Cellulose Nanofibrils Research Articles

Self-Assembly of Soft and Conformable Broadband Absorbing Nanocellulose-Gold Nanoparticle Composites.

Broadband light-absorbing materials are of large interest for numerous applications ranging from solar harvesting and photocatalysis to low reflection coatings. Fabrication of these materials is often complex and typically utilizes coating techniques optimized for flat and hard materials. Here, we show a self-assembly based strategy for generating robust but mechanically flexible broadband light-absorbing soft materials that can conform to curved surfaces and surface irregularities. The materials were fabricated by adsorbing large quantities of gold nanoparticles (AuNPs) on the nanofibrils of hydrated bacterial cellulose (BC) membranes by tailoring the interaction potential between the cellulose nanofibrils and the AuNPs. The highly efficient self-assembly process resulted in very dense multilayers of AuNPs on the nanofibrils, causing extensive broadening of the localized surface plasmon resonance band and a striking black appearance of the BC membranes. The nanocomposite materials showed an absorptance >96% in both the visible and the near-infrared wavelength range. The AuNP-functionalized BC membranes demonstrated excellent conformability to curved and structured surfaces and could adopt the shape of highly irregular surface structures without any obvious changes in their optical properties. The proposed self-assembly based strategy enables the fabrication of soft and conformable broadband light-absorbing nanocomposites with unique optical and mechanical properties using sustainable cellulose-based materials.

Dialdehyde cellulose nanofibrils/polyquaternium stabilized ultra-fine silver nanoparticles for synergistic antibacterial therapy

Dialdehyde cellulose nanofibrils (DACNF) and Polyquaternium-10 (PQ: chloro-2-hydroxy-3-(trimethylamino) propyl polyethylene glycol cellulose) have become increasingly favored as antibacterial substances due to their advantageous characteristics. DACNF exhibits exceptional mechanical properties and biocompatibility, whereas PQ demonstrates a positive charge that enhances its antibacterial activity. Combined in a DACNF/PQ mixture, they provide an excellent template material for preparing and stabilizing ultra-fine (~ 10.3 nm) silver nanoparticles (AgNPs) at room temperature. Here, the dialdehyde group of DACNF functions as a reducing agent, while the quaternary ammonium of PQ and carboxylate groups of DACNF synergistically helped in-situ generation of AgNPs uniformly. The synthesized nanocomposites, namely PQ@AgNPs, AgNPs@DACNF, and AgNPs@DACNF/PQ, were subjected to comprehensive characterization using various advanced analytical techniques. The films containing AgNPs@DACNF and AgNPs@DACNF/PQ, fabricated via vacuum filtration, exhibited excellent mechanical properties of 9.78 ± 0.21 MPa, and demonstrated superior antibacterial activity against both Escherichia coli and Staphylococcus aureus. Additionally, the silver ion leaching from the prepared composite films was well controlled. The fabricated nanocomposites also effectively inhibited bacterial biofilm formation. It was also found to be highly biocompatible and non-toxic to human skin fibroblast cells. Furthermore, the nanocomposites exhibited enhanced migration of human dermal fibroblasts, suggesting their potential in facilitating wound healing processes.

Fabrication of clickable bamboo-sourced cellulose nanofibrils for diverse surface modifications: Hydrophobicity and fluorescence functionalities

Surface functionalization of cellulose nanofibrils (CNF) is crucial for expanding their practical application. However, most functionalization processes are complicated and laborious. Herein, this work presents a facile surface engineering strategy to create a range of functionalized CNF via thiol-ene click reaction. Initially, clickable CNF was produced by grafting a compound with both carboxylate- and norbornene groups onto bamboo cellulose via norbornene-dicarboxylic anhydride esterification followed by homogenization. The introduction of negatively charged carboxylates facilitated nanofibrillation, resulting in CNF with a diameter of 3 nm and an aspect ratio of up to 600. The introduction of norbornenes enabled diverse functionalization of CNF through click reaction. Subsequently, hexadecanethiol successfully clicked with norbornene-grafting CNF, enhancing its hydrophobicity and dispersion in organic solvents. 7-mercapto-4-methyl coumarin was also able to click with norbornene-grafting CNF, yielding fluorescence-labeled CNF while maintaining excellent aqueous dispersibility. The fluorescence-labeled CNF was demonstrated to be utilized as an eco-friendly sensor for the detection of Fe3+ ions. Additionally, it could be converted into fluorescent films or intelligent inks suitable for anti-counterfeiting purposes. This study demonstrates that the proposed surface engineering strategy provides an effective approach for producing clickable CNF and fabricating cellulosic materials with diverse functionalities that meet the demands of various applications.

