ABSTRACT
Due to the diversity and variability of harmful ions in polluted water bodies, the selective removal and separation for specific ions is of great significance in water purification and resource processes. Capacitive deionization (CDI), an emerging desalination technology, shows great potential to selectively remove harmful ionic pollutants and further recover valuable ions because of the simple operation and low energy consumption. Researchers have done a lot of work to investigate ion selectivity utilizing CDI, including both theoretical and experimental studies. Nevertheless, in the investigation of selective mechanisms, phenomena where carbon materials exhibit entirely opposite selectivity require further analysis. Furthermore, there is a need to summarize the specific chemical reaction mechanisms, including the formation of hydrogen bonds, complexation reactions, and ligand exchanges, within selective electrodes, which have not been thoroughly examined in detail previously. In order to fill these gaps, in this review, we summarized the recent progress of CDI technologies for ion selective separation, and explored the selective separation mechanism of CDI from three aspects: selective physical adsorption, specific chemical reaction, and the utilization of selective barriers. Additionally, this review analyzes in detail the formation process of chemical bonds and ion conversion pathways when ions interact with electrode materials. Finally, some significant development prospects and challenges were offered for the future selective CDI systems. We believe the review will provide new insights for researchers in the field of ion selective separation.
Subject(s)
Carbon , Water Purification , Ions/chemistry , Electrodes , AdsorptionABSTRACT
Adsorption is one of the most common methods of pollution treatment. The selectivity for pollutants and recyclability of adsorbents are crucial to reduce the treatment cost. Layered double hydroxide (LDH) materials are one type of adsorbent with poor recyclability. Prussian blue (PB) is a sturdy and inexpensive metal-organic framework material that can be used as the precursor for synthesizing paramagnetic ferroferric oxide (Fe3O4). It is intriguing to build some reusable adsorbents with magnetic separation by integrating LDH and PB. In this work, paramagnetic Fe3O4-calcined LDH (Fe3O4@cLDH) core-shell adsorbent was designed and prepared by the calcination of PB-ZnAl layered double hydroxide (PB@LDH) core-shell precursor, which exhibits high anionic dyes selectivity in wastewater solutions. The paramagnetism and adsorption capability of Fe3O4@cLDH come from the Fe3O4 core and calcined ZnAl-LDH shell, respectively. Fe3O4@cLDH shows an adsorption capacity of 230 mg g-1 for acid orange and a high selectivity for anionic dyes in cation-anion mixed dye solutions. The regeneration process indicates that the high selectivity for anions is related to the specific hydration recovery process of ZnAl-LDH. The synergistic effect of the paramagnetic Fe3O4 core and calcined ZnAl-LDH shell makes Fe3O4@cLDH an excellent magnetic separation adsorbent with high selectivity to anions.
ABSTRACT
Due to substantial consumption and widespread contamination of the available freshwater resources, green, economical, and sustainable water recycling technologies are urgently needed. Recently, Faradic capacitive deionization (CDI), an emerging desalination technology, has shown great desalination potential due to its high salt removal ability, low consumption, and hardly any co-ion exclusion effect. However, the ion removal mechanisms and structure-property relationships of Faradic CDI are still unclear. Therefore, it is necessary to summarize the current research progress and challenges of Faradic CDI. In this review, the recent progress of Faradic CDI from five aspects is systematically reviewed: cell architectures, desalination mechanisms, evaluation indicators, operation modes, and electrode materials. The working mechanisms of Faradic CDI are classified as insertion reaction, conversion reaction, ion-redox species interaction, and ion-redox couple interaction in the electrolytes. The intrinsic and desalination properties of a series of Na+ and Cl- capturing materials are described in detail in terms of design concepts, structural analysis, and synthesis modulation. In addition, the effects of different cell architectures, operation modes, and electrode materials on the desalination performance of Faradic CDI are also investigated. Finally, the work summarizes the challenges remaining in Faradic CDI and provides the prospects and directions for future development.
ABSTRACT
Developing cost-effective electrocatalysts for water electrolysis is a promising strategy to enhance conversion and storage efficiency of sustainable energy. Transition metal oxides have been considered as alternative oxygen evolution reaction (OER) catalysts to replace noble metal-based catalysts. Here, we report a series of Fe-doped NiCo2O4 (NCO) nanowires with different Fe-doped concentrations, synthesized by a facile solvothermal and calcinations process, as high-efficiency electrocatalysts for OER. Due to abundant catalytically active sites, high-charge transport capability and specific surface area, these as-obtained NCO nanowires exhibit low overpotential and small Tafel slope. Specifically, NCO-0.1 shows the outstanding OER performance with a low overpotential of 297 mV at a current density of 10 mA cm-2 and a small Tafel slope of about 68 mV dec-1 in 1.0 M KOH. This study offers a promising electrocatalyst for the OER in water splitting.
ABSTRACT
As one of the promising clean and renewable technologies, water splitting has been a hot topic, especially the half-reaction of oxygen evolution reaction (OER) due to its sluggish and complex kinetics. Hence, Fe-doped NiCo2 O4 nanobelts were designed and prepared as catalysts toward OER. By increasing the Fe amount, the catalytic performances of the as-synthesized products went up and then decreased. Profiting from the synergistic effect between Fe atom and NiCo2 O4 , all the Fe-NiCo2 O4 catalysts exhibited superior catalytic activities to the corresponding NiCo2 O4 . In addition, the characteristic nanobelt architecture facilitates the conduction of electrons and the exposure of active sites. With the optimal Fe content, the 9.1 % Fe-NiCo2 O4 yielded the smallest overpotential and Tafel slope among the catalysts, distinctly lower than that of RuO2 .
ABSTRACT
The three-dimensional Bi2MoO6 mesoporous architectures constructed by nanosheets were synthesized through solvothermal method. The photocatalytic efficiency for tetracycline (TC) by the pristine Bi2MO6 and the BMO-450 (pristine Bi2MO6 was calcined at 450⯰C) reached 73% and 90% after 150â¯min light irradiation, respectively. Compared to the photocatalytic efficiency of pristine Bi2MoO6, the BMO-450 exhibited much higher photocatalytic performance owing to the presence of oxygen vacancies obvious change the band structure of BMO-450. The X-ray photoelectron spectroscopy (XPS) revealed that the presence of oxygen vacancy in the BMO-450 crystal, which endowed it outstanding photocatalytic performance. Moreover, the BMO-450 possess high crystallization degree, mesoporous structure and the decreasing band gap. The excellent photocatalytic performance for the degradation of TC aqueous solutions, which demonstrate that the calcined Bi2MoO6 mesoporous spheres would have potential applications in the fields of treating wastewater.
ABSTRACT
Water splitting as a greatly desired technology to produce clean renewable energy, but is hampered by the sluggish oxygen evolution reaction. So, the development of highly active and durable water oxidation electrocatalysts is of primarily significance for energy conversion. Here, a facial strategy to synthesize FeCoNi nanohybrids with adjustable morphological structures by using fluorine is introduced. The morphology and electrocatalytic activity of the sample is determined by the innovative introduction of fluorine. Among them, the overpotential at 10â mA cm-2 of the best sample is approximately 97â mV lower than the commercial RuO2 toward the oxygen evolution reaction in 1 m KOH. Additionally, the catalysts also have low Tafel slopes and remarkable stability.
