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Structure-Regulated SrTiO3 Catalyst for Efficient Electrocatalytic Degradation of Chlortetracycline 结构调控SrTiO3催化剂高效电催化降解氯四环素
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-27 DOI: 10.1002/cnma.202400645
Shuai Wang, Wenqi Cui, Changhao Yao, Yiyang He, Kun Lang, Yang Yang, Baojiang Jiang
{"title":"Structure-Regulated SrTiO3 Catalyst for Efficient Electrocatalytic Degradation of Chlortetracycline","authors":"Shuai Wang,&nbsp;Wenqi Cui,&nbsp;Changhao Yao,&nbsp;Yiyang He,&nbsp;Kun Lang,&nbsp;Yang Yang,&nbsp;Baojiang Jiang","doi":"10.1002/cnma.202400645","DOIUrl":"10.1002/cnma.202400645","url":null,"abstract":"<p>The rapid industrialization of modern society has resulted in the extensive release of persistent organic pollutants into aquatic ecosystems, necessitating innovative approaches for wastewater treatment. Herein, a perovskite oxide material, strontium titanate (SrTiO<sub>3</sub>, STO), is synthesized via a sol–gel method and employed for the first time as an efficient advanced electrocatalyst for the degradation of organic pollutants. The STO electrode annealed at 900 °C demonstrates superior degradation efficiency, achieving 86.3% removal of 60 mg L<sup>−1</sup> chlortetracycline. This outstanding activity stems from the optimized crystal structure and enhanced surface redox properties of STO, which significantly boost OH radical generation. Compared to recent electrocatalysts, STO achieves competitive degradation efficiency and lower energy consumption under mild conditions, highlighting a notable performance breakthrough. Mechanistic insights, obtained through liquid chromatography–mass spectrometry and radical scavenging experiments, reveal that hydroxyl radicals (·OH) play a dominant role in the degradation process. Moreover, STO demonstrates exceptional long-term stability and broad applicability in degrading various antibiotics, underscoring its versatility and potential for treating complex organic wastewater. This work establishes STO as a cost-effective and scalable electrocatalyst with high stability and energy efficiency, addressing key challenges in electrocatalytic degradation and advancing the use of perovskite materials in environmental remediation.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 7","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144598727","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Liquid Joule Heating Synthesis of Ultrafine Pd–Se Nanoparticles for Enhanced Oxygen Reduction Electrocatalysis 液体焦耳加热合成用于增强氧还原电催化的超细Pd-Se纳米颗粒
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-27 DOI: 10.1002/cnma.202500172
Zhenya Hu, Mengyuan Ma, Dong Chen, Shaonan Tian, Hui Liu, Yu Chen, Jun Yang
{"title":"Liquid Joule Heating Synthesis of Ultrafine Pd–Se Nanoparticles for Enhanced Oxygen Reduction Electrocatalysis","authors":"Zhenya Hu,&nbsp;Mengyuan Ma,&nbsp;Dong Chen,&nbsp;Shaonan Tian,&nbsp;Hui Liu,&nbsp;Yu Chen,&nbsp;Jun Yang","doi":"10.1002/cnma.202500172","DOIUrl":"10.1002/cnma.202500172","url":null,"abstract":"<p>The development of ultrafast synthesis strategies for nanomaterials is highly attractive for their applications in energy conversion and storage. Herein, a rapid strategy that couples Joule heating with wet chemistry for synthesizing carbon-supported Pd–Se nanoparticles with an ultrafine size of ≈3.83 nm, which exhibits superior catalytic performance for the oxygen reduction reaction, is demonstrated. In particular, the ultrafine Pd–Se nanoparticles at Pd/Se ratio of 17/15 on the carbon substrate exhibit mass and specific activities of 0.29 A <span></span><math></math> and 0.74 mA cm<sup>−2</sup>, respectively, significantly surpassing those of their commercial Pd/C counterparts and a number of Pd-based electrocatalysts reported recently. This liquid Joule heating (LJH) approach directly applies Joule heating to a liquid mixture of precursors, capping agents, reducing agents, and carbon substrates, enabling simultaneous optimization of particle size and reduction of reaction time. This study highlights the potential of solvent-involved Joule heating methodologies for the efficient synthesis of nanomaterials tailored for electrocatalytic applications.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 8","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144905318","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
3D Porous Activated Carbon Network Derived from Luffa Sponge for Sustainable High-Performance Supercapacitors 用于可持续高性能超级电容器的丝瓜海绵三维多孔活性炭网络
