High Pseudocapacitance Boosts Ultrafast, High-Capacity Sodium Storage of 3D Graphene Foam-Encapsulated TiO Architecture.

ACS Appl Mater Interfaces

Beijing Key Laboratory of Environmental Science and Engineering, School of Material Science & Engineering, Beijing Institute of Technology, Beijing 100081, China.

Published: May 2020

AI Article Synopsis

  • - Anatase TiO is a promising anode material for Li-ion and Na-ion batteries, but its low electrical conductivity and poor ion diffusivity limit its electrochemical performance.
  • - Researchers developed a lightweight 3D graphene aerogel-encapsulated anatase TiO that shows impressive performance, including a high reversible capacity of 390 mA h/g, excellent rate performance at 164.9 mA h/g, and strong cycling stability with 86.8% capacity retention after 7800 cycles.
  • - The 3D porous aerogel structure enhances energy storage by providing more active sites and improving ion access, making it a potential breakthrough for next-generation energy-storage technologies.

Article Abstract

Anatase TiO is an attractive anode for Li-ion batteries and Na-ion batteries because of its structural stability. However, the electrochemical capability of anatase TiO is unsatisfactory due to its intrinsically low electrical conductivity and poor ion diffusivity at the electrode/electrolyte interface. We prepared 3D lightweight graphene aerogel-encapsulated anatase TiO, which exhibits a high reversible capacity (390 mA h g at 50 mA g), a superior rate performance (164.9 mA h g at 5 A g), and a long-term cycling capability (capacity retention of 86.8% after 7800 cycles). The major energy-storage mechanism is surface capacitance dominated, which favors a high capacity and fast Na uptake. The inherent features of 3D porous aerogels provide additional active reaction sites and facilitate fast charge diffusion and easy ion access. This will enable the development of 3D interconnected, graphene-based, high-capacity active materials for the development of next-generation energy-storage applications.

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Source
http://dx.doi.org/10.1021/acsami.0c04481DOI Listing

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