Capacitive Deionization System Research Articles

Optimizing Sodium Ion Adsorption Through Robust d–d Orbital Modulation for Efficient Capacitive Deionization

AbstractUnraveling the fundamental mechanisms of sodium ion adsorption behavior is crucial for guiding the design of electrode materials and enhancing the performance of capacitive deionization systems. Herein, the optimization of sodium ion adsorption is systematically investigated through the robust d–d orbital interactions within zinc‐doped iron carbide, facilitated by a novel liquid nitrogen quenching treatment. Liquid nitrogen quenching treatment can enhance the coordination number, strengthen d–d orbital interactions, promote electron transfer, and shift the d‐band center of Fe closer to the Fermi level, thereby enhancing sodium ions adsorption energy. Consequently, the obtained electrode material achieves a superior gravimetric adsorption capacity of 121.1 mg g−1 and attractive cyclic durability. The adsorption capacity is highly competitive compared to the vast majority of related research works in the field of capacitive deionization. Furthermore, sodium ion adsorption/desorption mechanisms are substantiated through ex situ techniques, revealing dynamic atomic and electronic structure evolutions under operational conditions. This work demonstrates that optimizing sodium ion adsorption via robust d–d orbital modulation enabled by liquid nitrogen quenching treatment is an effective approach for developing efficient capacitive deionization electrode materials.

Off-grid photovoltaic-powered capacitive deionization for groundwater desalination in rural Africa

ABSTRACT In regions lacking centralized water supply and electricity grid connections, capacitive deionization (CDI) offers a promising approach with its modular and energy-efficient characteristics for low-salinity solutions. This research evaluates the feasibility of using a photovoltaic (PV)-powered CDI system as an off-grid, household-based water purification solution for groundwater desalination in rural Uganda. In this work, the CDI system was integrated with a PV system, comprising an ultrafiltration unit for pretreatment, a CDI stack for desalination, and a PV array for power supply. As evidenced by the performance analysis of the CDI stack in a single-pass mode, the system exhibited commendable desalination efficiency with a salt removal efficiency (>60%) and stable energy performance (0.110 ± 0.014 kWh/mol) observed under different influent conductivities (500–3,000 μS/cm). When applied to groundwater desalination, the CDI-based system successfully reduced the conductivity to meet Uganda's potable water standard (1,500 μS/cm), achieving a water recovery of 63%, and an energy consumption of less than 1.5 kWh/m3. Consequently, the CDI-based system effectively couples with the PV system to meet daily water needs solely through solar energy, demonstrating the practical implementation of innovative off-grid water desalination solutions in resource-constrained settings.

A two-pronged strategy to boost the capacitive deionization performance of nitrogen-doped porous carbon nanofiber membranes

Carbon-based capacitive deionization (CDI) systems are universally subject to the limited desalination capacity, due to the electrosorption characteristics and undesirable pore structures. Herein, a two-pronged strategy is proposed to boost the desalination performance of the electrospun carbon nanofibers (CNFs), where silicalite-1 nanoparticles as the internal porogen create mesopores and macropores, and zeolitic imidazolate framework (ZIF-L) leaves as the external carbon source provide micropores and mesopores. This combination results in the large surface area, well-developed graded pore structure, and increased nitrogen content of the core-shell polyacrylonitrile/silicalite-1@ZIF-L-derived CNFs (defined as PCNFs-SZ) electrode, which delivers a superior specific capacitance of 145.4 F g−1 in a neutral electrolyte. The symmetric CDI cell assembled by the self-supporting PCNFs-SZ membrane electrodes holds a prominent desalination capacity of 37.09 mg g−1 and a rapid salt removal rate of 10.36 mg g−1 min−1 at 1.2 V (initial NaCl concentration: 500 mg L−1), and demonstrates significant potential for real-world applications in the desalination and purification of reclaimed water. Furthermore, theory calculations confirm the enhanced Na+-capture capability of PCNFs-SZ. The present work highlights an effective and viable approach to enhance the desalination performance of carbon-based CDI cells.