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-26 DOI: 10.1002/cnma.202500147
Navaneethan Duraisamy, Krishna Shenniangirivalasu Kandasamy, Elumalai Dhandapani, Kavitha Kandiah, Sarojini Jeeva Panchu, Hendrik C Swart
{"title":"3D Porous Activated Carbon Network Derived from Luffa Sponge for Sustainable High-Performance Supercapacitors","authors":"Navaneethan Duraisamy,&nbsp;Krishna Shenniangirivalasu Kandasamy,&nbsp;Elumalai Dhandapani,&nbsp;Kavitha Kandiah,&nbsp;Sarojini Jeeva Panchu,&nbsp;Hendrik C Swart","doi":"10.1002/cnma.202500147","DOIUrl":"10.1002/cnma.202500147","url":null,"abstract":"<p>The development of efficient energy storage devices requires the exploration of new, economically feasible, and sustainable electrode materials. To develop high-performance electrode materials for supercapacitors (SCs), a microwave technique is employed to prepare activated carbon from luffa fibers (biowaste). As a result of the unique luffa network and its macroscopically shaped design, a 3D porous activated carbon electrode is fabricated, and its electrochemical performance is evaluated in a 1 <span>m</span> Na<sub>2</sub>SO<sub>4</sub> aqueous electrolyte using a three-electrode system. Due to the high specific surface area of 3D-porous microwave-activated carbons (PMACs) (380 m<sup>2</sup> g<sup>−1</sup>), the PMACs exhibit a specific capacitance of ≈290 F g<sup>−1</sup> at 2 A g<sup>−1</sup>, along with excellent cyclability of 89% over 5000 charging/discharging cycles at 20 A g<sup>−1</sup>. The enhanced electrochemical characteristics of PMACs are attributed to the formation of micro-/mesoporosity induced by microwave irradiation. A symmetric supercapacitor device (PMACs//PMACs) is constructed, demonstrating an excellent specific capacitance of 75.4 F g<sup>−1</sup> at 2 A g<sup>−1</sup>, a maximum energy density of 26.9 W h kg<sup>−1</sup> at 1307.6 W kg<sup>−1</sup>, and a power density of 48,941.2 W kg<sup>−1</sup> at 6.9 W h kg<sup>−1</sup>, with 80.6% capacitance retention after 5000 charge/discharge cycles.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 7","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cnma.202500147","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144598710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Borophene Oxide and Graphene Oxide for Renewable Energy: A Comparative Study on their Catalytic Performance in Sodium Borohydride Hydrolysis for Hydrogen Generation 用于可再生能源的氧化硼苯和氧化石墨烯:它们在硼氢化钠水解制氢催化性能的比较研究
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-26 DOI: 10.1002/cnma.202500031
Yen Yiin Lee, Shuen Lam, Swee Pin Yeap, Kah Hou Teng, Zaher Mundher Yaseen, Andy Shaw, Vijayakumar Karunamoothei, Yeah Hui Loh, Leong Sim Teh
{"title":"Borophene Oxide and Graphene Oxide for Renewable Energy: A Comparative Study on their Catalytic Performance in Sodium Borohydride Hydrolysis for Hydrogen Generation","authors":"Yen Yiin Lee,&nbsp;Shuen Lam,&nbsp;Swee Pin Yeap,&nbsp;Kah Hou Teng,&nbsp;Zaher Mundher Yaseen,&nbsp;Andy Shaw,&nbsp;Vijayakumar Karunamoothei,&nbsp;Yeah Hui Loh,&nbsp;Leong Sim Teh","doi":"10.1002/cnma.202500031","DOIUrl":"10.1002/cnma.202500031","url":null,"abstract":"<p>The recent rise of borophene as a new 2D material has triggered competition with the well-known graphene. The present work serves as the first attempt to compare the efficiency of borophene oxide (BO) and graphene oxide (GO) in catalyzing NaBH<sub>4</sub> hydrolysis for hydrogen generation. For a fair comparison, the BO and GO particles are synthesized using the same improved Hummers’ method. Morphological studies show that both BO and GO appear in plate-like shapes; however, GO exhibits a more scrunched and rippled structure with larger interlayer spacing. BO and GO exhibit more oxygen-containing groups than their bulk counterparts. X-ray diffraction analysis indicates that BO has a reduced crystallinity, while GO exhibits turbostratic disorder. Regarding catalytic properties, both BO and GO are found to be on par as catalysts, increasing hydrogen yield from NaBH<sub>4</sub> hydrolysis by 25 times in 30 s, offering new insights for the clean energy industry.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 7","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144598709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhancing Durability and Performance of Solid–Liquid Triboelectric Nanogenerators through Advanced Corrosion-Resistant Coatings 通过先进的耐腐蚀涂层提高固体-液体摩擦电纳米发电机的耐久性和性能
