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As a new electrochemical technology, capacitive deionization (CDI) has been increasingly applied in environmental water treatment and seawater desalination. In this study, functional groups modified porous hollow carbon (HC) were synthesized as CDI electrode material for removing Na+ and Cl- in salty water. Results showed that the average diameter of HC was approximately 180 nm, and the infrared spectrum showed that its surface was successfully modified with sulfonic and amino groups, respectively. The sulfonic acid functionalized HC (HC-S) showed better electrochemical and desalting performance than the amino-functionalized HC (HCN), with a maximum Faradic capacity of 287.4 F/g and an adsorptive capacity of 112.97 mg/g for NaCl. Additionally, 92.63% capacity retention after 100 adsorption/desorption cycles demonstrates the excellent stability of HC-S. The main findings prove that HC-S is viable as an electrode material for desalination by high-performance CDI applications.
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Carbono , Eletrodos , Purificação da Água , Purificação da Água/métodos , Carbono/química , Porosidade , Adsorção , Água do Mar/química , Salinidade , Cloreto de Sódio/químicaRESUMO
The Microbial Desalination Cell (MDC) stands out as an innovative and a sustainable technology for both renewable energy generation and water treatment. The choice of electron acceptor significantly influences the efficiency of electricity flow. This study focuses on exploring the MDC performance under different conditions, including variations in cathode electron acceptors, initial pH levels, and hydraulic retention time (HRT). The investigation assesses simultaneous reduction of TDS and power generation from Caspian Sea water, a prominent saline water source in northern Iran, in both open-circuit (OC) and closed-circuit (CC) modes. The findings reveal that sodium hypochlorite, potassium permanganate, and potassium bromate as catholyte achieved TDS reduction rates of 84%, 77%, and 72%, respectively, under CC conditions at pH 5. Furthermore, it was observed that increasing HRT and pH levels lead to a decrease in desalination efficiency and power generation. Notably, the study highlights that the maximum power density was attained using permanganate, hypochlorite, and bromate as catholyte in both OC and CC configurations. By showcasing the adaptability of MDC performance with different cathode electron acceptors under varying conditions, this research offers valuable insights for optimizing MDC efficiency when treating real saline water sources.
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This work is an effort to mitigate the existing environmental issues caused by brine discharge from Kuwait's desalination plants and to find an economical and efficient way of managing reject brine from local desalination plants. Low- and high-resistance membranes (LRMs and HRMs, respectively) were used to produce salt and low-salinity water from brine effluent utilizing an electrodialysis (ED)-evaporator hybrid system. The effect of high current densities of 300, 400, and 500 A/m2 and brine flowrates of 450 and 500 L/h on the quality of produced salt and diluate were investigated for LRM and HRM. The recovered salt purity for LRM is up to 90.58%. Results show that the low-resistance membrane (LRM) achieved higher water recovery, energy consumption, desalination rate, operation time and ion removal rate than those of the high-resistance membrane (HRM) under the same operating conditions. The difference in concentration for 300 A/m2 between LRM and HRM increased from 0.93% at 10 min to 8.28% at 140 min. The difference in diluate concentration effluent is negligible for both membranes, whereas LRM produced higher concentrate effluent than HRM for all current densities and low flowrate (400 L/h). The maximum difference between LRM and HRM (with LRM achieving higher concentrations) is 10.7% for 400 A/m2. The permselectivity of LRM for monovalent cations decreased with current density, whereas the effect on permselectivity for HRM was insignificant for the current density values. The addition of a neutral cell was effective in reducing the buildup of divalent ions on the inner membrane of the cathode side.
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In recent years, with the development of solar seawater desalination technology, many solar evaporators are affected by precipitated salts during the evaporation process, which can reduce efficiency. In this work, flexible fabrics made of polypyrrole (PPy)/MXene are obtained by impregnating the prepared PPy ink onto waffle like fabrics. The combination of PPy and fabric greatly improves the water absorption and evaporation performance of the fabric. The average evaporation rate of this structure is 1.43 kg m-2 h-1, and the average evaporation efficiency under a single light source is 85.13%. After a 15-h testing cycle and a total of 8 cycles, lasting nearly 120 h, the performance of the device remained stable. The structural characteristics of waffle fabric, based on the Marangoni thermal effect, make it possible to suppress salt precipitation during evaporation, avoiding large salt particles covering the evaporation surface and reducing efficiency. This experiment successfully demonstrated long-term stable water evaporation, providing new ideas for the development of fabric evaporators.