Low-Energy Desalination Techniques, Development of Capacitive Deionization Systems, and Utilization of Activated Carbon

Water desalination technology has emerged as a critical area of research, particularly with the advent of more cost-effective alternatives to conventional methods, such as reverse osmosis and thermal evaporation. Given the vital importance of water for life and the scarcity of potable water for agriculture and livestock—especially in the Kingdom of Saudi Arabia—the capacitive deionization (CDI) method for removing salt from water has been highlighted as the most economical choice compared to other techniques. CDI applies a voltage difference across two porous electrodes to extract salt ions from saline water. This study will investigate water desalination using CDI, utilizing a compact DC power source under 5 volts and a standard current of 2 amperes. We will convert waste materials like sunflower seeds, peanut shells, and rice husks into activated carbon through carbonization and chemical activation to improve its pore structure. Critical parameters for desalination, including voltage, flow rate, and total dissolved solids (TDS) concentration, have been established. The initial TDS levels are set at 2000, 1500, 1000, and 500 ppm, with flow rates of 38.2, 16.8, and 9.5 mL/min across the different voltage settings of 2.5, 2, and 1.5 volts, applicable to both direct and inverse desalination methods. The efficiency at TDS concentrations of 2000, 1500, and 1000 ppm remains between 18% and 20% for up to 8 min. Our results indicate that the desalination process operates effectively at a TDS level of 750 ppm, achieving a maximum efficiency of 45% at a flow rate of 9.5 mL/min. At voltages of 2.5 V, 2 V, and 1.5 V, efficiencies at 3 min are attained with a constant flow rate of 9.5 mL/min and a TDS of 500 ppm, with the maximum desalination efficiency reaching 56%.

Additive-Free, In Situ Rapid Repair of Vacancies in Fe[Fe(CN)6] Electrodes for Efficient Capacitive Deionization.

Fe[Fe(CN)6] (FeHCF) is considered a promising material for capacitive deionization-desalination of saline wastewater due to its excellent structure. However, additives are usually introduced during the synthesis of FeHCF in order to avoid [Fe(CN)6]3- vacancy defects filled by ligand water, which can result in the appearance of harmful byproducts and additional water treatment costs. In this study, an additive-free in situ vacancy repair strategy is proposed for the rapid synthesis of high-quality FeHCF in a saturated K3Fe(CN)6 solution. During the process of synthesizing FeHCF in solution, a high concentration of [Fe(CN)6]3- is found to facilitate the binding of Fe3+ to [Fe(CN)6]3- and hinder the hydrolysis and coordination reaction of Fe3+. After undergoing repair, FeHCF4 demonstrates an increased capacity and highly reversible electrochemical performance due to the robust structure. When utilized as Faraday cathodes in hybrid capacitive deionization (HCDI) systems, FeHCF4 exhibits a higher salt removal capacity (65.67 mg g-1) and lower energy consumption (0.68 kWh kg-1-NaCl) compared to unrepaired FeHCF1, while still maintaining excellent cycling performance. This environmentally friendly approach of repairing vacancies serves as a source of inspiration for the advancement of high-performance Prussian Blue analogues as capacitive sodium-removing materials.

Pilot-scale capacitive deionization for water softening: Performance, energy consumption, and ion selectivity

