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Morphology-dependent binder-free CuNiO_2electrode material with excellent electrochemical performances for supercapacitors

机译:形态依赖的无粘结剂CuNiO_2电极材料,具有超级电容器的优异电化学性能

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摘要

Rational design for structure and morphology of multi-component metal oxides is an efficient and promising way to enhance energy storage performance of electrode materials. In this present work, nanosheet-like CuNiO2 heterostructures are fabricated using facile one-step hydrothermal route by introducing various amounts of ammonium fluoride (NH4F) as structure-directing agent. The NH4F assisted synthesis of CuNiO2 materials on Ni foam current collector can be effectively utilized as binder-free battery-type electrode materials for supercapacitors. With an assistance of NH4F, the structural, morphological and composition evolutions of CuNiO2 electrodes are discussed effectively using X-ray diffraction, scanning electron microscopy and transmission electron microscopy and X-ray photoelectron spectroscopy characterizations. The CuNiO2 electrode material prepared with 0.4 M NH4F provides large number of active sites, superior conductivity and rapid charge transfer, which are promote fast Faradaic redox reactions. As a battery-type material, the optimized 0.4-CuNiO2 electrode material (NH4F is 0.4 M) exhibits a high specific capacity (similar to 153.02 mA h g at 2 A g(-1)), excellent rate capability (similar to 87.4% retains even at 10 A g(-1)), and outstanding cycling stability (similar to 94.14% at 6 A g(-1) over 3000 cycles), respectively. Thereby, this study paves the path into rational design for structure and morphology of multi-component metal oxides for improving energy storage performance.
机译:合理设计多组分金属氧化物的结构和形态是提高电极材料储能性能的有效途径。在本工作中,通过引入各种量的氟化铵(NH4F)作为结构导向剂,使用简便的一步式水热法制备了纳米片状CuNiO2异质结构。 NH4F辅助在Ni泡沫集电器上合成CuNiO2材料可有效用作超级电容器的无粘合剂电池型电极材料。借助NH4F,利用X射线衍射,扫描电子显微镜和透射电子显微镜以及X射线光电子能谱表征,有效地讨论了CuNiO2电极的结构,形态和组成演变。用0.4 M NH4F制备的CuNiO2电极材料具有大量的活性部位,优异的电导率和快速的电荷转移,可促进快速的法拉第氧化还原反应。作为电池型材料,经过优化的0.4-CuNiO2电极材料(NH4F为0.4 M)具有高比容量(在2 A g(-1)时类似于153.02 mA hg),优异的倍率能力(保留了87.4%)甚至在10 A g(-1)时)和出色的循环稳定性(类似于3000个循环中6 A g(-1)时的94.14%)。因此,本研究为合理设计多组分金属氧化物的结构和形态铺平了道路,以改善储能性能。

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