for tertiary wastewater treatment.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 3","pages":" 1027-1041"},"PeriodicalIF":4.6,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12778360/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934329","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}
Carbon dots (C-dots) have emerged as highly promising light-harvesting materials, particularly as photosensitizers, due to their eco-friendliness, biocompatibility, and cost-efficiency. Their adaptability as photosensitizers has garnered widespread attention, marking them as pivotal materials for future technological innovations. One of the key attributes of C-dots is their dual functionality in charge transfer, enabling them to serve as both electron donors and acceptors. This charge transfer process between C-dots and small organic molecules as quenchers plays a critical role in diverse applications such as photocatalysis, sensing, and optoelectronics. In this perspective, we have discussed the capability of C-dots in confined environments, doped C-dots, C-dots/molecular hybrids, and perovskite/C-dots composites as photosensitizers. This perspective includes the origin of fluorescence and carrier dynamics in full colour light-emitting C-dots, followed by a novel way to control the photosensitizer capability of C-dots via the transfer of electrons and holes in hybrids, composites, and doped C-dots, and the effects of the core and surface in the electron transfer process. The photosensitizer capability of C-dots was investigated via exploring the charge transfer dynamics using various advanced optical techniques like steady-state and time-resolved photoluminescence and ultrafast transient absorption (TA). This perspective also focuses on understanding the ultrafast dynamics of C-dots, such as charge transfer, charge transport, and charge recombination, in various environments, composites, and hybrid systems, with an emphasis on their development as effective photosensitizers. The extensive range of reported electron donor–acceptor systems underscores the versatility of C-dots as photosensitizers, with their tuneable electronic properties tailored to address the demands of emerging technological challenges.
{"title":"Carbon dots as photosensitizers: unraveling their ultrafast charge transfer, challenges, and future prospects","authors":"Somen Mondal","doi":"10.1039/D5NA00806A","DOIUrl":"10.1039/D5NA00806A","url":null,"abstract":"<p >Carbon dots (C-dots) have emerged as highly promising light-harvesting materials, particularly as photosensitizers, due to their eco-friendliness, biocompatibility, and cost-efficiency. Their adaptability as photosensitizers has garnered widespread attention, marking them as pivotal materials for future technological innovations. One of the key attributes of C-dots is their dual functionality in charge transfer, enabling them to serve as both electron donors and acceptors. This charge transfer process between C-dots and small organic molecules as quenchers plays a critical role in diverse applications such as photocatalysis, sensing, and optoelectronics. In this perspective, we have discussed the capability of C-dots in confined environments, doped C-dots, C-dots/molecular hybrids, and perovskite/C-dots composites as photosensitizers. This perspective includes the origin of fluorescence and carrier dynamics in full colour light-emitting C-dots, followed by a novel way to control the photosensitizer capability of C-dots <em>via</em> the transfer of electrons and holes in hybrids, composites, and doped C-dots, and the effects of the core and surface in the electron transfer process. The photosensitizer capability of C-dots was investigated <em>via</em> exploring the charge transfer dynamics using various advanced optical techniques like steady-state and time-resolved photoluminescence and ultrafast transient absorption (TA). This perspective also focuses on understanding the ultrafast dynamics of C-dots, such as charge transfer, charge transport, and charge recombination, in various environments, composites, and hybrid systems, with an emphasis on their development as effective photosensitizers. The extensive range of reported electron donor–acceptor systems underscores the versatility of C-dots as photosensitizers, with their tuneable electronic properties tailored to address the demands of emerging technological challenges.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 3","pages":" 782-793"},"PeriodicalIF":4.6,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12728738/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145834425","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}
Jaehong Park, Dongchul Sung, Junho Yun and Suklyun Hong
Two-dimensional valleytronics offers a promising platform for novel information processing and quantum technologies by harnessing the valley degree of freedom. A key challenge lies in lifting valley degeneracy, for which magnetic proximity effects provide a promising route. Here, we demonstrate substantial valley splitting in a MoTe2/CrSCl heterostructure via first-principles calculations. We show that interlayer charge transfer and interfacial orbital hybridization critically govern the valley physics at the interface. Under a moderate in-plane tensile strain (3%) and an applied out-of-plane electric field (0.2 V Å−1), a sizable valley splitting of 63 meV emerges at the valence band maximum. These conditions induce hole doping and a pronounced Berry curvature of −23 Å2 at the K valley, realizing an electrically tunable anomalous valley Hall effect. Our findings establish the MoTe2/CrSCl interface as a versatile platform for valley-selective charge transport, opening pathways for valleytronic device applications.