Exploring the effects of cellulose sources on silver reduction and the bacterial removal of nanocellulose-based hydrogel beads

With water access challenged, there is a need to develop efficient and sustainable alternatives for water purification. Here, cellulose nanofibrils (CNFs) isolated from three source materials (softwood, soybean hulls and oat straw) were compared for the generation of hydrogels beads, and compared as support and reducing agent for silver nanoparticles formation. The silver-functionalized hydrogel beads (Ag-CNFs) were characterized, and the surface energy and specific surface area were evaluated. Antimicrobial testing was conducted to assess the efficacy of the Ag-CNFs against E. coli. The results showed that the Ag-CNFs had a higher specific surface area and lower surface energy compared with unmodified CNFs. Softwood-based Ag-CNFs exhibited the highest silver content and specific surface area, while the soybean hull based showed the highest hydrophobic character. The silver-functionalized soybean hull beads (Ag-sbCNF) showed the highest efficacy in reducing the growth of bacteria. Overall, this study highlights the potential of silver-functionalized CNFs hydrogel beads as a promising environmentally friendly and sustainable material for water filtration and disinfection. The findings also suggest that lower surface energy of the Ag-CNFs play an important role in their antimicrobial effect on tested water by enabling shorter retention, providing useful insights into the design of future water filtration materials.

Humidity-responsive fiber actuators assembled from cellulose nanofibrils

Fiber actuators, particularly valuable in soft robotics and environmental sensing, are at the forefront of “smart” materials and materials innovation. In this realm, torsional and tensile biofiber actuators, notable for their cost-effectiveness and biodegradability, mark a critical gap in the development of next-generation functional systems and devices. To address this gap, this study showcased moisture-responsive fiber actuators made from cellulose nanofibrils (CNFs). The initial focus of this contribution was on an innovative torsional actuator, which capitalized on the hydrophilic nature of the CNFs filaments produced through wet-spinning processes. These robust filaments, with a mechanical strength of (237.0 ± 10.7) MPa, were twisted to form the torsional actuator. This actuator demonstrated a rapid rotational response, achieving up to 1180 rpm within merely 10 s of exposure to moisture, and maintained high durability over multiple cycles. Building upon this platform, the study continued and aimed to build up a tensile actuator, which ingeniously integrated a supercoiled nylon fiber core within a moisture-sensitive CNFs sheath. This design enhances the structural support and functionality of the actuator. The pursued transition from torsional to tensile actuator demonstrates an iterative and innovative approach in actuator technology, underscoring the versatility and potential of CNFs in the realm of “smart” actuation materials.

Characteristics of cellulose nanofibril films prepared by liquid- and gas-phase esterification processes

Abstract Cellulose nanofibrils (CNFs) are versatile materials, but their sensitivity to humidity affects performance. Esterification with fatty acids enhances the hydrophobicity of CNF films. This study compared gas- and liquid-phase esterification using three fatty acid chlorides at different dosages. Gas-phase esterification minimally affected cellulose crystallinity, maintaining a crystallinity index exceeding 55.8%, whereas liquid-phase esterification significantly reduced crystallinity. Gas-phase esterification achieved hydrophobicity (water contact angle >100°) with less fatty acid chlorides (0.50 eq/OH) compared to liquid-phase esterification (1.00 eq/OH). Tensile strength significantly dropped in the liquid phase (68.4–6 MPa) and up to an 8-fold decrease in the elastic modulus. Conversely, gas-phase esterification maintained tensile strength over 40 MPa, and elastic modulus increased by a minimum of 2.5 times. However, gas-phase esterification resulted in a 5-fold reduction in elongation at break (%). Thermogravimetric analysis indicated a high T max of 362°C for liquid-phase esterified samples and a substantial 24.9% residual weight for gas-phase esterified samples.

Cutting edge technology for wastewater treatment using smart nanomaterials: recent trends and futuristic advancements.