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This study presents a novel approach to integrating combined cooling, heating, and power (CCHP) systems with water desalination for enhanced energy and water management in educational buildings. Two distinct layouts for CCHP and desalination systems are introduced: one prioritizing efficient power generation to meet electricity demands while providing waste heat for desalination, and the other focusing on balancing cooling and heating loads alongside water desalination. Both layouts are tailored to meet the building's energy and water demands while considering operational efficiency. Optimization of these layouts against traditional systems using the bat search algorithm emphasizes economic viability and the gas engine's operational flexibility, which are crucial for partial load operation. In addition, an environmental assessment compares the proposed CCHP-desalination systems with conventional setups, assessing CO2 emission reductions and overall sustainability. The evaluation encompasses key environmental metrics, such as resource consumption and the integration of renewable energy sources. Results highlight significant CO2 emission reductions across various gas engine capacities, with notable enhancements in economic and environmental performance achieved by selecting a 3,250 kW gas engine within the CCHP-desalination system. This choice not only maximizes the annual profit but also reduces CO2 emissions by 57% compared to conventional systems, underscoring the system's sustainability benefits.
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Purificação da Água , Purificação da Água/métodos , Energia Renovável , Educação , Calefação , Conservação de Recursos Energéticos/métodosRESUMO
Solar-driven interfacial water evaporation (SIWE) has emerged as a promising avenue for cost-effective freshwater production from seawater or wastewater. However, the simultaneous evaporation of volatile organic compounds (VOCs) presents a limitation for the widespread implementation of this technique. Thus, developing dual-functional evaporators capable of both desalining seawater and degrading VOCs is challenging. Herein, we fabricated an iron-based metal-organic framework MIL-88A/carbon nanotubes (CNTs) poly(vinyl alcohol) hydrogel (MCH) evaporator via the conventional freezing method for solar-driven seawater desalination and simultaneous photo-Fenton VOC degradation. Because of the superior photothermal conversion capability of CNTs, reduced thermal conductivity and water evaporation enthalpy within the hydrogel, and the photo-Fenton activity of rod-shaped MIL-88A, the MCH evaporator exhibits a higher evaporation rate of 2.26 kg m-2 h-1 under 1 sun illumination with simultaneous VOC degradation. The higher hydrophilicity and vertical channels in the MCH evaporator enable its self-salt cleaning ability, facilitating consistent seawater desalination, even in high salt concentrations up to 10 wtâ¯%. The synergistic effects of localized heating from CNTs and hydrogen peroxide activation through reactive sites of MIL-88A allow the MCH evaporator to degrade more than 93% of the added phenol during evaporation. This work presents a sustainable and efficient approach for solar-driven seawater desalination, offering simultaneous VOC degradation.
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Elastic aerogels have become a research hot spot in both academia and industry recently. The reported elastic aerogels are all made of hard materials by controlling their shapes. Herein we report an elastic aerogel made of a polymer elastomer with entropy elasticity. In the aerogel, cross-linked carboxyl nitrile rubber nanoparticles with hydrophilicity are dispersed in hydrophobic derivative of styrene-maleic anhydride alternating copolymer, forming a very special micro-nano surface structure with hydrophilic protrusions and hydrophobic depressions on the aerogel wall; therefore, the aerogel is not only superelastic but also superamphiphilic. A leak-free phase-change composite was prepared using the aerogel and paraffin, which can maintain at phase change temperature of paraffin for a longer time than the traditional one. The aerogel is also extremely suitable for desalination evaporators in solar-driven interfacial evaporation technology due to its superamphiphilicity, superelasticity, and ability to absorb sunlight. Exceptional evaporation rate of 2.78 kg·m-2·h-1 and evaporation efficiency of 170% could be reached even without using expensive light-absorbing materials. The evaporation rate exceeds that of most evaporators with expensive light-absorbing materials, and the evaporation efficiency exceeds the theoretical limit of conventional 2D solar evaporators. Both the phase-change composite and the evaporator can be easily recovered because the novel superelastic aerogel reported in this work is also recyclable.