二维谷电子学通过利用谷自由度为新型信息处理和量子技术提供了一个有前途的平台。一个关键的挑战在于提升谷简并,磁邻近效应为提升谷简并提供了一条有希望的途径。在这里,我们通过第一性原理计算证明了MoTe2/CrSCl异质结构中存在大量的谷分裂。我们发现层间电荷转移和界面轨道杂化对界面谷物理有重要的控制作用。在中等的面内拉伸应变(3%)和面外电场(0.2 V Å-1)作用下,价带最大值处出现了较大的63 meV谷裂。这些条件诱导空穴掺杂和K谷明显的-23 Å2的Berry曲率,实现了电可调谐的异常谷霍尔效应。我们的研究结果建立了MoTe2/CrSCl接口作为谷选择电荷传输的通用平台,为谷电子器件应用开辟了途径。
{"title":"Valley splitting and anomalous valley Hall effect in MoTe2/CrSCl heterostructure","authors":"Jaehong Park, Dongchul Sung, Junho Yun and Suklyun Hong","doi":"10.1039/D5NA00834D","DOIUrl":"10.1039/D5NA00834D","url":null,"abstract":"<p >Two-dimensional valleytronics offers a promising platform for novel information processing and quantum technologies by harnessing the valley degree of freedom. A key challenge lies in lifting valley degeneracy, for which magnetic proximity effects provide a promising route. Here, we demonstrate substantial valley splitting in a MoTe<small><sub>2</sub></small>/CrSCl heterostructure <em>via</em> first-principles calculations. We show that interlayer charge transfer and interfacial orbital hybridization critically govern the valley physics at the interface. Under a moderate in-plane tensile strain (3%) and an applied out-of-plane electric field (0.2 V Å<small><sup>−1</sup></small>), a sizable valley splitting of 63 meV emerges at the valence band maximum. These conditions induce hole doping and a pronounced Berry curvature of −23 Å<small><sup>2</sup></small> at the K valley, realizing an electrically tunable anomalous valley Hall effect. Our findings establish the MoTe<small><sub>2</sub></small>/CrSCl interface as a versatile platform for valley-selective charge transport, opening pathways for valleytronic device applications.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 2","pages":" 580-587"},"PeriodicalIF":4.6,"publicationDate":"2025-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679478/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145700798","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}
Lingcong He, Hongyang Xu, Yonghui Yang and Xue-Bo Chen
With the overuse of antibiotics and the emergence of increasingly complex application scenarios, single-strategy bactericidal approaches are proving increasingly inadequate in today's environment. How to simultaneously attack multiple “targets” from multiple dimensions has become one of the hot topics in current research. This study proposes a multi-mechanism synergistic antibacterial platform based on Janus polystyrene–gold nanoparticle (AuNPs–PS) microspheres using COMSOL 6.3. This platform achieves the displacement motion of Janus AuNPs–PS microspheres through the UV-induced photothermal effect (PTT), and combines dielectrophoretic force (DEP) to enable controlled enrichment and directional arrangement of the microspheres. It achieves enhanced sterilization efficiency through the synergistic interaction of the photothermal effect and DEP based on Janus AuNPs. The study first simulated the light absorption–scattering model of AuNPs–PS microspheres under UV irradiation, verifying that the microspheres can generate a temperature field via the photothermal effect. Subsequently, the motion of the microspheres under thermophoresis and their effective separation under DEP were simulated to assess their feasibility in practical applications. Finally, the paper compares the bactericidal rates achieved by the microspheres under UV irradiation alone versus under multi-mechanism synergy. Simulation results indicate that the synergistic effect of multiple mechanisms yields a bactericidal efficacy approximately 30% higher than that of a single strategy. Among these, UV itself has a bactericidal effect. Relevant literature indicates that AuNPs can generate high temperatures under the photothermal effect, thereby disrupting bacterial membrane structures to a certain extent. Furthermore, the photocatalytic effect on the AuNP surface can catalyze the production of large amounts of reactive oxygen species (ROS) under appropriate conditions, facilitating the inactivation of certain bacteria. The