4.6 Article

Diacid Molecules Welding Achieved Self-Adaption Layered Structure Ti3C2 MXene toward Fast and Stable Lithium-Ion Storage

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 9, Issue 38, Pages 12930-12939

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.1c04210

Keywords

Ti3C2; enlarging interlayer spacing; self-adaption; diffusion coefficient; lithium-ion storage

Funding

  1. National Natural Science Foundation of China [52062030]
  2. Found of the State Key Laboratory of Advance Processing and Recycling of Nonferrous Metals, Lanzhou University of Technology [SKLAB02019008]
  3. Hongliu Youth Fund of Lanzhou University of Technology

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Ti3C2 has been considered a potential material for lithium-ion storage due to its abundant surface terminals, excellent metal-like conductivity, and modifiable layered structure. However, the Li+ diffusion rate in the interlayer is limited by the small interlayer spacing determined by van der Waals forces. A novel chemical welding approach involving dehydration condensation between amino-functionalized Ti3C2 and maleic acid molecules was employed to enlarge the interlayer spacing, resulting in enhanced Li+ diffusion rate and improved storage performance.
Ti3C2 has been considered as a potential material for lithium-ion storage because of its abundant surface terminals, excellent metal-like conductivity, and modifiable layered structure. However, the Li+ diffusion rate in interlayer is limited by the small interlayer spacing determined by the van der Waals forces. Herein, the dehydration condensation reaction between amino-functionalized Ti3C2 (Ti3C2-NH2) and maleic acid (MA) molecules was utilized to enlarge the interlayer spacing of Ti3C2. The MA molecules were successfully welded into interlayers of Ti3C2 by HN-C.O bonds (namely, chemical welding) and MA chemical welded Ti3C2 (MA-Ti3C2) with self-adaption layered structure were obtained. The MA molecules can contribute double effects to the layered structure of Ti3C2, and they act as chains to remit the volume change during Li+ insertion and serve as pillars to enhance the structure stability during Li+ extraction. The MA-Ti3C2 exhibits an interlayer spacing of 1.28 nm, a fast Li+ diffusion rate (1.4 x 10(-8) to 5.8 x 10(-7) cm(2) s(-1)), and improved Li+ storage performance. The MA-Ti3C2//AC lithium-ion capacitor (LIC) demonstrates an excellent energy density of 102.5 Wh kg(-1) at 200 W kg(-1) and cycle stability with 76.3% at 1.0 A g(-1) after 1000 cycles. This novel chemical welding delivers an effective perspective for modifying the layered structure, enhancing the structure stability, and achieving fast Li+ diffusion and high-rate capability of two-dimension materials.

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