Recent advances in NiO-based nanostructures for energy storage device applications

被引:19
|
作者
Pai, Shri Hari S. [1 ]
Pandey, Sarvesh Kumar [2 ]
Samuel, E. James Jebaseelan
Jang, Jin Uk [3 ]
Nayak, Arpan Kumar [1 ,3 ]
Han, HyukSu [4 ]
机构
[1] Vellore Inst Technol, Sch Adv Sci, Dept Phys, Vellore 632014, Tamil Nadu, India
[2] Manipal Univ Jaipur, Sch Basic Sci, Dept Chem, Jaipur 300307, Rajasthan, India
[3] Konkuk Univ, Dept Energy Engn, 120 Neungdong Ro, Seoul 05029, South Korea
[4] Sungkyunkwan Univ, Dept Energy Sci, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
Nickel oxide; Synthesis methods; Supercapacitors; Symmetric and Asymmetric; In-silico approach; REDUCED GRAPHENE OXIDE; ENHANCED ELECTROCHEMICAL PERFORMANCE; FLOWER-LIKE NIO; NICKEL-OXIDE; ELECTRODE MATERIAL; IN-SITU; CARBON CLOTH; ELECTROPHORETIC DEPOSITION; FACILE PREPARATION; OXYGEN VACANCIES;
D O I
10.1016/j.est.2023.109731
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In recent years, Nickel oxide (NiO) nanostructures gained more attention due to their excellent supercapacitive performances. The increasing global needs promote researchers to develop efficient energy storage devices to fulfill the requirements of mankind in an eco-friendly way. NiO-based energy storage devices are habitat-friendly and cost-effective. This review anchors the structure-property relationship of nickel oxide electrode materials, and the enhancement of structural designs to optimize the specific capacitance, and storage mechanism. An overview of various methods of preparation for NiO-based nanostructures is highlighted and discussed in detail. Moreover, various strategies to enhance the specific capacitance, capacitive retention, cyclic stability, energy density, and, power density have been summarized based on the experimental findings along with the incorporation of broadly used in-silico approaches. The present review reveals a concrete overview of the current status, challenges, and future perspective of NiO-based electrode materials for energy storage devices.
引用
收藏
页数:26
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