Pillared Mo 2 TiC 2 MXene for high-power and long-life lithium and sodium-ion batteries
Source abstract
Abstract
In this work, we apply an amine-assisted silica pillaring method to create the first example of a porous Mo2TiC2 MXene with nanoengineered interlayer distances. The pillared Mo2TiC2 has a surface area of 202 m2 g-1, which is among the highest reported for any MXene, and has a variable gallery height between 0.7 and 3 nm. The expanded interlayer distance leads to significantly enhanced cycling performance for Li-ion storage, with superior capacity, rate capably and cycling stability in comparison to the non-pillared analogue. The pillared Mo2TiC2 achieved a capacity over 1.7 times greater than multilayered MXene at 20 mA g-1 (≈320 mA h g-1) and 2.5 times higher at 1 A g-1 (≈150 mA h g-1). The fast-charging properties of pillared Mo2TiC2 are further demonstrated by outstanding stability even at 1 A g-1 (under 8 min charge time), retaining 80% of the initial capacity after 500 cycles. Furthermore, we use a combination of spectroscopic techniques (i.e. XPS, NMR and Raman) to show unambiguously that the charge storage mechanism of this MXene occurs by a conversion reaction through the formation of Li2O. This reaction increases by 2-fold the capacity beyond intercalation, and therefore, its understanding is crucial for further development of this family of materials. In addition, we also investigate for the first time the sodium storage properties of the pillared and non-pillared Mo2TiC2.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: MXene and MAX Phase Materials · Advancements in Battery Materials · Ferroelectric and Negative Capacitance Devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Engineering
Lancaster University
Lancaster
UK
Department of Chemistry
Department of Materials
University of Manchester
Manchester
Funding
Engineering and Physical Sciences Research Council · Royal Society · H2020 European Research Council · Lancaster University · European Regional Development Fund
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