Mohan Rao Tamtam, , , Gyu Sang Choi*, , , Sai Phani Kumar Vangala, , , Jaesool Shim*, , , Nhi Ngoc Nguyen*, , and , Nam Nguyen Dang,
{"title":"合理设计核壳型Mn-V MOF纳米结构,提高电荷存储性能","authors":"Mohan Rao Tamtam, , , Gyu Sang Choi*, , , Sai Phani Kumar Vangala, , , Jaesool Shim*, , , Nhi Ngoc Nguyen*, , and , Nam Nguyen Dang, ","doi":"10.1021/acs.jpclett.5c02501","DOIUrl":null,"url":null,"abstract":"<p >In this study, we synthesized a series of bimetallic Mn<sub><i>x</i></sub>V<sub><i>y</i></sub>-based metal organic frameworks directly on nickel foam (NF) substrates via an in situ hydrothermal interfacial growth method. By systematically varying the Mn:V ratio, we optimized the interactions between the two metals, thereby enhancing the electrochemical properties of the resulting electrode materials. Among the prepared materials, the M<sub>1</sub>V<sub>3</sub>/NF electrode showed the best capacitance (1826.4 F/g @ 1 A/g) due to its core–shell morphology, with superior rate performance, low internal resistance, and outstanding cycling stability (88% capacitance retention after 10,000 cycles). Furthermore, the assembled asymmetric hybrid supercapacitor device with M<sub>1</sub>V<sub>3</sub>/NF and activated carbon/NF electrodes in a coin-cell configuration delivered an energy density of 77.62 Wh/kg at 175 W/kg and showed reliable cycling performance. Thus, the proposed synthesis approach is a feasible route for designing advanced binary or ternary metal-based hybrid nanostructures with enhanced storage characteristics.</p>","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"16 41","pages":"10655–10668"},"PeriodicalIF":4.6000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rational Design of Core–Shell Mn–V MOF Nanostructures with Improved Charge Storage Performance\",\"authors\":\"Mohan Rao Tamtam, , , Gyu Sang Choi*, , , Sai Phani Kumar Vangala, , , Jaesool Shim*, , , Nhi Ngoc Nguyen*, , and , Nam Nguyen Dang, \",\"doi\":\"10.1021/acs.jpclett.5c02501\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In this study, we synthesized a series of bimetallic Mn<sub><i>x</i></sub>V<sub><i>y</i></sub>-based metal organic frameworks directly on nickel foam (NF) substrates via an in situ hydrothermal interfacial growth method. By systematically varying the Mn:V ratio, we optimized the interactions between the two metals, thereby enhancing the electrochemical properties of the resulting electrode materials. Among the prepared materials, the M<sub>1</sub>V<sub>3</sub>/NF electrode showed the best capacitance (1826.4 F/g @ 1 A/g) due to its core–shell morphology, with superior rate performance, low internal resistance, and outstanding cycling stability (88% capacitance retention after 10,000 cycles). Furthermore, the assembled asymmetric hybrid supercapacitor device with M<sub>1</sub>V<sub>3</sub>/NF and activated carbon/NF electrodes in a coin-cell configuration delivered an energy density of 77.62 Wh/kg at 175 W/kg and showed reliable cycling performance. Thus, the proposed synthesis approach is a feasible route for designing advanced binary or ternary metal-based hybrid nanostructures with enhanced storage characteristics.</p>\",\"PeriodicalId\":62,\"journal\":{\"name\":\"The Journal of Physical Chemistry Letters\",\"volume\":\"16 41\",\"pages\":\"10655–10668\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Physical Chemistry Letters\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jpclett.5c02501\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpclett.5c02501","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Rational Design of Core–Shell Mn–V MOF Nanostructures with Improved Charge Storage Performance
In this study, we synthesized a series of bimetallic MnxVy-based metal organic frameworks directly on nickel foam (NF) substrates via an in situ hydrothermal interfacial growth method. By systematically varying the Mn:V ratio, we optimized the interactions between the two metals, thereby enhancing the electrochemical properties of the resulting electrode materials. Among the prepared materials, the M1V3/NF electrode showed the best capacitance (1826.4 F/g @ 1 A/g) due to its core–shell morphology, with superior rate performance, low internal resistance, and outstanding cycling stability (88% capacitance retention after 10,000 cycles). Furthermore, the assembled asymmetric hybrid supercapacitor device with M1V3/NF and activated carbon/NF electrodes in a coin-cell configuration delivered an energy density of 77.62 Wh/kg at 175 W/kg and showed reliable cycling performance. Thus, the proposed synthesis approach is a feasible route for designing advanced binary or ternary metal-based hybrid nanostructures with enhanced storage characteristics.
期刊介绍:
The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.