摘要
The design of innovative faradaic electrode materials is crucial for improving the removal efficiency of contaminants in hybrid capacitive deionization (HCDI) systems. Organic compounds are a promising choice for faraday electrodes due to the sustainable production and tunable molecular structure. However, their high solubility in aqueous media and limited availability of redox-active sites for deionization greatly constrain the HCDI applications. Herein, we intentionally construct a conjugated polymer (IMP) with abundant imine groups, in which the strategic integration of N-heteroaromatic rings within the π-conjugated framework effectively prevents the disintegration of redox-active entities, while honing the energy bandgap and electronic characteristics. The copious redox-active C N sites within the imine groups along the polymeric chain markedly improve its capacity for the high-efficiency (de)intercalation of NH 4 + ions. As an electrode material, the IMP polymer exhibits a significant NH 4 + -storage capacitance of 257.1 F g −1 at 2 A g −1 and maintains an ultra-cycle stability of 96.1 % after 10,000 cycles (4 A g −1 ), as evidenced by the in-situ spectral analysis of electrolyte. For real applications, a HCDI configuration has been constructed with a high specific NH 4 + adsorption capacity of 119.0 mg g −1 and a fast removal rate of 27.0 mg g −1 min −1 with stable regeneration performance.
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