Two-Dimensional Mesoporous Heterostructure Delivering Superior Pseudocapacitive Sodium Storage via Bottom-Up Monomicelle Assembly

假电容 介孔材料 异质结 纳米技术 化学工程 超级电容器 单层 电解质 储能 化学 电化学 材料科学 电极 催化作用 光电子学 生物化学 功率(物理) 物理 物理化学 量子力学 工程类
作者
Kun Lan,Qiulong Wei,Ruicong Wang,Xia Yuan,Shuangshuang Tan,Yanxiang Wang,Ahmed A. Elzatahry,Pingyun Feng,Liqiang Mai,Dongyuan Zhao
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:141 (42): 16755-16762 被引量:140
标识
DOI:10.1021/jacs.9b06962
摘要

Two-dimensional (2D) heterostructures endowed with mesoporosities offer exciting opportunities in electrocatalysis, photocatalysis, energy storage, and conversion technologies due to their integrated functionalities, abundant active sites and shortened diffusion distance. However, layered mesostructures have not been combined due to the immense difficulties by conventional chemical, mechanical exfoliation or self-assembly approaches. Herein, we explore a bottom-up strategy, carried out under mild conditions, for the facile synthesis of monolayered mesoporous-titania-mesoporous-carbon vertical heterostructure with uniform mesopore size, which enables ultrahigh rate capability and cycling longevity for pseudocapacitive sodium-ion storage in nonaqueous electrolyte. Such a brand-new type of heterostructure consists of well-ordered monolayered mesoporous titania nanosheets and surrounding two mesoporous carbon monolayers assembled at both sides. Remarkably, the combination of interconnected large mesoporosity and heterointerface leads to highly promoted reversible pseudocapacitance (96.4% of total charge storage at a sweep rate of 1 mV s-1), and it enables the material to retain strong mechanical stability during the rapid sodiation and desodiation processes. This study reveals the importance of incorporating mesopores into heterointerface as a strategy for enhancing charge storage kinetics of electroactive materials.
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