Abstract
A Ti3C2Tx MXene film assembled by using conventional vacuum-assisted filtration has an outstanding volumetric performance due to its excellent pseudocapacitive and high density. However, the severely high energy and time consumption by vacuum-assisted filtration will limit its practical mass production as electrodes; meanwhile, the self-restacking of MXene nanosheets increases ion diffusion limitation, especially for thicker film electrodes. Herein, a simple strategy is employed to fabricate a compact and nanoporous MXene film with folded structure (CN-MX) by mechanically pressing a three-dimensional MXene aerogel, resulting in an increased packing density and electrical conductivity (8681 S m-1) while retaining sufficiently abundant ion-accessible active sites. In addition, the formed highly interconnected nanopore channels can facilitate more rapid ionic and electronic transport. When applied as additive-free electrodes for supercapacitors, the CN-MX delivers a comparable volumetric capacitance and much improved rate capability performance compared to the MXene film fabricated by vacuum-assisted filtration. More impressively, it can still exhibit an attractive volumetric capacitance even at practical levels of mass loading (above 10 mg cm-2). This study opens a feasible avenue forward toward commercial applications of MXene in portable and compact storage devices.
| Original language | English |
|---|---|
| Pages (from-to) | 1811-1820 |
| Number of pages | 10 |
| Journal | ACS Applied Energy Materials |
| Volume | 3 |
| Issue number | 2 |
| DOIs | |
| State | Published - 24 Feb 2020 |
Keywords
- folded structured MXene
- mass loading
- rate capability
- supercapacitors
- volumetric performance
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