Benzyl Acrylate Research Articles

The Valence-Dependent Activity of Colloidal Molecules as Ice Recrystallization Inhibitors.

Inspired by advances in cryopreservation techniques, which are essential for modern biomedical applications, there is a special interest in the ice recrystallization inhibition (IRI) of the antifreeze protein (AFPs) mimics. There are in-depth studies on synthetic materials mimicking AFPs, from simple molecular structure levels to complex self-assemblies. Herein, we report the valence-dependent IRI activity of colloidal organic molecules (CMs). The CMs were prepared through polymerization-induced particle-assembly (PIPA) of the ABC-type triblock terpolymer of poly(acryloxyethyl trimethylammonium chloride)-b-poly(benzyl acrylate)-b-poly(diacetone acrylamide) (PATAC-b-PBzA-b-PDAAM) at high monomer conversions. Stabilized by the cationic block of PATAC, the strong intermolecular H-bonding and incompatibility of the PDAAM block with PBzA contributed to the in situ formation of Janus particles (AX1) beyond the initial spherical seed particles (AX0), as well as the high valency clusters of linear AX2 and trigonal AX3. Their distribution was controlled mainly by the polymerization degrees (DPs) of PATAC and PDAAM blocks. IRI activity results of the CMs suggest that the higher fraction of AX1 results in the better IRI activity. Increasing the fraction of AX1 from 27% to 65% led to a decrease of the mean grain size from 39.8% to 10.9% and a depressed growth rate of ice crystals by 58%. Moreover, by replacing the PDAAM block with the temperature-responsive one of poly(N-isopropylacrylamide) (PNIPAM), temperature-adjustable IRI activity was observed, which is well related to the reversible transition of AX0 to AX1, providing a new idea for the molecular design of amphiphilic polymer nanoparticle-based IRI activity materials.

Strong and Thermo-Switchable Gel Adhesion Based on UCST-Type Phase Transition in Deep Eutectic Solvent.

It remains a great challenge to achieve strong and reversible hydrogel adhesion. Hydrogel adhesives also suffer from poor environmental stability due to dehydration. To overcome these problems, here reversible adhesive gels are designed using a new switching mechanism and new solvent. For the first time, the study observes UCST (upper critical solution temperature)-type thermosensitive behaviors of poly(benzyl acrylate) (PBnA) polymer and gel in menthol:thymol deep eutectic solvents (DESs). The temperature-induced phase transition allows adjusting cohesive force, and hence adhesion strength of PBnA gels by temperature. To further improve the mechanical and adhesion properties, a peptide crosslinker is used to allow energy dissipation when deforming. The resulting eutectogel exhibits thermal reversible adhesion with a high switching ratio of 14.0. The adhesion strength at attachment state reaches 0.627MPa, which is much higher than most reversible adhesive hydrogels reported before. The low vapor pressure of DES endows the gel excellent environmental stability. More importantly, the gel can be repeatedly switched between attachment and detachment states. The strong and reversible gel adhesive is successfully used to design soft gripper for the transport of heavy cargos and climbing robot capable of moving on vertical and inverted surface in a manner similar to gecko.

Synthesize uniform ZrO2 NPs by non-coordination solvents and modification for high refractive film