Water is a vital component of our existence. Many human activities, such as improper waste disposal from households, industries, hospitals, and synthetic processes, are major contributors to the contamination of water streams. It is the responsibility of every individual to safeguard water resources and reduce pollution. Among the various available wastewater treatment (WWT) methods, smart nanomaterials stand out for their effectiveness in pollutant removal through absorption and adsorption. This paper examines the application of valuable smart nanomaterials in treating wastewater. Various nanomaterials, including cellulose nanocrystals (CNC), cellulose nanofibrils (CNF), nanoadsorbents, nanometals, nanofilters, nanocatalysts, carbon nanotubes (CNTs), nanosilver, nanotitanium dioxide, magnetic nanoparticles, nanozero-valent metallic nanoparticles, nanocomposites, nanofibers, and quantum dots, are identified as promising candidates for WWT. These smart nanomaterials efficiently eliminate toxic substances, microplastics, nanoplastics, and polythene particulates from wastewater. Additionally, the paper discusses comparative studies on the purification efficiency of nanoscience technology versus conventional methods.

In Vitro Gastrointestinal Digestion of Corn-Oil-in-Water Pickering Emulsions: Influence of Lignin-Containing Cellulose Nanofibrils Loading.

There is a growing trend in incorporating biomass-based engineered nanomaterials into food products to enhance their quality and functionality. The zeta potential, droplet size, microstructure, and content of free fatty acid (FFA) release were determined to investigate the influence of a plant-derived particle stabilizer, i.e., lignin-containing cellulose nanofibrils (LCNFs). Remarkable differences were observed during digestion stages, which were found to be correlated with the concentrations of LCNFs. The gradual FFA release in the small intestine stage from LCNF-coated lipid droplets was monitored over time, with a final lowest release of FFAs amounting to 26.3% in the emulsion containing 20.0% (v/v) of the dispersed phase stabilized by 3 mg/mL of LCNFs. This release can be attributed to the physical barrier at lipid droplet surfaces and the network effect created by the free LCNFs in the continuous phase. This work provides a foundation for the potential application of nature-derived LCNF materials in reducing fat absorbance.

Improving the Concrete Compressive and Flexural Strength with a Low Fraction Addition of Carboxylated Nitro-oxidized Cellulose Nanofibrils from Banana Rachis

Conventionally, concrete strength depends on the bonding interface, especially in hydrated products such as calcium silicate hydrate (CSH). As a result, concrete is sensitive under tensile load. With its unique properties, a low fraction of carboxylated nitro-oxidized cellulose nanofibrils (NOCNF) from the banana rachis is employed to improve the mechanical performance of the concrete nano structurally. Compressive and flexural strength using the NOCNF content at 0, 0.05, and 0.1 wt. % cured in 7 and 28 days were evaluated. Notably, the compressive strength increased by 16% and flexural strength by 13% at 0.1% NOCNF compared to plain concrete after the 28 curing days. A low NOCNF fraction achieved a good, albeit impossible, performance with the microscale fibers. The nanostructured effect was discussed twofold: an excellent interaction between the NOCNF and the hydrated products and the carboxylic groups on the NOCNF surface enhanced the cement hydration. These data are better than the literature based on the small-diameter cellulose nanofibrils without the carboxyl groups. As a sustainable nanocomponent, NOCNF could be a perfect candidate to improve concrete performance under mechanical load.

Enhancing electricity generation from water evaporation through cellulose-based multiscale fibers network

Harvesting energy from the water − solid interface through natural water evaporation provides a promising approach for generating sustainable electricity to power self-powered electronics. Advancing the bio-based hydrovoltaic materials enhances sustainability, with wood as a viable candidate due to the inherent hydrophilic and charged properties. However, current wood-based water evaporation-induced electricity generators (WEIGs) mainly depend on the “top-down” construction strategies. Wherein, the improvement of power density is constrained by the limited structural regulation, nondiverse building blocks, and monolithic enhancement mechanisms. Here, the high-performance wood-based WEIGs based on multiscale fibers network (MFN) are reported by embedding the Ti4O7 nanofibers (T4NF) inside the assemblies of TEMPO-oxidized cellulose nanofibrils (TOCNF) through a “bottom-up” route. Benefiting from the large specific surface area, high surface potential, and photothermal effect of conductive T4NF, the WEIG achieves a high short-circuit current of ∼13.7 μA while delivering ∼0.94 V open-circuit voltage. This work presents an efficient method to boost performance while understanding the impact of functional MFN on water evaporation.

