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Ultrastrong MXene films via the synergy of intercalating small flakes and interfacial bridging

  • Sijie Wan
  • , Xiang Li
  • , Ying Chen
  • , Nana Liu
  • , Shijun Wang
  • , Yi Du
  • , Zhiping Xu
  • , Xuliang Deng
  • , Shixue Dou
  • , Lei Jiang
  • , Qunfeng Cheng*
  • *Corresponding author for this work
  • Beihang University
  • Peking University
  • National Center for Nanoscience and Technology
  • University of Wollongong
  • Tsinghua University
  • CAS - Technical Institute of Physics and Chemistry
  • Zhengzhou University

Research output: Contribution to journalArticlepeer-review

Abstract

Titanium carbide MXene combines high mechanical and electrical properties and low infrared emissivity, making it of interest for flexible electromagnetic interference (EMI) shielding and thermal camouflage film materials. Conventional wisdom holds that large MXene is the preferable building block to assemble high-performance films. However, the voids in the films comprising large MXene degrade their properties. Although traditional crosslinking strategies can diminish the voids, the electron transport between MXene flakes is usually disrupted by the insulating polymer bonding agents, reducing the electrical conductivity. Here we demonstrate a sequential densification strategy to synergistically remove the voids between MXene flakes while strengthening the interlayer electron transport. Small MXene flakes were first intercalated to fill the voids between multilayer large flakes, followed by interfacial bridging of calcium ions and borate ions to eliminate the remaining voids, including those between monolayer flakes. The obtained MXene films are compact and exhibit high tensile strength (739 MPa), Young’s modulus (72.4 GPa), electrical conductivity (10,336 S cm−1), and EMI shielding capacity (71,801 dB cm2 g−1), as well as excellent oxidation resistance and thermal camouflage performance. The presented strategy provides an avenue for the high-performance assembly of other two-dimensional flakes.

Original languageEnglish
Article number7340
JournalNature Communications
Volume13
Issue number1
DOIs
StatePublished - Dec 2022

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