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In Situ Preparation of ID Co@C Composite Nanorods as Negative Materials for Alkaline Secondary Batteries

机译:ID Co @ C复合纳米棒的原位制备作为碱性电池的负极材料

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Cobalt-based coordination compounds were successfully prepared via employing nitrilotriacetic acid (NTA) as a complexing agent through a mild surfactant-free solvothermal process. Cobalt ions are linked with the amino group or carboxyl groups of NTA to become one-dimensional nanorods that can be proved by Fourier transform infrared measurement findings. The morphologies of the precursor Co—NTA highly depend on the solvent composition, the reaction time and temperature. The probable growth mechanism has been proposed, After heat treatment, the Co—NTA precursor can be completely converted into Co@C nanorods assembled by numerous core—shell-like Co@C nanoparticles, which preserved the rodlike morphology. The as-prepared Co@C composites display a rodlike morphology with 4μm length and 100 nm diameter, The electrochemical performances of this novel Co@C material as the alkaline secondary Ni/Co battery negative electrode have been systematically researched. The discharge capacity of the Co@C-1 composite electrode can attain 609 mAh g~(-1) and retains about 383.3 mAh g~(-1) after 120 cycles (the discharge current density of 500 mA g~(-1)). The novel material exhibits a high discharge capacity of 610 and 470 mAh g~(-1) at discharge currents of 100 and 1000 mA g~(-1), respectively. This suggests that approximately 77% of the discharge capacity is kept when the discharge current density is increased to 1000 mA g~(-1) (10 times the initial current density of 100 mA g~(-1)). The excellent electrochemical properties could be ascribed to the porous channels of the novel Co(SC materials, which is beneficial to electrolyte difrusion and electrons and ions transportation.
机译:通过使用次氮基三乙酸(NTA)作为络合剂,通过温和的无表面活性剂溶剂热法成功制备了钴基配位化合物。钴离子与NTA的氨基或羧基相连,成为一维纳米棒,可以通过傅立叶变换红外测量发现来证明。前驱体Co-NTA的形态在很大程度上取决于溶剂组成,反应时间和温度。已经提出了可能的生长机理。热处理后,Co-NTA前体可以完全转化为由众多核壳状Co @ C纳米粒子组装而成的Co @ C纳米棒,从而保留了棒状形态。制备的Co @ C复合材料呈棒状形态,长度为4μm,直径为100nm。对该新型Co @ C材料作为碱性二次Ni / Co电池负极的电化学性能进行了系统的研究。 Co @ C-1复合电极的放电容量可达到609 mAh g〜(-1),经过120次循环后可保持约383.3 mAh g〜(-1)(放电电流密度为500 mA g〜(-1)) )。这种新型材料在100和1000 mA g〜(-1)的放电电流下分别具有610和470 mAh g〜(-1)的高放电容量。这表明,当放电电流密度增加到1000 mA g〜(-1)时(大约是100 mA g〜(-1)的初始电流密度的10倍),可以保持大约77%的放电容量。优异的电化学性能可归因于新型Co(SC)材料的多孔通道,这有利于电解质扩散和电子和离子传输。

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