{"title":"MXene集成金属-有机框架衍生磷化钴在超级电容器中的应用","authors":"Gaurav Pandey, Ankit Sharma, Meenakshi, Kamakshi Pandey, Prashanth W. Menezes, Kamlendra Awasthi","doi":"10.1002/cctc.202500430","DOIUrl":null,"url":null,"abstract":"<p>The development of high energy density electrode materials for supercapacitors is essential to address the growing energy demands and environmental concerns. Transition metal phosphides, particularly cobalt phosphide (CoP) have attracted significant interest due to their high theoretical capacity and excellent redox activity. However, their practical application is limited by poor cycling stability and lower electrical conductivity. To address these challenges, this study employs a metal-organic framework (ZIF-67) as a precursor to synthesize CoP, followed by the in- situ heterojunction formation (CoP/50-Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub>, CoP/100-Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub>, and CoP/150-Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub>) with different mass loading (50, 100, and 150 mg) of MXene (Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub>). The optimized electrode material CoP/100-Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> achieve the highest specific capacitance of 625.9 F/g at 0.25 A/g with a high rate performance of 260.2 F/g at 25 A/g. This performance significantly surpasses bare CoP (397.3 F/g at 0.25 A/g), Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> (106.3 F/g at 0.25 A/g), and other CoP/Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> composite. Additionally, it demonstrates a cycling stability of 78.13% for 10,000 cycles at 20 A/g. Furthermore, an asymmetric supercapacitor device was fabricated using CoP/100-Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> as positive electrode materials and activated carbon as the negative electrode. The as-fabricated device delivered an energy density of 22.59 Wh/kg at a power density of 399.99 W/kg with capacitance retention of 73.25% after 2000 cycles at 10 A/g and Coulombic efficiency close to 100%. The insight charge-discharge mechanism is explained in detail.</p>","PeriodicalId":141,"journal":{"name":"ChemCatChem","volume":"17 17","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"MXene Integrated Metal-Organic Framework Derived Cobalt Phosphide for Supercapacitor Applications\",\"authors\":\"Gaurav Pandey, Ankit Sharma, Meenakshi, Kamakshi Pandey, Prashanth W. 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The optimized electrode material CoP/100-Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> achieve the highest specific capacitance of 625.9 F/g at 0.25 A/g with a high rate performance of 260.2 F/g at 25 A/g. This performance significantly surpasses bare CoP (397.3 F/g at 0.25 A/g), Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> (106.3 F/g at 0.25 A/g), and other CoP/Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> composite. Additionally, it demonstrates a cycling stability of 78.13% for 10,000 cycles at 20 A/g. Furthermore, an asymmetric supercapacitor device was fabricated using CoP/100-Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> as positive electrode materials and activated carbon as the negative electrode. The as-fabricated device delivered an energy density of 22.59 Wh/kg at a power density of 399.99 W/kg with capacitance retention of 73.25% after 2000 cycles at 10 A/g and Coulombic efficiency close to 100%. 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引用次数: 0
摘要
为了解决日益增长的能源需求和环境问题,开发高能量密度的超级电容器电极材料是必不可少的。过渡金属磷化物,特别是磷化钴(CoP)由于其较高的理论容量和优异的氧化还原活性而引起了人们的极大兴趣。然而,它们的实际应用受到循环稳定性差和电导率低的限制。为了解决这些挑战,本研究采用金属有机骨架(ZIF-67)作为前体合成CoP,然后在不同质量负载(50、100和150 mg) MXene (Ti3C2Tx)的情况下原位形成CoP/50-Ti3C2Tx、CoP/100-Ti3C2Tx和CoP/150-Ti3C2Tx。优化后的电极材料CoP/100-Ti3C2Tx在0.25 A/g时的最高比电容为625.9 F/g,在25 A/g时的高倍率性能为260.2 F/g。该性能显著优于纯CoP(在0.25 A/g时为397.3 F/g)、Ti3C2Tx(在0.25 A/g时为106.3 F/g)和其他CoP/Ti3C2Tx复合材料。此外,在20 a /g下,它在10,000次循环中表现出78.13%的循环稳定性。在此基础上,以CoP/100-Ti3C2Tx为正极材料,活性炭为负极,制备了非对称超级电容器器件。在功率密度为399.99 W/kg时,该器件的能量密度为22.59 Wh/kg,在10 a /g下循环2000次后电容保持率为73.25%,库仑效率接近100%。详细解释了insight充放电机理。
MXene Integrated Metal-Organic Framework Derived Cobalt Phosphide for Supercapacitor Applications
The development of high energy density electrode materials for supercapacitors is essential to address the growing energy demands and environmental concerns. Transition metal phosphides, particularly cobalt phosphide (CoP) have attracted significant interest due to their high theoretical capacity and excellent redox activity. However, their practical application is limited by poor cycling stability and lower electrical conductivity. To address these challenges, this study employs a metal-organic framework (ZIF-67) as a precursor to synthesize CoP, followed by the in- situ heterojunction formation (CoP/50-Ti3C2Tx, CoP/100-Ti3C2Tx, and CoP/150-Ti3C2Tx) with different mass loading (50, 100, and 150 mg) of MXene (Ti3C2Tx). The optimized electrode material CoP/100-Ti3C2Tx achieve the highest specific capacitance of 625.9 F/g at 0.25 A/g with a high rate performance of 260.2 F/g at 25 A/g. This performance significantly surpasses bare CoP (397.3 F/g at 0.25 A/g), Ti3C2Tx (106.3 F/g at 0.25 A/g), and other CoP/Ti3C2Tx composite. Additionally, it demonstrates a cycling stability of 78.13% for 10,000 cycles at 20 A/g. Furthermore, an asymmetric supercapacitor device was fabricated using CoP/100-Ti3C2Tx as positive electrode materials and activated carbon as the negative electrode. The as-fabricated device delivered an energy density of 22.59 Wh/kg at a power density of 399.99 W/kg with capacitance retention of 73.25% after 2000 cycles at 10 A/g and Coulombic efficiency close to 100%. The insight charge-discharge mechanism is explained in detail.
期刊介绍:
With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.