PS matrix serves as an ideal carrier for AuNPs, with its excellent functionalization and dielectric properties providing the foundation for DEP manipulation. Furthermore, the spatial targeting and enrichment effect of DEP significantly enhances the local microsphere concentration and contact efficiency with bacteria. This multi-synergistic approach combining “physical enrichment–photothermal–photocatalysis” offers a potential strategy for overcoming bacterial resistance barriers. Under simulated conditions, it demonstrates promising removal potential against persistent biofilms, providing a theoretical mechanism for combating drug-resistant bacterial infections without readily inducing resistance. However, this inference requires validation through biological experiments. The study aims to provide theoretical foundations and simulation guidance for developing highly efficient sterilization technologies.
{"title":"Theoretical study on the multi-mechanism synergistic bactericidal effect of asymmetric Janus AuNPs–PS microspheres","authors":"Lingcong He, Hongyang Xu, Yonghui Yang and Xue-Bo Chen","doi":"10.1039/D5NA00955C","DOIUrl":"10.1039/D5NA00955C","url":null,"abstract":"<p >With the overuse of antibiotics and the emergence of increasingly complex application scenarios, single-strategy bactericidal approaches are proving increasingly inadequate in today's environment. How to simultaneously attack multiple “targets” from multiple dimensions has become one of the hot topics in current research. This study proposes a multi-mechanism synergistic antibacterial platform based on Janus polystyrene–gold nanoparticle (AuNPs–PS) microspheres using COMSOL 6.3. This platform achieves the displacement motion of Janus AuNPs–PS microspheres through the UV-induced photothermal effect (PTT), and combines dielectrophoretic force (DEP) to enable controlled enrichment and directional arrangement of the microspheres. It achieves enhanced sterilization efficiency through the synergistic interaction of the photothermal effect and DEP based on Janus AuNPs. The study first simulated the light absorption–scattering model of AuNPs–PS microspheres under UV irradiation, verifying that the microspheres can generate a temperature field <em>via</em> the photothermal effect. Subsequently, the motion of the microspheres under thermophoresis and their effective separation under DEP were simulated to assess their feasibility in practical applications. Finally, the paper compares the bactericidal rates achieved by the microspheres under UV irradiation alone <em>versus</em> under multi-mechanism synergy. Simulation results indicate that the synergistic effect of multiple mechanisms yields a bactericidal efficacy approximately 30% higher than that of a single strategy. Among these, UV itself has a bactericidal effect. Relevant literature indicates that AuNPs can generate high temperatures under the photothermal effect, thereby disrupting bacterial membrane structures to a certain extent. Furthermore, the photocatalytic effect on the AuNP surface can catalyze the production of large amounts of reactive oxygen species (ROS) under appropriate conditions, facilitating the inactivation of certain bacteria. The PS matrix serves as an ideal carrier for AuNPs, with its excellent functionalization and dielectric properties providing the foundation for DEP manipulation. Furthermore, the spatial targeting and enrichment effect of DEP significantly enhances the local microsphere concentration and contact efficiency with bacteria. This multi-synergistic approach combining “physical enrichment–photothermal–photocatalysis” offers a potential strategy for overcoming bacterial resistance barriers. Under simulated conditions, it demonstrates promising removal potential against persistent biofilms, providing a theoretical mechanism for combating drug-resistant bacterial infections without readily inducing resistance. However, this inference requires validation through biological experiments. The study aims to provide theoretical foundations and simulation guidance for developing highly efficient sterilization technologies.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 3","pages":" 1014-1026"},"PeriodicalIF":4.6,"publicationDate":"2025-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12723689/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145827628","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}