Capacitive deionization (CDI) has emerged as an efficient process for hardness control than traditional water-softening technologies. However, few systematic studies have been conducted on water softening using pilot-scale CDI systems. For industrial applications, it is essential to investigate deionization performance, energy consumption, and selectivity for divalent cations through pilot-scale studies. In this study, we examined the deionization performance and energy consumption of a pilot-scale CDI process for effective water softening. The key operational variables analyzed were the applied voltage (200–300 V (i.e., 1.0–1.5 V per pair)), feed concentration (550–1250 mg/L), recovery ratio (50–80 %), flow rate (3–5 L/min), and adsorption/desorption time (80–180 s). Within this range, a high voltage, low feed concentration, low recovery ratio, high flow rate, and long adsorption/desorption times are advantageous for the total dissolved solids (TDS) removal ratio. In terms of energy efficiency, expressed as TDS removal per unit energy consumption, a low voltage, low feed concentration, low recovery ratio, fast flow rate, and long adsorption/desorption time are beneficial. Additionally, we investigated the selective removal of Ca2+ over Na+ under various operating conditions, as well as its impact on enhancing energy efficiency. The pilot CDI system achieved a Ca/Na selectivity coefficient of approximately 2.4 and it was analyzed to achieve up to 45 % energy-saving efficiency compared to nonselective systems (i.e., selectivity coefficient = 1). The results of this study are expected to provide valuable data for the application of CDI to water softening and hardness control processes.

Efficacy of Capacitive Deionization Flow Cell Fabricated with Carbon Nanomaterial Modified Electrodes

The supply of freshwater is becoming a serious global challenge. Capacitive deionization (CDI) has been recognized as apromising and smart desalination technique to solve it. Carbonaceous materials, due to their non-toxic characteristics, areused for filtration, adsorption, and water deionization. In this study, a newly designed, homemade low CDI system wasfabricated, and carbon as electrode material was prepared from waste leather through a one-step activated pyrolysis process. Carbonaceous materials prepared at different temperatures were characterized by Fourier-transform infrared (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD) techniques. The charge storage capacity of the carbon materials casted on a glassy carbon electrode was evaluated using cyclic voltammetric and galvanostatic chargingdischarging techniques. The fabricated CDI system could be successfully used for the study of the removal capacity of NaCl from an aqueous solution. The removal capacity of carbon prepared at 600 °C from leather is 11.58 mgg1, which is about three times higher than commercial activated carbon at flow rate and applied potential of 23 mL min–1 and 1.0 V, respectively. Dhaka Univ. J. Sci. 72(2): 52-60, 2024 (July)

Investigation of the Deionization Rate of Asymmetric Capacitive Deionization Technology for the Treatment of Short-Chain Perfluoroalkyl Substances (PFAS)

Objectives : This study aims to introduce and evaluate the effectiveness of asymmetric membrane capacitive deionization (ACDI) in removing short-chain perfluoroalkyl substances (PFAS), specifically perfluorobutane sulfonic acid (PFBS), from aqueous solutions. This study offers important insights for the advancement of CDI technology in the sustainable treatment of industrial wastewater containing PFAS.Methods : ACDI was employed by removing the anion exchange membrane from conventional membrane capacitive deionization system. The effect of key operational parameters such as voltage (0.5~1.2 V), initial concentration (50~500 mg/L), and flow rate (1~5 ml/min) on PFBS removal efficiency was systematically investigated. Additionally, PFBS removal performance in the presence of chloride ions was also investigated to determine competing ion effects.Results and Discussion : The ACDI system significantly outperformed both CDI and MCDI, achieving a maximum deionization rate of 0.032 mg/g/s, compared to 0.012 mg/g/s for CDI and 0.01 mg/g/s for MCDI. Increasing the applied voltage from 0.5 V to 1.2 V enhanced the deionization rate, with the highest rate observed at 1.2 V. Higher initial PFBS concentrations also improved the deionization rate, increasing from 0.0009 mg/g/s at 50 mg/L to 0.032 mg/g/s at 500 mg/L. The optimal flow rate was found to be 2 ml/min, balancing ion contact time and throughput, resulting in the highest deionization rate. The presence of competing ions, such as chloride, reduced PFBS removal efficiency, as shown by the decrease in deionization rate when NaCl was added to the feed solution.Conclusion : Overall, the ACDI system demonstrated superior deionization capacity and energy efficiency for PFBS removal, highlighting its potential as a sustainable and efficient technology for treating water contaminated with short-chain PFAS. Future research should address the challenges posed by competing ions in real-world wastewater to further optimize the ACDI system’s performance.

