Metal-organic frameworks (MOFs) have emerged as versatile precursors and templates for developing high-performance electrode materials for aqueous zinc-ion batteries (ZIBs), owing to their adjustable porosity, abundant metal-coordination sites, and structural flexibility. Among the diverse array of MOFs investigated, those based on manganese, copper, and cobalt, as well as their derivatives, have shown exceptional potential, exhibiting enhanced redox activity, structural integrity, and advantageous zinc-ion storage kinetics compared with many other MOF systems. This study emphasizes the synthesis methodologies, structural characteristics, and electrochemical benefits of these three significant MOF families. After a succinct overview of MOF chemistry, synthesis methodologies, and fundamental design principles for ZIB electrode materials, the article presents a systematic, comparative evaluation of Mn-MOFs, Cu-MOFs, Co-MOFs and V-MOFs, along with their corresponding metal oxides, sulfides, phosphates, carbon composites, and multidimensional hybrid structures. Recent publications for each MOF type are detailed in separate tables, including synthesis methods, morphological development, electrochemical behavior, and performance metrics. The discourse highlights the distinct properties of each metal center, Mn's multivalent redox chemistry, Cu's superior electron transport and coordination adaptability, and Co's elevated activity and stable structures, which together facilitate improved ion diffusion, substantial reversible capacity, and prolonged cycling durability. Ultimately, existing obstacles and potential research avenues are delineated to advance MOF-based materials for next-generation aqueous ZIB systems.
{"title":"Critical Progress of Mn, Cu, Co, and V-MOFs and Their Derivatives as Promising Electrodes for Aqueous Zn-Ion Batteries.","authors":"Ramanadha Mangiri, Joonho Bae","doi":"10.3390/nano16010033","DOIUrl":"10.3390/nano16010033","url":null,"abstract":"<p><p>Metal-organic frameworks (MOFs) have emerged as versatile precursors and templates for developing high-performance electrode materials for aqueous zinc-ion batteries (ZIBs), owing to their adjustable porosity, abundant metal-coordination sites, and structural flexibility. Among the diverse array of MOFs investigated, those based on manganese, copper, and cobalt, as well as their derivatives, have shown exceptional potential, exhibiting enhanced redox activity, structural integrity, and advantageous zinc-ion storage kinetics compared with many other MOF systems. This study emphasizes the synthesis methodologies, structural characteristics, and electrochemical benefits of these three significant MOF families. After a succinct overview of MOF chemistry, synthesis methodologies, and fundamental design principles for ZIB electrode materials, the article presents a systematic, comparative evaluation of Mn-MOFs, Cu-MOFs, Co-MOFs and V-MOFs, along with their corresponding metal oxides, sulfides, phosphates, carbon composites, and multidimensional hybrid structures. Recent publications for each MOF type are detailed in separate tables, including synthesis methods, morphological development, electrochemical behavior, and performance metrics. The discourse highlights the distinct properties of each metal center, Mn's multivalent redox chemistry, Cu's superior electron transport and coordination adaptability, and Co's elevated activity and stable structures, which together facilitate improved ion diffusion, substantial reversible capacity, and prolonged cycling durability. Ultimately, existing obstacles and potential research avenues are delineated to advance MOF-based materials for next-generation aqueous ZIB systems.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787443/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933964","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}
Liya Qiao, Zhimin Tong, Yabing Xu, Chunliu Guan, Geyu Liang, Lu Kong
Male reproductive disorders and declining fertility rates play an important role in birth rates, and their impact on future populations makes them one of the most serious public health issues of this century. Defects in spermatogenesis are the most common manifestation of male infertility, and exposure to environmental pollutants has been suggested as a potential cause. Nanomaterials, due to their unique physicochemical properties and widespread application, have raised growing concerns about their potential reproductive toxicity. Studies have shown that nickel nanoparticles (Ni NPs) have reproductive toxicity in male rats and mice, especially sperm damage. This study aimed to explore the male reproductive toxicity of Ni NPs and the role of mitochondrial fission in mouse spermatocytes (GC-2). Our results showed that Ni NPs induced the damage of mitochondrial structure and function in GC-2 cells and disrupted intramitochondrial homeostasis, thereby resulting in enhanced Dynamin-related protein 1(Drp1)-mediated mitochondrial fission and cell apoptosis, along with aggravated cytotoxicity and obvious reproductive toxicity. The mitochondrial division inhibitor 1(Mdivi-1) and lentiviral-transfected low expression of Dnm1l can significantly alleviate the germ cell toxicity caused by Ni NPs, suggesting a certain therapeutic effect. The novelty of this study lies in its systematic demonstration that Drp1-mediated mitochondrial division is a core pathogenic mechanism of Ni NP-induced male reproductive toxicity, and the validation of both pharmacological inhibition and genetic silencing as effective intervention strategies. Therefore, this study offers a reference for expanding the reproductive toxicity effect of Ni NPs and potential molecular mechanisms and provides an important basis for finding potential targets and treatment of Ni NPs.
