Self-Floating Carbon Nanotube Membrane on Macroporous Silica Substrate for Highly Efficient Solar-Driven Interfacial Water Evaporation

Self-Healing Hydrophilic Porous Photothermal Membranes for Durable and Highly Efficient Solar-Driven Interfacial Water Evaporation

A high-efficiency solar water evaporation-photocatalysis system achieved by manipulating surface wettability and constructing heterojunction

An anion-counterion strategy is proposed to construct organic mono-radical charge-transfer cocrystals for near-infrared photothermal conversion and solar-driven water evaporation. Ionic compounds with halogen anions as the counterions serve as electron donors, providing the necessary electrons for efficient charge transfer with unchanged skeleton atoms and structures as well as the broad red-shifted absorption (200-2000 nm) and unprecedented photothermal conversion efficiency (~90.5 %@808 nm) for the cocrystals. Based on these cocrystals, an excellent solar-driven interfacial water evaporation rate up to 6.1±1.1 kg ⋅ m-2 ⋅ h-1 under 1 sun is recorded due to the comprehensive evaporation effect from the cocrystal loading in polyurethane foams and chimney addition, such performance is superior to the reported results on charge-transfer cocrystals or other materials for solar-driven interfacial evaporation. This prototype exhibits the great potential of cocrystals prepared by the one-step mechanochemistry method in practical large-scale seawater desalination applications.

Nano-structured urchin-like photothermal covalent organic frameworks for efficient Solar-Driven interfacial water evaporation

Herein, a bioinspired metal-organic framework (MOF) cocrystal produced from the co-assembly of a MOF [Ni3(hexaiminobenzene)2, Ni3(HIB)2] and p-chloranils (CHLs) is reported. Because of the 2D conjugation nature and the formation of persistent anion radicals, this cocrystal shows an excellent photothermal property, and is further used as an absorber in solar-driven interfacial water evaporation. The solar-driven interfacial water evaporation rate (4.04 kg m-2 h-1) is among the best compared with those of previously reported photothermal materials. Molecular dynamics simulation results suggested that the rotating of the CHL molecules relative to the MOF planes tuned the pore size to enable the ultra-fast water transporting, and thus ultra-high water transporting rates (1.11 × 1011 and 3.21 × 1011 H2O s-1 channel-1 at 298.2 and 323.0 K, respectively) for layered cocrystal structures, that are much higher than that of aquaporins (≈1.1 × 1010 H2O s-1 channel-1 at 298.2 K), are observed. The superior solar-driven water evaporation performance is thus attributed to the synergistic effect of the ultra-fast water transporting pores together with the excellent photothermal property of the cocrystal. This research provided a biomimetic strategy of rational design and production of charge transfer cocrystals to modulate their pores and photothermal properties for solar-driven interfacial water evaporation.

Co nanoparticles modified N-doped carbon nanosheets array as a novel bifunctional photothermal membrane for simultaneous solar-driven interfacial water evaporation and persulfate mediating water purification

In recent years, solar-driven photothermal water evaporation technology for seawater desalination and wastewater treatment has developed rapidly, which is of great significance for addressing the issue of freshwater scarcity. However, due to the high costs associated with the manufacturing, maintenance, and operation of such devices, their application remains challenging in remote and resource-scarce regions. Due to its excellent light absorption capability in the near-infrared region, high hydrophilicity, and stable chemical properties, coupled with the low cost of recycling waste carbonized polyphenylene sulfide, this material is an excellent choice as a photothermal material for solar-driven water evaporation devices. Ordinary wood in nature usually has a highly regenerative porous structure, which is a natural water transport channel that facilitates the transport of water from the bottom to the top, allowing it to be rapidly converted into vapor. Based on this characteristic, this article innovatively proposes to prepare waste polyphenylene sulfide from porous carbonized materials (KCP) as the photothermal conversion material for novel photothermal water evaporation devices, achieving solar-driven water evaporation. This material efficiently facilitates the conversion between solar and thermal energies and exhibits excellent hydrophilicity, thereby enabling the rapid utilization of absorbed solar energy for water evaporation on the surface of the evaporator. In this study, a porous carbonized polyphenylene sulfide photothermal water evaporator (KCP-wood) was fabricated by using freeze-drying and in situ coating to load the photothermal conversion material onto a wood substrate. Under simulated one-sun irradiation, this evaporator achieved a water evaporation rate of 2.41 kg m-2 h-1 and a photothermal conversion efficiency of 91.3%. Additionally, a systematic study was conducted on the photothermal performance of various light-water evaporators, encompassing photothermal conversion efficiency, stability, thermal conductivity, and anti-fouling capabilities. Finally, the practical performance of the light-water evaporator under various environmental conditions was validated, demonstrating its excellent stability and durability. It is capable of effectively applying to high-efficiency water resource utilization and solar energy conversion fields.