Enhancing anticorrosion performance of metals by incorporating cellulose nanofibrils/α-ZrP composite as nanofiller into water-based coating

The anticorrosion of metals has gain considerable interest in view of economic and environmental issues. Coating protection is one of the most effective and cost-effective methods for anticorrosion of metals. However, the traditional coatings often suffer from many issues such as poor performance or high cost. For the first time, a strategy was proposed by constructing cellulose nanofibrils (CNF)/alpha‑zirconium phosphate (α-ZrP) composite as nanofiller and incorporating into water-based coatings for anticorrosion of metals. The successful coordination of α-ZrP nanosheet and CNF were characterized. The effects of the resultant composite on anticorrosion performance were investigated. The results showed that, the as-prepared coating exhibited superior anticorrosion performance to commercial coatings. The impedance of the test sample coated with the as-prepared coating reached up to 4.38 × 105 Ω when it was immersed in 3.5 % NaCl solution with few corrosions fragmentation on metal surface, exhibiting a favorable long-term anticorrosion performance. Meanwhile, the anticorrosion mechanism was proposed. It is expected that this strategy would provide novel solutions for developing highly efficient water-based anticorrosive coatings of metals.

Can pure cellulose nanofibril films replace polyolefins as water vapor barriers in packaging?

Despite significant research into cellulose nanofibril (CNF) films as substitutes to synthetic plastic materials, commercial applications remain very limited. One major hindrance is the poor water vapor barrier properties of CNF films compared to polyolefins, a critical property for product protection, such as food safety and preservation. To date, it is unknown whether full moisture barrier properties can be achieved with materials made by the assembly of nanofibers and fibrils. A comprehensive understanding of the effect of film structure on water vapor transport properties is required. Here, over 200 films were produced with a wide range of grammages from 30 g/m2 to 580 g/m2 by casting and spray deposition. Their structures were quantified by µCT and SEM and related to their water vapor transmission rates (WVTRs). Porosity and pore connectivity decreased with increasing film grammage, which correlates with the exponential decrease in WVTR. However, the WVTR plateaued at 30 g/m2day, indicating that the known open space and adsorption diffusion mechanisms cannot be fully eliminated by producing high grammage films. Pure cellulose nanofibril films therefore cannot replace polyolefins in packaging applications, requiring modifications such as coating and nanofillers.

Exploiting the Properties of Non-Wood Feedstocks to Produce Tailorable Lignin-Containing Cellulose Nanofibers.

Lignin-containing cellulose nanofibrils (LCNFs) are mainly produced commercially from treated wood pulp, which can decrease some of the carbon-negative benefits of utilizing biomass feedstock. In this work, LCNFs are prepared from non-wood feedstocks, including agricultural residues such as hemp, wheat straw, and flax. These feedstocks allowed for the preparation of LCNFs with a variety of properties, including tailored hydrophobicity. The feedstocks and their subsequent LCNFs are extensively characterized to determine the roles that feedstocks play on the morphology and properties of their resultant LCNFs. The LCNFs were then incorporated into paper handsheets to study their usefulness in papermaking applications, which indicated good potential for the use of wheat straw LCNFs as a surface additive to improve the oil resistance coating.

The effect of nanocellulose and silica filler on the mechanical properties of natural fiber polymer matrix composites

Natural fiber-reinforced polymer matrix composites recently got great attention in biomedical applications due to their inherent characteristics such as biocompatibility, lightweight, and biodegradability. However, natural fiber composites suffer from poor mechanical properties and weak interfacial adhesion. It is well documented that the addition of nanofiller has improved the mechanical properties of different synthetic fibers such as glass and carbon composites. The main objective of this paper is to study nanofillers' effect on the mechanical properties of unidirectional false banana fibers reinforced polymer composites. The filler materials, crystalline nanocellulose fibrils, and crystalline nanosilica particles were extracted from sugarcane bagasse and its byproducts. The composite samples were fabricated by adding the nanofillers in unidirectional natural fibers arranged in four fiber orientations (0°, 0o/90o ±45o, and quasi-isotropic), and their tensile, flexural, compression strength, thermal stability, and void content were measured following ASTM standards. The results revealed that adding nanofillers increased the tensile, flexural, and compressive strengths by 16 % (98.83 Mpa), 11 % (161.60 Mpa), and 23 % (114.62 Mpa), respectively. Similarly, at 0° orientation, the addition of nanoparticles enhances the tensile, bending, and compressive modulus by 30 % (15.43 Gpa), 12 % (13.52 Gpa), and 60 % (42.6 Gpa), respectively. On the other hand, the void content was reduced with the addition of nanofillers. The results also revealed that composites with crystalline nanosilica particle fillers had superior thermal stability compared to crystalline nanocellulose fibril fillers. The overall results of this research give the confidence that nano particle-filled natural fiber composites can be used for bio-based engineering applications, such as prosthetic sockets.

