电容
超级电容器
材料科学
电解质
石墨烯
氧化物
电极
纳米技术
准固态
储能
电化学
化学工程
化学
冶金
工程类
物理化学
功率(物理)
物理
量子力学
色素敏化染料
作者
Xing Wei,Junru Wang,Rui Chen,Zhijiang Zhang,Qing Zhang
出处
期刊:Small
[Wiley]
日期:2025-04-08
标识
DOI:10.1002/smll.202501802
摘要
Abstract Graphene oxide‐based all‐solid‐state supercapacitors (GO ASSCs) provide a to‐the‐point opportunity of integrating miniaturized energy storage devices on a single chip with operation‐ability and safety superiority over liquid electrolyte‐based SCs, yet their capacitance needs to be improved. Based on the lamellar MXene‐GO ASSC structure energy density of the GO ASSCs can be brought up to the level comparable to their counterparts using liquid electrolytes via simple tuning the MXene/GO thickness. During analyzing how the GO and MXene thickness affects the electrochemical performance, a major paradox is noticed between the high capacitance of up to two hundreds of farads per gram achievable with specific MXene/GO thickness combination, and its seemly slow diffusion kinetics. In situ pressure test is designed, and a quick capacitance saturation validated enhanced “charge storage efficiency” of the specific MXene/GO thickness combination, further revealing a possible delicate balance acquired between the solid electrolyte and the electrodes to break the restriction on ion diffusion. The findings should provide a straightforward solution in achieving high capacitance performance for the ASSCs using GO solid electrolyte and MXene or other pseudocapacitive electrode materials.
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