男性生殖障碍和生育率下降在出生率方面起着重要作用,它们对未来人口的影响使它们成为本世纪最严重的公共卫生问题之一。精子发生缺陷是男性不育最常见的表现,暴露于环境污染物已被认为是一个潜在的原因。纳米材料由于其独特的物理化学性质和广泛的应用,引起了人们对其潜在生殖毒性的日益关注。研究表明,镍纳米颗粒对雄性大鼠和小鼠具有生殖毒性,尤其是精子损伤。本研究旨在探讨Ni NPs的雄性生殖毒性以及线粒体分裂在小鼠精母细胞(GC-2)中的作用。我们的研究结果表明,Ni NPs诱导GC-2细胞线粒体结构和功能损伤,破坏线粒体内稳态,从而导致动力蛋白相关蛋白1(Dynamin-related protein 1, Drp1)介导的线粒体分裂和细胞凋亡增强,细胞毒性加重,生殖毒性明显。线粒体分裂抑制剂1(Mdivi-1)和慢病毒转染低表达的Dnm1l可显著减轻Ni NPs引起的生殖细胞毒性,提示有一定的治疗作用。本研究的新颖之处在于系统论证了drp1介导的线粒体分裂是Ni np诱导的男性生殖毒性的核心致病机制,并验证了药物抑制和基因沉默作为有效的干预策略。因此,本研究为拓展Ni NPs的生殖毒性作用和潜在的分子机制提供了参考,为寻找Ni NPs的潜在靶点和治疗提供了重要依据。
{"title":"Promoting Drp1-Mediated Mitochondrial Division in Nickel Nanoparticles-Induced Reproductive Toxicity in GC-2 Cells.","authors":"Liya Qiao, Zhimin Tong, Yabing Xu, Chunliu Guan, Geyu Liang, Lu Kong","doi":"10.3390/nano16010034","DOIUrl":"10.3390/nano16010034","url":null,"abstract":"<p><p>Male reproductive disorders and declining fertility rates play an important role in birth rates, and their impact on future populations makes them one of the most serious public health issues of this century. Defects in spermatogenesis are the most common manifestation of male infertility, and exposure to environmental pollutants has been suggested as a potential cause. Nanomaterials, due to their unique physicochemical properties and widespread application, have raised growing concerns about their potential reproductive toxicity. Studies have shown that nickel nanoparticles (Ni NPs) have reproductive toxicity in male rats and mice, especially sperm damage. This study aimed to explore the male reproductive toxicity of Ni NPs and the role of mitochondrial fission in mouse spermatocytes (GC-2). Our results showed that Ni NPs induced the damage of mitochondrial structure and function in GC-2 cells and disrupted intramitochondrial homeostasis, thereby resulting in enhanced Dynamin-related protein 1(Drp1)-mediated mitochondrial fission and cell apoptosis, along with aggravated cytotoxicity and obvious reproductive toxicity. The mitochondrial division inhibitor 1(Mdivi-1) and lentiviral-transfected low expression of Dnm1l can significantly alleviate the germ cell toxicity caused by Ni NPs, suggesting a certain therapeutic effect. The novelty of this study lies in its systematic demonstration that Drp1-mediated mitochondrial division is a core pathogenic mechanism of Ni NP-induced male reproductive toxicity, and the validation of both pharmacological inhibition and genetic silencing as effective intervention strategies. Therefore, this study offers a reference for expanding the reproductive toxicity effect of Ni NPs and potential molecular mechanisms and provides an important basis for finding potential targets and treatment of Ni NPs.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12788166/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934430","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}
Nargish Parvin, Sang Woo Joo, Jae Hak Jung, Tapas K Mandal
In the original publication [...].
