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Correction to “Atomic Layer Etching of Titanium Nitride With O3 and NbCl5” 对“用O3和NbCl5原子层蚀刻氮化钛”的修正
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-27 DOI: 10.1002/cnma.70379
{"title":"Correction to “Atomic Layer Etching of Titanium Nitride With O3 and NbCl5”","authors":"","doi":"10.1002/cnma.70379","DOIUrl":"https://doi.org/10.1002/cnma.70379","url":null,"abstract":"<p>Ojala, J.; Chundak, M.; Vihervaara, A.; Ritala, M. Atomic Layer Etching of Titanium Nitride With O<sub>3</sub> and NbCl<sub>5</sub>. <i>ChemNanoMat</i> <b>2026</b>, <i>12</i> (5), e70264. https://doi.org/10.1002/cnma.70264.</p><p>In Figure 4b the Arrhenius plot was drawn using the base 10 logarithm. The figure should have used the natural logarithm:</p><p>As a result some values and conclusions in the discussion are incorrect.</p><p>On page 3, 8<sup>th</sup> paragraph of the “Etching experiments” section, the text: “The estimated activation energy for this etching process is 20 kJ/mol. This is lower but still on the same order of magnitude as in previous ALE studies on different materials where the Arrhenius-type temperature dependence is reported (36–56 kJ/mol).” was incorrect and should have read “The estimated activation energy for this etching process is 46 kJ/mol. This is similar to previous ALE studies on different materials where the Arrhenius-type temperature dependence is reported (36–56 kJ/mol).”</p><p>On page 4, 8<sup>th</sup> paragraph of the “Etching experiments” section, the text: “Coincidentally, the activation energy is close to the energy barrier reported for the dissociation of adsorbed O<sub>2</sub> molecules on the TiN (001) surface (19.3 kJ/mol) as calculated by DFT [35]. While the O<sub>3</sub> pulses contain O<sub>2</sub> as well, it is unlikely that the O<sub>2</sub> is significantly affecting the EPC.” was incorrect and should not have been included in the text.</p><p>On page 7, first paragraph of the “Conclusions” section, the text “At 200–300 °C the EPC follows the Arrhenius-like temperature dependence with estimated activation energy of 20 kJ/mol.” was incorrect and should have read: “At 200–300 °C the EPC follows the Arrhenius-like temperature dependence with estimated activation energy of 46 kJ/mol.”</p><p>We apologize for these errors.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cnma.70379","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146632","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
Low-Temperature Electrochemical Synthesis of Cubic Carbon Nitride via Co-Oxidation in Molten LiCl–KCl 熔融LiCl-KCl共氧化低温电化学合成立方氮化碳
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-27 DOI: 10.1002/cnma.70337
Yuta Shiomi, Masashi Morishima, Yuta Suzuki, Takuya Goto
{"title":"Low-Temperature Electrochemical Synthesis of Cubic Carbon Nitride via Co-Oxidation in Molten LiCl–KCl","authors":"Yuta Shiomi,&nbsp;Masashi Morishima,&nbsp;Yuta Suzuki,&nbsp;Takuya Goto","doi":"10.1002/cnma.70337","DOIUrl":"https://doi.org/10.1002/cnma.70337","url":null,"abstract":"<p>Carbon nitride materials, predicted to rival diamond in hardness and exhibit wide bandgaps, have long eluded direct synthesis in bulk crystalline form. We demonstrate the low-temperature electrochemical synthesis of cubic carbon nitride (c-C<sub>3</sub>N<sub>4</sub>) via co-oxidation of carbide (C<sub>2</sub><sup>2−</sup>) and nitride (N<sup>3−</sup>) ions in molten LiCl–KCl at 450 °C. Using CaC<sub>2</sub> and Li<sub>3</sub>N as stable precursors, we investigate the thermodynamic and electrochemical windows for C─N bond formation on nickel and platinum electrodes. Cyclic voltammetry, potentiostatic, and pulsed electrolysis reveal that co-oxidation enables