Latest development in salt removal from solar-driven interfacial saline water evaporators: Advanced strategies and challenges

Freshwater scarcity remains a critical global challenge, prompting the development of sustainable solutions like solar-driven interfacial water evaporation technology. Here, we present a scalable fabrication method for porous monolithic polymer evaporators through olefin metathesis polymerization coupled with NaCl templating. The large-area evaporator (800 × 600 mm²) incorporates amine-capped aniline trimer (ACAT) as a photothermal component within a dicyclopentadiene (DCPD)/cyclooctene (COE) polymer matrix, enabling efficient solar energy absorption and water transport. The optimized SDIE PDCPD-25%COE-10%ACAT exhibits notable performance in seawater desalination, wastewater treatment, and lithium salt enrichment. Under 1 sun irradiation, it achieves a pure water evaporation rate of 3.64 kg m⁻² h⁻¹ with a solar-thermal conversion efficiency of 96.7%, reflecting high energy utilization efficiency. Outdoor experiments under natural sunlight further confirm its operational feasibility, yielding an evaporation rate of 3.33 kg m⁻² h⁻¹. This work provides a viable route for the large-scale implementation of photothermal water treatment technologies, contributing to sustainable freshwater production and resource recovery.

Economic and environmental protection high efficiency solar steam generator: Carbonized starch with porous structure

Enhanced waste water purification performance of solar-driven interfacial water evaporation through the integration of electrocatalysis

A self-floating photothermal membrane with simultaneous mechanical stability and antibacterial activity is facilely prepared for efficient solar-driven interfacial water evaporation.

Thermally localized solar-driven water evaporation (SWE) in recent years has increasingly been developed due to the potential of cost-efficient freshwater production from small-scale portable devices. In particular, the multistage SWE has attracted much attention as the systems possess mostly a simple foundational structure and high solar-to-thermal conversion output rates, enough to produce freshwater from 1.5 L m−2h−1 (LMH) to 6 LMH. In this study, the currently designed multistage SWE devices were reviewed and examined based on their unique characteristics as well as their performances in freshwater production. The main distinguishing factors in these systems were the condenser staging design and the spectrally selective absorbers either in a form of high solar absorbing material, photovoltaic (PV) cells for water and electricity co-production, and coupling of absorber and solar concentrator. Other elements of the devices involved differences such as the direction of water flow, the number of layers constructed, and the materials used for each layer of the system. The key factors to consider for these systems include the heat and mass transport in the device, solar-to-vapor conversion efficiency, gain output ratio (representing how many times the latent heat has been reused), water production rate/number of stages, and kWh/number of stages. It was evident that most of the studied devices involved slightly different mechanisms and material compositions to draw out higher efficiency rates from the current limitations. The reviewed designs showed the ability to be adopted into small-scale solar desalination allowing for accessibility of sufficient freshwater in needing regions.

Solar-driven water evaporation is of great importance for freshwater production via solar distillation and has attracted growing attention recently by the development of heat localization strategies. Yet, when polluted water is used as the source water, solar-driven water evaporation might further deteriorate the pollution. In this study, we report the facile preparation of multifunctional Ag3PO4-reduced graphene oxide (Ag3PO4-rGO) nanocomposite-coated textiles for clean water production by solar-driven water evaporation, photocatalysis, and disinfection. The multifunctional textiles are obtained through coating Ag3PO4-rGO nanocomposites onto cotton textile substrates. The resulting textile can float on the water surface, absorb solar light, and convert it into heat, enhancing the water surface temperature and promoting water evaporation. We show that with Ag3PO4-rGO nanocomposite-coated textiles on the water surface, a high water evaporation rate of 1.31 kg/(m2 h) can be reached under solar light irradiation. Furthermore, the textiles can simultaneously decompose organic dyes and disinfect pathogenic microbes in water, purifying the raw water during solar-driven water evaporation. Such an all-in-one multifunctional textile provides a facile yet sustainable strategy for freshwater production.

Hierarchical Cu dendrites@ CuO multifunctional nanowire mesh for solar-thermal clean water production