High Rate Production of Clean Water Based on the Combined Photo‐Electro‐Thermal Effect of Graphene Architecture

The use of abundant solar energy for regeneration and desalination of water is a promising strategy to address the challenge of a global shortage of clean water. Progress has been made to develop photothermal materials to improve the solar steam generation performance. However, the mass production rate of water is still low. Herein, by a rational combination of photo‐electro‐thermal effect on an all‐graphene hybrid architecture, solar energy can not only be absorbed fully and transferred into heat, but also converted into electric power to further heat up the graphene skeleton frame for a much enhanced generation of water vapor. As a result, the unique graphene evaporator reaches a record high water production rate of 2.01–2.61 kg m^?2 h^?1 under solar illumination of 1 kW m^?2 even without system optimization. Several square meters of the graphene evaporators will provide a daily water supply that is enough for tens of people. The combination of photo‐electro‐thermal effect on graphene materials offers a new strategy to build a fast and scalable solar steam generation system, which makes an important step towards a solution for the scarcity of clean water.     

Sandwich Photothermal Membrane with Confined Hierarchical Carbon Cells Enabling High‐Efficiency Solar Steam Generation

Solar‐driven vaporization is a sustainable solution to water and energy scarcity. However, most of the present evaporators are still suffering from inefficient utilization of converted thermal energy. Herein, a universal sandwich membrane strategy is demonstrated by confining the hierarchical porous carbon cells in two energy barriers to obtain a high‐efficiency evaporator with a rapid water evaporation rate of 1.87 kg m^?2 h^?1 under 1 sun illumination, which is among the highest performance for carbon‐based and wood‐based evaporators. The significantly enhanced evaporation rate is mainly attributed to the inherently optimized porous evaporation mode derived from the hierarchical hollow structures of pollen carbon cells, and the synergistically regulated water transporting and thermal management performance of the sandwich membrane. Moreover, the constructed sandwich membrane also exhibits excellent self‐regenerating performance in simulated seawater and high salinity water. The developed device can maintain an average evaporation rate of 4.3 L m^?2 day^?1 in a 25 day consecutive outdoor test.     

Portable Low‐Pressure Solar Steaming‐Collection Unisystem with Polypyrrole Origamis

Solar steaming has emerged as a promising green technology that can address the global issue of scarcity of clean water. However, developing high‐performance, cost‐effective, and manufacturable solar‐steaming materials, and portable solar steaming‐collection systems for individuals remains a great challenge. Here, a one‐step, low‐cost, and mass‐producible synthesis of polypyrrole (PPy) origami‐based photothermal materials, and an original portable low‐pressure controlled solar steaming‐collection unisystem, offering synergetic high rates in both water evaporation and steam collection, are reported. Due to enhanced areas for vapor dissipation, the PPy origami improves the water evaporation rate by at least 71% to 2.12 kg m^?2 h^?1 from that of a planar structure and exhibits a solar–thermal energy conversion efficiency of 91.5% under 1 Sun. When further controlling the pressure to ≈0.17 atm in the steaming‐collection unisystem, the water collection rate improves by up to 52% systematically and dramatically. Although partial energy is utilized toward obtaining low‐pressure, evaluations show that the overall energy efficiency is improved remarkably in the low‐pressure system compared to that in ambient pressure. Furthermore, the device demonstrates effective decontamination of heavy metals, bacteria, and desalination. This work can inspire new paradigms toward developing high‐performance solar steaming technologies for individuals and households.     

Bioinspired Aerogel with Vertically Ordered Channels and Low Water Evaporation Enthalpy for High-Efficiency Salt-Rejecting Solar Seawater Desalination and Wastewater Purification