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-23 DOI: 10.1002/cnma.202500054
Syeda Shahir Bano, Qunfeng Zeng, Muhammad Arslan
{"title":"Enhancing Durability and Performance of Solid–Liquid Triboelectric Nanogenerators through Advanced Corrosion-Resistant Coatings","authors":"Syeda Shahir Bano,&nbsp;Qunfeng Zeng,&nbsp;Muhammad Arslan","doi":"10.1002/cnma.202500054","DOIUrl":"10.1002/cnma.202500054","url":null,"abstract":"<p>The creation of renewable energy sources needs to happen so that they can address the issue of energy deficits. These problems have been addressed by triboelectric nanogenerators that convert droplets, waves, and flows of mechanical power into electricity. This paper aims to review the antecedents of solid–liquid triboelectric nanogenerators (SL-TENG) while focusing on lightweight, cost efficiency, and sustainability. SL-TENGs are appropriate for industrial, environmental, and marine environments because of their capacity to convert liquid flow into electrical power. However, they have drawbacks, including material degradation, biofouling, corrosion, and ecological effects that constrain their performance and durability. It has been suggested that advanced materials and coatings, such as superhydrophobic surfaces, self-healing layers, and composites, be featured to overcome these challenges. Processes such as solgel deposition, plasma-enhanced techniques, and spray coatings boost their sturdiness and functionality. The paper focuses on performance reviews involving triboelectric output, corrosion, mechanical stability, and the ability to demonstrate how new designs and coatings have determined SL-TENG efficiency. Therefore, this review will be a clear roadmap to realize efficient and durable SL-TENG technologies for future energy harvesting systems.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 8","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144905641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recycling Spent Synthesis Liquor for Enhanced Production of ZIF-67: Characterization and Morphological Insights 回收废合成液以提高ZIF-67的产量:表征和形态学见解
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-19 DOI: 10.1002/cnma.202500100
Lucas Battiston, Barbara Gerbelli, Fabiano Yokaichiya, Ivan Barros, Kátia Oliveira, Cícero Ávila-Neto
{"title":"Recycling Spent Synthesis Liquor for Enhanced Production of ZIF-67: Characterization and Morphological Insights","authors":"Lucas Battiston,&nbsp;Barbara Gerbelli,&nbsp;Fabiano Yokaichiya,&nbsp;Ivan Barros,&nbsp;Kátia Oliveira,&nbsp;Cícero Ávila-Neto","doi":"10.1002/cnma.202500100","DOIUrl":"10.1002/cnma.202500100","url":null,"abstract":"<p>This study reports the preparation and characterization of zeolitic imidazolate framework-67 (ZIF-67) through the recycling of spent synthesis liquor containing unreacted 2-methylimidazole. The recycling enhances the yield of ZIF-67 while maintaining the dodecahedral rhombic morphology of the particles. In the first synthesis, a molar ratio of 1:26 (Co<sup>2</sup>:2-methylimidazole) results in particles with an average diameter of 230 nm and a surface area of 1374 m<sup>2</sup> g<sup>−1</sup>. The first recycling step produces ZIF-67 particles that doubl in diameter and surface area, reaching 520 nm and 1690 m<sup>2</sup> g<sup>−1</sup>, respectively. In the second recycling step, the particles further increase to 1040 nm in diameter and 1806 m<sup>2</sup> g<sup>−1</sup> in surface area. This increase in diameter is attributed to changes in the metal-to-ligand ratio, which affects the nucleation and growth rates. Increased surface area is linked to a reduction in the average micropore diameter, which decreases from 1.42 nm (first synthesis) to 1.37 nm (second recycling step). There is a 6 m<sup>2</sup> g<sup>−1</sup> increase in surface area for every 0.001 cm<sup>3</sup> g<sup>−1</sup> increase in the volume of micropores. This indicates that the spent liquor can be utilized in consecutive batches to produce ZIF-67, minimizing reagent waste.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 7","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cnma.202500100","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144598471","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Corn Cob-Derived Carbon-Modified NiFe Layered Double Hydroxides as Electrode Material for Supercapacitors 玉米棒子衍生碳修饰NiFe层状双氢氧化物作为超级电容器电极材料
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-19 DOI: 10.1002/cnma.202500155