the nucleation of C─N bonded phases, with substrate selection critically influencing phase composition and crystallinity. X-ray diffraction (XRD) revealed reflections consistent with a cubic C<sub>3</sub>N<sub>4</sub> candidate phase on Pt electrodes under pulsed conditions, while scanning electron microscopy/energy-dispersive X-ray spectroscopy, Raman spectroscopy, and nanoindentation supported the formation of a dense carbon nitride-containing layer with hardness values up to 9.56 GPa. These findings show that molten-salt electrochemistry provides a low-temperature route to carbon nitride-containing deposits with XRD reflections consistent with a c‑C<sub>3</sub>N<sub>4</sub> candidate phase at 450 °C, a temperature substantially lower than those required in conventional high-pressure or vapor-phase approaches.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cnma.70337","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149146630","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
Magnetic Metal Organic Framework-Based Nanocomposite as an Efficient Magneto-Adsorbent for Rapid Congo Red Removal and Germination Toxicity Assessment in Cicer arietinum 基于磁性金属有机框架的纳米复合材料快速去除刚果红及其萌发毒性评价
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-23 DOI: 10.1002/cnma.70376
Rinku Nayak,  Archana, Janhavi Manu, Amit Ahlawat, Zimad Hashmi, Anees Ahmed Ansari, Pratima R. Solanki
{"title":"Magnetic Metal Organic Framework-Based Nanocomposite as an Efficient Magneto-Adsorbent for Rapid Congo Red Removal and Germination Toxicity Assessment in Cicer arietinum","authors":"Rinku Nayak,&nbsp; Archana,&nbsp;Janhavi Manu,&nbsp;Amit Ahlawat,&nbsp;Zimad Hashmi,&nbsp;Anees Ahmed Ansari,&nbsp;Pratima R. Solanki","doi":"10.1002/cnma.70376","DOIUrl":"https://doi.org/10.1002/cnma.70376","url":null,"abstract":"<p>The quality of water decreases due to hazardous pollutants such as dyes, including Congo red (CR), a nonbiodegradable, toxic, and synthetic azo dye commonly used in paper, textile, chemical industries, etc. Therefore, removing CR from water is essential. Adsorption using an effective adsorbent is highly efficient for remediation of organic dye molecules. In this work, a cost-effective magnetite nanoparticle@zirconium benzenedicarboxylate (Fe<sub>3</sub>O<sub>4</sub>/Zr-BDC MOF) nanocomposite was synthesized hydrothermally for the removal of CR. As per our knowledge, the synthesized Fe<sub>3</sub>O<sub>4</sub>/Zr-BDC MOF nanocomposite for CR removal has not been reported yet. X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy and energy dispersive X-ray spectroscopy, vibrating sample magnetometry, characterizations were performed to determine material property. The maximum adsorption efficiency of Fe<sub>3</sub>O<sub>4</sub>/Zr-BDC MOF was 96% for 20 parts per million (ppm) of CR in 5 min. The reusability of Fe<sub>3</sub>O<sub>4</sub>/Zr-BDC MOF was also observed over five successive adsorption cycles. The effect on seed germination assay was performed on <i>Cicer arietinum</i> (black gram) seeds to assess the dye toxicity before and after adsorption. The magnetic and highly porous properties of the synthesized Fe<sub>3</sub>O<sub>4</sub>/Zr-BDC MOF nanocomposite make them synergistically more effective and efficient toward the adsorption and removal of CR dye.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149048201","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
A Comparative Study of 2D MoSe2/NbX2 (X = S, Se) vdW Heterostructures as Anode Materials for Sodium-Ion Battery: A First-Principles Calculations Approach 二维MoSe2/NbX2 (X = S, Se) vdW异质结构作为钠离子电池负极材料的比较研究:第一性原理计算方法
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-20 DOI: 10.1002/cnma.70377
