Hoang Anh Nguyen, Thi Thuy Linh Le, Minh Dai To, Anh Tuan Dao, Le Hoang Tan Doan, Van Vien Nguyen, Thai Hoang Nguyen, Viet Hai Le, Le Thanh Nguyen Huynh
{"title":"Preparation of layered structure MnO2/CNTs composites for high-performance salt removal by hybrid capacitive deionization","authors":"Hoang Anh Nguyen, Thi Thuy Linh Le, Minh Dai To, Anh Tuan Dao, Le Hoang Tan Doan, Van Vien Nguyen, Thai Hoang Nguyen, Viet Hai Le, Le Thanh Nguyen Huynh","doi":"10.1007/s10008-024-05998-0","DOIUrl":null,"url":null,"abstract":"<div><p>Capacity deionization (CDI), which combines capacitive carbon electrodes and redox-active electrodes, has emerged as a promising method for water desalination. It enables higher ion removal capacity than CDI-containing carbonaceous electrodes. Our work aimed to synthesize layered structure δ-MnO<sub>2</sub>/CNTs composites via the sol-gel method, examining their suitability for hybrid capacitive deionization (HCDI). The XRD results showed a layered structure birnessite for all composites with a distance interlayer over 7.0 Å, while the SEM images confirmed the intercopration of MnO<sub>2</sub> particles and CNT fibers. The electrochemical evaluations evidenced the role of CNTs in enhancing the charge transfer and ionic diffusion in composites. Composite δ-MnO<sub>2</sub>/CNTs presented a specific capacitance of 160 F g<sup>−1</sup> at a charge-discharge rate of 1 A g<sup>-1</sup> upon 1600 cycles. In salt removal performance, the asymmetric cell AC||δ-MnO<sub>2</sub>/CNTs-1 showed the highest salt adsorption capacity (SAC) of 30.2 mg g<sup>−1</sup> and fast average salt adsorption rate (ASAR) of 3 mg g<sup>−1</sup> s<sup>−1</sup> under a constant applied potential 1.4 V in 200 ppm NaCl, rendering it a promising candidate for efficient and sustainable desalination technology.</p></div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"28 10","pages":"3961 - 3972"},"PeriodicalIF":2.6000,"publicationDate":"2024-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid State Electrochemistry","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10008-024-05998-0","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Capacity deionization (CDI), which combines capacitive carbon electrodes and redox-active electrodes, has emerged as a promising method for water desalination. It enables higher ion removal capacity than CDI-containing carbonaceous electrodes. Our work aimed to synthesize layered structure δ-MnO2/CNTs composites via the sol-gel method, examining their suitability for hybrid capacitive deionization (HCDI). The XRD results showed a layered structure birnessite for all composites with a distance interlayer over 7.0 Å, while the SEM images confirmed the intercopration of MnO2 particles and CNT fibers. The electrochemical evaluations evidenced the role of CNTs in enhancing the charge transfer and ionic diffusion in composites. Composite δ-MnO2/CNTs presented a specific capacitance of 160 F g−1 at a charge-discharge rate of 1 A g-1 upon 1600 cycles. In salt removal performance, the asymmetric cell AC||δ-MnO2/CNTs-1 showed the highest salt adsorption capacity (SAC) of 30.2 mg g−1 and fast average salt adsorption rate (ASAR) of 3 mg g−1 s−1 under a constant applied potential 1.4 V in 200 ppm NaCl, rendering it a promising candidate for efficient and sustainable desalination technology.
期刊介绍:
The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry.
The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces.
The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis.
The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.