Accelerating ion diffusion kinetics with an intensified interfacial electric field for efficient hybrid capacitive deionization

The interfacial electric field (IEF) represents a cutting-edge strategy for enhancing ion diffusion kinetics, pivotal in various technological applications. Despite its extensive use, the mechanisms and strategies for regulating IEF remain underexplored. In this study, we enhanced the IEF in a MnO2-x/g-C3N4 (CN) heterostructure by engineering oxygen vacancies in MnO2, which increased the work function difference between MnO2 and CN. The increased work function difference effectively lowers the energy barrier for electron transfer at the heterostructure interface, thereby intensifying the IEF. The enhanced IEF subsequently provides a more potent driving force, facilitating ion movement within the electrode materials during the desalination process. The modified MnO2-x/CN heterostructure demonstrates a notable salt removal capacity of 45.5 mg g−1 and an impressive salt removal rate of 4 mg g−1 min−1, under an operational voltage of 1.2 V in a 500 mg/L NaCl solution. This research not only deepens our understanding of IEF modulation in materials but also sets the stage for the development of high-performance electrodes for hybrid capacitive deionization systems.

Seed strategy synthesis of porous NASICON structured NaTi2(PO4)3/carbon aerogel nanocomposites for high-performance hybrid capacitive deionization

The limited capacity of conventional carbon electrode materials hinders the practical application of capacitive deionization (CDI). Hence, it is imperative to develop electrode materials with high sodium ion adsorption and reliable stability to facilitate the construction of hybrid CDI (HCDI) systems. Notably, NaTi2(PO4)3 (NTP) has received significant attention due to its high capacity and rapid transportation ability of sodium ions. However, the poor electrical conductivity and limited electrolyte contact area of NTP have prevented further improvement in its deionization capacity. Herein, we report a seed strategy to synthesize NTP/carbon aerogel (CA). P25 was used as a seed crystal to prepare TiO2/CA via the sol–gel method and supercritical CO2 drying. NTP/CA was then obtained from TiO2/CA by hydrothermal synthesis and calcination. This strategy preserved the rational network skeleton of CA and endowed NTP/CA with a high specific surface area of 420 m2/g. The enhanced electrical conductivity provided by CA yielded a remarkable salt adsorption capacity of 43.3 mg/g in a 500 mg/L NaCl solution and a stable cycle desalination capability. This work provides a new perspective for constructing three-dimensional, highly efficient and stable HCDI electrode materials.

Selective mono/divalent ion separation in bifunctional ionomeric capacitive deionization incorporated with counter-charge ionomer layer

In this study, a carbon-based bifunctional ionomeric capacitive deionization (BICDI) system was successfully developed by applying a counter-charge ionomer layer to the BICDI electrode without the need of a monovalent ion exchange membrane (M-IEM) for the selective separation of mono/divalent ions. The counter-charge ionomer layer facilitates the selective separation of mono/divalent ions through a combination of mechanisms involving electrostatic repulsion, steric hindrance, and hydrophobic interactions. Meanwhile, the BICDI electrode matrix serves as an ion transport channel, enabling seamless ion transport and improving the electrosorption capacity of the electrode. SEM and EDS analyses have confirmed the presence of a counter-charge ionomer layer encapsulating the BICDI electrode. Notably, BICDI-C cell with counter-charge ionomer layer exhibits higher Li+ ion adsorption capacity and selectivity (321.6 μmol/g, βMg2+Li+=6.6) compared to commercial monovalent cation exchange membrane CDI (MCDI-C) cell (206.4 μmol/g, βMg2+Li+=1.4). The selectivity of the BICDI-C cell for mono/divalent ions can be optimized by adjusting various testing parameters, including flow rate, voltage, etc. More importantly, this versatile method is not only applicable for the separation of monovalent cation, but can also enhance the monovalent anion adsorption capacity and selectivity of BICDI-A (43.6 μmol/g, βSO42-Cl-=7.3) cell by incorporating a counter-charge ionomer layer onto the BICDI cathode. This approach allows for the efficient separation of both cationic and anionic species, broadening the range of potential applications for BICDI technology.

