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通过自下而上的单胶束组装实现卓越赝电容钠存储的二维介孔异质结构

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

作者信息

Lan Kun, Wei Qiulong, Wang Ruicong, Xia Yuan, Tan Shuangshuang, Wang Yanxiang, Elzatahry Ahmed, Feng Pingyun, Mai Liqiang, Zhao Dongyuan

机构信息

Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) , Fudan University , Shanghai 200433 , PR China.

Department of Chemistry , University of California , Riverside , California 92521 , United States.

出版信息

J Am Chem Soc. 2019 Oct 23;141(42):16755-16762. doi: 10.1021/jacs.9b06962. Epub 2019 Oct 11.

Abstract

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), 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.

摘要

具有介孔的二维(2D)异质结构因其集成功能、丰富的活性位点和缩短的扩散距离,在电催化、光催化、能量存储及转换技术方面提供了令人兴奋的机遇。然而,由于传统化学、机械剥离或自组装方法存在巨大困难,层状介观结构尚未得到结合。在此,我们探索了一种在温和条件下进行的自下而上策略,用于轻松合成具有均匀介孔尺寸的单层介孔二氧化钛-介孔碳垂直异质结构,该结构在非水电解质中实现了赝电容钠离子存储的超高倍率性能和循环寿命。这种全新类型的异质结构由排列有序的单层介孔二氧化钛纳米片和两侧组装的两个介孔碳单层组成。值得注意的是,相互连接的大介孔和异质界面的结合导致可逆赝电容显著提高(在扫描速率为1 mV s时占总电荷存储的96.4%),并且使材料在快速的 sodiation 和 desodiation 过程中保持强大的机械稳定性。这项研究揭示了将介孔引入异质界面作为增强电活性材料电荷存储动力学策略的重要性。

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