Layered hydrated-titanium-oxide-laden reduced graphene oxide composite as a high-performance negative electrode for selective extraction of Li via membrane capacitive deionizationopen access
- Authors
- Bhaskaran, Gokul; Rethinasabapathy, Muruganantham; Shin, Junho; Ranjith, Kugalur Shanmugam; Lee, Hyun Uk; Son, Won Keun; Han, Young-Kyu; Ryu, Taegong; Huh, Yun Suk
- Issue Date
- Nov-2023
- Publisher
- Elsevier Inc
- Keywords
- Lithium extraction; Membrane capacitive deionization; Hydrated titanium oxide; Graphene oxide; Lithium-ion sieves; Desalination; Electrosorption
- Citation
- Journal of Colloid and Interface Science, v.650, pp 752 - 763
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Colloid and Interface Science
- Volume
- 650
- Start Page
- 752
- End Page
- 763
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/25873
- DOI
- 10.1016/j.jcis.2023.07.029
- ISSN
- 0021-9797
1095-7103
- Abstract
- In this work, we initially prepared layered lithium titanate (Li2TiO3) using a solid-state reaction. Then Li+ of Li2TiO3 were acid-eluded with Hydrochloric acid to obtain hydrated titanium oxide (H2TiO3). Different weight percentages (50%, 60%, 70%, 80%, and 90%) of the as-prepared H2TiO3 were deposited on a conductive reduced graphene oxide (rGO) matrix to obtain a series of rGO/ H2TiO3 composites. Of the prepared composites, rGO/ H2TiO3-60% showed excellent current density, high specific capacitance, and rapid ion diffusion. An asymmetric MCDI (membrane capacitive deionization) cell fabricated with activated carbon as the anode and rGO/H2TiO3- 60% as the cathode displayed outstanding Li+ electrosorption capacity (13.67 mg g-1) with a mean removal rate of 0.40 mg g-1 min-1 in a 10 mM LiCl aqueous solution at 1.8 V. More importantly, the rGO/H2TiO3-60% composite electrode exhibited exceptional Li+ selectivity, superior cyclic stability up to 100,000 s, and a Li+ sorption capacity retention of 96.32% after 50 adsorption/desorption cycles. The excellent Li+ extraction ob-tained by MCDI using the rGO/H2TiO3-60% negative electrode was putatively attributed to: (i) ion exchange between Li+ and H+ of H2TiO3; (ii) the presence of narrow lattice spaces in H2TiO3 suitable for selective Li+ capture; (iii) capture of Li+ by isolated and hydrogen-bonded hydroxyl groups of H2TiO3; and (iv) enhanced interfacial contact and transfer of large numbers of Li+ ions from the electrolyte to H2TiO3 achieved by compositing H2TiO3 with a highly conductive rGO matrix.
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