Zirconia nanoparticles (ZrO2 NPs) are considered promising functional materials due to their high refractive index, thermal stability, and relatively wide bandgap. They can be particularly valuable when blended with monomer resins to create transparent composite materials with tunable refractive indices. However, the challenge of synthesizing uniformly sized and transparently dispersible ZrO2 NPs in organic resin monomers has been an ongoing research problem. In this study, we proposed an improved method based on an existing synthesis route for the production of ZrO2 NPs. We employed a sol-gel approach and introduced a simple yet effective strategy to synthesize ZrO2 NPs. Using high-boiling non-coordinating solvent squalane to adjust the concentration of oil amine ligands in the solution, helped to balance the nucleation and growth of ZrO2, thereby improving the size uniformity of ZrO2 NPs. In addition, the addition of sodium hydroxide (NaOH) to the reaction system effectively promoted the crystal growth of ZrO2 without affecting its crystal structure and crystallinity. Simultaneously, this addition significantly reduced the content of surface oleylamine (OAm) ligands. Finally, ZrO2 was modified using 2-Ethylhexanoic acid (EHA) and 3-methacryloxypropyltrimethoxysilane (KH-570), achieving successful transparent dispersion within the high refractive index acrylic monomer, benzyl acrylate (BZA). In-situ polymerization was used with a UV initiator to produce a refractive index continuously tunable BZA/ZrO2 composite film.

Photorefractivity and photocurrent dynamics of triphenylamine-based polymer composites

The photorefractive properties of triphenylamine polymer-based composites with various composition ratios were investigated via optical diffraction, response time, asymmetric energy transfer, and transient photocurrent. The composite consisted of a photoconductive polymer of poly((4-diphenylamino)benzyl acrylate), a photoconductive plasticizer of (4-diphenylamino)phenyl)methanol, a sensitizer of [6,6]-phenyl-C61-butyric acid methyl ester, and a nonlinear optical dye of (4-(azepan-1-yl)-benzylidene)malononitrile. The photorefractive properties and related quantities were dependent on the composition, which was related to the glass transition temperature of the photorefractive polymers. The quantum efficiency (QE) of photocarrier generation was evaluated from the initial slope of the transient photocurrent. Transient photocurrents were measured and showed two unique peaks: one in the range of 10−4 to 10−3 s and the other in the range of 10−1 to 1 s. The transient photocurrents was well simulated (or reproduced) by the expanded two-trapping site model with two kinds of photocarrier generation and recombination processes and two different trapping sites. The obtained photorefractive quantity of trap density was significantly related to the photoconductive parameters of QE.

Correlation between the Chemical Structure of (Meth)Acrylic Monomers and the Properties of Powder Clear Coatings Based on the Polyacrylate Resins.

This paper presents studies on the influence of the chemical structure of (meth)acrylic monomers on the properties of powder coatings based on polyacrylate resins. For this purpose, a wide range of monomers were selected-2-hydroxyethyl methacrylate (HEMA), methyl methacrylate (MMA), n-butyl acrylate (nBA), tert-butyl acrylate (tBA), dodecyl acrylate (DA), ethyl acrylate (EA) and benzyl acrylate (BAZ)-for the synthesis of the polyacrylate resin. The average molecular mass and molecular mass distribution of the synthesized resins were measured by gel permeation chromatography (GPC). The glass transition temperature (Tg) and viscosity of polyacrylate resins were determined by using differential scanning calorimetry (DSC) and a Brookfield viscometer. These parameters were necessary to obtain information about storage stability and behavior during the application of powder clear coatings. Additionally, DSC was also used to checked the course of the low-temperature curing reaction between the hydroxyl group contained in the polyacrylate resin and the blocked polyisocyanate group derived from a commercial agent such as Vestanat B 1358/100. The properties of the cured powder clear coatings were tested, such as: roughness, gloss, adhesion to the steel surface, hardness, cupping, scratch resistance, impact resistance and water contact angle. The best powder clear coating based on the polyacrylate resin L_HEMA/6MMA/0.5nBA/0.5DA was characterized as having good scratch resistance (550 g) and adhesion to the steel surface, a high water contact angle (93.53 deg.) and excellent cupping (13.38 mm). Moreover, its crosslinking density (CD) and its thermal stability was checked by using dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA).

Iron Heme Enzyme-Catalyzed Cyclopropanations with Diazirines as Carbene Precursors: Computational Explorations of Diazirine Activation and Cyclopropanation Mechanism.

