Activating an MXene as a host for EMIm by electrochemistry-driven Fe-ion pre-intercalation
EMIm + , as a substitute for Li + , can solve the initial problems that accompany lithiation/delithiation processes on an anode. However, the larger size of EMIm + limits the options when it comes to electrode materials. Herein, a multilayered Ti 3 C 2 T x MXene was electrochemically pre-intercalate...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-08, Vol.8 (32), p.16265-1627 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
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Zusammenfassung: | EMIm
+
, as a substitute for Li
+
, can solve the initial problems that accompany lithiation/delithiation processes on an anode. However, the larger size of EMIm
+
limits the options when it comes to electrode materials. Herein, a multilayered Ti
3
C
2
T
x
MXene was electrochemically pre-intercalated with Fe ions to achieve EMIm
+
hosting abilities. As a result, a pre-intercalated MXene electrode exhibited enhanced EMIm
+
transport and storage capabilities. When integrated with an EMIm
+
[PF6]
−
ionic liquid electrolyte, the assembled DIB provides an energy density of 76 W h kg
−1
at a power density of 360 W kg
−1
, and 94.3% of the energy density is retained after 50 cycles. Compared with a pristine example, the Fe pre-intercalated Ti
3
C
2
T
x
MXene showed a significant increase in electrochemical performance. Employing this approach to optimize layered materials may open up a new route for accurately tuning intercalated materials.
An electrochemistry-driven Fe-ion pre-intercalated MXene with superior EMIm
+
reversible storage abilities for dual-ion battery use was shown. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d0ta05151a |