Enhancing capacitive deionization performance and cyclic stability of nitrogen-doped activated carbon by the electro-oxidation of anode materials

Electrode materials with high desalination capacity and long-term cyclic stability are the focus of capacitive deionization(CDI) community. Understanding the causes of performance decay in traditional carbons is crucial to design a high-performance material. Based on this, here, nitrogen-doped activated carbon(NAC) was prepared by pyrolyzing the blend of activated carbon powder(ACP) and melamine for the positive electrode of asymmetric CDI. By comparing the indicators changes such as conductivity, salt adsorption capacity, pH, and charge efficiency of the symmetrical ACP-ACP device to the asymmetric ACP-NAC device under different CDI cycles, as well as the changes of the electrochemical properties of anode and cathode materials after long-term operation, the reasons for the decline of the stability of the CDI performance were revealed. It was found that the carboxyl functional groups generated by the electro-oxidation of anode carbon materials make the anode zero-charge potential(E_(pzc)) shift positively,which results in the uneven distribution of potential windows of CDI units and affects the adsorption capacity. Furthermore, by understanding the electron density on C atoms surrounding the N atoms, we attribute the increased cyclic stability to the enhanced negativity of the charge of carbon atoms adjacent to quaternary-N and pyridinic-oxide-N.

Boosting Capacitive Deionization Performance of Commercial Carbon Fibers Cloth via Structural Regulation Based on Catalytic-Etching Effect

Monolithic carbon electrodes with robust mechanical integrity and porous architecture are highly desired for capacitive deionization but remain challenging.Owing to the excellent mechanical strength and electroconductivity,commercial carbon fibers cloth demonstrates great potential as high-performance electrodes for ions storage.Despite this,its direct application on capacitive deionization is rarely reported in terms of limited pore structure and natural hydrophobicity.Herein,a powerful metal-organic framework-engaged structural regulation strategy is developed to boost the desalination properties of carbon fibers.The obtained porous carbon fibers features hierarchical porous structure and hydrophilic surface providing abundant ions-accessible sites,and continuous graphitized carbon core ensuring rapid electrons transport.The catalytic-etching mechanism involving oxidation of Co and subsequent carbonthermal reduction is proposed and highly relies on annealing temperature and holding time.When directly evaluated as a current collector-free capacitive deionization electrode,the porous carbon fibers demonstrates much superior desalination capability than pristine carbon fibers,and remarkable cyclic stability up to 20 h with negligible degeneration.Particularly,the PCF-1000 showcases the highest areal salt adsorption capacity of 0.037 mg cm^(−2) among carbon microfibers.Moreover,monolithic porous carbon fibers-carbon nanotubes with increased active sites and good structural integrity by in-situ growth of carbon nanotubes are further fabricated to enhance the desalination performance(0.051 mg cm^(−2)).This work demonstrates the great potential of carbon fibers in constructing high-efficient and robust monolithic electrode for capacitive deionization.

Exploration of the Exceptional Capacitive Deionization Performance of CoMn_(2)O_(4) Microspheres Electrode

The“battery type”inorganic electrode has been demonstrated the highly efficient sodium ion intercalation capacity for capacitive deionization.In this work,the CoMn_(2)O_(4)(CMO)microspheres with porous core-shell structure are prepared via co-precipitation and followed by annealing.The effects of annealing temperatures on the morphology,pore structure,valence state,and electrochemical behavior of CMO are explored.As electrode for capacitive deionization,the salt removal capacity and current efficiency of optimized AC||CMO device reaches up to 60.7 mg g^(−1) and 97.6%,respectively,and the capacity retention rate is 74.1%after 50 cycles.Remarkably,both the in-situ X-ray diffraction and ex-situ X-ray diffraction analysis features that the intercalation/de-intercalation of sodium ions are governed by(103)and(221)crystal planes of CMO.Accordingly,the density functional theory calculations realize that the adsorption energies of Na+onto(103)and(221)crystal planes are higher than that of any other crystal planes,manifesting the priorities in adsorption of sodium atoms.Furthermore,the X-ray photoelectron spectra of pristine and post-CMO electrode highlights that the reversible conversion of Mn^(3+)/Mn^(4+)couple is resulted from the intercalation/de-intercalation of Na^(+),while this is irreversible for Co^(3+)/Co^(2+)couple.Beyond that,the CMO electrode has been proven the selectivity removal of Na^(+) over K^(+)and Mg^(2+)in a multi-cation stream.