Fluorescent cellulose nanofibrils hydrogels for sensitive detection and efficient adsorption of Cu2+ and Cr6+

Increasing chromium and copper pollution poses a significant threat to the global environment and human health. It is crucial to detect and remove Cu (II) and Cr (VI) from water. Cellulose nanofibrils (CNF)-based hydrogels were a natural, abundant, and biocompatible material that has attracted great attention for bio adsorption applications. In this work, a new fluorescent CNF-based hydrogel (PAA-CNF-W) was prepared for the high-efficiency adsorption and sensitive detection of Cu (II) and Cr (VI). CNF was introduced as a natural backbone to construct a three-dimensional porous structure, which increased the specific surface area and provided additional active sites, exhibiting excellent adsorption properties for Cu (II) (159.24 mg/g) and Cr (VI) (173.87 mg/g). Moreover, the synthesized dansyl chloride derivatives with fluorescent properties were introduced to the hydrogel and formed chelates with the metals leading to fluorescence quenching. PAA-CNF-W hydrogels showed high sensitivity to the detection limit (LOD) of Cu (II) (28.70 mg/L) and Cr (VI) (1.45 mg/L). The kinetic study revealed that pseudo-second order kinetics was the best-fitting model. The Langmuir isotherm was the best adjustment model. The study provides a new idea for efficient detection and removal of Cu (II) and Cr (VI) from wastewater by cellulose materials.

On the determination of charge and nitrogen content in cellulose fibres modified to contain quaternary amine functionality

Research interest in quaternization of cellulose fibres has increased considerably over the past decades. However, there is little or no consensus regarding how to characterize the material in terms of degree of substitution (DS), and the literature suggests a range of different methods focusing on charge determination as well as nitrogen content quantification. This work aims to fill the knowledge gap regarding how the different methods perform in relation to each other, and for what cellulosic systems each method has advantages, disadvantages and even potential pitfalls. FT-IR and NMR measurements are used to establish successful modification and determine the relative number of substituent groups. Another six methods are compared for the determination of the DS of cellulosic fibres and nanofibrils. The methods include Kjeldahl measurements, nitrogen determination by chemiluminescence, determination of molecular nitrogen by the Dumas method, colloidal titration, conductometric titration and polyelectrolyte adsorption. It can be concluded that most techniques investigated are reliable within certain ranges of DS and/or when using appropriate post-treatment of the quaternized material and suitable sample preparation techniques. The results from the present work hence provide recommendations to make an educated choice of method, and experimental protocol, based on the technique at hand.

Enhanced buoyancy and propulsion in 3D printed swimming micro-robots based on a hydrophobic nano-fibrillated cellulose aerogel and porous lead-free piezoelectric ceramics

This paper provides the first demonstration of additively manufactured swimming micro-robots which combine a hydrophobic nanofibrillated cellulose aerogel, to provide long-term buoyancy, with a low acoustic impedance porous piezoelectric ceramic for improved propulsion. The hydrophobic nanocellulose aerogel is shown to exhibit a high and stable contact angle that was maintained for extended periods of time, which facilitates long-term and stable buoyancy of the micro-robot. To quantify the benefits of introducing porosity into the active piezoelectric element, a new analysis model was developed to inform material design and maximize the acoustic propulsion force. Detailed characterisation and modelling of the swimming robots demonstrated that a swimming robot based on a lead-free porous Ba0.85Ca0.15Zr0.1Ti0.9O3 (BCZT) ceramic exhibited a higher acoustic radiation propulsion force and a faster swimming speed compared to a robot fabricated using a dense ceramic element. These benefits were associated with the lower elastic modulus, density and acoustic impedance of the porous piezoelectric material. The lower dielectric constant, reduced device capacitance, and lower resonant frequency of the porous piezoelectric element also significantly reduced the driving current and power requirements of the robot. This work therefore provides new insights on the impact of hydrophobic and acoustically matched piezoelectric materials on the performance of swimming micro-robots, and successfully demonstrates the use of porosity to improve acoustic impedance matching of resonant piezoelectric devices, such as micro-robots and ultrasonic transducers.

