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Abstract The ion exchange membrane (IEM) is a key component that helps achieve good performance in membrane capacitive deionization (MCDI). However, systematic researches have been limitedly conducted regarding the effect of IEM characteristics on MCDI performance. The aim of this study is to investigate the effects of the characteristics of the cation exchange membrane (CEM) on MCDI performance. Salt adsorption capacity (SAC), maximum average deionization rate (MADR), and charge efficiency were chosen to demonstrate MCDI performances. Only MADR was significantly affected by CEM characteristics. Additionally, MADR showed a positive relationship with the transport number divided by total electrical resistance (R 2 = 0.83). Therefore, CEM should have a high transport number and low electrical resistance for fast rate-capable MCDI. The correlations between CEM characteristics and MCDI performances revealed through this study are expected to further develop high-performance MCDI. Highlights • Cation exchange membrane (CEM) properties for membrane CDI (MCDI) were examined. • Tested performance of MCDI were capacity, rate, and efficiency. • Among them, the rate performance was the most sensitive to CEM properties. • CEM with high transport number and low resistance showed good rate performance. [ABSTRACT FROM AUTHOR]

[Display omitted] • Divergent/convergent CDI cells are established and compared with straight ones. • The spacer geometry shifts the location of the initial adsorption and the depletion zone. • The channel slope mainly affects the desalination output rate. • Convergent channels show a faster ASAR than the regular straight geometry. • Steeper slopes give larger benefits. This research aims to explore the impact of tilted channel configurations of CDI cells on desalination performance. The results reveal that the titled convergent channels have a faster average salt adsorption rate (ASAR) than the regular straight geometry. For desalination operations that end at a quarter of the equilibrium salt adsorption capacity (SAC), the convergent spacer with a slight slope of 1.5 degrees has a 20 % higher ASAR than the typical straight geometry (0.15 mg/g/min for convergent and 0.12 mg/g/min for straight). This gain increases to about 24, 29.5, and 33%, respectively, for slopes of 3.5, 5.5, and 7 degrees, compared to the straight geometry with the same spacer thickness. By looking at the underlying mechanisms, the spacer geometry is found to shift the location of the initial adsorption. This affects how quickly the device outputs the cleaned water. Interestingly, the geometry angle can also affect the location of the depletion zone, so tilted spacers can also affect the behavior during electrode starvation. Specifically, the convergent geometry has the depletion zone in the middle of the electrode instead of the corner near the outlet, as seen for straight and divergent channels. Together, these findings indicate how to construct tilted spacers to enhance CDI performance. [ABSTRACT FROM AUTHOR]

[Display omitted] • Charging time plays a decisive role in CDI performance improvement. • UQ analysis quantitively provides guidance for CDI optimization. • The pore distribution and connectivity are highlighted. Capacitive deionization (CDI) is considered to be one of the most promising technologies to deionize water with low/medium concentration. Great attention has been paid to improve its performance by optimizing electrode architectures and operation conditions. However, no guidelines are built for developing such strategies due to the nonlinear impact of the parameters concerning electrodes and operations. Therefore, our work quantitatively reveals the influence of some key parameters involving electrode characteristics, operation conditions and ion properties using the statistical analysis based on uncertainty quantification. We find the porosity solely has a small influence on all the performance metrics. But the pore might play a significant role by the pore size distribution and connectivity that greatly determine the effective diffusion coefficient of salt ions. The high diffusion coefficient obviously raises the salt adsorption by facilitating ion transport, which also reduces the energy consumption while most of the consumed energy could even be recovered. The current exerts an opposite influence by shortening the charging period in the constant current (CC) mode. The salt concentration in the inflow water increases the adsorption capacity but decreases the removal efficiency. The decreased removal efficiency requires less external energy, enabling the usage of CDI as an economic pre-treatment unit. We highlight the ion transport resistance and its influence on CDI performance by acting upon charging time in the CC mode. We also suggest the application of the constant voltage mode to the low-salinity wastewater instead of the CC mode due to the high resistance. Our work addressed the importance of proper electrode and operation condition for high desalination performance and energy efficiency. [ABSTRACT FROM AUTHOR]