The mechanism of cyclopropanations with diazirines as air-stable and user-friendly alternatives to commonly employed diazo compounds within iron heme enzyme-catalyzed carbene transfer reactions has been studied by means of density functional theory (DFT) calculations of model systems, quantum mechanics/molecular mechanics (QM/MM) calculations, and molecular dynamics (MD) simulations of the iron carbene and the cyclopropanation transition state in the enzyme active site. The reaction is initiated by a direct diazirine-diazo isomerization occurring in the active site of the enzyme. In contrast, an isomerization mechanism proceeding via the formation of a free carbene intermediate in lieu of a direct, one-step isomerization process was observed for model systems. Subsequent reaction with benzyl acrylate takes place through stepwise C-C bond formation via a diradical intermediate, delivering the cyclopropane product. The origin of the observed diastereo- and enantioselectivity in the enzyme was investigated through MD simulations, which indicate a preferred formation of the cis-cyclopropane by steric control.

A novel pour point depressant with diesel cold-flow properties: Performance evaluation of benzene-containing ternary copolymers

The addition of pour point depressants (PPDs) represents the most direct and efficient approach for improving the cold-flow properties of diesel. Nevertheless, the high doses of additives have consistently been a constraining factor. To address this challenge, the study synthesized tetradecyl methacrylate–N-hydroxymethacrylamide–benzyl acrylate (C14MC–NMA–BA), tetradecyl methacrylate–N-hydroxymethacrylamide–4-pentenoic acid benzyl ester (C14MC–NMA–PB), and tetradecyl methacrylate–N-hydroxymethacrylamide–10-undecenoic acid benzyl ester (C14MC–NMA–UB) at various molar ratios (1:1:1, 5:1:1, 10:1:1, 15:1:1, and 20:1:1) as PPDs for diesel. The aim of these PPDs is to efficiently improve the cold-flow properties of diesel at low doses. The cold filter plugging point (CFPP) and solidification point (SP) of diesel were tested before and after treatment with PPDs. The results confirmed that C14MC–NMA–UB with longer carbon chains exhibited superior performance compared to C14MC–NMA–PB and C14MC–NMA–BA. Considering both cost-effectiveness and performance metrics, 400 ppm C14MC–NMA–UB (5:1:1) was identified as the optimal choice for significantly enhancing diesel cold-flow properties, leading to reductions of CFPP and SP by 11 °C and 25 °C, respectively. Furthermore, the study delved into the inhibitory mechanisms of PPDs by examining the crystallization behavior of diesel at low temperatures, utilizing techniques such as differential scanning calorimetry, viscosity-temperature profiles, and polarized optical microscopy.

Adsorption Kinetics of Poly(benzyl acrylate) Chains onto Alumina Interface during the Flow-Driven Translocation through Cylindrical Nanochannels.

In this work, the adsorption kinetics of the PBAN/AAO system under flushing condition has been investigated, where PBAN and AAO represent poly(benzyl acrylate) and anodic alumina oxide (AAO, average pore radius R0 ≈ 10 nm) nanochannel, respectively. Our specially designed double-pump flushing system is proved to eliminate the overshoot phenomenon and in situ monitor transmembrane pressure (ΔP) as a function of flushing time (t) and flow rate (Q), which gives the effective pore radius (R), cross-sectional coverage factor (χ = [1 - (R/R0)2]), and characteristic ratio (rc) of the increments of χ during each adsorption/desorption cycle at a given bulk solution concentration (Cbulk). Our findings include: (1) by gradient increasing Cbulk from 10 to 200 mg/L at Q = 10 mL/h, the shortest PBA40 displays a saturation adsorption behavior when Cbulk ≥ 80 mg/L and t ≥ 2000 s, which agrees well with the prediction of blob model, whereas for the longer PBAN chains, the chain length (N) and concentration-dependent adsorption tendency get stronger as N increases from 40 to 620 at t ≥ 2000 s, in particular, R/R0 ∼ N-0.20 is observed at Cbulk = 140 mg/L; (2) by focusing on the platform χ in the saturation adsorption regime (χsat), the longer PBAN displays a stronger adsorption trend with partially reversible feature at Q = 5.0 mL/h, namely, as N increases from 40 to 620, χsat increases from 0.15 to 0.83 at Cbulk = 100 mg/L, where rc changes from 0.25 ± 0.10 to 0.80 ± 0.10 as the adsorption/desorption flushing cycle increases from 1 to 8 at Cbulk = 100 mg/L; (3) by further assuming a solvent nonpenetrating and nondraining adsorption layer, χsat determined in the case of curved surface can be comparable to the physical meaning of adsorption thickness (Δad) in the case of flat-surface adsorption, and the fitting result indicates χsat ∼ Δad ∼ N0.58, falling between Δad ∼ N1/2 and Δad ∼ N1.0 predicted by the mean-field and scaling theories for real multichain adsorption, respectively. Overall, the present work not only clarifies some controversies but also provides unambiguous evidence supporting the existence of tightly adsorbed internal and loosely adsorbed external layers.