Integration of pore structure modulation and B,N co-doping for enhanced capacitance deionization of biomass-derived carbon

Biomass-derived carbon has demonstrated great potentials as advanced electrode for capacitive deionization(CDI),owing to good electroconductivity,easy availability,intrinsic pores/channels.However,conventional simple pyrolysis of biomass always generates inadequate porosity with limited surface area.Moreover,biomass-derived carbon also suffers from poor wettability and single physical adsorption of ions,resulting in limited desalination performance.Herein,pore structure optimization and element co-doping are integrated on banana peels(BP)-derived carbon to construct hierarchically porous and B,N co-doped carbon with large ions-accessible surface area.A unique expansionactivation(EA)strategy is proposed to modulate the porosity and specific surface area of carbon.Furthermore,B,N co-doping could increase the ions-accessible sites with improved hydrophilicity,and promote ions adsorption.Benefitting from the synergistic effect of hierarchical porosity and B,N co-doping,the resultant electrode manifest enhanced CDI performance for NaCl with large desalination capacity(29.5 mg g^(-1)),high salt adsorption rate(6.2 mg g^(-1)min^(-1)),and versatile adsorption ability for other salts.Density functional theory reveals the enhanced deionization mechanism by pore and B,N co-doping.This work proposes a facile EA strategy for pore structure modulation of biomass-derived carbon,and demonstrates great potentials of integrating pore and heteroatoms-doping on constructing high-performance CDI electrode.

Development of Cd-doped Co Nanoparticles Encapsulated in Graphite Shell as Novel Electrode Material for the Capacitive Deionization Technology

Because of the low energy requirement and the environmentally safe byproducts, the capacitive deionization water desalination technology has attracted the attention of many researchers. The important requirements for electrode materials are good electrical conductivity, high surface area, good chemical stability and high specific capacitance. In this study, metallic nanoparticles that are encapsulated in a graphite shell(Cd doped Co/C NPs) are introduced as the new electrode material for the capacitive deionization process because they have higher specific capacitance than the pristine carbonaceous materials. Cd doped Co/C NPs perform better than graphene and the activated carbon. The introduced nanoparticles were synthesized using a simple sol gel technique. A typical sol gel composed of cadmium acetate, cobalt acetate and poly(vinyl alcohol)was prepared based on the polycondensation property of the acetates. The physiochemical characterizations that were used confirmed that the drying, grinding and calcination in an Ar atmosphere of the prepared gel produced the Cd doped Co nanoparticles, which were encapsulated in a thin graphite layer. Overall, the present study suggests a new method to effectively use the encapsulated bimetallic nanostructures in the capacitive deionization technology.

Atomic layer deposition of TiO_(2) on carbon-nanotubes membrane for capacitive deionization removal of chromium from water

Chromium(Cr)is a common heavy metal that has severe impacts on the ecosystem and human health.Capacitive deionization(CDI)is an environment-friendly and energy-efficient electrochemical purification technology to remove Cr from polluted water.The performance of CDI systems relies primarily on the properties of electrodes.Carbon-nanotubes(CNTs)membranes are promising candidates in creating advanced CDI electrodes and processes.However,the low electrosorption capacity and high hydrophobicity of CNTs greatly impede their applications in water systems.In this study,we employ atomic layer deposition(ALD)to deposit TiO_(2) nanoparticulates on CNTs membranes for preparing electrodes with hydrophilicity.The TiO_(2)-deposited CNTs membranes display preferable electrosorption performance and reusability in CDI processes after only 20 ALD cycles deposition.The total Cr and Cr(VI)removal efficiencies are significantly improved to 92.1%and 93.3%,respectively.This work demonstrates that ALD is a highly controllable and simple method to produce advanced CDI electrodes,and broadens the application of metal oxide/carbon composites in the electrochemical processes.