Solar energy-driven water evaporation is a promising sustainable strategy to purify seawater and contaminated water. However, developing solar evaporators with high water evaporation rates and excellent salt resistance still faces a great challenge. Herein, inspired by the long-range ordered structure and water transportation capability of lotus stem, a biomimetic aerogel with vertically ordered channels and low water evaporation enthalpy for high-efficiency solar energy-driven salt-resistant seawater desalination and wastewater purification is developed. The biomimetic aerogel consists of ultralong hydroxyapatite nanowires as heat-insulating skeletons, polydopamine-modified MXene as a photothermal material with broadband sunlight absorption and high photothermal conversion efficiency, polyacrylamide, and polyvinyl alcohol as reagents to lower the water evaporation enthalpy and as glues to enhance the mechanical performance. The honeycomb porous structure, unidirectionally aligned microchannels, and nanowire/nanosheet/polymer pore wall endow the biomimetic aerogel with excellent mechanical properties, rapid water transportation, and excellent solar water evaporation performance. The biomimetic aerogel exhibits a high water evaporation rate (2.62 kg m⁻² h⁻¹) and energy efficiency (93.6%) under one sun irradiation. The superior salt-rejecting ability of the designed water evaporator enables stable and continuous seawater desalination, which is promising for application in water purification to mitigate the global water crisis.     

MOF‐Based Hierarchical Structures for Solar‐Thermal Clean Water Production

Solar‐thermal water evaporation, as a promising method for clean water production, has attracted increasing attention. However, solar water evaporators that exhibit both high water vapor generation ability and anti‐oil‐fouling ability have not been reported. Here, a unique metal–organic‐framework‐based hierarchical structure, referred to as MOF‐based hierarchical structure (MHS), is rationally designed and prepared, which simultaneously displays a high solar absorption and a superhydrophilic and underwater superoleophobic surface property. As a proof‐of‐concept application, a device prepared from the MHS can achieve a high solar‐thermal water evaporation rate of 1.50 kg m^?2 h^?1 under 1 sun illumination. Importantly, the MHS also possesses an excellent anti‐oil‐fouling property, ensuring its superior water evaporation performance even in oil‐contaminated water. The high solar‐thermal water evaporation rate and anti‐oil‐fouling property make the MHS a promising material for the solar‐thermal water production.     

An Interfacial Solar‐Driven Atmospheric Water Generator Based on a Liquid Sorbent with Simultaneous Adsorption–Desorption

Water scarcity is one of the greatest challenges facing human society. Because of the abundant amount of water present in the atmosphere, there are significant efforts to harvest water from air. Particularly, solar‐driven atmospheric water generators based on sequential adsorption–desorption processes are attracting much attention. However, incomplete daytime desorption is the limiting factor for final water production, as the rate of water desorption typically decreases very quickly with decreased water content in the sorbents. Hereby combining tailored interfacial solar absorbers with an ionic‐liquid‐based sorbent, an atmospheric water generator with a simultaneous adsorption–desorption process is generated. With enhanced desorption capability and stabilized water content in the sorbent, this interfacial solar‐driven atmospheric water generator enables a high rate of water production (≈0.5 L m^?2 h^?1) and 2.8 L m^?2 d^?1 for the outdoor environment. It is expected that this interfacial solar‐driven atmospheric water generator, based on the liquid sorbent with a simultaneous adsorption–desorption process opens up a promising pathway to effectively harvest water from air.     

Engineering Metal–Phenolic Networks for Solar Desalination with Directional Salt Crystallization

Solar desalination is one of the most promising strategies to address the global freshwater shortage crisis. However, the residual salt accumulated on the top surface of solar evaporators severely reduces light absorption and steam evaporation efficiency, thus impeding the further industrialization of this technology. Herein, a metal–phenolic network (MPN)-engineered 3D evaporator composed of photothermal superhydrophilic/superhydrophobic sponges and side-twining hydrophilic threads for efficient desalination with directional salt crystallization and zero liquid discharge is reported. The MPN coatings afford the engineering of alternating photothermal superhydrophilic/superhydrophobic sponges with high heating efficiency and defined vapor escape channels, while the side-twining threads induce site-selective salt crystallization. The 3D evaporator exhibits a high and stable indoor desalination rate (≈2.3 kg m⁻² h⁻¹) of concentrated seawater (20 wt%) under simulated sun irradiation for over 21 days without the need for salt crystallization inhibitors. This direct desalination is also achieved in outdoor field operations with a production rate of clean water up to ≈1.82 kg m⁻² h⁻¹ from concentrated seawater (10 wt%). Together with the high affinity and multiple functions of MPNs, this work is expected to facilitate the rational design of solar desalination devices and boost the research translation of MPN materials in broader applications.     