Eco-friendly and novel tannin-based wood adhesive enhanced with cellulose nanofibrils grafted by hyperbranched polyamides

Tannin-based adhesives, as a natural biobased adhesive, have the potential to expand their application in wood industry as substitutes for traditional adhesives. In this study, cellulose nanofibrils and hyperbranched polyamides (HBPA) were studied to address the challenges associated with the low crosslinking degree and poor water resistance characteristics of condensed tannin-based wood adhesives. The modification strategy focuses on grafting oxidized cellulose nanofibrils with hyperbranched polyamides through the Schiff base reaction. Comprehensive analyses, including FTIR, XPS, XRD, and TG, confirm the successful binding of oxidized cellulose nanofibrils with hyperbranched polyamides, demonstrating their potential to enhance the properties of tannin adhesives. Furthermore, the investigation about bonding strength, and water resistance of tannin adhesives reveal significant improvements in the mechanical and water resistance properties through this modification strategy. In particular, the maximum wet shear strength is 0.7 MPa, meeting the requirements for Class II plywood. This study provides valuable insights into improving the performance of tannin adhesives, offering promising implications for broader applications and contributing to eco-friendly practices in the wood industry.

Self-assembly of mixed-linkage glucan hydrogels formed following EG16 digestion

Mixed-linkage glucans are major components of grassy cell-walls and cereal endosperm. Recently identified plant endo-β-glucanase from the EG16 family cleaves MLGs with strong specificity towards regions with at least four sequential β(1,4)-linked glucose residues. This activity yields a low molecular-weight MLG with a repeating structure of β(1,3)-linked cellotriose that gels rapidly at concentrations as low as 1.0 % w/v. To understand the gelation mechanism, we investigated the structure and behavior using rheology, microscopy, X-ray scattering, and molecular dynamics simulations. Upon digestion, the material's rheological behavior changes from typical polymeric material to a fibrillar network behavior seen for e.g. cellulose nanofibrils. Scanning electron microscopy and confocal microscopy verifies these changes in micro- and nanostructure. Small-angle X-ray scattering shows in-solution self-assembly of MLG through ~10 nm elemental structures. Wide-angle X-ray scattering data indicate that the polymer association is similar to cellulose II, with dominant scattering at d-spacing of 0.43 nm. Simulations of two interacting glucan chains show that β(1,3)-linkages prevent the formation of tight helices that form between β(1,4)-linked d-glucan chains, leading to weaker interactions and less ordered inter-chain assembly. Overall, these data indicate that digestion drives gelation not by enhancement of interactions driving self-assembly, but by elimination of unproductive interactions hindering self-assembly.

Dual-functional paper-like evaporator for boosting interfacial evaporation synchronized with organic pollutant degradation

Solar-driven interfacial evaporation is a sustainable method to produce freshwater, but volatile organic compounds (VOCs) inevitable accumulate in the condensed water, causing secondary pollution. Herein, paper-like photothermal evaporators were constructed by fixing zeolitic diazoate frameworks-8 derived N-doped carbon with different morphologies on the interwoven cellulose nanofibrils (CNFs) membranes for simultaneous steam generation and organic pollutant degradation. The results showed that the evaporator incorporated porous N-doped carbon with rhombic dodecahedron (NC-RD) into CNFs membranes not only increases the roughness to achieve broad spectrum solar absorption, but also capable of ensuring continuous evaporation of water, and maintaining a sufficient water supply. The NC-RD/CNFs membranes exhibit the high evaporation rate of 1.46 kg·m−2·h−1 under one sun. Meanwhile, N-doped carbon enable photothermal-synergistic peroxymonosulfate (PMS) activation to promote the generation of abundant 1O2 and O2∙– for degradation of methylene blue, tetracycline and phenol. Furthermore, the solar-vapor conversion efficiency and the evaporation rate are stable in a simulated seawater environment with 15 wt% NaCl solution. Importantly, an outdoor NC-RD/CNFs-based device was constructed, which realizes a high evaporation rate of 0.659 kg∙m−2∙h−1 under natural light irradiation for 10 h. The present study highlights that the NC-RD/CNFs membranes successfully coupled interfacial evaporation with PMS based-advanced oxidation processes to provide a subtlety strategy to solve the problem of VOCs accumulation in the evaporation process.