Environmental pollution and sewage surges necessitate effective water purification methods. Solar interfacial evaporation offers a promising solution, which needs advancements in salt resistance, efficiency, and stability. Herein, inspired by the structure of wood, the unidirectional freeze-drying method was used to develop the vertically aligned channels and antioil-fouling poly(vinyl alcohol)-CNTs-waste carton fiber@polydopamine (PVA-CNTs-WCF@PDA) aerogel for desalination and wastewater treatment. The anisotropic three-dimensional porous structure of the aerogel enables it to rapidly transport water to the evaporation interface and resist salt deposition. Meanwhile, its unique structure is combined with CNTs and PDAs with excellent broadband spectral absorption capacity because the composite aerogels can interact with water molecules to reduce their water vaporization enthalpy. The composite aerogel shows an excellent photothermal evaporation rate (2.626 kg m-2 h-1) and efficiency (94.24%) under one-sun irradiation. Additionally, the composite aerogel interface evaporator can conduct 10 consecutive evaporations in 3.5% brine, indicating that it has the ability to desalination. Finally, it is also used to purify an oil-in-water emulsion and mine wastewater. It can be seen that there are no obvious oil droplets in the treated emulsion and that the treatment effect of mine wastewater reaches 89.13%. The composite aerogel showed excellent application prospects in the field of water purification.

With the increasing demand for effective methods to address environmental pollution, piezocatalysis has emerged as a promising approach for pollutant degradation under mechanical energy. However, the development of highly efficient piezocatalytic materials remains a challenge. This study aimed to increase the piezocatalytic activity of bismuth titanate (Bi4Ti3O12) by modifying it with zinc stannate (ZnSnO3) nanocubes. The composite catalysts were synthesized using a straightforward deposition and calcination process. The calcination process ensured the tight adhesion of ZnSnO3 nanocubes to the Bi4Ti3O12 surface, while facilitating strong interactions between ZnSnO3 and Bi4Ti3O12, which enhanced electron transfer and heterojunction structure formation. Band structure analysis indicated that Bi4Ti3O12 has higher conduction band and valence band potentials than ZnSnO3, forming a type-II heterojunction. Bi4Ti3O12 possesses a higher Fermi level than ZnSnO3, resulting in interfacial electron drift and formation of a built-in electric field, which further promotes the directional transfer and separation efficiency of charge carriers within the composite catalyst. This hypothesis was confirmed by surface photovoltage spectroscopy, piezoelectric current response, and electrochemical analysis. Consequently, the ZnSnO3/Bi4Ti3O12 composite exhibited significantly improved piezocatalytic performance in RhB degradation, achieving a degradation efficiency of 80 % within 90 min under ultrasonic vibration. The degradation rate of the optimal sample was 8.2 times that of Bi4Ti3O12 and 6.3 times that of ZnSnO3. Additionally, experiments to detect reactive species were conducted to elucidate the mechanism behind the piezocatalytic RhB degradation. Holes and hydroxyl radicals were the main reactive species. This study may offer new insights into the design of efficient piezocatalytic materials.

The main pressing problems should be solved for heterogeneous catalysts in activation of peroxymonosulfate (PMS) are sluggish mass transfer kinetics and low intrinsic activity. Here, oxygen vacancies (Vo)-rich of Co3O4 nanosheets were anchored on the superficies of spirulina-based reduced graphene oxide-konjac glucomannan (KGM) aerogel (R-Co3O4-x/SRGA). The porous structure and superhydrophilicity conferred by KGM maximized the diffusion and transport of reactant. More interestingly, R-Co3O4-x/SRGA came true self-suspension rather than conventional self-floating without the aid of external force, maximizing space utilization and facilitating catalysts recovery. Anchored R-Co3O4-x nanosheets acted as "engines" to drive the reaction. Density functional theory (DFT) manifested Vo was capable of breaking the symmetry of the electronic structure of Co3O4. The formation of asymmetric active sites (Vo) was revealed to modulate the d-band center, enhanced affinity for PMS, and promoted evolution of high-valent cobalt-oxo (Co(IV)=O) species. R-Co3O4-x/SRGA achieved complete removal of sulfamethoxazole (SMX) within 12 min. Furthermore, R-Co3O4-x/SRGA demonstrated exceptional stability in the presence of various environmental interference factors and continuous flow device. This insightful work cleverly integrates the macroscopic design of structure, and the microscopic regulation of active sites is expected to open up new opportunities for the development of water treatment.

