Gayle Jessica, Roy Soumyabrata, Gupta Shashikant, Hassan Sakib, Rao Adwitiya, Demingos Pedro Guerra, Miller Kristen, Guo Galio, Wang Xu, Garg Ashish, Singh Chandra Veer, Vajtai Robert, Robinson Jacob T, Ajayan Pulickel M
Department of Materials Science and NanoEngineering, Rice University, Houston, Texas 77005, United States.
Department of Materials Science and Engineering, Indian Institute of Technology Kanpur, Kanpur 208016, India.
ACS Appl Mater Interfaces. 2024 Jan 17;16(2):2726-2739. doi: 10.1021/acsami.3c14825. Epub 2024 Jan 3.
Two-dimensional (2D) films of conjugated porous organic polymers (C-POPs) can translate the rich in-plane functionalities of conjugated frameworks into diverse optical and electronic applications while addressing the processability issues of their crystalline analogs for adaptable device architectures. However, the lack of facile single-step synthetic routes to obtain large-area high-quality films of 2D-C-POPs has limited their application possibilities so far. Here, we report the synthesis of four mechanically robust imine-linked 2D-C-POP free-standing films using a single-step fast condensation route that is scalable and tunable. The rigid covalently bonded 2D structures of the C-POP films offer high stability for volatile gas sensing in harsh environments while simultaneously enhancing site accessibility for gas molecules due to mesoporosity by structural design. Structurally, all films were composed of exfoliable layers of 2D polymeric nanosheets (NSs) that displayed anisotropy from disordered stacking, evinced by out-of-plane birefringent properties. The tunable in-plane conjugation, different nitrogen centers, and porous structures allow the films to act as ultraresponsive colorimetric sensors for acid sensing via reversible imine bond protonation. All the films could detect hydrogen chloride (HCl) gas down to 0.05 ppm, far exceeding the Occupational Safety and Health Administration's permissible exposure limit of 5 ppm with fast response time and good recyclability. Computational insights elucidated the effect of conjugation and tertiary nitrogen in the structures on the sensitivity and response time of the films. Furthermore, we exploited the exfoliated large 2D NSs and anisotropic optoelectronic properties of the films to adapt them into micro-optical and triboelectric devices to demonstrate their real-time sensing capabilities.
共轭多孔有机聚合物(C-POPs)的二维(2D)薄膜可以将共轭骨架丰富的面内功能转化为多样的光学和电子应用,同时解决其晶体类似物在可适配器件架构方面的加工性问题。然而,缺乏简便的单步合成路线来获得大面积高质量的二维C-POP薄膜,这限制了它们目前的应用可能性。在此,我们报告了使用一种可扩展且可调谐的单步快速缩合路线合成四种机械坚固的亚胺连接二维C-POP独立薄膜。C-POP薄膜刚性的共价键合二维结构为恶劣环境中的挥发性气体传感提供了高稳定性,同时通过结构设计产生的介孔性提高了气体分子的位点可及性。在结构上,所有薄膜均由二维聚合物纳米片(NSs)的可剥离层组成,这些纳米片由于无序堆叠而呈现各向异性,这通过面外双折射特性得以证明。可调节的面内共轭、不同的氮中心和多孔结构使这些薄膜能够通过可逆的亚胺键质子化作为对酸传感的超灵敏比色传感器。所有薄膜都能检测低至0.05 ppm的氯化氢(HCl)气体,远远超过美国职业安全与健康管理局规定的5 ppm的允许暴露限值,且响应时间快、可回收性好。计算分析阐明了结构中共轭和叔氮对薄膜灵敏度和响应时间的影响。此外,我们利用薄膜剥离后的大尺寸二维纳米片和各向异性的光电特性,将它们应用于微光学和摩擦电器件,以展示其实时传感能力。