Wen Yu, Xinru Dong, Baolan Ma, Guorong Wang
{"title":"Corn Cob-Derived Carbon-Modified NiFe Layered Double Hydroxides as Electrode Material for Supercapacitors","authors":"Wen Yu,&nbsp;Xinru Dong,&nbsp;Baolan Ma,&nbsp;Guorong Wang","doi":"10.1002/cnma.202500155","DOIUrl":"10.1002/cnma.202500155","url":null,"abstract":"<p>Biomass waste is a potential source of energy storage materials. Herein, a biomass-based carbon (CSC) is prepared using postconsumption corn cobs as the precursor through a solvothermal carbonization strategy. This carbon is further utilized to improve nickel–iron layered double hydroxide (NiFe LDHs) to enhance its electrochemical energy storage capacity. As a result, the specific capacitance of NiFe LDHs is significantly increased to a value of 1775 F g<sup>−1</sup> at a current density of 1 A g<sup>−1</sup>, after the addition of CSC. This remarkable improvement indicates the broad application prospects of biomass waste in the field of energy storage and paves the way for the development of environmentally friendly and sustainable energy materials. Additionally, the asymmetric supercapacitor assembled with CSC/NiFe LDHs-15 and AC electrodes exhibits an outstanding energy density of 15.6 Wh kg<sup>−1</sup> and a power density of 961.9 W kg<sup>−1</sup>, representing a significant enhancement compared to traditional supercapacitor systems. After 10 000 charge–discharge cycles at a high current density of 10 A g<sup>−1</sup>, it still retains 64.47% of its capacity. The excellent electrochemical performance and stability of this electrode material highlight the great potential of biomass waste in electrochemical energy storage.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 8","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144905535","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Boosting Aqueous Zn-Ion Battery Performances with Mg-Vanadate Positive and Cu-Metal Organic Framework Negative Electrodes in Inorganic Gel Electrolyte 无机凝胶电解质中钒酸镁正极和铜金属有机骨架负极提高锌离子电池性能
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-19 DOI: 10.1002/cnma.202500077
Subhrajyoti Debnath, Apurba Maiti, Pappu Naskar, Arijit Dey, Sourav Laha, Anjan Banerjee
{"title":"Boosting Aqueous Zn-Ion Battery Performances with Mg-Vanadate Positive and Cu-Metal Organic Framework Negative Electrodes in Inorganic Gel Electrolyte","authors":"Subhrajyoti Debnath,&nbsp;Apurba Maiti,&nbsp;Pappu Naskar,&nbsp;Arijit Dey,&nbsp;Sourav Laha,&nbsp;Anjan Banerjee","doi":"10.1002/cnma.202500077","DOIUrl":"10.1002/cnma.202500077","url":null,"abstract":"<p>Aqueous Zn-ion batteries (AZIBs) are attractive, cost-effective, safe, and environmentally friendly energy storage solutions for stationary solar energy applications; offering a balanced combination of energy, power, and durability. A key challenge for AZIBs is the slow diffusion kinetics of divalent Zn<sup>2+</sup> ions within the host lattices. To address this, Mg<sub>x</sub>V<sub>2</sub>O<sub>5</sub> (MgVO) as the positive and Cu-BTC metal organic framework (Cu-BTC MOF) (BTC: benzene-1,3,5-tricarboxylic acid) as the negative electrodes are designed, both of which support Zn<sup>2+</sup> ion intercalation/deintercalation. The incorporation of Mg<sup>2+</sup> into the V<sub>2</sub>O<sub>5</sub> layer improves Zn<sup>2+</sup> ion diffusion and enhances electrode stability, mitigating common issues such as layer-collapse. The Cu-BTC framework, with its open structure, facilitates efficient Zn<sup>2+</sup> intercalation, significantly improving energy and power characteristics. A MgVO//Cu-BTC full cell, utilizing a ZnSO<sub>4</sub>-silica gel electrolyte, delivers a high energy-density of 305 Wh kg<sup>−1</sup> (@ 394 W kg<sup>−1</sup>) and a notable power-density of 1773 W kg<sup>−1</sup> (@ 87 Wh kg<sup>−1</sup>), with stable cycling performance (≈86% capacity retention) over 200 cycles at 600 mAh g<sup>−1</sup>. Additionally, the successful demonstration of a 4.5 V AZIB prototype powering a 3 V light-emitting-diode setup under solar charging shows its practical potential. With superior performance, safety, and cost-effectiveness, this AZIB offers great promise for large-scale solar energy storage.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145101869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Optimized Electrochemical Behavior of Carbon-Coated Ti-Doped Na3V2(PO4)2F3 Cathodes for Sodium-Ion Batteries 钠离子电池碳包覆ti掺杂Na3V2(PO4)2F3阴极电化学性能优化
