Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Optimizing charge transfer and alleviating volume expansion in electrode materials are critical to maximize electrochemical performance for energy storage systems. Herein, an atomically thin soft-rigid Co
S
@MoS
core-shell heterostructure with dual cation vacancies at the atomic interface is constructed as a promising anode for high-performance sodium-ion batteries. The dual cation vacancies involving V
and V
in the heterostructure and the soft MoS
shell afford ionic pathways for rapid charge transfer, as well as the rigid Co
S
core acts as the dominant active component and resists structural deformation during charge/discharge. Electrochemical testing and theoretical calculations demonstrate both excellent Na
transfer kinetics and pseudocapacitive behavior. Consequently, the soft-rigid heterostructure delivers extraordinary sodium storage performance (389.7 mA h g
after 500 cycles at 5.0 A g
), superior to those of the single-phase counterparts; and the assembled Na
V
(PO
)
||d-Co
S
@MoS
/S-Gr full cell achieves an energy density of 235.5 Wh kg
at 0.5 C. Our finding opens up a new strategy of soft-rigid heterostructure and broadens the horizons of material design in energy storage and conversion. This article is protected by copyright. All rights reserved.