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Experimental study demonstrates record ammonium removal using a nitro-functionalized organic electrode, highlighting a molecular pathway for sustainable nitrogen recovery.
The increasing discharge of ammonium‐rich wastewater has become a critical challenge for aquatic ecosystems and sustainable nitrogen management, creating an urgent need for efficient NH 4 + removal and recovery technologies. Among emerging electrochemical approaches, capacitive deionization (CDI) is attractive because of its low energy consumption and mild operating conditions, yet its practical performance is still largely limited by electrode materials. In this study, we developed a nitro‐functionalized organic electrode based on dinitro‐isoquinoxaline (DNIQ), featuring a rigid fused‐ring π‐conjugated framework and well‐defined redox‐active sites. The introduced nitro groups markedly lower the LUMO energy level and redistribute electron density within the conjugated framework, while enhancing the interaction of the C═N and NO 2 sites with NH 4 + . Experimental results show that the DNIQ electrode retains 81.84% of its capacity after 6000 cycles. When assembled into a CDI system, it delivers a record NH 4 + removal capacity of 273.89 mg g −1 and an ultrafast removal rate of 42.39 mg g −1 min −1 at 1.4 V, while maintaining 100% capacity retention over 100 cycles. This work provides a molecular‐level strategy for efficient ammonium capture and sustainable nitrogen recovery.
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Liu et al. (2026) studied this question.
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