The increasing burden of toxic heavy metals, dyes, pharmaceuticals, and pathogenic microorganisms in aquatic environments necessitates the development of sustainable purification strategies. This review comprehensively elucidates recent progress in the synthesis, characterization, and application of phytogen-based synthesis of functionalized magnetic nanoparticles (phytogen@MNPs) for eco-friendly wastewater treatment. Plant-derived bioactive compounds serve as green capping agents, facilitating the synthesis of multifunctional, biocompatible, and surface-reactive MNPs. This review details diverse phytogenic sources, synthesis methodologies, and advanced characterization techniques, highlighting the influence of surface modification on stability, adsorption efficiency, and superparamagnetic behavior. Applications in the adsorption and catalytic degradation of inorganic, organic, and microbial contaminants are critically discussed, along with the kinetics, isotherms, and thermodynamics of pollutant removal. The antibacterial properties, reusability, and impact of real water matrices are covered, highlighting the superior performance and cost-effectiveness of phytogen@MNPs. Mechanistic insights into pollutant–nanoparticle interactions reveal the decisive roles of surface functionalization and particle size. This review also encompasses the advantages of phytogen@MNPs over conventional materials, while also identifying the need for standardized protocols, evaluation of long-term stability, and strategies for scalable production to fully realize their potential in environmental remediation in future work.
{"title":"Magnetically driven, plant-extract-modified Fe3O4 nanoparticles for sustainable and eco-friendly wastewater detoxification: recent developments","authors":"Chanchal Das and Goutam Biswas","doi":"10.1039/D5NA00893J","DOIUrl":"10.1039/D5NA00893J","url":null,"abstract":"<p >The increasing burden of toxic heavy metals, dyes, pharmaceuticals, and pathogenic microorganisms in aquatic environments necessitates the development of sustainable purification strategies. This review comprehensively elucidates recent progress in the synthesis, characterization, and application of phytogen-based synthesis of functionalized magnetic nanoparticles (phytogen@MNPs) for eco-friendly wastewater treatment. Plant-derived bioactive compounds serve as green capping agents, facilitating the synthesis of multifunctional, biocompatible, and surface-reactive MNPs. This review details diverse phytogenic sources, synthesis methodologies, and advanced characterization techniques, highlighting the influence of surface modification on stability, adsorption efficiency, and superparamagnetic behavior. Applications in the adsorption and catalytic degradation of inorganic, organic, and microbial contaminants are critically discussed, along with the kinetics, isotherms, and thermodynamics of pollutant removal. The antibacterial properties, reusability, and impact of real water matrices are covered, highlighting the superior performance and cost-effectiveness of phytogen@MNPs. Mechanistic insights into pollutant–nanoparticle interactions reveal the decisive roles of surface functionalization and particle size. This review also encompasses the advantages of phytogen@MNPs over conventional materials, while also identifying the need for standardized protocols, evaluation of long-term stability, and strategies for scalable production to fully realize their potential in environmental remediation in future work.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 3","pages":" 743-781"},"PeriodicalIF":4.6,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12723263/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145827601","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}