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In this current investigation, the experimental performance of a solar still basin was significantly enhanced by incorporating snail shell biomaterials. The outcomes of the snail shell-augmented solar still basin (SSSS) are compared with those of a conventional solar still (CSS). The utilization of snail shells proved to facilitate the reduction of saline water and enhance its temperature, thereby improving the productivity of the SSSS. Cumulatively, the SSSS productivity was improved by 4.3% over CSS. Furthermore, the SSSS outperformed in energy and exergy efficiency of CSS by 4.5 and 3.5%, respectively. Economically, the cost per liter of distillate (CPL) for the CSS was 3.4% higher than SSSS. Moreover, the SSSS showed a shorter estimated payback period (PBP) of 141 days which was 6 days less than CSS. Considering the environmental impact, the observed CO2 emissions from the SSSS were approximately 14.6% higher than CSS over its 10-year lifespan. Notably, the SSSS exhibited a substantial increase in the estimated carbon credit earned (CCE) compared to the CSS. Ultimately, the research underscores the efficacy of incorporating snail shells into solar still basins as a commendable approach to organic waste management, offering economic benefits without compromising environmental considerations.
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Caramujos , Animais , Exoesqueleto/química , Materiais Biocompatíveis/química , Luz Solar , Conservação dos Recursos Naturais/métodos , Purificação da Água/métodosRESUMO
Solar-driven interfacial evaporation technology is a novel and efficient desalination process that helps alleviate the global shortage of freshwater resources. We developed a Janus evaporator assembled from cotton hydrogel, hydrophilic polyester fabric (PF), and Hydrophobic Wood (PW). By doping graphene oxide and TiO2 as light-absorbing materials within the hydrogel, we achieved a high absorptivity of over 90% across the entire solar spectrum. The hydrophilically modified PF, combined with the PW substrate, provided robust water transport and reduced thermal losses. Subsequent optical path simulations using TracePro74 software verified that the sawtooth light-trapping design of the wood substrate increased multiple light reflections and absorption (compared to a flat structure), enhancing light absorption capabilities. The sawtooth interface also enlarged the evaporation area, further boosting evaporation performance. The cleverly designed evaporator exhibited an evaporation rate of 1.722 kg m-2 h-1 and an efficiency of 83.1% under 1 sun irradiation. Additionally, after applying polydimethylsiloxane to the single surface of the photothermal hydrogel for low surface energy treatment, the resulting Janus structure demonstrated asymmetric wettability that prevented salt ions from accumulating on the irradiated interface. After 8 h of continuous evaporation in saline water (10 wt %), only slight salt crystallization occurred at the edges. The evaporator maintained long-term stability during a 15 day cyclic test, and the produced freshwater fully met the relevant drinking water standards. The components of the evaporator are characterized by simple fabrication, low cost, and eco-friendliness, offering significant application potential in the global context of energy conservation and emission reduction initiatives.
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This study introduces draw solutions for application in forward osmosis (FO) processes, combining mono propylene glycol propyl ether (PGPE) with the cellulose derivative hydroxypropyl cellulose (HPC). A total of 16 unique single-solute and ternary organic draw solutions were prepared and evaluated, leading to the selection of three promising solutions for further investigation. Notably, eight of the initial organic draw solutions demonstrated osmotic pressures exceeding 2.4 MPa. The dynamic viscosities of all draw solutions exhibited a significant reduction with increasing temperature. Among the investigated solutions, the 0.25HPC-3.75PGPE demonstrated the most favorable FO performance, achieving average experimental water fluxes of 11.062 and 9.852 Lm-2 h-1 (LMH) against a 1 g/L NaCl brackish feed solution across two FO runs. PRACTITIONER POINTS: Hydroxypropyl cellulose (HPC, MW ~100,000) was mixed with propylene glycol propyl ether (PGPE) as draw solutes for FO processes. Seven combinations of HPC and PGPE produced osmolalities greater than 1000 mOsm/kg. 0.5HPC-7.5PGPE ternary draw solution achieved experimental water fluxes of 11.062 and 9.852 LMH against 1 g/L NaCl brackish feed solution. Leveraging the LCSTs of these ternary organic solutions holds promise for improved separation and regeneration processes.