Polymeric Surfactants Bearing Divalent Carboxy Pendants for Stable Color Dispersions with High Redispersibility

Inkjet printing of ink requires dyes or pigments insoluble in water but uniformly dispersing as fine particles for a long period. In addition, redispersibility after solidification by solvent vaporization around the jetting heads is also important for performance. In this study, thus, a series of amphiphilic copolymers were prepared for a dispersant of inkjet using reversible addition fragmentation chain-transfer copolymerization of styrene (St), benzyl acrylate (BnA), and phenoxyethyl acrylate (PEA) as a hydrophobic monomer with acrylic acid (AA) and itaconic acid (IA) as a hydrophilic monomer. To understand the fundamental properties and potentials as a polymer dispersant, the surface parameters and rheology of the copolymers and their color dispersions in aqueous media were investigated. The aqueous solutions were typical Newtonian fluids, whereas the color dispersions were non-Newtonian fluids with shear-thinning properties and yield values ranging from 0.57 to 1.04 Pa. Although the surface parameters, such as surface tension (γ), molecular occupied area (Amin), and zeta potential (ζ), did not show clear correlation with polymer structures, their behaviors as a dispersant were significantly different. The color dispersants containing the copolymer of St or BnA as a hydrophobic monomer and IA and AMPS as hydrophilic monomers exhibited sufficient redispersion both for yellow and cyan inks, even after the aging test at 60 °C for 5 days, whereas other copolymers did not exhibit such superior performances. In addition, the color dispersions of the copolymer of St, IA, and AMPS (St-IA-AMPS) showed lower viscosity and yield value and became closer to Newtonian fluid compared with that of St, AA, and AMPS (St-AA-AMPS). Thus, St-IA-AMPS provided good redispersibility and avoided sedimentation. These results suggest that the most suitable dispersant for inkjet inks among the polymers investigated was the copolymer of St, IA, and AMPS.

Aggregation induced luminescence chromism molecule for preparation of physically unclonable function labels

Organic stimuli-responsive luminescent materials have attracted much attention due to their great potential in security fields such as fluorescent inks and information security. However, the widespread aggregation quenching effect limits the organics’ practical application in anti-counterfeiting technology. To overcome this challenge, this study developed a novel molecule 4-(4-phenyl-6-(pyren-1-yl)-1,3,5-triazin-2-yl)benzyl acrylate (PPTBA) which exhibits high luminescence efficiency in both monodisperse and aggregated states, with an obvious aggregation-induced emission color change. The copolymer P(NIPAM-PPTBA) was obtained by copolymerizing PPTBA and NIPAM (N-Isopropyl acrylamide). The polymer exhibits a blue-to-yellow luminescence chromism upon adding an appropriate amount of water. The polymer film can perfectly hide letters when combined with stamp technology and can be developed with water for general-purpose anti-counterfeiting verification. The polymer is utilized to prepare fluorescence physically unclonable functions (PUF) labels with a high-security level by using a convenient spraying technique. The random localization of polymeric domains yields unclonable surfaces with moderate uniformity, uniqueness, and good coding capacity. In particular, this PUF exhibits good temperature stability and photostability, and the luminescent hydrochromism of the polymer further enhances the encryption level. This work demonstrates the practicality and reliability of an organic light-emitting system for anti-counterfeiting applications and provides a realistic solution for preparing low-cost PUF.