在原出版物中[…]。
{"title":"Correction: Parvin et al. Multimodal AI in Biomedicine: Pioneering the Future of Biomaterials, Diagnostics, and Personalized Healthcare. <i>Nanomaterials</i> 2025, <i>15</i>, 895.","authors":"Nargish Parvin, Sang Woo Joo, Jae Hak Jung, Tapas K Mandal","doi":"10.3390/nano16010036","DOIUrl":"10.3390/nano16010036","url":null,"abstract":"<p><p>In the original publication [...].</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787616/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934016","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}
Functional steel surfaces engineered through tailored micro-nano structures are increasingly vital for various applications such as high-performance aerospace components, energy conversion systems and defense equipment. Femtosecond laser filament processing is a recently proposed remote fabrication technique, showing the capability of fabricating micro-nano structures on irregular and large-area surfaces without the need of tight focusing. Nevertheless, the mechanisms underlying the formation of filament-induced structures remain not fully understood. Here we systematically investigate the formation mechanisms of filament-induced micro-nano structures on stainless steel surfaces by processing stainless steel in three manners: point, line, and area. We clarify the decisive role of the unique core-reservoir energy distribution of the filament in the formation of filament-induced micro-nano structures, and reveal that ablation, molten metal flow, and metal vapor condensation jointly drive the structure evolution through a dynamic interplay of competition and coupling, giving rise to the sequential morphological transitions of surface structures, from laser-induced periodic surface structures to ripple-like, crater-like, honeycomb-like, and ultimately taro-leaf-like structures. Our work not only clarifies the mechanisms of femtosecond laser filament processed morphological structures on steels but also provides insights onto intelligent manufacturing and design of advanced functional steel materials.
{"title":"Formation Mechanisms of Micro-Nano Structures on Steels by Strong-Field Femtosecond Laser Filament Processing.","authors":"Liansheng Zheng, Shuo Wang, Yingbo Cong, Chenxing Wang, Haowen Li, Hongyin Jiang, Helong Li, Hongwei Zang, Huailiang Xu","doi":"10.3390/nano16010037","DOIUrl":"10.3390/nano16010037","url":null,"abstract":"<p><p>Functional steel surfaces engineered through tailored micro-nano structures are increasingly vital for various applications such as high-performance aerospace components, energy conversion systems and defense equipment. Femtosecond laser filament processing is a recently proposed remote fabrication technique, showing the capability of fabricating micro-nano structures on irregular and large-area surfaces without the need of tight focusing. Nevertheless, the mechanisms underlying the formation of filament-induced structures remain not fully understood. Here we systematically investigate the formation mechanisms of filament-induced micro-nano structures on stainless steel surfaces by processing stainless steel in three manners: point, line, and area. We clarify the decisive role of the unique core-reservoir energy distribution of the filament in the formation of filament-induced micro-nano structures, and reveal that ablation, molten metal flow, and metal vapor condensation jointly drive the structure evolution through a dynamic interplay of competition and coupling, giving rise to the sequential morphological transitions of surface structures, from laser-induced periodic surface structures to ripple-like, crater-like, honeycomb-like, and ultimately taro-leaf-like structures. Our work not only clarifies the mechanisms of femtosecond laser filament processed morphological structures on steels but also provides insights onto intelligent manufacturing and design of advanced functional steel materials.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787824/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933982","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}
Wenjing Wu, Zichao Yang, Min Zhang, Zhongjie Guan, Jianjun Yang
Photocatalytic reduction of carbon dioxide is a very effective strategy to address the energy crisis and greenhouse effect. TiO2 is a widely used semiconductor photocatalyst, which has excellent catalytic activity, excellent chemical stability and low toxicity. Nevertheless, TiO2 still has some inherent limitations, such as: wide band gap, high carrier recombination rate, and low adsorption activation ability for carbon dioxide. These drawbacks severely restrict its further application in the photocatalytic reduction of CO2. In this study, cotton-like blue C/TiO2 NTs are successfully synthesized through the in situ growth of TiO2 nanotubes on the MIL-125(Ti)-derived C/TiO2 precursor. The experimental results revealed that the CO production rate of the cotton-like blue C/TiO2 NTs was 1.84 times that of C/TiO2 and 3.78 times that of TiO2 nanotubes. These results clearly demonstrate that the cotton-like blue C/TiO2 NTs exhibit a broad spectral response, a large specific surface area, and an abundance of oxygen vacancies. This research provides new insights into the design of titanium dioxide-based photocatalytic materials and opens up a promising avenue for enhancing the performance of titanium dioxide in the photocatalytic reduction of carbon dioxide.