Capacitive deionization: Capacitor and battery materials, applications and future prospects

Water scarcity all over the world attracts alternative methods to purify saline water and supplement the available dwindling freshwater resources. Capacitive deionization (CDI) is hopeful to supply water to the population due to operation at low potential along with low energy expenditure when low salinity (5 mM NaCl) feed water solutions are desalinated. Electrode material is the main controlling factor in CDI system and a lot of efforts are devoted to develop excellent materials for better CDI performance. So far, carbon materials are widely used as the electrode for CDI, though limitations such as co-ion expulsion and faradaic reactions hinder their full utilization. Alternatively, battery materials are used since their performance is great due to mitigation of co-ions ejection as well as faradaic reactions. In 2019 our group reviewed factors affecting the performance of activated carbon electrode materials and revealed lack of selectivity, co-ion expulsion, low electrical conductivity and inappropriate pore size distribution to largely contribute to its low salt removal capacity [1]. Therefore, herein, we extend the discussion beyond AC to include other carbons such as aerogels, nanotubes, graphenes etc., and battery materials such as MXenes, sodium super ionic conductors, and BiOCl to mention the few. This article also discusses the extent CDI is applied in the laboratory scale as well as in the field for desalination of real water, wastewater remediation and removal of harmful contaminants to substantiate what it can offer beyond the laboratory experiments. The work is expected to save as a complete reference for the progress of CDI electrode materials and its applications in water purification.

Heavy metal removal performance of capacitive deionization technology studied by machine learning

Capacitive deionization (CDI) technology is utilized for efficient treatment of industrial wastewater, characterized by low energy consumption and environmental protection. In order to comprehend the correlation between key experimental parameters and the electrosorption capacity (EC) of heavy metals in CDI technology, this paper employs a genetic algorithm (GA) to optimize a backpropagation artificial neural network (BPANN) for predicting the EC of CDI technology for heavy metal ions, with the characteristics of electrode materials converted into numerical characteristics for further analysis. Compared to the BPANN, the optimized GABPANN model demonstrates superior predictive accuracy. It achieves automatic adjustment of the hidden layer structure, neuron count, and transfer functions. Furthermore, the grey relational analysis indicates that the electrode material and the initial pH value of the solution are pivotal in determining the EC of heavy metal ions. This underscores the efficacy of machine learning (ML) algorithms in forecasting the nonlinear dynamics of CDI systems and elucidates the influence of individual parameters on the efficacy of heavy metal removal.

Commercialization Efforts of Capacitive Deionization Technology in Water Treatment Processes

AbstractAlthough capacitive deionization (CDI) technology has been studied intensively for more than 20 years, its commercialization remains in the initial stage, which is partly caused by the insufficient knowledge exchange between academia and industry. This concept reviews multiple scaling‐up efforts in the CDI technology for treating real water streams, following a case‐by‐case fashion. While the cell architecture in pilot scales is limited to the membrane CDI, highlighting the necessary role of ion‐exchange components during scaling‐ups, different ways of electrode stacking, i. e., monopolar and bipolar, are available. The performance indicators of these CDI systems when treating real water streams are summarized to gain insights into industrial practices. Importantly, key discrepancies in cell components and performances between pilot‐scale and lab‐scale studies are emphasized. The main challenges in large‐scale CDI systems for industrial purposes are discussed, providing hints for a better integration of research and applications.