Ionic Group Derivitized Nano Porous Carbon Electrodes for Capacitive Deionization

Capacitance for electrostatic adsorption forms primarily within a Debye length of the electrode surface. Capacitive carbon electrodes were derivatized with ionic groups by means of adsorbing a surfactant in order to test the theory that attached ionic groups would exclude co-ions and increase coulombic efficiency without the need for an added charge barrier membrane. It has been discovered that capacitive electrodes surface derivatized with ionic groups become polarized and intrinsically more coulombically efficient.

Effective Modified Carbon Nanofibers as Electrodes for Capacitive Deionization Process

Carbon materials have the advantages of good electrical conductivity and excellent chemical stability, so many carbon materials have been introduced as electrodes for the capacitive deionization (CDI) process. Due to the low surface area compared to the other nanocarbonaceous materials, CNFs performance as electrode in the CDI units is comparatively low. This problem has been overcome by preparing high surface area carbon nanofibers and by creating numerous long pores on the nanofibers surface. The modified CNFs have been synthesized using low cost, high yield and facile method;electrospinning technique. Stabilization and graphitization of electrospun nanofiber mats composed of polyacrylonitrile (PAN) and poly (methyl methacrylate) (PMMA) leads form longitudinal pores CNFs. The utilized characterizations indicated that the CNFs obtained from electrospun solution having 50% PMMA have surface area of 181 m2/g which are more than the conventional CNFs. Accordingly, these nanofibers revealed salt removal efficiency of ~90% and specific capacitance of 237 F/g.

Adsorption properties of Ⅴ(Ⅳ) on resin-activated carbon composite electrodes in capacitive deionization

Composite electrodes prepared by cation exchange resins and activated carbon(AC)were used to adsorb Ⅴ(Ⅳ)in capacitive deionization(CDI).The electrode made of middle resin size(D860/AC M)had the largest specific surface area and mesoporous content than two other composite electrodes.Electrochemical analysis showed that D860/AC M presents higher specific capacitance and electrical double layer capacitor than the others,and significantly lower internal diffusion impedance.Thus,D860/AC M exhibits the highest adsorption capacity and rate of Ⅴ(Ⅳ)among three electrodes.The intra-particle diffusion model fits well in the initial adsorption stage,while the liquid film diffusion model is more suitable for fitting at the later stage.The pseudo-second-order kinetic model is suited for the entire adsorption process.The adsorption of Ⅴ(Ⅳ)on the composite electrode follows that of the Freundlich isotherm.Thermodynamic analysis indicates that the adsorption of Ⅴ(Ⅳ)is an exothermic process with entropy reduction,and the electric field force plays a dominant role in the CDI process.This work aims to improve our understanding of the ion adsorption behaviors and mechanisms on the composite electrodes in CDI.

Desalination Alternative Technology in Conjunction with Membrane Capacitive Deionization (MCDI): A Literature Review Article

Water and energy shortages came due to rapid population growth, living standards and rapid development in the agriculture and industrial sectors. Desalination tends to be one of the most promising water solutions;however, it is a process of intense energy. Membrane Capacitive Deionization (MCDI) has received considerable interest as a promising desalination technology, and MCDI research has increased significantly over the last 10 years. In addition, there are no guidelines for the design of Capacitive Deionization (CDI) implementation strategies for individual applications. This study, therefore;provides an alternative of CDI’s recent application developments, with emphasis placed on hybrid systems to address the technological needs of different relevant fields. The MCDI’s energy consumption is compared with the reverse osmosis literature data based on experimental data from laboratory-scale system. The study demonstrates that MCDI technology is a promising technology in the next few years with an extreme competition in water recovery, energy consumption and salt removal for reverse osmosis.

