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使用还原氧化石墨烯锚定的溶胶-凝胶衍生Ni/NiO纳米复合材料的固态混合储能装置的性能

Performance of Solid-state Hybrid Energy-storage Device using Reduced Graphene-oxide Anchored Sol-gel Derived Ni/NiO Nanocomposite.

作者信息

Das Himadri Tanaya, Mahendraprabhu Kamaraj, Maiyalagan Thandavarayan, Elumalai Perumal

机构信息

Electrochemical Energy and Sensors Lab, Department of Green Energy Technology, Madanjeet School of Green Energy Technologies, Pondicherry University, Puducherry, 605014, India.

Department of Bioelectronics and Biosensors, Alagappa University, Karaikudi, 630003, Tamilnadu, India.

出版信息

Sci Rep. 2017 Nov 10;7(1):15342. doi: 10.1038/s41598-017-15444-z.

Abstract

The influence of (nickel nitrate/citric acid) mole ratio on the formation of sol-gel end products was examined. The formed Ni/NiO nanoparticle was anchored on to reduced graphene-oxide (rGO) by means of probe sonication. It was found that the sample obtained from the (1:1) nickel ion: citric acid (Ni: CA) mole ratio resulted in a high specific capacity of 158 C/g among all (Ni: CA) ratios examined. By anchoring Ni/NiO on to the rGO resulted in enhanced specific capacity of as high as 335 C/g along with improved cycling stability, high rate capability and Coulombic efficiency. The high conductivity and increased surface area seemed responsible for enhanced electrochemical performances of the Ni/NiO@rGO nanocomposite. A solid-state hybrid energy-storage device consisting of the Ni/NiO@rGO (NR) as a positive electrode and the rGO as negative electrode exhibited enhanced energy and power densities. Lighting of LED was demonstrated by using three proto-type (NR|| rGO) hybrid devices connected in series.

摘要

研究了(硝酸镍/柠檬酸)摩尔比对溶胶-凝胶最终产物形成的影响。通过探针超声处理将形成的镍/氧化镍纳米颗粒锚定在还原氧化石墨烯(rGO)上。发现在所有研究的(镍:柠檬酸)比例中,从(1:1)镍离子:柠檬酸(Ni:CA)摩尔比获得的样品具有158 C/g的高比容量。通过将镍/氧化镍锚定在rGO上,导致比容量提高到高达335 C/g,同时循环稳定性、高倍率性能和库仑效率得到改善。高导电性和增加的表面积似乎是镍/氧化镍@rGO纳米复合材料电化学性能增强的原因。由镍/氧化镍@rGO(NR)作为正极和rGO作为负极组成的固态混合储能装置表现出增强的能量和功率密度。通过串联连接三个原型(NR||rGO)混合装置演示了发光二极管的点亮。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ebb/5681587/51e03810aba8/41598_2017_15444_Fig1_HTML.jpg

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