Improved Photo-Excited Carriers Transportation of WS2-O-Doped-Graphene Heterostructures for Solar Steam Generation (Small 19/2023)

Two-dimensional (2D) transition metal dichalcogenides and graphene have revealed promising applications in optoelectronic and energy storage and conversion. However, there are rare reports of modifying the light-to-heat transformation via preparing their heterostructures for solar steam generation. In this work, commercial WS₂ and sucrose are utilized as precursors to produce 2D WS₂-O-doped-graphene heterostructures (WS₂-O-graphene) for solar water evaporation. The WS₂-O-graphene evaporators demonstrate excellent average water evaporation rate (2.11 kg m⁻² h⁻¹) and energy efficiency (82.2%), which are 1.3- and 1.2-fold higher than WS₂ and O-doped graphene-based evaporators, respectively. Furthermore, for the real seawater with different pH values (pH 1 and 12) and rhodamine B pollutants, the WS₂-O-graphene evaporators show great average evaporation rates (≈2.08 and 2.09 kg m⁻² h⁻¹, respectively) for producing freshwater with an extremely low-grade of dye residual and nearly neutral pH values. More interestingly, due to the self-storage water ability of WS₂-O-graphene evaporators, water evaporation can be implemented without the presence of bulk water. As a result, the evaporation rate reaches 3.23 kg m⁻² h⁻¹, which is ≈1.5 times higher than the regular solar water evaporation system. This work provides a new approach for preparing 2D transition metal dichalcogenides and graphene heterostructures for efficient solar water evaporation.     

Hierarchical Porous SWCNT Stringed Carbon Polyhedrons and PSS Threaded MOF Bilayer Membrane for Efficient Solar Vapor Generation

Interfacial solar vapor generation is considered to be an efficient and eco‐friendly technology for harvesting solar energy and providing freshwater. However, the efficient and long‐term steady evaporation of seawater under 1 sun becomes a critical issue when it comes to practical applications. Based on this issue, a special double‐layer structure, which contains a metal–organic‐framework‐derived hierarchical porous carbon membrane (HPCM) for solar absorption and a polystyrene sulfonate (PSS)@Cu₃(BTC)₃?3H₂O (HKUST‐1)/single‐walled carbon nanotube (SWCNT) (PHS) membrane for water supply and salt blocking, is designed in this work. The converted heat is utilized efficiently in situ to drive the evaporation of water‐trapped HPCM. The PHS membrane with PSS modified channels successfully prevents the deposition of salt. Due to the synergistic combination of the HPCM and PHS membranes, the device exhibits a remarkably high water evaporation rate of 1.38 kg m^?2 h^?1 and solar‐vapor generation efficiency of 90.8% under 1 sun.     

Tree‐Inspired Design for High‐Efficiency Water Extraction

The solar steam process, akin to the natural water cycle, is considered to be an attractive approach to address water scarcity issues globally. However, water extraction from groundwater, for example, has not been demonstrated using these existing technologies. Additionally, there are major unaddressed challenges in extracting potable water from seawater including salt accumulation and long‐term evaporation stability, which warrant further investigation. Herein, a high‐performance solar steam device composed entirely of natural wood is reported. The pristine, natural wood is cut along the transverse direction and the top surface is carbonized to create a unique bilayer structure. This tree‐inspired design offers distinct advantages for water extraction, including rapid water transport and evaporation in the mesoporous wood, high light absorption (≈99%) within the surface carbonized open wood channels, a low thermal conductivity to avoid thermal loss, and cost effectiveness. The device also exhibits long‐term stability in seawater without salt accumulation as well as high performance for underground water extraction. The tree‐inspired design offers an inexpensive and scalable solar energy harvesting and steam generation technology that can provide clean water globally, especially for rural or remote areas where water is not only scarce but also limited by water extraction materials and methods.     