Desalination technologies can increase potable water supplies worldwide. One possible approach, capacitive deionization (CDI), could prove optimal for brackish water treatment. At present, CDI development has largely focused on increasing salt adsorption capacity and desalination rates of materials and devices. In addition to these metrics, ultimately, optimizing salt rejection and throughput will be essential. In this work, we present a framework for the design of flow-between CDI cells for maximum salt rejection. We developed a model that is dependent on device specific parameters (system volume, flow rate, inlet and outlet water quality), to generalize the design of a cell for any given requirement. We showed that decreasing the advection-diffusion Péclet number and increasing the aspect ratio of the electrode compared to the channel space yield the highest salt rejection. In addition, tuning the cycle frequency time for salt rejection instead of complete electrode charging can yield faster water production rates and optimal salt rejection. These modeling results were validated through experimental prototypes that made use of vertically-aligned carbon nanotube (VA-CNT) electrodes. This framework to maximize salt rejection can be extended to a multitude of porous electrodes used in flow-between CDI devices. [ABSTRACT FROM AUTHOR]

Capacitive deionization (CDI) has been considered as the most promising and environmentally friendly electrical desalination technology owing to its low energy consumption and no secondary pollution. CDI is based on the principle of electric double layer for salt ion adsorption, but the existence of co-ions repulsion reduce the charge efficiency, leading to the low salt adsorption capacity. To prevent the intrinsic "co-ion effect" inside the porous carbon electrodes, membrane capacitive deionization (MCDI) by applying an ion-exchange membrane (IEM) to the surface of electrode is of increasing interest. However, MCDI brings various resistances, such as the internal and interface resistances of membrane, as well as the contact resistance between membrane and carbon electrode. More recently, by integrating "membrane" with carbon electrode without the introduction of free-standing IEM, integrated-MCDI has shown great merits to enhance counter-ion selectivity of electrode and decrease resistance, resulting in improving adsorption rate and reducing energy consumption. In this review, the preparation methods of innovative electrodes, the working mechanisms and performances of integrated-MCDIs, and the advanced advantages are summarized. It is hoped that this work will provide insight into integrated-MCDI and shed light on the future direction of water desalination based on CDI technology. [Display omitted] • Integrated-MCDI has been developed without using free-standing IEM on electrode. • Integrated-MCDI outperforms MCDI on energy consumption, cost, and kinetic rate. • Integrated-MCDI has the potential of anti-organic pollution and ion-selective removal. • Review summarized current status of integrated-MCDI for water desalination. • The mechanisms of integrated-MCDI with different fabrication methods are analyzed. [ABSTRACT FROM AUTHOR]

• Porous carbon nanoflakes were prepared by carbonizing xylose with KHCO 3. • Porous carbon nanoflakes exhibited a satisfactory salt adsorption capacity. • Porous carbon nanoflakes have great potential for large-scale application. Capacitive deionization (CDI) works by using the electrical double layer on various materials including nanoporous carbons to separate ions from saline water. To help realize industrial application, there has been an increasing interest in the exploration of carbon materials from low cost, eco-friendly and abundant biomass for CDI to align with the demands of sustainable development strategies. Herein we report pyrolysis of xylose with KHCO 3 to prepare hierarchically porous carbon nanoflakes which display a satisfactory salt adsorption capacity of 16.29 mg g−1. This novel strategy can design highly efficient carbon materials from naturally-developed biomass materials with its low preparation cost, environmentally friendliness and superior desalination performance. Our xylose-derived hierarchically porous carbon nanoflakes are promising for potential industrial application for CDI. [ABSTRACT FROM AUTHOR]