Kernel Godwin G. Enriquez, Darwin B. Putungan
{"title":"A Comparative Study of 2D MoSe2/NbX2 (X = S, Se) vdW Heterostructures as Anode Materials for Sodium-Ion Battery: A First-Principles Calculations Approach","authors":"Kernel Godwin G. Enriquez,&nbsp;Darwin B. Putungan","doi":"10.1002/cnma.70377","DOIUrl":"https://doi.org/10.1002/cnma.70377","url":null,"abstract":"<p>This study investigates two-dimensional (2D) MoSe<sub>2</sub>/NbX<sub>2</sub> (X = S, Se) van der Waals heterostructures as anode materials for sodium-ion batteries using density functional theory. It focuses on how the chalcogen atom in NbX<sub>2</sub> affects structural, electronic, and electrochemical properties. Both MoSe<sub>2</sub>/NbS<sub>2</sub> and MoSe<sub>2</sub>/NbSe<sub>2</sub> are energetically stable with low-strain configurations and binding energies of –125.60 and –130.07 meV per unit cell. Both systems exhibit metallic behavior, favorable for charge transport. Sodium adsorption is stronger in MoSe<sub>2</sub>/NbS<sub>2</sub> (–1.83 eV) than in MoSe<sub>2</sub>/NbSe<sub>2</sub> (–1.01 eV). Accordingly, MoSe<sub>2</sub>/NbS<sub>2</sub> shows a higher storage capacity (188 mAh/g) and lower open-circuit voltage (0.35 V) than MoSe<sub>2</sub>/NbSe<sub>2</sub> (106 mAh/g, 0.87 V), both within the desirable range. Simulations confirm thermal stability at 300 K, while CI-NEB results indicate faster Na-ion diffusion in MoSe<sub>2</sub>/NbS<sub>2</sub>. The superior performance of MoSe<sub>2</sub>/NbS<sub>2</sub> is attributed to a larger work function difference, generating a stronger interfacial electric field that enhances sodium adsorption and diffusion. Overall, chalcogen selection in NbX<sub>2</sub> offers an effective strategy for optimizing 2D heterostructure anodes.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149047950","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
Imidazole-Linked Covalent Organic Polymers: Sustainable Materials for Greenhouse Gas Capture, Iodine Vapor Adsorption, and CO2 Cycloaddition 咪唑共价有机聚合物:温室气体捕获,碘蒸气吸附和CO2环加成的可持续材料
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-10 DOI: 10.1002/cnma.70374
Noorullah Baig, Hassan H. Hammud, Suchetha Shetty, Badvel Pallavi, Anuvasita Parikh, Fatemah M. Al-Douseri, Ali Shuaib, Ajay K. Sah, Bassam Alameddine
{"title":"Imidazole-Linked Covalent Organic Polymers: Sustainable Materials for Greenhouse Gas Capture, Iodine Vapor Adsorption, and CO2 Cycloaddition","authors":"Noorullah Baig,&nbsp;Hassan H. Hammud,&nbsp;Suchetha Shetty,&nbsp;Badvel Pallavi,&nbsp;Anuvasita Parikh,&nbsp;Fatemah M. Al-Douseri,&nbsp;Ali Shuaib,&nbsp;Ajay K. Sah,&nbsp;Bassam Alameddine","doi":"10.1002/cnma.70374","DOIUrl":"https://doi.org/10.1002/cnma.70374","url":null,"abstract":"<p>Addressing the dual challenges of radioiodine pollution and rising CO<sub>2</sub> emissions, we report a series of five robust imidazole-based covalent organic polymers (<b>iCOP1–5</b>) synthesized via a microwave-assisted, one-pot [3 + 2] cyclopentannulation reaction. The design strategy leverages a nitrogen-rich tetra-ethynyl imidazole synthon (<b>DIA</b>) and diverse dibrominated polycyclic aromatic hydrocarbons (PAHs) (<b>2–6</b>), enabling efficient heteroatom incorporation and extended π-conjugation. Comprehensive porosity analysis using argon sorption measurements revealed high surface areas of up to 545 m<sup>2</sup> g<sup>−1</sup> and average pore volumes of 0.33 cm<sup>3</sup> g<sup>−1</sup>. The presence of nitrogen heteroatoms and PAH backbones facilitates strong guest–host interactions, leading to outstanding CO<sub>2</sub> uptake of 221 mg g<sup>−1</sup> at 273 K under ambient pressure. Remarkably, these materials also demonstrated exceptional iodine vapor adsorption capacities, reaching up to 3.25 g g<sup>−1</sup>. Furthermore, <b>iCOP1–5</b> function as highly active heterogeneous catalysts for the cycloaddition of CO<sub>2</sub> with styrene oxide, delivering cyclic carbonate (4-phenyl-1,3-dioxolan-2-one) with excellent yields (up to 97%) and selectivity. The polymers exhibit excellent thermal and chemical stability and retain structural integrity over multiple adsorption–desorption cycles, highlighting their potential as multifunctional platforms for gas capture and catalytic CO<sub>2</sub> valorization.