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Celulose , Osmose , Águas Salinas , Purificação da Água , Celulose/química , Celulose/análogos & derivados , Purificação da Água/métodos , Águas Salinas/química , Propilenoglicóis/químicaRESUMO
Membrane distillation (MD) has great potential in the management of hypersaline water for zero liquid discharge (ZLD) due to its high salinity tolerance. However, the membrane wetting issue significantly restricts its practical application. In this study, a composite membrane tailored for extreme concentrations and even crystallization of hypersaline water is synthesized by coating a commercial hydrophobic porous membrane with a composite film containing a dense polyamide layer, a cation exchange layer (CEL), and an anion exchange layer (AEL). When used in direct contact MD for treating a 100 g L-1 NaCl hypersaline solution, the membrane achieves supersaturation of feed solution and a salt crystal yield of 38.0%, with the permeate concentration at <5 mg L-1. The composite membrane also demonstrates ultrahigh antiwetting stability in 360 h of long-term operation. Moreover, ion diffusion analysis reveals that the ultrahigh wetting resistance of the composite membrane is attributed to the bipolar AEL and CEL that eliminate ion crossover. The literature review elucidates that the composite membrane is superior to state-of-the-art membranes. This study demonstrates the great potential of the composite membrane for direct crystallization of hypersaline water, offering a promising approach to filling the gap between reverse osmosis and conventional thermal desalination processes for ZLD application.
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Cristalização , Destilação , Membranas Artificiais , Salinidade , Água/química , Purificação da Água/métodosRESUMO
Cellulose in the nano regime, defined as nanocellulose, has been intensively used for water treatment. Nanocellulose can be produced in various forms, including colloidal, water redispersible powders, films, membranes, papers, hydrogels/aerogels, and three-dimensional (3D) objects. They were reported for the removal of water contaminants, e.g., heavy metals, dyes, drugs, pesticides, pharmaceuticals, microbial cells, and other pollutants from water systems. This review summarized the recent technologies for water treatment using nanocellulose-based materials. A scientometric analysis of the topic was also included. Cellulose-based materials enable the removal of water contaminants, and salts offer advanced technologies for water desalination. They are widely used as substrates, adsorbents, and catalysts. They were applied for pollutant removal via several methods such as adsorption, filtration, disinfection, coagulation/flocculation, chemical precipitation, sedimentation, filtration (e.g., ultrafiltration (UF), nanofiltration (NF)), electrofiltration (electrodialysis), ion-exchange, chelation, catalysis, and photocatalysis. Processing cellulose into commercial products enables the wide use of nanocellulose-based materials as adsorbents and catalysts.
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Celulose , Poluentes Químicos da Água , Purificação da Água , Celulose/química , Purificação da Água/métodos , Poluentes Químicos da Água/química , Poluentes Químicos da Água/isolamento & purificação , Adsorção , Nanoestruturas/química , CatáliseRESUMO
Extracting clean water from oily wastewater and seawater is one of the effective strategies to alleviate the freshwater crisis. However, achieving both high separation efficiency and excellent salt resistance remain challenges for materials. Herein, a novel methyltrichlorosilane-modified polyvinyl alcohol/cellulose aerogel (MPCA) was prepared by freeze drying, chemical cross-linking, and chemical vapor deposition (CVD) methods. The superwetting MPCA presented an asymmetric structure, in which the small dense pores at the top surface facilitated the efficient separation of water-in-oil (W/O) emulsions and the large pores on the bottom surface were beneficial for brine exchange. The as-prepared superwetting aerogel was suitable for the separation of various W/O emulsions with excellent separation flux (631.9-2368.7 L·m-2·h-1) and outstanding separation efficiency (99.5 %). In addition, MPCA achieved a high evaporation efficiency of 1.39 kg·m-2·h-1 and a satisfactory energy conversion efficiency of 89.7 %. Moreover, the unique asymmetric structure endowed the evaporator excellent salt resistance and could self-dissolve the accumulated salt in 20 min. The as-prepared MPCA could achieve efficient W/O emulsion separation as well as produce freshwater in seawater, providing a new strategy for oily waste seawater purification.