Electrosorptive desalination is a very simple and appealing approach to satisfy the increasing demand for drinking water. The large-scale application of this technology calls for the development of easy-to-produce, cheap and highly performing electrode materials and for the identification and tailoring of their most influential properties, as well. Here, biosynthesised bacterial cellulose is used as a carbon precursor for the production of three-dimensional nanostructures endowed with hierarchically porous architecture and different density and type of intrinsic and hetero-atom induced lattice defects. The produced materials exhibit unprecedented desalination capacities for carbon-based electrodes. At an initial concentration of 585 mg L−1 (10 mmol L−1), they are able to remove from 55 to 79 mg g−1 of salt; as the initial concentration rises to 11.7 g L−1 (200 mmol L−1), their salt adsorption capacity reaches values ranging between 1.03 and 1.35 g g−1. The results of the thorough material characterisation by complementary techniques evidence that the relative amount of oxygenated surface functional species enhancing the electrode wettability play a crucial role at lower NaCl concentrations, whereas the availability of active non- sp 2 defect sites for adsorption is mainly influential at higher salt concentrations. • Bacterial-cellulose (BC) is biosynthesised by using Gluconacetobacter medellinensis as a strain. • By carbonising BC, microporous nanocarbons with different amount and type of defects are produced. • BC-derived nanocarbons are tested as electrodes for the capacitive deionization of water. • The BC-based electrodes remove 55–79 mg g−1 of NaCl from a solution with a 585 mg L−1 initial concentration. • The C network defectiveness plays a key role in the electrode capacitive and electrosorptive behaviour. [ABSTRACT FROM AUTHOR]

Capacitive deionization (CDI) is an emerging technology for energy-efficient water desalination, and attracts more and more attention in recent years. It has been concluded that CDI technology shows competitiveness and perspectives on seawater desalination and wastewater treatment. The ionic adsorption mechanism can be clarified by electric double-layer capacitive adsorption and pseudocapacitive adsorption. The performance of CDI depends on both device and materials. The adsorption capacity and energy efficiency was improved significantly with fast growth of researches on material and novel energy storage techniques. This review summarizes researches on CDI technologies with an emphasis on electrode material design and improved adsorption performance. This review outlines the ion storage mechanisms and electrode materials of capacitive deionization. Unlabelled Image • Electrochemical extraction of ions from seawater/brine was reviewed systematically. • An emphasis on electrode material design thought has been analyzed. • The performance of various extraction devices has been summarized and compared. • Future challenge on this technology has been clarified. [ABSTRACT FROM AUTHOR]

Introduction of new nanomaterials with conductivity, salt adsorption capacity (SAC) and rate (SAR) exceeding that of carbon electrodes may greatly improve capacitive deionization of water. However, those materials show a different electrochemical behavior, which must be studied and optimized for practical use. Here, effects of operating conditions on desalination performance of pre-conditioned Ti 3 C 2 T x -MXene-based electrodes in a symmetric membrane capacitive deionization (MCDI) system were investigated. Specifically, influences of discharge potential, half-cycle length (HCL), and flow rate were systematically studied. Results showed different degrees of performance dependence on operating conditions. For instance, lower discharge potentials increased SAC and SAR by 152%. However, longer HCL increased SAC by 32% while decreasing SAR by 54%. Finally, faster flow rates decreased both SAC and SAR by 20%. Desalination performances of symmetric pre-conditioned MXene and activated carbon cloth (ACC) electrodes were gravimetrically and volumetrically compared in MCDI system. Pre-conditioned MXene electrodes gravimetrically performed 30% lower than ACC due to their notably higher density. Yet, pre-conditioned MXene electrodes volumetrically outperformed ACC by 162%. Results suggest that although MXenes offer high electrochemical activity and hydrophilicity, making them promising candidates for CDI applications, the strong dependence of desalination performance of MXenes on operating conditions requires in-depth understanding and warrants further research. Unlabelled Image • Pre-conditioned MXene outperforms ACC by 162% due to bulk volume ion storage. • Pre-conditioned MXene MCDI system has shown steady SAC for 100 cycles. • Lower discharge potentials enable more effective ion deintercalation. • Improved ion deintercalation leads to up to 152% increase in SAC and SAR. • Longer half-cycle length increases SAC by 32% and decreases SAR by 54%. [ABSTRACT FROM AUTHOR]