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148942984","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
Decoding Atmospheric Influence on Defect-Mediated Luminescence and Charge Storage Mechanisms in 2D BCNO 解码大气对二维BCNO缺陷介导发光和电荷存储机制的影响
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-10 DOI: 10.1002/cnma.70371
Hariprasad V N, S. Sekar, S. Venkataprasad Bhat
{"title":"Decoding Atmospheric Influence on Defect-Mediated Luminescence and Charge Storage Mechanisms in 2D BCNO","authors":"Hariprasad V N,&nbsp;S. Sekar,&nbsp;S. Venkataprasad Bhat","doi":"10.1002/cnma.70371","DOIUrl":"https://doi.org/10.1002/cnma.70371","url":null,"abstract":"<p>Boron carbon oxynitride (BCNO) has emerged as a promising material for optoelectronic and energy-related applications owing to its tunable chemical, optical, and electronic properties. However, a clear understanding of its structural nature remains under debate. In this work, the influence of synthesis atmosphere (nitrogen, open air, and vacuum) on the structural, optical, and electrochemical properties of BCNO is systematically investigated. X-ray diffraction and FTIR analyses indicate the coexistence of turbostratic BN and cubic B<sub>2</sub>O<sub>3</sub> phases in all samples, with their relative contributions strongly dependent on the synthesis environment. Photoluminescence studies reveal defect-mediated tunable emission behavior, with nitrogen-related defects dominating the red emission (~650 nm) and oxygen-related centers contributing to the blue emission (~450 nm), while the open-air samples exhibit a broadband emission (400–800 nm) due to overlapping defect states. Mott–Schottky analysis reveals an atmosphere-dependent shift in flat-band potential, enabling estimation of band alignment. Notably, the vacuum-based sample exhibits superior electrochemical performance with an areal capacitance of ~57 mF cm<sup>−2</sup>, attributed to its defect-rich structure and increased surface sites. These findings support a structure-defect-property relationship and suggest atmospheric control enables tuning of BCNO and provides a rational strategy for its optimization in luminescence and energy storage applications.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148943259","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
Effect of Ionic Surfactants for Tetrapod-Shaped CdSe Quantum Dots 离子表面活性剂对四足形CdSe量子点的影响
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-08 DOI: 10.1002/cnma.70370
Sucheta Banerjee
{"title":"Effect of Ionic Surfactants for Tetrapod-Shaped CdSe Quantum Dots","authors":"Sucheta Banerjee","doi":"10.1002/cnma.70370","DOIUrl":"https://doi.org/10.1002/cnma.70370","url":null,"abstract":"<p>We explore the effect of ionic surfactants on the photoluminescence (PL) of single emissive CdSe nano-tetrapods. In the presence of the cationic surfactant cetyltrimethylammonium bromide (CTAB), effective quenching of PL is observed for tetrapods. X-ray photoelectron spectroscopy (XPS) reveals the adsorption of negatively charged Br<sup>−</sup> ions onto the nanocrystal surface, which leads to efficient PL quenching. In particular, the longer-lived trap-state emission is suppressed due to the accumulation of surfactant counterions at the tetrapod surface. In contrast, sodium dodecyl sulfate (SDS), an anionic surfactant, shows negligible interaction with the negatively charged Se<sup>2−</sup>-terminated surface, resulting in sustained PL intensity. These results demonstrate that the immediate surface environment and counterion adsorption play a critical role in modulating the photoluminescence properties of CdSe nano-tetrapods.