Unraveling the Ion Uptake Capacitive Deionization of Sea- and Highly Saline-Water by Sulfur and Nitrogen Co-Doped Porous Carbon Modified with Molybdenum Sulfide

电容去离子 材料科学 硫黄 氮气 硫化物 化学工程 离子 电化学 多孔性 兴奋剂 碳纤维 电极 无机化学 冶金 复合材料 化学 有机化学 物理化学 工程类 复合数 光电子学
作者
Hanieh Sharifpour,Farzaneh Hekmat,Saeed Shahrokhian
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (36): 42568-42584 被引量:17
标识
DOI:10.1021/acsami.3c07809
摘要

In parallel to the depletion of potable water reservoirs, novel technologies have been developed for seawater softening, as it is the most abundant source for generating deionized water. Although salt removal at subosmotic pressures and ambient temperatures by applying low-operating potentials with high energy efficiency made capacitive deionization (CDI) an advantageous water-softening process, its practical application is limited by insufficient ion removal capacity and low concentration influent. The performance of a CDI system is in progress with engineering the electrode active materials, also facilitating the advance design in highly saline- and seawater study. Herein, an innovative strategy was developed to provide high-performance CDI systems based on efficient and electrochemical ion-uptake active materials with a simple initial preparation. Nitrogen-doped porous carbons (N-pCs) received benefits from a high specific surface area and good surface wettability. The N-pCs were modified with molybdenum oxide/sulfide intercalative array and developed as CDI electrode active materials for desalination of both low/medium saline- and seawater. The MoS2/S,N-pC electrode materials exhibited perfect optimized salt adsorption capacity (SACs) of 47.9 mg g-1 when compared to N-pC (37.9 mg g-1) and MoO3/N-pC (39.6 mg g-1) counterparts at 1.4 V in a 750 ppm NaCl solution. In addition, the assembled CDI cells exhibited reasonable cycle stability and retained 96.7% of their initial SAC in continuous CDI cycles for 128,000 s. The fabricated CDI cell rendered an excellent salt removal efficiency (SRE, %) of 13.34% from the real seawater sample at 1.2 V. In detail, the SRE % of the NaCl, KCl, MgCl2, and CaCl2 soluble salts with respect to seawater sample exhibited a remarkable SRE % of 30.8%, 36%, 32.6%, and 19.3%, respectively. These SRE % values (>13.34%) provide convincing evidence on the reasonable ion uptake capability of the fabricated CDI cells for removing Na+, K+, Mg2+, and Ca2+ ions compared to other soluble component. The advanced cell design parallel to the promising outcomes provided herein makes these CDI systems immensely propitious for efficient water softening.
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