Priyanka Goel, Christoffer Kauppinen, Ramesh Raju and Ilkka Tittonen
Titanium nitride (TiN) thin films demonstrate high electrical conductivity and thermal stability up to 400 °C in ambient conditions, with stability extending to 600–800 °C under inert or vacuum environments. Unlike many metals and transition metal nitrides, TiN combines high carrier mobility with moderate carrier concentration, making it ideal for thermal management and power-efficient applications in nanoelectronics and energy harvesting. This study systematically investigates the thermoelectric and electronic transport properties of TiN films grown by plasma-enhanced atomic layer deposition (PEALD), comparing them to those produced using traditional thermal atomic layer deposition (thermal ALD). These properties are studied as a function of growth temperature and the number of growth cycles. In particular, TiN films deposited by PEALD at 400 °C for 2000 ALD cycles exhibited a remarkable power factor of 512 µW m−1 K−2 at room temperature compared to a power factor of 4.95 µW m−1 K−2 measured for thermal ALD films fabricated under the same deposition conditions. Additionally, thermal conductivity was also measured for thicker TiN films (86 nm), yielding values of 26.96 W m−1 K−1 for PEALD and 7.01 W m−1 K−1 for thermal ALD, marking the first such report for ALD-grown TiN. These values offer an upper estimate of the thermal behavior in thinner films. Based on these measured properties, the thermoelectric figure of merit (zT) at room temperature was calculated to be 0.0056 for PEALD TiN films which is significantly higher than the value of 0.0002 obtained for thermal ALD TiN films. Our findings provide critical insights into transport properties of TiN, offering guidance for the development of conductive nanolayers in thermoelectric, nanoelectronic, and on-chip cooling applications, where precise control over thermal and electronic behavior is vital, thereby expanding the relevance of ALD TiN in high-performance applications.
氮化钛(TiN)薄膜在环境条件下具有高达400°C的高导电性和热稳定性,在惰性或真空环境下稳定性可扩展到600-800°C。与许多金属和过渡金属氮化物不同,TiN结合了高载流子迁移率和适度载流子浓度,使其成为纳米电子和能量收集领域热管理和节能应用的理想选择。本研究系统地研究了等离子体增强原子层沉积(PEALD)制备的TiN薄膜的热电和电子输运特性,并将其与传统热原子层沉积(thermal atomic layer deposition, ALD)制备的TiN薄膜进行了比较。研究了这些性质与生长温度和生长循环次数的关系。特别是,在400°C下经过2000次ALD循环,PEALD沉积的TiN薄膜在室温下的功率因数为512µW m-1 K-2,而在相同沉积条件下制备的热ALD薄膜的功率因数为4.95µW m-1 K-2。此外,还测量了较厚的TiN薄膜(86 nm)的导热系数,PEALD的导热系数为26.96 W m-1 K-1,热ALD的导热系数为7.01 W m-1 K-1,这是首次报道ALD生长TiN的导热系数。这些值提供了较薄薄膜中热行为的上限估计。根据这些测量的性能,计算出PEALD TiN薄膜在室温下的热电性能值(zT)为0.0056,明显高于热ALD TiN薄膜的0.0002。我们的研究结果为TiN的输运特性提供了重要的见解,为热电、纳米电子和片上冷却应用中导电纳米层的开发提供了指导,在这些应用中,对热和电子行为的精确控制至关重要,从而扩大了ALD TiN在高性能应用中的相关性。
{"title":"Thermoelectric and electronic transport properties of thermal and plasma-enhanced ALD grown titanium nitride thin films","authors":"Priyanka Goel, Christoffer Kauppinen, Ramesh Raju and Ilkka Tittonen","doi":"10.1039/D5NA00914F","DOIUrl":"10.1039/D5NA00914F","url":null,"abstract":"<p >Titanium nitride (TiN) thin films demonstrate high electrical conductivity and thermal stability up to 400 °C in ambient conditions, with stability extending to 600–800 °C under inert or vacuum environments. Unlike many metals and transition metal nitrides, TiN combines high carrier mobility with moderate carrier concentration, making it ideal for thermal management and power-efficient applications in nanoelectronics and energy harvesting. This study systematically investigates the thermoelectric and electronic transport properties of TiN films grown by plasma-enhanced atomic layer deposition (PEALD), comparing them to those produced using traditional thermal atomic layer deposition (thermal ALD). These properties are studied as a function of growth temperature and the number of growth cycles. In particular, TiN films deposited by PEALD at 400 °C for 2000 ALD cycles exhibited a remarkable power factor of 