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-19 DOI: 10.1002/cnma.202500070
Pathak Rajkumar Babunar, Sameer Tirkey, Ananta Sarkar
{"title":"Optimized Electrochemical Behavior of Carbon-Coated Ti-Doped Na3V2(PO4)2F3 Cathodes for Sodium-Ion Batteries","authors":"Pathak Rajkumar Babunar,&nbsp;Sameer Tirkey,&nbsp;Ananta Sarkar","doi":"10.1002/cnma.202500070","DOIUrl":"10.1002/cnma.202500070","url":null,"abstract":"<p>Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>2</sub>F<sub>3</sub> (NVPF) has emerged as a very promising cathode material for sodium-ion batteries (SIBs), on account of its durable structural reliability and impressive electrochemical performance. However, their practical use is limited by low capacity, poor conductivity, slow Na-ion transport, and capacity fading, requiring structural and surface modifications. To overcome its inherent low conductivity, carbon-coated Ti-doped NVPF (designated as NVPF-Ti-x) is prepared via a sol–gel process, with x values of 0, 0.01, 0.02, 0.03, 0.04, and 0.05. Among these variants, NVPF-Ti-0.02 demonstrates the most remarkable electrochemical behavior of high reversible capacity and rate capability. NVPF-Ti-0.02 achieves an exceptional stabilized specific capacity of 133 mAh g<sup>−1</sup> at a current density of 50 mA g<sup>−1</sup> after the first cycle onward. It shows a high reversible capacity retention of 94.76% after 100 cycles and 81% after 300 cycles. These results highlight the effectiveness of Ti doping and carbon coating in significantly boosting the conductivity and mechanical stability of NVPF. The improved performance of NVPF-Ti-0.02 underscores its potential as a leading candidate for advanced SIB technologies, offering both high capacity and robust cycling stability.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 7","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144598470","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Facile Synthesis of a Heterojunction of Snowflake Dendritic Cu2S-2D g-C3N4: An Efficient Photocatalyst for Degradation of Several Textile Dyes and Antibiotics under Solar Light 雪花树枝状Cu2S-2D g-C3N4异质结的快速合成:一种在日光下降解几种纺织染料和抗生素的高效光催化剂
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2025-05-19 DOI: 10.1002/cnma.202500156
Darshana Anand Upar, Narendra Nath Ghosh
{"title":"Facile Synthesis of a Heterojunction of Snowflake Dendritic Cu2S-2D g-C3N4: An Efficient Photocatalyst for Degradation of Several Textile Dyes and Antibiotics under Solar Light","authors":"Darshana Anand Upar,&nbsp;Narendra Nath Ghosh","doi":"10.1002/cnma.202500156","DOIUrl":"10.1002/cnma.202500156","url":null,"abstract":"<p>The pollution of aquatic environments by industrial effluents is a significant challenge and intensifies the rapid pace of industrialization and globalization. In this work, a heterojunction is created by forming a hierarchical structure composed of a p-type semiconductor Cu<sub>2</sub>S having a dendritic snowflake structure and n-type semiconductor 2D g-C<sub>3</sub>N<sub>4</sub>. Initially, the photocatalytic (PC) performances of Cu<sub>2</sub>S-g-C<sub>3</sub>N<sub>4</sub> (p–n heterojunction) are evaluated toward the degradation of a model dye methyl orange (MO) under the simulated solar light exposure. To optimize the composition of the photocatalyst, this reaction is performed using the photocatalysts with varying amounts of Cu<sub>2</sub>S and g-C<sub>3</sub>N<sub>4</sub>, and among several compositions, 10Cu<sub>2</sub>S-90 g-C<sub>3</sub>N<sub>4</sub> heterostructure demonstrates the highest PC activity, achieving complete degradation of MO within ≈30 min, with an apparent rate constant of <i>k</i><sub>app</sub> = 2.05 × 10<sup>−3</sup> s<sup>−1</sup>. This performance is superior to many reported photocatalysts. The PC activities of this photocatalyst are assessed toward the degradation of different textile dyes and various antibiotics. 10Cu<sub>2</sub>S-90 g-C<sub>3</sub>N<sub>4</sub> exhibits excellent PC performances by degrading the aforementioned commercial dyes and antibiotics, which are real examples of water pollutants and present in different wastewater effluents. Thus, this photocatalyst demonstrates its potential to be used in water pollution remediation processes.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"11 8","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144905537","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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