Issue 10, 2019

A rough endoplasmic reticulum-like VSe2/rGO anode for superior sodium-ion capacitors

Abstract

Sodium ion capacitors (SICs) exhibit both high energy and power density, offering potential as a new type of energy device. However, the fabrication of highly effective SICs is limited by the sluggish kinetics and large-volume expansion of ion insertion/extraction in the anode materials. In this featured work inspired by the structure and function of the rough endoplasmic reticulum in living cells, layer-structured vanadium diselenide (VSe2) was downsized and confined on both sides of reduced graphene oxide (rGO) sheets and further assembled into a porous 3-dimensional (3D) VSe2/rGO aerogel. The biomimetic-structured porous 3D rGO skeleton provides a stable host to fix VSe2, can accelerate the diffusion and adsorption of electrolyte in the electrode materials, and buffers the volume expansion of VSe2 during long cycles. As the anode materials of SICs, the as-prepared VSe2/rGO aerogel delivered a far higher reversible capacity and superior long-life stability than those of pure VSe2. We further analyzed the VSe2/rGO charge and discharge mechanism by ex situ XRD. By pairing the VSe2/rGO anode with active carbon (AC) as the cathode, the as-assembled SIC displayed both high power density and high energy density (106 W h kg−1 at 125 W kg−1, 68 W h kg−1 at 5000 W kg−1). Overall, the superior electrochemical performance and unique biomimetic-inspired architecture of the VSe2/rGO aerogel offer a promising platform for designing other ion insertion/extraction host electrode materials.

Graphical abstract: A rough endoplasmic reticulum-like VSe2/rGO anode for superior sodium-ion capacitors

Supplementary files

Article information

Article type
Research Article
Submitted
03 Jul 2019
Accepted
27 Aug 2019
First published
30 Aug 2019

Inorg. Chem. Front., 2019,6, 2935-2943

A rough endoplasmic reticulum-like VSe2/rGO anode for superior sodium-ion capacitors

Y. Wu, H. Chen, L. Zhang, Q. Li, M. Xu and S. Bao, Inorg. Chem. Front., 2019, 6, 2935 DOI: 10.1039/C9QI00809H

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