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148942689","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
Fabrication of Effective Room Temperature Chemiresistive Gas Sensor by Utilizing p-type CuO @ n-type g-C3N4 Heterojunction Nanocomposite 利用p型CuO @ n型g-C3N4异质结纳米复合材料制备有效的室温化学阻性气体传感器
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-08 DOI: 10.1002/cnma.70342
Sana Balal, Levent Sendogdular
{"title":"Fabrication of Effective Room Temperature Chemiresistive Gas Sensor by Utilizing p-type CuO @ n-type g-C3N4 Heterojunction Nanocomposite","authors":"Sana Balal,&nbsp;Levent Sendogdular","doi":"10.1002/cnma.70342","DOIUrl":"https://doi.org/10.1002/cnma.70342","url":null,"abstract":"<p>A low-cost and sensitive chemiresistive gas sensor based on a p-type CuO and n-type g-C<sub>3</sub>N<sub>4</sub> (copper oxide and graphitic carbon nitride) nanocomposite is described. A simple hydrothermal process was used to create the CuO@g-C<sub>3</sub>N<sub>4</sub> heterostructure, which was then applied as a sensing layer on interdigitated electrodes. CuO nanoparticles successfully formed a porous p–n heterojunction on g-C<sub>3</sub>N<sub>4</sub> sheets, as demonstrated by structural, morphological, and compositional investigations. At room temperature (RT), both reducing (H<sub>2</sub>) and oxidizing (CO<sub>2</sub>) gases were tested by the newly fabricated sensor with outstanding performance. With response times of 10 s for H<sub>2</sub> and 8 s for CO<sub>2</sub>, as well as recovery times of 10 and 7 s, respectively, the device showed quick response and recovery characteristics. High sensitivity was also demonstrated by the sensor's low limit of detection (LOD), which was 44.98 sccm for H<sub>2</sub> and 13.23 sccm for CO<sub>2</sub>. Increased surface area, the creation of an efficient p–n heterojunction, and the synergistic effect of CuO and g-C<sub>3</sub>N<sub>4</sub> are all responsible for the improved sensing behavior.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cnma.70342","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148942750","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
In Situ Formation of N-Doped Mn3O4/Carbon Composites via Linoleic Acid-Assisted Solvothermal Synthesis for Enhanced Pseudocapacitance 亚油酸辅助溶剂热合成原位制备n掺杂Mn3O4/碳复合材料增强赝电容
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-08 DOI: 10.1002/cnma.70369
Hae Woong Park, Jung Min Choi, Hyo-Jun Ahn, Kwang Chul Roh
{"title":"In Situ Formation of N-Doped Mn3O4/Carbon Composites via Linoleic Acid-Assisted Solvothermal Synthesis for Enhanced Pseudocapacitance","authors":"Hae Woong Park,&nbsp;Jung Min Choi,&nbsp;Hyo-Jun Ahn,&nbsp;Kwang Chul Roh","doi":"10.1002/cnma.70369","DOIUrl":"https://doi.org/10.1002/cnma.70369","url":null,"abstract":"<p>In this study, we report the synthesis of nitrogen-doped Mn<sub>3</sub>O<sub>4</sub>/amorphous carbon (N–Mn<sub>3</sub>O<sub>4</sub>/AC) composites via a one-step solvothermal method, employing linoleic acid (LA) and N,N-dimethylacetamide (DMAc) as dual-functional agents for carbon templating and nitrogen doping, respectively. The presence of high-valent manganese-oxo (Mn─O) moieties (terminal Mn<sup>4+</sup>═O), graphitic domains, and redox-active nitrogen functional groups