Enhanced Removalof Cu<sup>2+</sup> and Pb<sup>2+</sup> Ions from Wastewater via aHybrid Capacitive Deionization Platformwith MnO<sub>2</sub>/N-Doped Mesoporous Carbon Nanocomposite Electrodes

Integrating MnO<sub>2</sub> with carbon is a reliable strategy to improve capacitive deionization (CDI) performance by leveraging the unique properties of both components (i.e., MnO<sub>2</sub> and carbon). However, the influences of preliminary functionalization of carbon (e.g., nitrogen doping, KOH activation) and pairing of cathodes and anodes on the CDI performance have yet to be systematically explored. Herein, we prepared a group of MnO<sub>2</sub>-decorated mesoporous carbon composites with nitrogen as a dopant (i.e., MK-NMCS, K-NMCS, NMCS, and CS), and systematically evaluated the desalination performance of various cathode//anode pairs in a hybrid capacitive deionization (HCDI) for capturing Na<sup>+</sup>, Cu<sup>2+</sup>, and Pb<sup>2+</sup>, respectively. Of all electrodes, the MK-NMCS//K-NMCS pair demonstrates the optimum desalination performance based on salt adsorption capacity (SAC) and cycling stability, offering a SAC of 25.4 mg g<sup>–1</sup> and a SAC retention of 102.4% after 50 consecutive charge–discharge cycles at 1.2 V in 500 ppm of NaCl solution. In addition, the MK-NMCS//K-NMCS electrodes also show the maximum ion adsorption capacity (IAC) toward Cu<sup>2+</sup> and Pb<sup>2+</sup> ions compared to other cathode//anode pairs, attaining an IAC of 37.0 and 30.0 mg Cu<sup>2+</sup> per gram electrode materials at 1.2 V in 500 and 200 ppm of Cu<sup>2+</sup> solutions, respectively (cf. 32.2 mg of Pb<sup>2+</sup> per gram of electrode materials in 200 ppm of Pb<sup>2+</sup> solution). Besides, these electrodes exhibit excellent cycling stability when applied in removing each heavy metal ion separately, with IAC retentions of 90.0 and 98.5% after 50 cycles toward Cu<sup>2+</sup> and Pb<sup>2+</sup> ions, respectively. Mechanical analysis reveals that both heavy metals are likely to be sequestered via capacitive electrosorption by carbon, intercalation with MnO<sub>2</sub>, and surface complexation at the external surface of the [MnO<sub>6</sub>] octahedral layers. Our results demonstrated a great potential of the MnO<sub>2</sub>-decorated N-doped carbon//prefunctionalized carbon pairs, in particular, the MK-NMCS//K-NMCS electrode pair for capturing heavy metal ions via HCDI platforms. Such prefunctionalization and pairing strategies are very promising for screening high-performance composite electrodes for wastewater remediation.

Publication Details

Journal
Figshare
Published
2025-02-21
DOI
https://doi.org/10.1021/acsami.4c18755.s001
Primary Topic
Membrane-based Ion Separation Techniques
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article
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article

Enhanced Removalof Cu2+ and Pb2+ Ions from Wastewater via aHybrid Capacitive Deionization Platformwith MnO2/N-Doped Mesoporous Carbon Nanocomposite Electrodes

Figshare
Membrane-based Ion Separation Techniques
article

Enhanced Removalof Cu2+ and Pb2+ Ions from Wastewater via aHybrid Capacitive Deionization Platformwith MnO2/N-Doped Mesoporous Carbon Nanocomposite Electrodes

article en

Abstract

Integrating MnO<sub>2</sub> with carbon is a reliable strategy to improve capacitive deionization (CDI) performance by leveraging the unique properties of both components (i.e., MnO<sub>2</sub> and carbon). However, the influences of preliminary functionalization of carbon (e.g., nitrogen doping, KOH activation) and pairing of cathodes and anodes on the CDI performance have yet to be systematically explored. Herein, we prepared a group of MnO<sub>2</sub>-decorated mesoporous carbon composites with nitrogen as a dopant (i.e., MK-NMCS, K-NMCS, NMCS, and CS), and systematically evaluated the desalination performance of various cathode//anode pairs in a hybrid capacitive deionization (HCDI) for capturing Na<sup>+</sup>, Cu<sup>2+</sup>, and Pb<sup>2+</sup>, respectively. Of all electrodes, the MK-NMCS//K-NMCS pair demonstrates the optimum desalination performance based on salt adsorption capacity (SAC) and cycling stability, offering a SAC of 25.4 mg g<sup>–1</sup> and a SAC retention of 102.4% after 50 consecutive charge–discharge cycles at 1.2 V in 500 ppm of NaCl solution. In addition, the MK-NMCS//K-NMCS electrodes also show the maximum ion adsorption capacity (IAC) toward Cu<sup>2+</sup> and Pb<sup>2+</sup> ions compared to other cathode//anode pairs, attaining an IAC of 37.0 and 30.0 mg Cu<sup>2+</sup> per gram electrode materials at 1.2 V in 500 and 200 ppm of Cu<sup>2+</sup> solutions, respectively (cf. 32.2 mg of Pb<sup>2+</sup> per gram of electrode materials in 200 ppm of Pb<sup>2+</sup> solution). Besides, these electrodes exhibit excellent cycling stability when applied in removing each heavy metal ion separately, with IAC retentions of 90.0 and 98.5% after 50 cycles toward Cu<sup>2+</sup> and Pb<sup>2+</sup> ions, respectively. Mechanical analysis reveals that both heavy metals are likely to be sequestered via capacitive electrosorption by carbon, intercalation with MnO<sub>2</sub>, and surface complexation at the external surface of the [MnO<sub>6</sub>] octahedral layers. Our results demonstrated a great potential of the MnO<sub>2</sub>-decorated N-doped carbon//prefunctionalized carbon pairs, in particular, the MK-NMCS//K-NMCS electrode pair for capturing heavy metal ions via HCDI platforms. Such prefunctionalization and pairing strategies are very promising for screening high-performance composite electrodes for wastewater remediation.

Figshare
Clean water and sanitation
Openalex Percentile: Top 54%
Membrane-based Ion Separation Techniques
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