Vertically aligned reduced graphene oxide/Ti3C2Tx MXene hybrid hydrogel for highly efficient solar steam generation

Effective utilization of abundant solar energy for desalination of seawater and purification of wastewater is one of sustainable techniques for production of clean water, helping relieve global water resource shortage. Herein, we fabricate a vertically aligned reduced graphene oxide/Ti₃C₂T_x MXene (A-RGO/MX) hybrid hydrogel with aligned channels as an independent solar steam generation device for highly efficient solar steam generation. The vertically aligned channels, generated by a liquid nitrogen-assisted directional-freezing process, not only rapidly transport water upward to the evaporation surface for efficient solar steam generation, but also facilitate multiple reflections of solar light inside the channels for efficient solar light absorption. The deliberate slight reduction endows the RGO with plenty of polar groups, decreasing the water vaporization enthalpy effectively and hence accelerating water evaporation efficiently. The MXene sheets, infiltrated inside the A-RGO hydrogel on the basis of Marangoni effect, enhance light absorption capacity and photothermal conversion performance. As a result, the A-RGO/MX hybrid hydrogel achieves a water evaporation rate of 2.09 kg·m⁻²·h⁻¹ with a high conversion efficiency of 93.5% under 1-sun irradiation. Additionally, this photothermal conversion hydrogel rapidly desalinates seawater and purifies wastewater to generate clean water with outstanding ion rejection rates of above 99% for most ions.

     

Charged Layered Boron Nitride‐Nanoflake Membranes for Efficient Ion Separation and Water Purification

2D layered nanomaterials have attracted considerable attention for their potential for highly efficient separations, among other applications. Here, a 2D lamellar membrane synthesized using hexagonal boron nitride nanoflakes (h‐BNF) for highly efficient ion separation is reported. The ion‐rejection performance and the water permeance of the membrane as a function of the ionic radius, ion valance, and solution pH are investigated. The nonfunctionalized h‐BNF membranes show excellent ion rejection for small sized salt ions as well as for anionic dyes (>97%) while maintaining a high water permeability, ≈1.0 × 10^?3 L m m^?2 h^?1 bar^?1). Experiments show that the ion‐rejection performance of the membrane can be tuned by changing the solution pH. The results also suggest that the rejection is influenced by the ionic size and the electrostatic repulsion between fixed negative charges on the BN surface and the mobile ions, and is consistent with the Donnan equilibrium model. These simple‐to‐fabricate h‐BNF membranes show a unique combination of excellent ion selectivity and high permeability compared to other 2D membranes.     

Cellular Structured CNTs@SiO2 Nanofibrous Aerogels with Vertically Aligned Vessels for Salt-Resistant Solar Desalination

The emerging solar desalination technology is considered as one of the most promising strategies to ensure water security. However, with the proceeding of solar desalination, salt crystallization on the surface of solar evaporators caused by increasing salinity of seawater will result in a decrease in the evaporation rate. Thus, it is still challenging to fabricate solar evaporators with superior salt resistance. In this work, elastic ceramic-based nanofibrous aerogels with a cellular architecture are fabricated by the combination of electrospinning and fiber freeze-shaping technologies, which are composed of vertically aligned vessels and porous vessel walls. Under the action of convection and diffusion promoted by this unique cellular architecture, the aerogels exhibit a superior salt-resistance without any salt crystals on the surface of aerogels even in 20% brine and under 6-sun irradiation. Moreover, by virtue of the synergistic effect of the promising structure and light absorbance of carbon nanotubes, aerogels possess a high light absorbance of up to 98% and excellent evaporation performance achieving 1.50 kg m⁻² h⁻¹ under 1-sun irradiation. This work may provide a fascinating avenue for the desalination of seawater in a salt-resistance and efficient manner.     