Recently, the solar-driven interfacial evaporation desalination has attracted more and more attentions due to the advantages of low cost, zero energy consumption, and high water purification rate, etc. One of the bottlenecks of this emerging technique lies in a lack of simple and low-cost ways to construct three-dimensional (3D) hierarchical microstructures for photothermal membranes. To this end, a two-step strategy is carried out by combining surface functionalization with substrate engineering. Firstly, a silane coupling agent 3-aminopropyltriethoxysilane (APTES) is grafted onto an ideal photothermal material of Ti3C2Tx MXene, to improve the nanochannel sizes and hydrophilicity, which are attributed to enlarged interspaces of MXene and introduced hydrophilic group e.g., -NH2 and -OH, respectively. Secondly, a low-cost and robust nonwoven fiber (NWF) substrate, which has a 3D micron-sized mesh structure with interlaced fiber stacks, is employed as the skeleton to load enough APTES-grafted MXene by a simple soaking method. Benefited from above design, the Ti3C2Tx-APTES/NWF composite membrane with a 3D hierarchical structure shows enhanced light scattering and utilization, water transport and vapor escape. A remarkable evaporation rate of 1.457 kg m-2 h-1 and an evaporation efficiency of 91.48 % are attained for a large-area (5 × 5 cm2) evaporator, and the evaporation rate is further increased to 1.672 kg m-2 h-1 for a small-area (2 × 2 cm2) device. The rejection rates of salt ions and heavy metal ions are higher than 99 % and 99.99 %, respectively, and the removal rates of organic dye molecules are nearly to 100 %. Besides, the composite photothermal membrane exhibits great stabilities in harsh conditions such as high salinities, long cycling, large light intensities, strong acid/alkali environments, and mechanical bending. Most importantly, the photothermal membrane shows a considerable cost-effectiveness of 89.4 g h-1/$. Hence, this study might promote the commercialization of solar-driven interfacial evaporation desalination by collaboratively considering surface modification and substrate engineering for MXene.

Spent coffee grounds are recognized as a green and sustainable resource of cellulose nanofiber (CNF), which can further form aerogels with rGO for solar-driven interfacial desalination via directional freezing technology. The vertically arranged channels provide better photothermal conversion performance and salt tolerance of rGO/CNF aerogels. Their max evaporation rate can reach to 2.729 kg·m-2·h-1 under natural sunlight. In terms of long-term application (10 days), the aerogels exhibit a stable evaporation property in outdoor environments. The optimum daily average water yield is 15.00 L·m-2, which can fulfill the daily water requirement of six people.

Reverse water gas shift (RWGS) reaction is an intriguing strategy to realize carbon neutrality, however, the endothermic process usually needs high temperature that supplied by non-renewable fossil fuels, resulting in secondary energy and environmental issues. Photothermal catalysis are ideal substitutes for the conventional thermal catalysis, providing that high reaction efficiency is achievable. Two-dimensional (2D) materials are highly active as RWGS catalysts, however, their industrial application is restricted by the preparation cost. In this study, a series of 2D Co-based catalysts for photothermal RWGS reaction with tunable selectivity were prepared by self-assembly method based on cheap amylum, by integrating the 2D catalysts with our homemade photothermal device, sunlight driven efficient RWGS reaction was realized. The prepared 2D Co0.5Ce0.5Oxexhibited a full selectivity toward CO (100%) and could be heated to 318 °C under 1 kW m-2irradiation with the CO generation rate of 14.48 mmol g-1h-1, pointing out a cheap and universal method to prepare 2D materials, and zero consumption CO generation from photothermal RWGS reaction.

The present study was done to investigate and compare the photocatalytic and antibacterial activity of two in situ Manganese doped ternary nanocomposites. The dual ternary hybrid systems comprised Mn-doped Ag₂WO₄ coupled with MoS₂-GO and Mn-doped MoS₂ coupled with Ag₂WO₄-GO. Both hierarchical alternate Mn-doped ternary heterojunctions formed efficient plasmonic catalysts for wastewater treatment. The novel nanocomposites were well-characterized using XRD, FTIR, SEM-EDS, HR-TEM, XPS, UV-VIS DRS, and PL techniques confirming the successful insertion of Mn⁺² ions in respective host substrates. The bandgap of the ternary nanocomposites evaluated by the tauc plot showed them visible light-active nanocomposites. The photocatalytic ability of both Mn-doped coupled nanocomposites was investigated against the dye methylene blue. Both ternary nanocomposites showed excellent sunlight harvesting ability for dye degradation in 60 min. The maximum catalytic efficiency of both photocatalysts was obtained at a solution pH value of 8, photocatalyst dose and oxidant dose of 30 mg/100 mL and 1 mM for Mn-Ag₂WO₄/MoS₂-GO, 50 mg/100 mL, 3 mM for Mn-MoS₂/Ag₂WO₄-GO keeping IDC of 10 ppm for all photocatalysts. The nanocomposites showed excellent photocatalytic stability after five successive cycles. The response surface methodology was used as a statistical tool for the evaluation of the photocatalytic response of several interacting parameters for dye degradation by ternary composites. The antibacterial activity was determined by the inactivation of gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli) bacteria by support-based doped ternary hybrids.