Regulating the Flow-Driven Translocation of Macromolecules through Nanochannels by Interfacial Physical Adsorption

By using a model system composed of an anodic aluminum oxide nanopore (AAO), poly(benzyl acrylate) (PBAN) adsorbent, and polystyrene (PSN) probe, where N represents the degree of polymerization, this work has explored how the physical adsorption of PBA onto the surface of the AAO nanopore (rp ≈ 10 nm) influences the flow-driven translocation of PS in toluene. In the low flow rate range (Q = 0.02 mL/h), the translocation of PS chains is purely diffusive, and the partially reversible adsorption behavior of PBAN is observed only when N < ∼360, showing a strong chain length dependence. In the partially reversible regime, the interfacial thickness (δ) of the adsorption layer is estimated to be from ∼1.5 to ∼2.9 nm depending on the chain length. In the mixed solutions, when N increases from 0 to 75 and 150 for PBAN, the cut-off size (COS) of the membrane for broadly distributed PSB-285K (Mw/Mn ≈ 2.48) is estimated to decrease from ∼10.0 to ∼8.0 and ∼6.0 nm, respectively; in addition, the introduction of PBA360 can promote the separation of narrowly distributed PS655 and PS1200 by regulating re, whereas in the high flow rate range (Q > 0.02 mL/h), the translocation for PS long chains is based on the mechanism of molecular deformation, and the flow rate-dependent translocation shows a strong dependence on the chain length of PBAN. Namely, in mixed solutions, when N increases from 150 to 360, the critical flow rate (Qc) is found to slightly increase from ∼0.30 to ∼0.45 mL/h for PS1500 translocation; in addition, the cut-off performance of PSB-285K displays dependence both on flow rate and PBAN chain length. Our result has demonstrated a novel strategy to regulate the cut-off performance during the translocation of (bio)macromolecules through nanopores via partially reversible interfacial physical adsorption.

Stepwise photoassisted decomposition of carbohydrates to H2

Stepwise photoassisted decomposition of carbohydrates to H2

Synthesis of pyrazoles from sulfonyl hydrazone and benzyl acrylate under transition-metal-free conditions.

Pyrazoles as an important class of heterocyclic compounds, are widely found in pharmaceuticals and bioactive natural products. Herein we report a [3 + 2] cycloaddition reaction for the synthesis of a series of pyrazoles, with the yield up to 77%. This approach exhibits many notable features, such as convenient operating conditions, excellent functional group compatibility and readily accessible raw materials, providing an alternative route for the construction of pyrazole derivatives.

Photoelectron Yield Spectroscopy and Transient Photocurrent Analysis for Triphenylamine-Based Photorefractive Polymer Composites

The photocurrent for poly(4-(dimethylamino)benzyl acrylate) (PDAA) photorefractive composites with (4-(diphenylamino)phenyl)methanol (TPAOH) photoconductive plasticizers was measured to be two orders of magnitude higher than that obtained with (2,4,6-trimethylphenyl)diphenylamine (TAA) photoconductive plasticizers. In this study, to determine the reason for the large difference in the photocurrent measured for PDAA photorefractive composites containing two different photoconductive plasticizers of TPAOH and TAA, the highest occupied molecular orbital (HOMO) level identical to the ionization potential (Ip) and the width of the density of states (DOS) were evaluated using photoelectron yield spectroscopy, and the transient photocurrent was analyzed using a two-trap model. The estimated hole mobility was also rationalized using a Bässler formalism together with the energetic disorder of the width of the DOS and the positional disorder of the scattering situation for carrier hopping.

