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In situ preparation of cobalt doped ZnO@C/CNT composites by the pyrolysis of a cobalt doped MOF for high performance lithium ion batteries

机译:钴掺杂MOF热解原位制备钴掺杂ZnO @ C / CNT复合材料用于高性能锂离子电池

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Co doped ZnO embedded in carbon/carbon nanotube composites (CZO@C/CNT) was prepared in situ during the calcination of Co-MOF-105 at 600 degrees C. A lower crystallinity demonstrated weaker binding force in Co-MOF-105, which made it possible for Co ions to break away from the crystal and reduce to metal Co during the pyrolysis process. The formation of CNTs was catalyzed by Co metal and the carbon source was terephthalic acid, which acted as the organic linker in the MOF. Moreover, the sp(2) hybridization of the carbon atoms in terephthalic acid decreased the energy barrier during the growth of CNTs. From TEM and SEM observation, the CNTs were interspersed in the material and connected the CZO@C nanoparticles together, which made the electron transfer easier. The other advantages of Co doping were enhancing the conductivity of ZnO and increasing the graphitization degree of the carbon on the surface of the CZO@C nanoparticles. When the CZO@C/CNT composite was used as an anode material for lithium ion batteries, an enhanced electrochemical performance of 758 mA h g(-1) after 100 cycles at a current density of 100 mA g(-1) was obtained.
机译:在600摄氏度的Co-MOF-105煅烧过程中原位制备嵌入到碳/碳纳米管复合材料(CZO @ C / CNT)中的Co掺杂的ZnO。较低的结晶度表明Co-MOF-105中的结合力较弱,这使得Co离子在热解过程中可能脱离晶体并还原为金属Co。碳纳米管的形成是由钴金属催化的,碳源是对苯二甲酸,它是MOF中的有机连接基。此外,对苯二甲酸中碳原子的sp(2)杂化降低了CNT生长过程中的能垒。从TEM和SEM观察,碳纳米管散布在材料中,并将CZO @ C纳米颗粒连接在一起,这使电子转移更加容易。 Co掺杂的其他优点是增强了ZnO的电导率,并提高了CZO @ C纳米颗粒表面碳的石墨化程度。当CZO @ C / CNT复合材料用作锂离子电池的负极材料时,在100 mA g(-1)的电流密度下经过100次循环后,电化学性能达到758 mA h g(-1)。

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