Kinetic-Thermodynamic Promotion Engineering toward High-Density Hierarchical and Zn-Doping Activity-Enhancing ZnNiO@CF for High-Capacity Desalination

Despite the promising potential of transition metal oxides(TMOs)as capacitive deionization(CDI)electrodes,the actual capacity of TMOs electrodes for sodium storage is significantly lower than the theoretical capacity,posing a major obstacle.Herein,we prepared the kinetically favorable Zn_(x)Ni_(1−x)O electrode in situ growth on carbon felt(Zn_(x)Ni_(1−x)O@CF)through constraining the rate of OH^(−)generation in the hydrothermal method.Zn_(x)Ni_(1−x)O@CF exhibited a high-density hierarchical nanosheet structure with three-dimensional open pores,benefitting the ion transport/electron transfer.And tuning the moderate amount of redox-inert Zn-doping can enhance surface electroactive sites,actual activity of redox-active Ni species,and lower adsorption energy,promoting the adsorption kinetic and thermodynamic of the Zn_(0.2)Ni_(0.8)O@CF.Benefitting from the kinetic-thermodynamic facilitation mechanism,Zn_(0.2)Ni_(0.8)O@CF achieved ultrahigh desalination capacity(128.9 mgNaCl g^(-1)),ultra-low energy consumption(0.164 kW h kgNaCl^(-1)),high salt removal rate(1.21 mgNaCl g^(-1) min^(-1)),and good cyclability.The thermodynamic facilitation and Na^(+)intercalation mechanism of Zn_(0.2)Ni_(0.8)O@CF are identified by the density functional theory calculations and electrochemical quartz crystal microbalance with dissipation monitoring,respectively.This research provides new insights into controlling electrochemically favorable morphology and demonstrates that Zn-doping,which is redox-inert,is essential for enhancing the electrochemical performance of CDI electrodes.

A novel flow electrode capacitive deionization device with spindle-shaped desalting chamber

Flow-electrode capacitive deionization(FCDI)is an innovative technology in which an intermediate chamber plays an important role in the desalination process.However,relatively few studies have been conducted on the structures of these intermediate chambers.In this study,we propose a novel flow-electrode capacitive deionization device with a spindle-shaped inlet chamber(S-FCDI).The desalination rate of the S-FCDI under optimal operating conditions was 36%higher than that of the FCDI device with a conventional rectangular chamber(R-FCDI).The spindle-shaped chamber transferred 1.2μmol more ions than the rectangular chamber,based on energy per joule.Additionally,we performed a detailed analysis of different inlet chamber shapes using computational fluid dynamics software.We concluded that S-FCDI has a relatively low flow resistance and almost no stagnation zone.This provides unique insights into the development of intermediate chambers.This study may contribute to the improvement of the desalination performance in industrial applications of FCDI.

Tailoring interlayer spacing in MXene cathodes to boost the desalination performance of hybrid capacitive deionization systems

Capacitive deionization(CDI)is a promising technology to satisfy the global need for fresh water,since it can be both economical and sustainable.While two-dimensional transition metal carbides/nitrides(MXenes)exhibit great characteristics for use as CDI electrode materials,their tightly spaced layered structure renders intercalation inefficiency.In this study,the interlayer distance of MXenes is precisely modulated by inserting different quantity of one-dimensional bacterial fibers(BC),forming freestanding MXene/BC composite electrodes.Among the studied samples,MXene/BC-33%electrode with the interlayer spacing of 15.2Åcan achieve an optimized tradeoff among various desalination performance metrics and indicators.The salt adsorption capacity(SAC),the average salt adsorption rate(ASAR),the energy normalized adsorbed salt(ENAS),and the thermodynamic energy efficiency(TEE)of the MXene/BC-33%electrode are improved by 24%,46%,13%,and 66%respectively compared with those of pure MXene electrode.While the insertion of BC improves the ion diffusion pathways and facilitates the intercalation kinetics,the desalination performance decreases when the insertion amount of BC exceeds 40%.This is attributed to the overlarge resistance of the composite and the resulting increased energy consumption.This study reveals the desalination performance tradeoffs of MXene-based electrodes with different interlayer distances and also sheds light on the fundamental ion storage mechanisms of intercalation materials in a CDI desalination system.

