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Morphology-dependent magnetic role of ZIFs in nitrogen-doped MXene as metallic conductor microwave absorber

  • East China Normal University
  • Tongji University

科研成果: 期刊稿件文章同行评审

摘要

The suboptimal impedance matching characteristics exhibited by MXene, attributable to its elevated conductivity, in conjunction with the propensity of MXene flakes to agglomerate, has imposed significant limitations on the pragmatic applicability of MXene derivatives within the realm of electromagnetic wave (EMW) absorption. To decrease conductivity and induce dipolar polarization, the introduction of nitrogen-doped defects into a MXene (Ti3C2Tx) was accomplished by utilizing acetonitrile as a source of liquid nitrogen. The metallic conductivity of N-Ti3C2Tx at a nitrogen doping content of 5.31 at% has been uncovered through first-principles calculations. To mitigate the restacking of 2D MXene flakes and enhance their absorption performance in the low-frequency band, the insertion of magnetic intercalators has been implemented. The application of Co-Zn-coordinated zeolitic imidazole frameworks (ZIFs) as magnetic intercalators has demonstrated a substantial enhancement in polar units. The resulting structure of calcined ZIF-67@ZIF-8 showcases a hollow morphology and exhibits a high saturation magnetization, facilitating significant magnetic loss. For instance, ZIF-67@ZIF-8/N-Ti3C2Tx reaches the widest EBA of 5.36 GHz (2.273 mm, 13.00 GHz, RLmin = −65.03 dB), and the strongest value RLmin of −70.43 dB (3.350 mm, 7.64 GHz, EAB = 3.16 GHz), respectively. Furthermore, the present study employs COMSOL simulations to investigate the behavior of ZIF-67@ZIF-8/N-Ti3C2Tx in response to current field, as well as its electrical shielding attributes and EWM field patterns. This innovative multilayer microstructure effectively attains a desirable equilibrium between dielectric and magnetic properties, thereby showcasing immense promise in the domain of consecutive multi-band EMW absorption.

源语言英语
文章编号145817
期刊Chemical Engineering Journal
474
DOI
出版状态已出版 - 15 10月 2023
已对外发布

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