A High‐Performance Self‐Regenerating Solar Evaporator for Continuous Water Desalination

Emerging solar desalination by interfacial evaporation shows great potential in response to global water scarcity because of its high solar‐to‐vapor efficiency, low environmental impact, and off‐grid capability. However, solute accumulation at the heating interface has severely impacted the performance and long‐term stability of current solar evaporation systems. Here, a self‐regenerating solar evaporator featuring excellent antifouling properties using a rationally designed artificial channel‐array in a natural wood substrate is reported. Upon solar evaporation, salt concentration gradients are formed between the millimeter‐sized drilled channels (with a low salt concentration) and the microsized natural wood channels (with a high salt concentration) due to their different hydraulic conductivities. The concentration gradients allow spontaneous interchannel salt exchange through the 1–2 µm pits, leading to the dilution of salt in the microsized wood channels. The drilled channels with high hydraulic conductivities thus function as salt‐rejection pathways, which can rapidly exchange the salt with the bulk solution, enabling the real‐time self‐regeneration of the evaporator. Compared to other salt‐rejection designs, the solar evaporator exhibits the highest efficiency (≈75%) in a highly concentrated salt solution (20 wt% NaCl) under 1 sun irradiation, as well as long‐term stability (over 100 h of continuous operation).     

3D Solar Evaporation Enhancement by Superhydrophilic Copper Foam Inverted Cone and Graphene Oxide Functionalization Synergistic Cooperation

Solar evaporation has become a promising and sustainable technique for harvesting freshwater from seawater and wastewater. However, the applicability and efficacy of solar evaporation need further improvement to achieve high production closer to theoretical limits in compact systems. A 3D (three-dimensional) hierarchical inverted conical solar evaporation is developed, which consists of a 3D copper foam skeleton cone decorated with micro-/nano-structures functionalized with graphene oxide, fabricated via easy and scalable wet oxidation, impregnation, and drying at room temperature. The proposed configuration empowers high-efficiency solar absorption, continuous liquid film spreading and transport, enhanced interfacial local evaporation, and rapid vapor diffusion through the pores. More notably, the 3D conical evaporator realizes thermal localization at the skeleton interface and allows evaporation to occur along the complete structure with unimpeded liquid and vapor rapid diffusion. The solar–thermal evaporation efficiency under 1-Sun is as high as 93% with a maximum evaporation rate per unit area of 1.71 kg·m⁻²·h⁻¹. This work highlights the benefits of synergistic cooperation of an easily scalable 3D hierarchical functiomicro-/nano-structured copper foam skeletons and functionalized graphene oxide for high-efficient solar evaporation of interest to numerous applications.     

3D‐Printed,All‐in‐One Evaporator for High‐Efficiency Solar Steam Generation under 1 Sun Illumination

Using solar energy to generate steam is a clean and sustainable approach to addressing the issue of water shortage. The current challenge for solar steam generation is to develop easy‐to‐manufacture and scalable methods which can convert solar irradiation into exploitable thermal energy with high efficiency. Although various material and structure designs have been reported, high efficiency in solar steam generation usually can be achieved only at concentrated solar illumination. For the first time, 3D printing to construct an all‐in‐one evaporator with a concave structure for high‐efficiency solar steam generation under 1 sun illumination is used. The solar‐steam‐generation device has a high porosity (97.3%) and efficient broadband solar absorption (>97%). The 3D‐printed porous evaporator with intrinsic low thermal conductivity enables heat localization and effectively alleviates thermal dissipation to the bulk water. As a result, the 3D‐printed evaporator has a high solar steam efficiency of 85.6% under 1 sun illumination (1 kW m^?2), which is among the best compared with other reported evaporators. The all‐in‐one structure design using the advanced 3D printing fabrication technique offers a new approach to solar energy harvesting for high‐efficiency steam generation.     

Oriented Arrangement: The Origin of Versatility for Porous Graphene Materials

Macroscopic porous graphene materials composed of graphene sheets have demonstrated their advantageous aspects in diverse application areas. It is essential to maximize their excellent performances by rationally controlling the sheet arrangement and pore structure. Bulk porous graphene materials with oriented pore structure and arrangement of graphene sheets are prepared by marrying electrolyte‐assisted self‐assembly and shear‐force‐induced alignment of graphene oxide sheets, and the super elasticity and anisotropic mechanical, electrical, and thermal properties induced by this unique structure are systematically investigated. Its application in pressure sensing exhibits ultrahigh sensitivity of 313.23 kPa^?1 for detecting ultralow pressure variation below 0.5 kPa, and it shows high retention rate for continuously intercepting dye molecules with a high flux of ≈18.7 L m^?2 h^?1 bar^?1 and a dynamic removal rate of 510 mg m^?2 h^?1.     