{"title":"Photocatalytic CO<sub>2</sub> Reduction over Cotton-like Blue C/TiO<sub>2</sub> Nanotubes: Enhanced Performance via Structural Engineering.","authors":"Wenjing Wu, Zichao Yang, Min Zhang, Zhongjie Guan, Jianjun Yang","doi":"10.3390/nano16010035","DOIUrl":"10.3390/nano16010035","url":null,"abstract":"<p><p>Photocatalytic reduction of carbon dioxide is a very effective strategy to address the energy crisis and greenhouse effect. TiO<sub>2</sub> is a widely used semiconductor photocatalyst, which has excellent catalytic activity, excellent chemical stability and low toxicity. Nevertheless, TiO<sub>2</sub> still has some inherent limitations, such as: wide band gap, high carrier recombination rate, and low adsorption activation ability for carbon dioxide. These drawbacks severely restrict its further application in the photocatalytic reduction of CO<sub>2</sub>. In this study, cotton-like blue C/TiO<sub>2</sub> NTs are successfully synthesized through the in situ growth of TiO<sub>2</sub> nanotubes on the MIL-125(Ti)-derived C/TiO<sub>2</sub> precursor. The experimental results revealed that the CO production rate of the cotton-like blue C/TiO<sub>2</sub> NTs was 1.84 times that of C/TiO<sub>2</sub> and 3.78 times that of TiO<sub>2</sub> nanotubes. These results clearly demonstrate that the cotton-like blue C/TiO<sub>2</sub> NTs exhibit a broad spectral response, a large specific surface area, and an abundance of oxygen vacancies. This research provides new insights into the design of titanium dioxide-based photocatalytic materials and opens up a promising avenue for enhancing the performance of titanium dioxide in the photocatalytic reduction of carbon dioxide.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787468/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934443","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}
A monolithic all-fiber high-energy chirped pulse amplification (CPA) system with a managed large dispersion is demonstrated. Considering the nonlinearity in the amplification system, two temperature-tuning cascaded chirped fiber Bragg gratings (CFBGs) with a large dispersion of 200 ps/nm are employed as stretchers to stretch the pulse duration to more than 2 ns in the time domain. The main amplifier, with centimeter-level length, a large mode area, and high-gain silicate glass fiber, increases the energy to 293 μJ at 100 kHz. A reflective grating pair with a high density of 1740 lines/mm is used to compress the large-dispersion chirped pulse into a compact structure. Owing to the high-order dispersion pre-compensation by the CFBGs and the large-sized grating with high diffraction efficiency, we achieved a compressed pulse duration of 466 fs with a maximum pulse energy of 250 μJ, corresponding to a compression efficiency of more than 85% and a well-preserved beam quality of M2 < 1.3. To the best of our knowledge, this is the highest pulse energy ever reported in a monolithic fiber femtosecond amplifier.
{"title":"Nonlinearity- and Dispersion-Controlled High-Energy All-Fiber Femtosecond Laser System with Peak Power Exceeding 0.5 GW.","authors":"Feng Li, Qianglong Li, Jixin Xing, Xue Cao, Wenlong Wen, Lei Wang, Yufeng Wei, Hualong Zhao, Yishan Wang, Yuxi Fu, Wei Zhao","doi":"10.3390/nano16010032","DOIUrl":"10.3390/nano16010032","url":null,"abstract":"<p><p>A monolithic all-fiber high-energy chirped pulse amplification (CPA) system with a managed large dispersion is demonstrated. Considering the nonlinearity in the amplification system, two temperature-tuning cascaded chirped fiber Bragg gratings (CFBGs) with a large dispersion of 200 ps/nm are employed as stretchers to stretch the pulse duration to more than 2 ns in the time domain. The main amplifier, with centimeter-level length, a large mode area, and high-gain silicate glass fiber, increases the energy to 293 μJ at 100 kHz. A reflective grating pair with a high density of 1740 lines/mm is used to compress the large-dispersion chirped pulse into a compact structure. Owing to the high-order dispersion pre-compensation by the CFBGs and the large-sized grating with high diffraction efficiency, we achieved a compressed pulse duration of 466 fs with a maximum pulse energy of 250 μJ, corresponding to a compression efficiency of more than 85% and a well-preserved beam quality of M<sup>2</sup> < 1.3. To the best of our knowledge, this is the highest pulse energy ever reported in a monolithic fiber femtosecond amplifier.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787619/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934344","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}
We report a novel approach to fabricating high-performance and robust quantum dot light-emitting diodes (QLEDs) utilizing sputtered SnO2 thin films as the electron transport layer (ETL). While conventional solution-processed ZnMgO NP ETLs face limitations in mass production, the sputtering process offers advantages for uniform and reproducible thin film deposition. Herein, the structural, optical, and electrical properties of SnO2 thin films were optimized by controlling the Ar/O2 ratio and substrate heating temperature during sputtering. SnO2 thin films with O2 gas improve charge balancing in QLEDs by lowering the conduction band minimum. Furthermore, it was observed that oxygen vacancies in SnO2 function as exciton quenching sites, which directly impacts the long-term stability of the device. QLEDs fabricated under optimal conditions (Ar/O2 = 35:5, 200 °C heating) achieved a peak luminance of 99,212 cd/m2 and a current efficiency of 21.17 cd/A with excellent device stability. The findings suggest that sputtered SnO2 ETLs are a highly promising technology for the commercial production of QLEDs.