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Ion back-diffusion hinders the practical application of conventional flow-electrode capacitive deionization (FCDI) under long-term operational conditions. To address this challenge, the present study integrated cation intercalation deionization (CID) with FCDI. A novel PFCDI-CID system was developed by utilizing a modified Prussian blue analogues owing to their enhanced rheological and electrochemical properties. The PFCDI-CID system achieved a high charge efficiency of 89.77% and an energy-normalized removal salt of 0.69 mol kJ-1 in single-cycle (SC) mode with the flow electrodes mass fraction of 2% and a desalinized water chamber-to-concentrated saline water chamber ratio of 2:1. Furthermore, under continuous operation for 12 h in SC mode, the PFCDI-CID system maintained stable desalination performance within the first 2 h. Over an extended duration, the average charge efficiency of the PFCDI-CID system was maintained at 88.44%, with an average energy-normalized removal salt of 0.65 mol kJ-1. The mechanism revealed that the desalination process involving the Prussian blue analogues primarily involves Na+ intercalation, accompanied by a small amount of electro-sorption process. This system exhibits the characteristics of conventional FCDI while enabling desalination and concentration of simulated saline water during brine discharge, thereby mitigating the impact of ion back-diffusion and broadening the application scope of FCDI.
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Cátions , Eletrodos , Ferrocianetos , Purificação da Água , Purificação da Água/métodos , Ferrocianetos/químicaRESUMO
Electrosorption (ES) is a research frontier in electrochemical separation, with proven potential applications in desalination, wastewater treatment, and selective resource extraction. However, due to the limited adsorption capacity of film electrodes, ES requires short circuiting or circuit reversal, accompanied by a solution switch between the feed solution and receiving solution, to sustain desalination over many charge-discharge cycles. In previously reported studies, solution switches have been commonly ignored to simplify experimental procedures, and their impacts on separation performance are thus not well understood. This study aims to provide a quantitative analysis of the impacts of mixing due to a solution switch on the performance of ES-based desalination. A numerical model of ES has been employed to evaluate the adverse effects of the solution switch on the desalination performance in three commonly used operation modes. The analysis reveals that the impacts of mixing due to solution-switch are more severe with a larger concentration difference between the desalinated water and the brine and provides insights into the effectiveness of increasing electrode loading or specific capacity in mitigating the detrimental impacts of mixing. Even with state-of-the-art systems, producing freshwater from seawater or even brackish water with medium-to-high salinity is practically challenging due to the presence of solution switch.
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Salinidade , Purificação da Água , Purificação da Água/métodos , Água do Mar/química , Adsorção , Eletrodos , SoluçõesRESUMO
The use of hydrogel-based interfacial solar evaporators for desalination is a green, sustainable, and extremely concerned freshwater acquisition strategy. However, developing evaporators that are easy to manufacture, cheap, and have excellent porous structures still remains a considerable challenge. This work proposes a novel strategy for preparing a self-assembling sponge-like poly(vinyl alcohol)/graphite composite hydrogel based on the Hofmeister effect for the first time. The sponge-like hydrogel interfacial solar evaporator (PGCNG) is successfully obtained after combining with graphite. The whole process is environmental-friendly and of low-carbon free of freezing process. The PGCNG can be conventionally dried and stored. PGCNG shows impressive water storage performance and water transmission capacity, excellent steam generation performance and salt resistance. PGCNG has a high evaporation rate of 3.5 kg m-2 h-1 under 1 kW m-2 h-1 solar irradiation and PGCNG demonstrates stable evaporation performance over both 10 h of continuous brine evaporation and 30 cycles of brine evaporation. Its excellent performance and simple, scalable preparation strategy make it a valuable material for practical interface solar seawater desalination devices.
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The morphological adjustments of euhalophytes are well-known to be influenced by the soil-soluble salt variation; however, whether and how these changes in morphological traits alter the biomass allocation pattern remains unclear, especially under different NaCl levels. Therefore, an allometric analysis was applied to investigate the biomass allocation pattern and morphological plasticity, and the carbon (C), nitrogen (N), and phosphorus (P) stoichiometric characteristics of the euhalophyte Suaeda Salsa (S. salsa) at the four soil-soluble salt levels of no salt (NS), light salt (LS), moderate salt (MS), and heavy salt (HS). The results showed that soil-soluble salts significantly change the biomass allocation to the stems and leaves (p < 0.05). With the growth of S. salsa, the NS treatment produced a downward leaf mass ratio (LMR) and upward stem mass ratio (SMR); this finding was completely different from that for the salt treatments. When S. salsa was harvested on the 100th day, the HS treatment had the highest LMR (61%) and the lowest SMR (31%), while the NS treatment was the opposite, with an LMR of 44% and an SMR of 50%. Meanwhile, the soil-soluble salt reshaped the morphological characteristics of S. salsa (e.g., root length, plant height, basal stem diameter, and leaf succulence). Combined with the stoichiometric characteristics, N uptake restriction under salt stress is a vital reason for inhibited stem growth. Although the NS treatment had the highest biomass (48.65 g root box-1), the LS treatment had the highest salt absorption (3.73 g root box-1). In conclusion, S. salsa can change its biomass allocation pattern through morphological adjustments to adapt to different saline-alkali habitats. Moreover, it has an optimal biological desalting effect in lightly saline soil dominated by NaCl.