Enhancing the efficiency and stability of p-i-n triple cation perovskite solar cells using benzyl cyanoacetate passivation agent

It is extremely difficult to realize high-performance perovskite solar cells (PeSCs) due to a large number of defects of perovskite. Thus, perovskite defects should be passivated as much as possible. In this study, effective cyano (CN), benzene ring, and carbonyl (CO) functional groups were newly introduced to benzyl cyanoacetate (BCA) to prepare a multifunctional BCA passivation agent. The influence of functional group of BCA passivation molecule on perovskite and PeSCs was systemically studied using cyanoethyl acrylate (CA) with CN without benzene ring and benzyl acrylate (BA) with benzene ring without CN as reference molecules. Through various analyses, we found that the novel BCA passivation agent with both CN and benzene ring passivated perovskite defects the most efficiently. Thus, the combination of each effective functional group can synergistically passivate more perovskite defects. As a result, PeSCs created using BCA showed improved power conversion efficiency (PCE) from 18.38 % to 20.23 %. Additionally, PeSC with BCA retained 70 % of the initial PCE after ∼2034 h of air exposure test, 80 % of the initial PCE after ∼193 h of heat aging test, and 60 % of the initial PCE after ∼72 h of light-soaking test, demonstrating better stability than PeSC without BCA in air/heat/light-soaking stability.

Dual responsive block copolymer coated hollow mesoporous silica nanoparticles for glucose-mediated transcutaneous drug delivery

A self-regulated anti-diabetic drug release device mimicking pancreatic cells is highly desirable for the therapy of diabetes. Herein, a glucose-mediated dual-responsive drug delivery system, which combines pH- and H 2 O 2 -responsive block copolymer grafted hollow mesoporous silica nanoparticles (HMSNs) with microneedle (MN) array patch, has been developed to achieve self-regulated administration. The poly[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl acrylate]- b -poly[2-(dimethylamino)ethyl methacrylate] (PPBEM- b -PDM) polymer serves as gate keeper to prevent drug release from the cavity of HMSNs at normoglycemic level. In contrast, the drug release rate is significantly enhanced upon H 2 O 2 and pH stimuli due to the chemical change of H 2 O 2 sensitive PPBEM block and acid responsive PDM block. Therefore, incorporation of anti-diabetic drug and glucose oxidase (GOx, which can oxidize glucose to gluconic acid and in-situ produce H 2 O 2 ) into stimulus polymer coated HMSNs results in a glucose-mediated MN device after depositing the drug-loaded nanoparticles into MN array patch. Both in vitro and in vivo results show this MN device presents a glucose mediated self-regulated drug release characteristic, which possesses a rapid drug release at hyperglycemic level but retarded drug release at normoglycemic level. The result indicates that the fabricated smart drug delivery system is a good candidate for the therapy of diabetes.

Switching Frontal Polymerization Mechanisms: FROMP and FRaP

Two frontal polymerization (FP) mechanisms, frontal ring-opening metathesis polymerization (FROMP) of dicyclopentadiene and frontal radical polymerization (FRaP) of benzyl acrylate and hexanediol diacrylate, were combined for rapid manufacturing of welded thermoset materials. Leveraging the immiscibility of the two different FP resins, welded thermosets and gradient foams of varying composition were achieved by switching of FP mechanisms. The adhesion strength of the welded thermoset materials differed depending on the originating mechanism. Finally, welded thermoset foams of varying porosity and homogeneity were generated through initiation from the bottom of the two resins.

