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Carbonization of polymers of intrinsic microporosity to microporous heterocarbon: Capacitive pH measurements

机译:具有固有微孔性的聚合物碳化为微孔杂碳:电容pH测量

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摘要

A nitrogen-containing polymer of intrinsic microporosity (PIM-EA-TB-H2; nitrogen adsorption surface area 846 m2 g−1) is vacuum carbonized at 700 °C and thereby directly without post-treatment converted into a microporous heterocarbon (cPIM; N2 adsorption surface area 425 m2 g−1). Nitrogen functionalities in the polymer backbone are retained in the heterocarbon and appear responsible for unusual time-, electrolyte-, and pH-dependent properties. Electrochemical characterization suggests a high specific capacitance (typically 50 F g−1) but only after prolonged immersion in aqueous HClO4. The time-dependent increase in capacitance during immersion is assigned to slow hydration and ingress of HClO4 into hydrophobic micropores (H2SO4 or H3PO4 are more hydrophilic and much less effective). Once hydrated, the microporous heterocarbon exhibits pH-dependent capacitance “switching” over a wide pH range and analytical applications as “capacitive” pH sensor are proposed.
机译:具有固有微孔性的含氮聚合物(PIM-EA-TB-H2;氮吸附表面积846 m2 g-1)在700°C下真空碳化,因此无需后处理即可直接转化为微孔杂碳(cPIM; N2吸附表面积425 m2 g-1)。聚合物主链中的氮官能团保留在杂烃中,并表现出与时间,电解质和pH有关的异常特性。电化学特性表明其具有较高的比电容(通常为50 F g-1),但仅在长时间浸泡在HClO4水溶液中之后才可以。浸入过程中电容随时间的增加是由于缓慢的水合作用和HClO4进入疏水性微孔(H2SO4或H3PO4的亲水性更高,效果更差)所致。一旦水合,微孔杂烃就会在很宽的pH范围内表现出与pH值相关的电容“转换”,因此有人提出了将其作为“电容性” pH传感器的分析应用。

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