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In this study, we report the robust hydrophobicity, lower fouling propensity, and high thermal efficiency of the 1H,1H,2H,2H-perfluorooctyltriethoxysilane (FAS)-coated, carbon nanotube-immobilized membrane (CNIM) when applied to desalination via membrane distillation. Referred to as FAS-CNIM, the membrane was developed through a process that combined the drop-casting of nanotubes flowed by a dip coating of the FAS layer. The membranes were tested for porosity, surface morphology, thermal stability, contact angle, and flux. The static contact angle of the FAS-CNIM was 153 ± 1°, and the modified membrane showed enhancement in water flux by 18% compared to the base PTFE membrane. The flux was tested at different operating conditions and the fouling behavior was investigated under extreme conditions using a CaCO3 as well as a mixture of CaCO3 and CaSO4 solution. The FAS-CNIM showed significantly lower fouling than plain PTFE or the CNIM; the relative flux reduction was 34.4% and 37.6% lower than the control for the CaCO3 and CaCO3/CaSO4 mixed salt solution. The FAS-CNIM exhibited a notable decrease in specific energy consumption (SEC). Specifically, the SEC for the FAS-CNIM measured 311 kwh/m3 compared to 330.5 kwh/m3 for the CNIM and 354 kwh/m3 for PTFE using a mixture of CaCO3/CaSO4. This investigation underscores the significant contribution of the carbon nanotubes' (CNTs) intermediate layer in creating a durable superhydrophobic membrane, highlighting the potential of utilizing carbon nanotubes for tailored interface engineering to tackle fouling for salt mixtures. The innovative design of a superhydrophobic membrane has the potential to alleviate wetting issues resulting from low surface energy contaminants present in the feed of membrane distillation processes.
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Microbial desalination cells (MDCs) are considered as a sustainable technology for water desalination, wastewater treatment, and power generation. However, this neoteric technology suffers from different challenges, including sluggish oxygen reduction reaction and poor electron transfer from microbes to electrodes, ultimately leading to less power generation and desalination efficiency. This review delves into the intricate roles of both abiotic and biocatalysts in enhancing performance of MDCs through ion removal and charge transfer mechanisms. Detailed discussions highlight the comparative advantages and limitations of different catalyst types and insights into electrode modifications to optimise catalytic activity and biofilm formation. Further, recent advancements in electrode engineering, including surface coatings and integration of nanomaterial, geared towards enhancing efficiency of MDC and performance stability are discussed. Finally, future recommendations are provided, focusing on innovative catalyst designs, material integration, and considerations for scale-up and commercialisation, thereby offering a comprehensive roadmap for the continued advancement of MDC.
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Eletrodos , Purificação da Água , Purificação da Água/métodos , Catálise , Salinidade , Águas Residuárias/química , Biofilmes , Fontes de Energia BioelétricaRESUMO
Interfacial solar evaporation (ISE) holds considerable promise to solve fresh water shortage, but it is challenging to achieve high evaporation rate (Reva) and fresh water yield in close system. Here, we report design and preparation of MOF-based solar evaporators with hierarchical microporous/nanobridged/nanogranular structures for rapid ISE and fresh water collection in close system. The evaporators are fabricated by growing silicone nanofilaments with variable length as nanobridges on a microporous silicone sponge followed by grafting with polydopamine nanoparticles and Cu-MOF nanocrystals. Integration of the unique structure and excellent photothermal composites endows the evaporators with high Reva of 3.5-20 wt% brines (3.60-2.90 kg m-2 h-1 in open system and 2.38-1.44 kg m-2 h-1 in close system) under simulated 1 sun, high Reva under natural sunlight, excellent salt resistance and high fresh water yield, which surpass most state-of-the-art evaporators. Moreover, when combined with a superhydrophilic cover, the evaporators show much higher average Reva of real seawater, remarkable fresh water yield and excellent long-term stability over one month continuous ISE under natural sunlight. The findings here will promote the development of advanced evaporators via microstructure engineering and their real-world ISE applications.