膜
质子化
堆积
共价键
脱质子化
材料科学
欺骗
化学工程
质子
纳米技术
化学
有机化学
离子
生物化学
量子力学
计算机科学
物理
工程类
程序设计语言
作者
Ping Li,Bo He,Xuan Li,Yunfei Lin,Shaokun Tang
标识
DOI:10.1016/j.gee.2024.07.008
摘要
Covalent organic framework nanosheets (CONs) with porous crystalline features and ultrathin thickness are ideal candidates as membrane building blocks to form well-defined transfer nanochannels. The formidable challenge behind self-supporting CONs membrane lies in weak non-covalent interlayer interactions and thus loose stacking, insufficient strength and structure stabilities. Herein, we propose the fabrication of interlayer force-strengthened freestanding CONs membrane through the electrostatic attraction bridge effect of positively-charged amino-rich CONs (CON-NH2) to negatively-charged sulfonated CONs (CON-SO3H). Ultrathin and large lateral sized CON-SO3H and CON-NH2 are synthesized, followed by restacking to prepare freestanding CONs membrane with CON-SO3H as the membrane bulk. Benefiting from effective interlayer interconnection due to strong electrostatic interaction, the obtained CON-SO3H/CON-NH2 membrane displays features of ultrahigh integrity, dense stacking, eminent water/acid/base/organic solvents stabilities and mechanical strength (109 MPa). The shortened −SO3H distance contributes to construct site-continuous transfer pathways, and the deprotonated −SO3H and protonated –NH2 form acid-base pairs to decrease interfacial resistance, which impart membrane superior proton conductivity of 486 mS cm-1 (80 oC, 100% RH). This interlayer force enhancement strategy offers a promising perspective on achieving densely-stacked CONs membrane with ultrahigh mechanical property and conduction performance for fuel cell application.
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