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Asymmetrically Coordinated Cu–N 1 C 2 Single‐Atom Catalyst Immobilized on Ti 3 C 2 T x MXene as Separator Coating for Lithium–Sulfur Batteries
Lithium–sulfur (Li–S) batteries are receiving great attention owing to their large theoretical energy density, but the shuttle effect and sluggish kinetic conversion of lithium polysulfides (LiPSs) seriously restrict their practical applications. Herein, various metal single‐atom catalysts immobiliz...
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Published in: | Advanced energy materials 2023-05, Vol.13 (20) |
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Main Authors: | , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Lithium–sulfur (Li–S) batteries are receiving great attention owing to their large theoretical energy density, but the shuttle effect and sluggish kinetic conversion of lithium polysulfides (LiPSs) seriously restrict their practical applications. Herein, various metal single‐atom catalysts immobilized on nitrogen‐doped Ti
3
C
2
T
x
(
M
SA/N‐Ti
3
C
2
T
x
,
M
= Cu, Co, Ni, Mn, Zn, In, Sn, Pb, and Bi) are successfully prepared by a neoteric vacancy‐assisted strategy, applied as polypropylene (PP) separator coatings to facilitate the fast redox conversion and adsorption of LiPSs for boosting Li–S batteries. Of particular note, among the
M
SA/N‐Ti
3
C
2
T
x
s, Cu SA/N‐Ti
3
C
2
T
x
/PP exhibits amazing properties, involving excellent rate performance (925 mAh g
−1
at 3 C), superb cycling stability over 1000 cycles, and ultra‐high sulfur utilization even at large sulfur loadings (7.19 mg cm
−2
; an areal capacity of 5.28 mAh cm
−2
). X‐ray absorption fine spectroscopy and density functional theory calculations reveal that the asymmetrically coordinated Cu–N
1
C
2
moieties act as the active sites, which possess a higher binding energy and a larger electron cloud with LiPSs than pristine Ti
3
C
2
T
x
, facilitating the adsorption and kinetic conversion of LiPSs effectively. This work may provide new insights into single atom‐decorated ultrathin 2D materials for enhancing electrochemical performance of advanced batteries for energy storage and conversion. |
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ISSN: | 1614-6832 1614-6840 |
DOI: | 10.1002/aenm.202204014 |