N-doped carbon achieved by pyrolyzing urea and active carbon for the capacitive deionization coupled PMS oxidation system

Tetracyclines are among the most widely used antibiotics, and the saline organic wastewater generated during their production has caused serious environmental problems. Thus, it is imperative to develop effective methods for treating this antibiotic wastewater. In this study, we examined the structural characteristics and electrochemical performance of nitrogen-doped carbon materials and assessed the effects of nitrogen doping on the performance of a peroxymonosulfate (PMS)-coupled membrane capacitive deionization (MCDI) system for removing tetracycline (TC) and salt. Having optimized the carbonization temperature and system operating parameters, we observed that in response to an increase in carbonization temperature, there was an increase in the abundance of surface functional groups in the material, which promoted the ion migration capacity of the electrode and PMS activation sites. In addition, we observed that nitrogen doping can alter the electrical properties of carbon materials, provide a larger number of adsorption sites, and enhance the interactions between carbon structures and salt ions, thereby improving material properties. Under optimal operating conditions, the salt adsorption and tetracycline removal rates reached 30.2 % and 61.8 %, respectively. Our findings in this study provide a feasible method for the treatment of saline tetracycline wastewater.

Selective capacitive removal of Pb(II) ions from industrial wastewater using NF/Mn2CoO4@MoO2 electrodes

To achieve targeted removal of Pb2+ from industrial wastewater, a NF/Mn2CoO4@MoO2 composite electrode, synthesised using the hydrothermal method combined with electrodeposition technology, was employed to construct an asymmetric capacitive deionization (CDI) system to selectively electro-adsorb and desorb Pb2+ ions. The electrode exhibited pseudocapacitive characteristics in solutions containing Pb2+, facilitating rapid and reversible redox reactions. The asymmetric CDI system, utilising graphite paper as the positive electrode and NF/Mn2CoO4@MoO2 as the negative electrode, displayed exceptional adsorption performance at 1.4 V for 1 h, decreasing the Pb2+ concentration from 50 ppm to 4 ppb, achieving an adsorption capacity of 156.24 mg g−1, and displaying outstanding cyclic stability. Moreover, the electrode demonstrated preferential adsorption of Pb2+ in mixed solutions containing multiple heavy metal ions, with relative removal coefficients of 4.48 − 19.86 compared with other ions. Analysis of the adsorption mechanism indicated that during the adsorption process, Pb2+ was embedded between MoO2 layers, disrupting the electron cloud symmetry and triggering an oxidation reaction. Octahedral MoO2 then lost electrons and transformed into tetrahedral [MoO4]2-, forming PbMoO4 with embedded Pb2+ between the layers, and achieving effective removal of Pb2+ with high selectivity. Molecular dynamics simulations and density functional theory (DFT) calculations confirmed the high selectivity of the prepared electrode for Pb2+ ions based on stronger binding of Pb2+ to MoO2 than other ions. The electrode has application potential for the capacitive removal of Pb2+ from industrial effluent through CDI technology.

Imine-based conjugated polymer enables efficient removal of ammonium ion via capacitive deionization

The design of innovative faradaic electrode materials is crucial for improving the removal efficiency of contaminants in hybrid capacitive deionization (HCDI) systems. Organic compounds are a promising choice for faraday electrodes due to the sustainable production and tunable molecular structure. However, their high solubility in aqueous media and limited availability of redox-active sites for deionization greatly constrain the HCDI applications. Herein, we intentionally construct a conjugated polymer (IMP) with abundant imine groups, in which the strategic integration of N-heteroaromatic rings within the π-conjugated framework effectively prevents the disintegration of redox-active entities, while honing the energy bandgap and electronic characteristics. The copious redox-active CN sites within the imine groups along the polymeric chain markedly improve its capacity for the high-efficiency (de)intercalation of NH4+ ions. As an electrode material, the IMP polymer exhibits a significant NH4+-storage capacitance of 257.1 F g−1 at 2 A g−1 and maintains an ultra-cycle stability of 96.1 % after 10,000 cycles (4 A g−1), as evidenced by the in-situ spectral analysis of electrolyte. For real applications, a HCDI configuration has been constructed with a high specific NH4+ adsorption capacity of 119.0 mg g−1 and a fast removal rate of 27.0 mg g−1 min−1 with stable regeneration performance.

