Naqvi Shabbir Madad, Hassan Tufail, Iqbal Aamir, Jung Sungmin, Jeong Seunghwan, Zaman Shakir, Zafar Ujala, Hussain Noushad, Cho Sooyeong, Koo Chong Min
School of Advanced Materials Science and Engineering, Sungkyunkwan University, Seobu-ro 2066, Jangan-gu, Suwon-si, Gyeonggi-do 16419, Republic of Korea.
School of Chemical Engineering, Sungkyunkwan University, Seobu-ro 2066, Jangan-gu, Suwon-si, Gyeonggi-do 16419, Republic of Korea.
ACS Appl Mater Interfaces. 2025 Apr 2;17(13):20149-20161. doi: 10.1021/acsami.4c21997. Epub 2025 Mar 20.
MXenes have gained significant attention as multifunctional fillers in MXene-polymer nanocomposites. However, their inherently hydrophilic surfaces pose challenges in compatibility with hydrophobic polymers such as epoxy, potentially limiting composite performance. In this study, high-crystalline TiCT MXenes were functionalized with alkylated 3,4-dihydroxy-l-phenylalanine ligands, transforming the hydrophilic MXene flakes into a more hydrophobic form, thus significantly enhancing compatibility with the epoxy matrix. This surface functionalization enabled uniform dispersion and supported the formation of a percolation network within the epoxy matrix at a low filler loading of just 0.12 vol %. Consequently, the functionalized MXene-epoxy nanocomposites exhibited remarkable performance, including an electrical conductivity of 8200 S m, outstanding electromagnetic interference (EMI) shielding effectiveness (SE) of 100 dB at 110 GHz (61 dB at 8.2 GHz), improved thermal conductivity of 1.37 W m K, and a 300% increase in tensile toughness (271 KJ m). These properties substantially outperformed those of their nonfunctionalized counterparts and surpassed previously reported MXene-polymer nanocomposites. This study underscores the critical role of surface functionalization in unlocking the full potential of two-dimensional (2D) MXenes in polymer composites, providing a pathway to advanced multifunctional nanocomposite materials.
MXenes作为MXene-聚合物纳米复合材料中的多功能填料已受到广泛关注。然而,其固有的亲水性表面在与诸如环氧树脂等疏水性聚合物的相容性方面带来了挑战,这可能会限制复合材料的性能。在本研究中,高结晶度的TiCT MXenes用烷基化的3,4-二羟基-L-苯丙氨酸配体进行功能化,将亲水性的MXene薄片转变为更疏水的形式,从而显著增强了与环氧基质的相容性。这种表面功能化实现了均匀分散,并在仅0.12体积%的低填料负载量下支持了环氧基质中渗流网络的形成。因此,功能化的MXene-环氧纳米复合材料表现出卓越的性能,包括8200 S m的电导率、在110 GHz时100 dB(在8.2 GHz时61 dB)的出色电磁干扰(EMI)屏蔽效能(SE)、1.37 W m K的改善热导率以及拉伸韧性提高300%(271 KJ m)。这些性能大大优于其未功能化的对应物,并且超过了先前报道的MXene-聚合物纳米复合材料。本研究强调了表面功能化在释放二维(2D)MXenes在聚合物复合材料中的全部潜力方面的关键作用,为先进的多功能纳米复合材料提供了一条途径。