Enhanced Removal of Cu2+ and Pb2+ Ions from Wastewater via a Hybrid Capacitive Deionization Platform with MnO2/N-Doped Mesoporous Carbon Nanocomposite Electrodes

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Jie Jin, Yang Bao, Feihu Li
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引用次数: 0

Abstract

Integrating MnO2 with carbon is a reliable strategy to improve capacitive deionization (CDI) performance by leveraging the unique properties of both components (i.e., MnO2 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 MnO2-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+, Cu2+, and Pb2+, 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–1 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 Cu2+ and Pb2+ ions compared to other cathode//anode pairs, attaining an IAC of 37.0 and 30.0 mg Cu2+ per gram electrode materials at 1.2 V in 500 and 200 ppm of Cu2+ solutions, respectively (cf. 32.2 mg of Pb2+ per gram of electrode materials in 200 ppm of Pb2+ 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 Cu2+ and Pb2+ ions, respectively. Mechanical analysis reveals that both heavy metals are likely to be sequestered via capacitive electrosorption by carbon, intercalation with MnO2, and surface complexation at the external surface of the [MnO6] octahedral layers. Our results demonstrated a great potential of the MnO2-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.

Abstract Image

MnO2/ n掺杂介孔碳纳米复合电极复合电容去离子平台对废水中Cu2+和Pb2+离子的去除效果研究
将MnO2与碳集成是一种可靠的策略,通过利用两种成分(即MnO2和碳)的独特性质来提高电容性去离子(CDI)性能。然而,碳的初步功能化(如氮掺杂、KOH活化)和阴极、阳极配对对CDI性能的影响还没有系统的探讨。本文制备了一组以氮为掺杂剂的mno2修饰的介孔碳复合材料(即MK-NMCS、K-NMCS、NMCS和CS),并系统地评估了不同阴极/阳极对在杂化电容去离子(HCDI)中分别捕获Na+、Cu2+和Pb2+的脱盐性能。在所有电极中,基于盐吸附容量(SAC)和循环稳定性,MK-NMCS//K-NMCS对表现出最佳的脱盐性能,在500 ppm NaCl溶液中,在1.2 V下连续50次充放电循环后,SAC为25.4 mg g-1, SAC保留率为102.4%。此外,MK-NMCS//K-NMCS电极对Cu2+和Pb2+离子的最大离子吸附量(IAC)也高于其他阴极/阳极对,在500和200 ppm的Cu2+溶液中,在1.2 V电压下,每克电极材料的Cu2+吸附量分别为37.0和30.0 mg(参见:在200 ppm的Pb2+溶液中,每克电极材料的Pb2+吸附量为32.2 mg)。此外,这些电极在分别去除每种重金属离子时表现出优异的循环稳定性,循环50次后,对Cu2+和Pb2+离子的IAC保留率分别为90.0和98.5%。力学分析表明,这两种重金属都可能通过碳的电容性电吸附、MnO2的插层以及[MnO6]八面体层外表面的表面络合而被隔离。我们的研究结果表明,mno2修饰的n掺杂碳//预官能化碳对,特别是MK-NMCS//K-NMCS电极对,具有通过HCDI平台捕获重金属离子的巨大潜力。这种预功能化和配对策略在筛选用于废水修复的高性能复合电极方面非常有前景。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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