4.7 Article

Flexible nitrogen-doped carbon nanofiber-reinforced hierarchical hollow iron oxide nanorods as a binder-free electrode for efficient capacitive deionization

Journal

DESALINATION
Volume 549, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.desal.2022.116360

Keywords

Free-standing electrode; Iron oxide; Capacitive deionization; Desalination; Density functional theory

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This study focuses on the development of a nitrogen-doped carbon nanofiber-reinforced hierarchical hollow iron oxide nanorods (Fe2O3@CNFs) material for efficient capacitive deionization desalination. The Fe2O3@CNFs material exhibits a unique hierarchical porous structure and prevents the agglomeration of Fe2O3 nanorods, leading to improved ionic/electronic transport. Without the addition of any binders or conductive additives, this material shows a high adsorption capacity (114.97 mg/g) and a rapid salt adsorption rate (7.79 mg/g min).
Abundant endeavors have been undertaken to explore high-quality and inexpensive materials for capacitive deionization desalination. However, one major problem is the sluggish adsorption rate and inferior adsorption performance of these materials in practical applications. Herein, nitrogen-doped carbon nanofiber-reinforced hierarchical hollow iron oxide nanorods grown on electrospinning carbon nanofibers (denoted Fe2O3@CNFs) were rationally designed and synthesized for high-efficiency capacitive deionization. Such composition and distinctive hierarchical porous structure prevent agglomeration of Fe2O3 nanorods, boosting the ionic/electronic transport through the synergistic effect between the Fe2O3 nanorods and N-doped carbon nanofibers. When employed as a cathode for capacitive deionization without adding any polymeric binder or conductive additives, this material exhibits a high adsorption capacity of 114.97 mg/g and a rapid salt adsorption rate (7.79 mg/g min). Moreover, the sodium storage mechanism was revealed through ex situ XRD, EDX mapping and ex situ XPS. Density functional theory (DFT) calculations reveal that the electrons are redistributed at the heterojunction interface, refining the electrochemical activity. This work is anticipated to afford an innovative path for the development of porous transition metal oxide-based fibers with outstanding effectiveness and stability toward environmental research of high-performance capacitive deionization.

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