Emerging MXene-based electrode materials for efficient capacitive deionization: A comprehensive review

Capacitive deionization (CDI) has been considered a potential desalination technology because of its simple operation, high repeatability and low energy consumption. It is well known that electrode materials play a crucial role in the performance of CDI. As an emerging two-dimensional material, MXene have shown great application potential in CDI due to the unique two-dimensional structure, abundant surface functional groups and excellent physicochemical properties. In order to further improve the desalination performance of CDI, MXene-based electrode materials have received extensive attention and research. In this review, the structure, properties and synthesis strategies of MXene are analyzed to clarify the relationship between properties and desalination performance. The excellent electrical conductivity, mechanical property and hydrophilicity of MXene lay the foundation for the efficient desalination of MXene-based electrode materials. Then, the latest advance of MXene-based electrode materials in CDI is summarized. The optimization strategies of MXene-based materials include surface functional group regulation, in situ derivation and heterostructure construction. Finally, the current challenges and future prospects are presented from the perspectives of novel MXene-based CDI system, desalination mechanism, CDI battery and real water environment, which provides new inspiration and insight for the further development of CDI.

Reactive P and S co-doped porous hollow nanotube arrays for high performance chloride ion storage

Developing stable, high-performance chloride-ion storage electrodes is essential for energy storage and water purification application. Herein, a P, S co-doped porous hollow nanotube array, with a free ion diffusion pathway and highly active adsorption sites, on carbon felt electrodes (CoNiPS@CF) is reported. Due to the porous hollow nanotube structure and synergistic effect of P, S co-doped, the CoNiPS@CF based capacitive deionization (CDI) system exhibits high desalination capacity (76.1 mgCl– g–1), fast desalination rate (6.33 mgCl– g–1 min–1) and good cycling stability (capacity retention rate of > 90%), which compares favorably to the state-of-the-art electrodes. The porous hollow nanotube structure enables fast ion diffusion kinetics due to the swift ion transport inside the electrode and the presence of a large number of reactive sites. The introduction of S element also reduces the passivation layer on the surface of CoNiP and lowers the adsorption energy for Cl– capture, thereby improving the electrode conductivity and surface electrochemical activity, and further accelerating the adsorption kinetics. Our results offer a powerful strategy to improve the reactivity and stability of transition metal phosphides for chloride capture, and to improve the efficiency of electrochemical dechlorination technologies.

Novel flow-electrode capacitive deionization system employing modified MOF-derived carbon electrodes for metal ion removal

Activated carbon (AC) as an electrode for capacitive deionization (CDI) is constrained by its low specific surface area and specific capacitance, leading to electrical double layer overlap (EDL). To address this issue, a flow electrode capacitive deionization system (MDC-FCDI) was developed, which used modified MOFs-derived carbon (MDC) as the electrode. The MDC electrode exhibited enhanced specific capacitance (145.78 F/g) and specific surface area (2458.44 m2/g). Compared to conventional FCDI, the MDC-FCDI system demonstrated a 35–39 % improvement in heavy metal removal efficiency from wastewater containing Pb2+, Cu2+, Cd2+, and Zn2+. The selectivity of MDC-FCDI for heavy metals exhibited a unique “two-step phenomenon” that differed from what was observed in conventional CDI systems. In the MDC-FCDI system, high-valent ions experienced stronger electric field forces and preferentially occupied active sites on the electrode surface prior to the adsorption of ions with lower valence. The selectivity of the MDC-FCDI system for heavy metal ions is determined by three factors in the following order of priority: ionic charge, hydration radius, and ion feed concentration. This study offers a practical approach for expanding the range of MDC-FCDI applications.