Constructing visible-light driven semiconductor heterojunction with high redox bifunctional characteristics is a promising approach to deal with the increasingly serious environmental pollution problems, especially the coexistence of organic/heavy metal pollutants. Herein, a simple in-situ interfacial engineering strategy for the fabrication of 0D/3D hierarchical Bi₂WO₆@CoO (BWO) heterojunction with an intimate contact interface was successfully developed. The superior photocatalytic property was reflected not only in individual tetracycline hydrochloride (TCH) oxidation or Cr(VI) reduction, but also in their simultaneous redox reaction, which could be predominantly attributed to the outstanding light-harvesting, high carrier separation efficiency and enough redox potentials. In the simultaneous redox system, TCH acted as a hole-scavenger for Cr(VI) reduction, replacing the additional reagent. Interestingly, superoxide radical (·O₂^-) played the role as oxidants in TCH oxidation but as electron transfer media in Cr(VI) reduction. On account of the interlaced energy band and tight interfacial contact, a direct Z-scheme charge transfer model was established, which was verified by the active species trapping experiments, spectroscopy, and electrochemical tests. This work provided a promising strategy for the design/fabrication of highly efficient direct Z-scheme photocatalysts in environmental remediation.

Although many concerns have been put into photocatalytic hydrogen peroxide (H₂O₂) production, multifunctional catalysis suitable for continuously in-situ H₂O₂ consumption in the field has rarely been investigated. Herein, Cu⁰@CuO_x@nitrogen-doped graphitic carbon (Cu⁰@CuO_x-NC) decorated Zn₂In₂S₅ was successfully prepared for in-situ production and activation H₂O₂, which could achieve effectively photocatalytic self-Fenton degradation of tetracycline (TC). Under visible light irradiation, 5wt% Cu⁰@CuO_x-NC/Zn₂In₂S₅ (CuZS-5) efficiently generated a high yield of H₂O₂ (0.13 mmol L^-1), and Cu⁰@CuO_x-NC could in-situ consume H₂O₂ to generate hydroxyl radicals (•OH), accelerating the oxidation of TC. As a result, the 5 wt% Cu⁰@CuO_x-NC/Zn₂In₂S₅ degraded about 89.3% of TC within 60 min, and the cycle experiments also exhibited sufficient stability. This study achieves a delicate combination of in-situ production and activation of H₂O₂, which is regarded as a promising strategy to eco-friendly promote pollutant degradation in wastewater.

In this work, spherical photocatalytic floaters were fabricated by depositing TiO₂:Bi (TBi) particles on polypropylene (PP) spheres (recycled from beer cans). These particles were deposited on the sphere (TBi-sphere) by the spray coating technique and evaluated their performance for the photocatalytic degradation of 2,4,6-trichlorophenol (2,4,6-TCP) herbicide. SEM images demonstrated that the BTi powders consisted in conglomerated grains with sizes of 20-80 nm and the analysis by X-ray diffraction confirmed the presence of rutile and anatase phases in the BTi. The photocatalytic experiments showed that the TBi and TBi-sphere produced maximum degradation of 90 and 97% for 2,4,6-TCP, respectively, after 4 h under UV-Vis light. The photocatalytic powders/composites were reused 3 times and the loss of degradation efficiency was 3 and 16% for the TBi powder and TBi-sphere, respectively. This means that the TBi-sphere is more stable for the continuous degradation of the 2,4,6-TCP contaminant. The TiO₂:Bi powder was compared with the commercial TiO₂ (P25) and found that the TiO₂:Bi powder had higher light absorption (≈42%) and higher surface area (≈105%) than the P25. Therefore, the degradation percentage for the 2,4,6-TCP was 52% higher in the sample doped with Bi. Also, scavenger experiments were carried out and found that the main oxidizing agents produced for the degradation of 2,4,6-TCP were •OH^- radicals and •O₂^- anions. Other species such as h⁺ were also produced at lower amount. Hence, our results demonstrated that spherical/floatable photocatalytic composites are a viable option to remove herbicide residuals from the water, which is of interest in water-treatment-plants.