512 µW m<small><sup>−1</sup></small> K<small><sup>−2</sup></small> at room temperature compared to a power factor of 4.95 µW m<small><sup>−1</sup></small> K<small><sup>−2</sup></small> measured for thermal ALD films fabricated under the same deposition conditions. Additionally, thermal conductivity was also measured for thicker TiN films (86 nm), yielding values of 26.96 W m<small><sup>−1</sup></small> K<small><sup>−1</sup></small> for PEALD and 7.01 W m<small><sup>−1</sup></small> K<small><sup>−1</sup></small> for thermal ALD, marking the first such report for ALD-grown TiN. These values offer an upper estimate of the thermal behavior in thinner films. Based on these measured properties, the thermoelectric figure of merit (<em>zT</em>) at room temperature was calculated to be 0.0056 for PEALD TiN films which is significantly higher than the value of 0.0002 obtained for thermal ALD TiN films. Our findings provide critical insights into transport properties of TiN, offering guidance for the development of conductive nanolayers in thermoelectric, nanoelectronic, and on-chip cooling applications, where precise control over thermal and electronic behavior is vital, thereby expanding the relevance of ALD TiN in high-performance applications.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 2","pages":" 612-622"},"PeriodicalIF":4.6,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12687283/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145724641","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}
Catherine E. Araneda, Aldo A. Campos, Monica Soler and Marcelo J. Kogan
A stable and controllable coating can be formed on the surface of gold nanorods (AuNRs) by using metal–organic frameworks (MOFs), which avoids the agglomeration of the nanohybrid AuNR@MOF and also expands the functionality of the plasmon nanoparticles. In this review, we discuss the chemical role of the different components of the nanohybrid, i.e., AuNR, surface ligand or mesoporous nanostructure (MN) and the MOF around the AuNR. The methodologies used in the different synthesis stages and the factors to be considered to maintain stability in the construction of this type of nanostructures are also reported. Furthermore, we observed that there are a wide variety of MOF morphologies that can be built around AuNRs, even using the same components for their formation, which vary depending on the synthesis methodology. Finally, we discuss about the broad range of applications, of the AuNR@MOF nanohybrids, mainly in the biological field.
{"title":"Synthetic methodologies of gold nanorod@MOF nanohybrids focused on biological applications","authors":"Catherine E. Araneda, Aldo A. Campos, Monica Soler and Marcelo J. Kogan","doi":"10.1039/D5NA00832H","DOIUrl":"10.1039/D5NA00832H","url":null,"abstract":"<p >A stable and controllable coating can be formed on the surface of gold nanorods (AuNRs) by using metal–organic frameworks (MOFs), which avoids the agglomeration of the nanohybrid AuNR@MOF and also expands the functionality of the plasmon nanoparticles. In this review, we discuss the chemical role of the different components of the nanohybrid, <em>i.e.</em>, AuNR, surface ligand or mesoporous nanostructure (MN) and the MOF around the AuNR. The methodologies used in the different synthesis stages and the factors to be considered to maintain stability in the construction of this type of nanostructures are also reported. Furthermore, we observed that there are a wide variety of MOF morphologies that can be built around AuNRs, even using the same components for their formation, which vary depending on the synthesis methodology. Finally, we discuss about the broad range of applications, of the AuNR@MOF nanohybrids, mainly in the biological field.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 3","pages":" 794-810"},"PeriodicalIF":4.6,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12758404/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145900836","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}