Polymerization-Induced Self-Assembly Toward Micelle-Crosslinked Tough and Ultrastretchable Hydrogels

As a promising class of tough and ultrastretchable hydrogels, micelle-crosslinked hydrogels have been restrained by the scarcity of micellar crosslinkers with a high concentration, controlled nanostructure, and uniform size distribution. Herein, polymerization-induced self-assembly (PISA) was demonstrated to be a general and powerful platform for micellar crosslinkers, affording micelle-crosslinked hydrogels with tailorable chemical structures, mechanics, and functionality. Poly(N,N-dimethylacrylamide)-b-poly(diacetone acrylamide) (PDMAc-b-PDAAM) micellar crosslinkers with a controlled nanostructure and uniform size distribution were prepared via PISA and one-step post-polymerization modification at high concentrations. Copolymerization of these micellar crosslinkers with acrylamide generated tough and ultrastretchable hydrogels, whose mechanical properties were found correlated with the concentration, nanostructure, and chemical composition of the micelles. The energy dissipation mechanism of these micelle-crosslinked hydrogels was analyzed via cyclic mechanical tests and stress relaxation experiments. The general feasibility of PISA toward micelle-crosslinked hydrogels was verified by systematic evaluation of both aqueous (including 2-methoxyethyl acrylate, tetrahydro-2-furanylmethyl acrylate, and 4-hydroxybutyl acrylate) and alcoholic (including benzyl methacrylate, lauryl methacrylate, styrene, and benzyl acrylate) PISA formulations, producing hydrogels with diverse chemical structures, mechanics, and functionalities depending on the micellar crosslinkers. The modularity of this strategy was further demonstrated by the fabrication of fluoro-functionalized hydrogels with fluoro-containing micellar crosslinkers. This strategy has significantly enlarged the scope and application of micelle-crosslinked hydrogels.

Photoinduced Cross Linkable Polymerization of Flexible Perovskite Solar Cells and Modules by Incorporating Benzyl Acrylate

AbstractFlexible perovskite solar cells possess huge application potential in both outdoor (sunlight) and indoor scenes (artificial low light) owing to their high optoelectronic conversion efficiency and agile integration advantages. In order to further establish their feasibility to meet multi‐scenario applications, here a facile “internal packaging” interface strategy is developed, where a selective light‐cured cross‐linking molecule is leveraged to effectively heal the interface defects over perovskite films. Moreover, the cross‐linked interfacial layer can act as an airtight “protective wall”, preventing the device from water and oxygen corrosion and lead leakage. The flexible devices aided by this strategy show considerable performance ranging from small size to scalable modules (20.86%‐0.07 cm2, 16.75%‐24 cm2). More importantly, the optimal devices yield excellent moisture resistance, light soaking resistance, and lead leakage prevention stability. Based on the common light source environment of indoor scenes, the excellence of flexible modules (30.73% under white light‐emitting diode (LED), 26.48% under yellow LED) is further validated. It is expected that this gentle strategy can underline simultaneous promoting of the efficiency and stability of flexible perovskite modules, thereby accelerating the application of flexible perovskite in advanced industrial fields.

Facile adjustment on cellulose nanocrystals composite films with glycerol and benzyl acrylate copolymer for enhanced UV shielding property

In the present work, cellulose nanocrystals (CNCs) composite films with suitable applicable capabilities were prepared by facilely incorporating glycerol (Gly) and poly(benzyl acrylate) (PBA). Chemical and morphological variations during the fabrication of the films were systematically characterized. The properties of modified CNCs composite films including UV blocking ability, mechanical strength and thermal properties were characterized to assess their applicable potentials. As a result, the composite films have good UV shielding property in UVC (220–280 nm) region and UVB (280–320 nm) region. The shielding performance of the modified film in the ultraviolet absorption region reached 92.77% to 95.49% respectively, without damaging the original chiral nematic structure of the films. Along with the modification, BACNC film improved the mechanical properties, presenting the tensile strength 16 times higher compared to pure CNCs film. The nanocomposite films proposed in this work showed promising potentials in broad fields, such as food preservation, medical protection, and surface coating applications.