Abstract:In
capacitive deionization (CDI), coion repulsion and Faradaic
reactions during charging reduce the charge efficiency (CE), thus
limiting the salt adsorption capacity (SAC) and energy efficiency.
To overcome these issues, membrane CDI (MCDI) based on the enhanced
permselectivity of the anode and cathode is proposed using the ion-exchange
polymer as the independent membrane or coating. To develop a novel
and cost-effective MCDI system, we fabricated an integrated membrane
electrode using a thin layer of the ino… Show more
“…For example, directly utilizing redox-active organic ligands to connect the adjacent Fe trinuclear secondary building units can be an effective strategy to shorten the redox-active bridge and thus improve the redox efficiency between multiple active sites. As for the counter electrode, an integrated membrane assembly (i.e., an ion exchange layer coated on the electrode, with the layer thickness being less than 1/10 of the free-standing CEM) can be used as a cost-effective alternative to facilitate the wider application of the proposed technology. , The development of more highly selective and highly conductive platform materials is also critical to improve the selective removal efficiency of As(III). A new type of iron-based conductive MOF is a potential electrode material.…”
Section: Resultsmentioning
confidence: 99%
“…As for the counter electrode, an integrated membrane assembly (i.e., an ion exchange layer coated on the electrode, with the layer thickness being less than 1/10 of the free-standing CEM) can be used as a cost-effective alternative to facilitate the wider application of the proposed technology. 62,63 The development of more highly selective and highly conductive platform materials is also critical to improve the selective removal efficiency of As(III). A new type of iron-based conductive MOF is a potential electrode material.…”
Section: Mechanisms Of the Selectivity And Catalytic Activity Ofmentioning
Selective removal of trace, highly toxic arsenic from water is vital to ensure an adequate and safe drinking water supply for over 230 million people around the globe affected by arsenic contamination. Here, we developed an Fe-based metal−organic framework (MOF) with a ferrocene (Fc) redox-active bridge (termed Fe-MIL-88B-Fc) for the highly selective removal of As(III) from water. At a cell voltage of 1.2 V, Fe-MIL-88B-Fc can selectively separate and oxidize As(III) into the less harmful As(V) state in the presence of a 100-to 1250-fold excess of competing electrolyte, with an uptake capacity of >110 mg-As g −1 adsorbent. The high affinity between the uncharged As(III) and the μ 3 -O trimer (−36.55 kcal mol −1 ) in Fe-MIL-88B-Fc and the electron transfer between As(III) and redox-active Fc + synergistically govern the selective capture and conversion of arsenic. The Fe-based MOF demonstrates high selectivity and capacity to remediate arsenic-contaminated natural water at a low energy cost (0.025 kWh m −3 ). This study provides valuable guidance for the tailoring of effective and robust electrodes, which can lead to a wider application of electrochemical separation technologies.
“…For example, directly utilizing redox-active organic ligands to connect the adjacent Fe trinuclear secondary building units can be an effective strategy to shorten the redox-active bridge and thus improve the redox efficiency between multiple active sites. As for the counter electrode, an integrated membrane assembly (i.e., an ion exchange layer coated on the electrode, with the layer thickness being less than 1/10 of the free-standing CEM) can be used as a cost-effective alternative to facilitate the wider application of the proposed technology. , The development of more highly selective and highly conductive platform materials is also critical to improve the selective removal efficiency of As(III). A new type of iron-based conductive MOF is a potential electrode material.…”
Section: Resultsmentioning
confidence: 99%
“…As for the counter electrode, an integrated membrane assembly (i.e., an ion exchange layer coated on the electrode, with the layer thickness being less than 1/10 of the free-standing CEM) can be used as a cost-effective alternative to facilitate the wider application of the proposed technology. 62,63 The development of more highly selective and highly conductive platform materials is also critical to improve the selective removal efficiency of As(III). A new type of iron-based conductive MOF is a potential electrode material.…”
Section: Mechanisms Of the Selectivity And Catalytic Activity Ofmentioning
Selective removal of trace, highly toxic arsenic from water is vital to ensure an adequate and safe drinking water supply for over 230 million people around the globe affected by arsenic contamination. Here, we developed an Fe-based metal−organic framework (MOF) with a ferrocene (Fc) redox-active bridge (termed Fe-MIL-88B-Fc) for the highly selective removal of As(III) from water. At a cell voltage of 1.2 V, Fe-MIL-88B-Fc can selectively separate and oxidize As(III) into the less harmful As(V) state in the presence of a 100-to 1250-fold excess of competing electrolyte, with an uptake capacity of >110 mg-As g −1 adsorbent. The high affinity between the uncharged As(III) and the μ 3 -O trimer (−36.55 kcal mol −1 ) in Fe-MIL-88B-Fc and the electron transfer between As(III) and redox-active Fc + synergistically govern the selective capture and conversion of arsenic. The Fe-based MOF demonstrates high selectivity and capacity to remediate arsenic-contaminated natural water at a low energy cost (0.025 kWh m −3 ). This study provides valuable guidance for the tailoring of effective and robust electrodes, which can lead to a wider application of electrochemical separation technologies.
“…To address this issue, Wu et al attempted to prepare AC electrode coated with a thin layer of ionexchange polymer for mCDI (Figure 9). [120] In this direction, they have employed montmorillonite (MT, Al 2 O 9 Si 3 ) as an anion-exchange material and hydrotalcite (HT, Mg 6 Al 2 -(CO 3 )(OH) 16 .4H 2 O) as a cation-exchange material for the preparation of electrode. A charge efficiency of 90.5 % and SAC value of 15.8 mg g À 1 , compared to the pristine sample (CE of 55 % and SAC of 10.2 mg g À 1 ), suggest the potential of montmorillonite and hydrotalcite as ion exchange materials for the fabrication of high-performance charge efficient electrodes for mCDI.…”
Recent years have seen the emergence of capacitive deionization (CDI) as a promising desalination technique for converting sea and wastewater into potable water, due to its energy efficiency and eco‐friendly nature. However, its low salt removal capacity and parasitic reactions have limited its effectiveness. As a result, the development of porous carbon nanomaterials as electrode materials have been explored, while taking into account of material characteristics such as morphology, wettability, high conductivity, chemical robustness, cyclic stability, specific surface area, and ease of production. To tackle the parasitic reaction issue, membrane capacitive deionization (mCDI) was proposed which utilizes ion‐exchange membranes coupled to the electrode. Fabrication techniques along with the experimental parameters used to evaluate the desalination performance of different materials are discussed in this review to provide an overview of improvements made for CDI and mCDI desalination purposes
“…Moreover, the coating method using the membrane precursor solution is feasible to adjust the thickness of the layer, has controllable cost, and can build module integration in scale, playing a crucial role in the industrial realization of MCDI. However, the desalination capacity by IEM coatings achieves only 5–25 mg g –1 and the endurance time is too short or not mentioned in previous reports. − The exploration of high-performance ion-exchange materials for MCDI devices, hence, is necessary and challenging.…”
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