Light‐Driven Active Proton Transport through Photoacid‐ and Photobase‐Doped Janus Graphene Oxide Membranes

Biological electrogenic systems use protein‐based ionic pumps to move salt ions uphill across a cell membrane to accumulate an ion concentration gradient from the equilibrium physiological environment. Toward high‐performance and robust artificial electric organs, attaining an antigradient ion transport mode by fully abiotic materials remains a great challenge. Herein, a light‐driven proton pump transport phenomenon through a Janus graphene oxide membrane (JGOM) is reported. The JGOM is fabricated by sequential deposition of graphene oxide (GO) nanosheets modified with photobase (BOH) and photoacid (HA) molecules. Upon ultraviolet light illumination, the generation of a net protonic photocurrent through the JGOM, from the HA‐GO to the BOH‐GO side, is observed. The directional proton flow can thus establish a transmembrane proton concentration gradient of up to 0.8 pH units mm^?2 membrane area at a proton transport rate of 3.0 mol h^?1 m^?2. Against a concentration gradient, antigradient proton transport can be achieved. The working principle is explained in terms of asymmetric surface charge polarization on HA‐GO and BOH‐GO multilayers triggered by photoisomerization reactions, and the consequent intramembrane proton concentration gradient. The implementation of membrane‐scale light‐harvesting 2D nanofluidic system that mimics the charge process of the bioelectric organs makes a straightforward step toward artificial electrogenic and photosynthetic applications.     

Biomass-Derived Hybrid Hydrogel Evaporators for Cost-Effective Solar Water Purification

Solar vapor generation has presented great potential for wastewater treatment and seawater desalination with high energy conversion and utilization efficiency. However, technology gaps still exist for achieving a fast evaporation rate and high quality of water combined with low-cost deployment to provide a sustainable solar-driven water purification system. In this study, a naturally abundant biomass, konjac glucomannan, together with simple-to-fabricate iron-based metal-organic framework-derived photothermal nanoparticles is introduced into the polyvinyl alcohol networks, building hybrid hydrogel evaporators in a cost-effective fashion ($14.9 m⁻² of total materials cost). With advantageous features of adequate water transport, effective water activation, and anti-salt-fouling function, the hybrid hydrogel evaporators achieve a high evaporation rate under one sun (1 kW m⁻²) at 3.2 kg m⁻² h⁻¹ out of wastewater with wide degrees of acidity and alkalinity (pH 2–14) and high-salinity seawater (up to 330 g kg⁻¹). More notably, heavy metal ions are removed effectively by forming hydrogen and chelating bonds with excess hydroxyl groups in the hydrogel. It is anticipated that this study offers new possibilities for a deployable, cost-effective solar water purification system with assured water quality, especially for economically stressed communities.     

Nitrogen‐Superdoped 3D Graphene Networks for High‐Performance Supercapacitors

An N‐superdoped 3D graphene network structure with an N‐doping level up to 15.8 at% for high‐performance supercapacitor is designed and synthesized, in which the graphene foam with high conductivity acts as skeleton and nested with N‐superdoped reduced graphene oxide arogels. This material shows a highly conductive interconnected 3D porous structure (3.33 S cm^?1), large surface area (583 m² g^?1), low internal resistance (0.4 Ω), good wettability, and a great number of active sites. Because of the multiple synergistic effects of these features, the supercapacitors based on this material show a remarkably excellent electrochemical behavior with a high specific capacitance (of up to 380, 332, and 245 F g^?1 in alkaline, acidic, and neutral electrolytes measured in three‐electrode configuration, respectively, 297 F g^?1 in alkaline electrolytes measured in two‐electrode configuration), good rate capability, excellent cycling stability (93.5% retention after 4600 cycles), and low internal resistance (0.4 Ω), resulting in high power density with proper high energy density.