{"title":"Highly Efficient and Stable Quantum Dot Light-Emitting Diodes Employing Sputtered SnO<sub>2</sub> Layer as Electron Transport Layers.","authors":"Jaehwi Choi, Jiwan Kim","doi":"10.3390/nano16010031","DOIUrl":"10.3390/nano16010031","url":null,"abstract":"<p><p>We report a novel approach to fabricating high-performance and robust quantum dot light-emitting diodes (QLEDs) utilizing sputtered SnO<sub>2</sub> thin films as the electron transport layer (ETL). While conventional solution-processed ZnMgO NP ETLs face limitations in mass production, the sputtering process offers advantages for uniform and reproducible thin film deposition. Herein, the structural, optical, and electrical properties of SnO<sub>2</sub> thin films were optimized by controlling the Ar/O<sub>2</sub> ratio and substrate heating temperature during sputtering. SnO<sub>2</sub> thin films with O<sub>2</sub> gas improve charge balancing in QLEDs by lowering the conduction band minimum. Furthermore, it was observed that oxygen vacancies in SnO<sub>2</sub> function as exciton quenching sites, which directly impacts the long-term stability of the device. QLEDs fabricated under optimal conditions (Ar/O<sub>2</sub> = 35:5, 200 °C heating) achieved a peak luminance of 99,212 cd/m<sup>2</sup> and a current efficiency of 21.17 cd/A with excellent device stability. The findings suggest that sputtered SnO<sub>2</sub> ETLs are a highly promising technology for the commercial production of QLEDs.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12788106/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934149","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}
Perovskite crystals, nanocrystals, quantum dots (QDs), and two-dimensional (2D) materials are at the forefront of optoelectronics and quantum optics, offering groundbreaking potential for a wide range of applications, including photovoltaics, light-emitting devices, and quantum information technologies. Perovskite materials, with their remarkable, tunable bandgaps, high absorption coefficients, and efficient charge transport, have revolutionized the field of light-emitting diodes, photodetectors, and solar cells. QDs, owing to their size-dependent quantum confinement and high photoluminescence quantum yields, are crucial for applications in display technologies, imaging, and quantum computing. The synthesis of QDs from perovskite-based materials yields a significant enhancement in the performance of optoelectronics devices. Furthermore, 2D perovskites have recently exhibited extraordinary carrier mobility, strong light-matter interactions, and mechanical flexibility, making them highly attractive for next-generation optoelectronic applications. Additionally, this review discusses the synergistic potential of hybrid material architectures, where perovskite crystals, QDs, and 2D materials are combined to enhance optoelectronic performance and their role in quantum optics. By analyzing the effects of material structure, surface modifications, and fabrication techniques, this review provides a valuable resource for harnessing the transformative potential of these advanced materials in modern optoelectronic applications.
