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Tunable Surface Selenization on MoO 2 ‐Based Carbon Substrate for Notably Enhanced Sodium‐Ion Storage Properties
Author(s) -
Zeng Fanyan,
Yu Maohui,
Cheng Wanting,
He Wenxiu,
Pan Yang,
Qu Yaohui,
Yuan Cailei
Publication year - 2020
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.202001905
Subject(s) - materials science , substrate (aquarium) , anode , heterojunction , chemical engineering , carbon fibers , transition metal , nanotechnology , agglomerate , ion , electrode , optoelectronics , catalysis , composite number , chemistry , composite material , biochemistry , oceanography , organic chemistry , engineering , geology
Transition metal chalcogenides with high theoretical capacity are promising conversion‐type anode materials for sodium ion batteries (SIBs), but often suffer from unsatisfied cycling stability (hundreds of cycles) caused by structural collapse and agglomerate. Herein, a rational strategy of tunable surface selenization on highly crystalline MoO 2 ‐based carbon substrate is designed, where the sheet‐like MoSe 2 can be coated on the surface of bundle‐like N‐doped carbon/granular MoO 2 substrate, realizing partial transformation from MoO 2 to MoSe 2 , and creating b ‐NC/g‐MoO 2 @s‐MoSe 2 ‐10 with robust hierarchical MoO 2 @MoSe 2 heterostructures and strong chemical couplings (MoC and MoN). Such well‐designed architecture can provide signally improved reaction kinetics and reinforced structural integrity for fast and stable sodium‐ion storage, as confirmed by the ex situ results and kinetic analyses as well as the density functional theory calculations. As expected, the b ‐NC/g‐MoO 2 @s‐MoSe 2 ‐10 delivers splendid rate capability and ultralong cycling stability (254.2 mAh g −1 reversible capacity at 5.0 A g −1 after 6000 cycles with ≈ 89.0% capacity retention). Therefore, the tunable surface strategy can provide new insights for designing and constructing heterostructures of transition metal chalcogenides toward high‐performance SIBs.