Cu@Cu_(2)O/carbon for efficient desalination in capacitive deionization

Electrode materials with strong desalting ability is an important research direction of capacitive deionization.In this study,HKUST-1 was successfully synthesized by the solvothermal method,and MOFsderived porous carbon/Cu@Cu_(2)O composites were prepared by simple pyrolysis as cathode materials for CDI.After high-temperature pyrolysis,the Cu^(+) site with unsaturated coordination is generated,and the structure changes from micropores to the coexistence of mesoporous and micropores.The complex pore structure is conducive to strengthening ion migration and diffusion.The results show that the porous carbon/Cu@Cu_(2)O materials derived from MOFs depend on the pseudocapacitance behavior for capacitive deionization and desalination.At a voltage window of-1.2V~1.2V,a current density of 40mA/g.and 5 mmol/L NaCl,the HDC-1100 exhibited the best desalting capacity of 30.9 mg/g.HDC-1100 also has good cycle stability.After 20 cycles of adsorption and desorption,the desalting capacity almost does not decrease.Therefore,MOFs derived porous carbon/Cu@Cu_(2)O composites are expected to be an excellent choice for CDI cathode materials.

Mechanism of ball milled activated carbon in improving the desalination performance of flow-and fixed-electrode in capacitive deionization desalination

Capacitive deionization(CDI)is a novel electrochemical water-treatment technology.The electrode material is an important factor in determining the ion separation efficiency.Activated carbon(AC)is extensively used as an electrode material;however,there are still many deficiencies in commercial AC.We adopted a simple processing method,ball milling,to produce ball milled AC(BAC)to improve the physical and electrochemical properties of the original AC and desalination efficiency.The BAC was characterized in detail and used for membrane capacitive deionization(MCDI)and flow-electrode capacitive deionization(FCDI)electrode materials.After ball milling,the BAC obtained excellent pore structures and favorable surfaces for ion adsorption,which reduced electron transfer resistance and ion migration resistance in the electrodes.The optimal ball-milling time was 10 h.However,the improved effects of BAC as fixed electrodes and flow electrodes are different and the related mechanisms are discussed in detail.The average salt adsorption rates(ASAR)of FCDI and MCDI were improved by 134%and 17%,respectively,and the energy-normalized removal salt(ENRS)were enhanced by 21%and 53%,respectively.We believe that simple,low-cost,and environmentally friendly BAC has great potential for practical engineering applications of FCDI and MCDI.

Boron and nitrogen co-doped porous carbon derived from sodium alginate enhanced capacitive deionization for water purification

Capacitive deionization can alleviate water shortage and water environmental pollution, but performances are greatly determined by the electrochemical and desalination properties of its electrode materials. In this work, B and N co-doped porous carbon with micro-mesoporous structures is derived from sodium alginate by a carbonization, activation, and hydrothermal doping process, which exhibits large specific surface area (2587 m^(2)·g^(‒1)) and high specific capacitance (190.7 F·g^(‒1)) for adsorption of salt ions and heavy metal ions. Furthermore, the materials provide a desalination capacity of 26.9 mg·g−1 at 1.2 V in 500 mg·L^(‒1) NaCl solution as well as a high removal capacity (239.6 mg·g^(‒1)) and adsorption rate (7.99 mg·g^(‒1)·min^(‒1)) for Pb2+ with an excellent cycle stability. This work can pave the way to design low-cost porous carbon with high-performances for removal of salt ions and heavy metal ions.

Penicillin fermentation residue biochar as a high-performance electrode for membrane capacitive deionization

Membrane capacitive deionization(MCDI)is an efficient desalination technology for brine.Penicillin fermentation residue biochar(PFRB)possesses a hierarchical porous and O/N-doped structure which could serve as a high-capacity desalination electrode in the MCDI system.Under optimal conditions(electrode weight,voltage,and concentration)and a carbonization temperature of 700℃,the maximum salt adsorption capacity of the electrode can reach 26.4 mg/g,which is higher than that of most carbon electrodes.Furthermore,the electrochemical properties of the PFRB electrode were characterized through cyclic voltammetry(CV)and electrochemical impedance spectroscopy(EIS)with a maximum specific capacitance of 212.18 F/g.Finally,biotoxicity tests have showed that PFRB was non-biotoxin against luminescent bacteria and the MCDI system with the PFRB electrode remained stable even after 27 adsorption–desorption cycles.This study provides a novel way to recycle penicillin residue and an electrode that can achieve excellent desalination.