{"title":"Perovskite Nanocrystals, Quantum Dots, and Two-Dimensional Structures: Synthesis, Optoelectronics, Quantum Technologies, and Biomedical Imaging.","authors":"Kamran Ullah, Anwar Ul Haq, Sergii Golovynskyi, Tarak Hidouri, Junle Qu, Iuliia Golovynska","doi":"10.3390/nano16010030","DOIUrl":"10.3390/nano16010030","url":null,"abstract":"<p><p>Perovskite crystals, nanocrystals, quantum dots (QDs), and two-dimensional (2D) materials are at the forefront of optoelectronics and quantum optics, offering groundbreaking potential for a wide range of applications, including photovoltaics, light-emitting devices, and quantum information technologies. Perovskite materials, with their remarkable, tunable bandgaps, high absorption coefficients, and efficient charge transport, have revolutionized the field of light-emitting diodes, photodetectors, and solar cells. QDs, owing to their size-dependent quantum confinement and high photoluminescence quantum yields, are crucial for applications in display technologies, imaging, and quantum computing. The synthesis of QDs from perovskite-based materials yields a significant enhancement in the performance of optoelectronics devices. Furthermore, 2D perovskites have recently exhibited extraordinary carrier mobility, strong light-matter interactions, and mechanical flexibility, making them highly attractive for next-generation optoelectronic applications. Additionally, this review discusses the synergistic potential of hybrid material architectures, where perovskite crystals, QDs, and 2D materials are combined to enhance optoelectronic performance and their role in quantum optics. By analyzing the effects of material structure, surface modifications, and fabrication techniques, this review provides a valuable resource for harnessing the transformative potential of these advanced materials in modern optoelectronic applications.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787781/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934336","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 present study targets key limitation 'separation after the process' that is responsible for the loss of the photocatalyst in water treatment during heterogeneous photocatalysis. Therefore, eco-friendly nanostructured ZnO coatings were engineered by the doctor blade technique through the immobilization of green ZnO nanomaterials onto alumina substrate. ZnO/BPE 30 and ZnO/BPE 60 coatings were obtained from banana peel extract-based ZnO powder (ZnO/BPE). Likewise, ZnO/GTE 30 and ZnO/GTE 60 were prepared using green tea extract-based ZnO powder (ZnO/GTE). XRD characterization verified hexagonal wurtzite ZnO phase, while HRSEM analysis revealed that the flat surface of ZnO/BPE had rod-like nanostructures below 120 nm, and ZnO/GTE had spherical, porous nanoparticle networks with less than 70 nm. According to UV-vis spectrometry, all four coatings have bandgaps of ~5 eV. The highest efficiency for the solar-driven photocatalytic degradation of emerging organic pollutants was for ciprofloxacin (among pesticides clomazone and tembotrione; pharmaceuticals ciprofloxacin and 17α-ethinylestradiol; and mycotoxin zearalenone) in ultrapure water with the presence of all studied ZnO-based coatings, after 60 min of simulated solar irradiation. Its highest removal (89.1%) was achieved with ZnO/GTE 30, also having good reusability across three consecutive cycles in river water, thus supporting the application of eco-friendly, immobilized ZnO nanomaterials for wastewater treatment and environmental remediation.
{"title":"Eco-Friendly ZnO Nanomaterial Coatings for Photocatalytic Degradation of Emerging Organic Pollutants in Water Systems: Characterization and Performance.","authors":"Dušica Jovanović, Szabolcs Bognár, Nina Finčur, Vesna Despotović, Predrag Putnik, Branimir Bajac, Sandra Jakšić, Bojan Miljević, Daniela Šojić Merkulov","doi":"10.3390/nano16010023","DOIUrl":"10.3390/nano16010023","url":null,"abstract":"<p><p>The present study targets key limitation 'separation after the process' that is responsible for the loss of the photocatalyst in water treatment during heterogeneous photocatalysis. Therefore, eco-friendly nanostructured ZnO coatings were engineered by the doctor blade technique through the immobilization of green ZnO nanomaterials onto alumina substrate. ZnO/BPE 30 and ZnO/BPE 60 coatings were obtained from banana peel extract-based ZnO powder (ZnO/BPE). Likewise, ZnO/GTE 30 and ZnO/GTE 60 were prepared using green tea extract-based ZnO powder (ZnO/GTE). XRD characterization