in the carbon matrix and onto the Mn<sub>3</sub>O<sub>4</sub> surface effectively enhanced the electrical conductivity and redox activity of the resulting composite. Electrochemical performance revealed that the N-doped Mn<sub>3</sub>O<sub>4</sub>/AC delivered a high specific capacitance of 293.3 F g<sup>−1</sup> at a current density of 0.5 A g<sup>−1</sup> in 1 M Na<sub>2</sub>SO<sub>4</sub> electrolyte, while maintaining an excellent rate capability of 79% at 5 A g<sup>−1</sup>. Remarkably, this N-doped Mn<sub>3</sub>O<sub>4</sub>/AC electrode achieved 4.4 times higher capacitance than undoped Mn<sub>3</sub>O<sub>4</sub>. Moreover, the composite retained over 80% of its initial capacitance after 2000 charge–discharge cycles at 0.5 A g<sup>−1</sup>, underscoring its excellent long-term stability. Electrochemical impedance spectroscopy (EIS) revealed low charge transfer resistance and favorable ion diffusion kinetics. These findings establish N-doped Mn<sub>3</sub>O<sub>4</sub>/AC composites as a promising and scalable electrode material for high-performance supercapacitors and hybrid energy storage systems.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148942688","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
Fabrication of Boron Nitride@Polydopamine/Polyvinyl Alcohol/Polyvinylidene Fluoride Composite Film With Good Thermal Stability and Thermal Conductivity via Electrospinning and Hot Pressing Treatment 静电纺丝和热压法制备热稳定性和导热性良好的硼Nitride@Polydopamine/聚乙烯醇/聚偏氟乙烯复合薄膜
IF 2.6 4区 材料科学
ChemNanoMat Pub Date : 2026-09-04 DOI: 10.1002/cnma.70359
Zengxi Wang, Haorui Jin, Huidi Liu, Xiang Cai, Shaozao Tan, Shaoyuan Zhou, Jinglin Zhang
{"title":"Fabrication of Boron Nitride@Polydopamine/Polyvinyl Alcohol/Polyvinylidene Fluoride Composite Film With Good Thermal Stability and Thermal Conductivity via Electrospinning and Hot Pressing Treatment","authors":"Zengxi Wang,&nbsp;Haorui Jin,&nbsp;Huidi Liu,&nbsp;Xiang Cai,&nbsp;Shaozao Tan,&nbsp;Shaoyuan Zhou,&nbsp;Jinglin Zhang","doi":"10.1002/cnma.70359","DOIUrl":"https://doi.org/10.1002/cnma.70359","url":null,"abstract":"<p>The field of thermal conductivity is one of the important applications of polymers. However, polymer material generally possesses low thermal conductivity due to its internal characteristic, which cannot meet the heat dissipation requirement of device. Therefore, the preparation of polymer material with high thermal conductivity has broad application prospect and important significance. To achieve this goal, a new-type composite film was fabricated via electrospinning and hot pressing treatment. Utilizing the self-polymerization of dopamine under alkaline condition, polydopamine (PDA) was deposited on the surface of boron nitride (BN). The obtained BN@PDA acted as filler for polyvinyl alcohol (PVA). In addition, polyvinylidene fluoride (PVDF) was introduced into PVA through coaxial spinning. The results indicated that the thermal conductive filler was uniformly distributed and well adhered on the fiber. Moreover, thanks to the intermolecular force between PVA and PVDF, the acquired composite film had good thermal stability with the decomposition temperature over 300 °C. On the other hand, the got composite film exhibited good thermal conductivity at low filling ratio. It could quickly transfer the heat generated during the operation of the LED light, which could reduce the operating temperature of the equipment in actual use, demonstrating its good heat dissipation capability.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"12 9","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148878316","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}
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