电容去离子碳基电极材料的研究进展

电容去离子(CDI)技术具有能耗低、再生效率高、无二次污染、易于操作等优点,在解决水资源短缺和水环境污染方面应用广泛。开发具有高电化学性能和盐吸附能力的电极材料是CDI脱盐的关键。碳材料因其高比表面积、丰富的孔隙结构、优异的导电性和良好的稳定性而被广泛用作CDI电极。本文在介绍CDI技术基本原理的基础上,综述了5类典型碳基电极材料的研究进展,重点是材料设计和改进的吸附性能。对比分析了不同种类电极材料之间的优缺点,探讨了工业化存在的问题及改进方向。

氮氧双掺杂多孔碳对四环素的电吸附及其机制

四环素(TC)约占抗生素总产量和使用量的三分之一,且在水体中难以被降解,导致其在环境中的浓度越来越高而引发难以预估危害的细菌耐药性.因此,开发有效途径对水中四环素进行高效去除具有重要现实意义.本文通过简单的分散聚合物制备了具有高四环素吸附效率的聚酰亚胺衍生碳材料(FCPI).FCPI独特的分级多孔结构、丰富的氧(14.6%)、氮(4.7%)掺杂量和边缘缺陷等可为四环素的吸附提供丰富的活性位点;较大的比表面积、良好的导电性和化学稳定性,可提供稳定的双电层吸附界面.因此,将FCPI制备成电容去离子(CDI)器件的电极片后,FCPI对TC的电吸附容量高达989.5 mg·g^(-1),是传统自吸附的2.3倍(430.2 mg·g^(-1)).FCPI在自然水体中,经过200次吸-脱附循环后吸附容量仍可保持70%以上,具有优异的再生性和循环稳定性.且FCPI在不同水体中均表现出高效的TC吸附性能和同步去除水体中硬度离子的能力,使其在处理复杂水体污染与环境保护方面具有重要的实际意义.

木质基N,P共掺杂氧化石墨烯改性泡沫炭制备及电容去离子性能研究

以落叶松木屑为原料,磷酸二氢铵(NH_(4)H_(2)PO_(4))为掺杂剂,氧化石墨烯(GOs)为改性剂,经过液化、树脂化、发泡、炭化以及CO_(2)活化制备出木质基N、P共掺杂氧化石墨烯改性泡沫炭(N,P-GCF)。采用SEM、XRD、Raman、XPS、接触角测量仪分别对N,P-GCF的表面形态、晶体结构、化学性质、亲水性能进行分析,通过改变NH_(4)H_(2)PO_(4)的添加量探究其对泡沫炭孔结构、电化学性能及电容去离子性能(CDI)的影响。结果表明:经GOs改性与NH_(4)H_(2)PO_(4)掺杂后,孔泡尺寸下降,无序性提高。N,P-GCF具有分级孔结构。当NH_(4)H_(2)PO_(4)掺杂量为2 g时,具有最高的比表面积(2684.11 m^(2)·g^(-1))、总孔容(1.42 cm^(3)·g^(-1))和介孔率(49.45%),N、P质量分数分别为2.48%和3.46%。N元素主要以N-5、N-6、N-X形式存在,P元素主要为P-C、P-N。相比于CF,N,P-GCF2.0具有优异的润湿性及力学性能。在1 mol·L^(-1)NaCl电解液的三电极体系中,1 A·g^(-1)的电流密度时N,P-GCF2.0的比电容为256.48 F·g^(-1),当电流密度增加至15 A·g^(-1)时,比电容保持率达72.51%。在500 mg·L^(-1)的初始NaCl溶液、1.2 V的工作电压下,N,P-GCF2.0具有最佳脱盐能力(29.97 mg·g^(-1))及盐吸附速率(1.84 mg·g^(-1)·min^(-1)),10次循环后脱盐能力保留率为90.12%,具有较好的循环稳定性。