verified hexagonal wurtzite ZnO phase, while HRSEM analysis revealed that the flat surface of ZnO/BPE had rod-like nanostructures below 120 nm, and ZnO/GTE had spherical, porous nanoparticle networks with less than 70 nm. According to UV-vis spectrometry, all four coatings have bandgaps of ~5 eV. The highest efficiency for the solar-driven photocatalytic degradation of emerging organic pollutants was for ciprofloxacin (among pesticides clomazone and tembotrione; pharmaceuticals ciprofloxacin and 17α-ethinylestradiol; and mycotoxin zearalenone) in ultrapure water with the presence of all studied ZnO-based coatings, after 60 min of simulated solar irradiation. Its highest removal (89.1%) was achieved with ZnO/GTE 30, also having good reusability across three consecutive cycles in river water, thus supporting the application of eco-friendly, immobilized ZnO nanomaterials for wastewater treatment and environmental remediation.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787899/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933969","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}
Jipu Guo, Xiaolong Wei, Meiyan Wang, Xu Li, Bin Yan, Xiaotong Pan, Zhe Zhang, Yao Wu, Bofang Shi, Honghui Yang
Addressing the global shortage of freshwater resources necessitates the development of efficient and economical photothermal evaporation materials. Herein, an Fe/polyaniline/graphite felt (Fe/PANI/GF) composite was fabricated by combining electrochemical deposition and impregnation. The structural characteristics, photothermal conversion efficiency, and interfacial evaporation performance of the composite were systematically investigated. Results demonstrate that Fe/PANI/GF exhibits a remarkably high solar absorption rate of 95% across the 300-2000 nm wavelength range. Under 1 kW m-2 illumination, the surface temperature of Fe/PANI/GF rapidly increased from ambient temperature to 60.3 °C within 5 min. The composite achieved an evaporation rate of 2.05 kg m-2 h-1, corresponding to an interfacial evaporation efficiency of 70.3%. This exceptional performance is attributed to the synergistic effect between the broad-spectrum light absorption of PANI and the enhanced light absorption induced by Fe coordination, which collectively promote the photothermal conversion process. This study provides valuable insights for the development of high-performance solar interfacial evaporation materials.
解决全球淡水资源短缺问题需要开发高效、经济的光热蒸发材料。本文采用电化学沉积和浸渍相结合的方法制备了Fe/聚苯胺/石墨毡(Fe/PANI/GF)复合材料。系统地研究了该复合材料的结构特性、光热转换效率和界面蒸发性能。结果表明,Fe/PANI/GF在300 ~ 2000 nm波长范围内具有较高的太阳吸收率,达到95%。在1 kW m-2光照条件下,Fe/PANI/GF的表面温度在5 min内从环境温度迅速升高到60.3℃。复合材料的蒸发速率为2.05 kg m-2 h-1,对应的界面蒸发效率为70.3%。这种优异的性能归因于聚苯胺的广谱光吸收与铁配位诱导的光吸收增强之间的协同效应,共同促进了光热转换过程。该研究为高性能太阳能界面蒸发材料的开发提供了有价值的见解。
{"title":"Preparation of Fe/PANI/GF Composite and Study on Its Interfacial Evaporation Performance.","authors":"Jipu Guo, Xiaolong Wei, Meiyan Wang, Xu Li, Bin Yan, Xiaotong Pan, Zhe Zhang, Yao Wu, Bofang Shi, Honghui Yang","doi":"10.3390/nano16010024","DOIUrl":"10.3390/nano16010024","url":null,"abstract":"<p><p>Addressing the global shortage of freshwater resources necessitates the development of efficient and economical photothermal evaporation materials. Herein, an Fe/polyaniline/graphite felt (Fe/PANI/GF) composite was fabricated by combining electrochemical deposition and impregnation. The structural characteristics, photothermal conversion efficiency, and interfacial evaporation performance of the composite were systematically investigated. Results demonstrate that Fe/PANI/GF exhibits a remarkably high solar absorption rate of 95% across the 300-2000 nm wavelength range. Under 1 kW m<sup>-2</sup> illumination, the surface temperature of Fe/PANI/GF rapidly increased from ambient temperature to 60.3 °C within 5 min. The composite achieved an evaporation rate of 2.05 kg m<sup>-2</sup> h<sup>-1</sup>, corresponding to an interfacial evaporation efficiency of 70.3%. This exceptional performance is attributed to the synergistic effect between the broad-spectrum light absorption of PANI and the enhanced light absorption induced by Fe coordination, which collectively promote the photothermal conversion process. This study provides valuable insights for the development of high-performance solar interfacial evaporation materials.</p>","PeriodicalId":18966,"journal":{"name":"Nanomaterials","volume":"16 1","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12787383/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145934378","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}