Bilayer Structure Research Articles

Efficient evaporation of seawater desalination by novel double-interface evaporator: Photothermal conversion, water transfer and salt-resistant

Interfacial solar-driven water evaporation emerged as an established eco-friendly method for seawater desalination to combat water scarcity, yet the low water evaporation rate and cost-effectiveness limit the practicable application. Herein, we presented a double-interface evaporator with a bilayer structure (BCCu@FC). The upper layer was constructed using carbonized copper-doped biochar (BCCu), which exhibited broadband sunlight absorption and effective photothermal conversion capability for the localized surface plasmon resonance (LSPR) effect. Meanwhile, the lower layer was constructed by felt fabric (FC), which featured a large spatial network structure, guaranteeing sufficient water transportation. Therefore, BCCu@FC exhibited a high photothermal conversion efficiency of 87.05% with a 1.571 kg m-2 h-1 water evaporation rate under 1 sun illumination. Moreover, BCCu@FC further exhibited high stability and salt resistance, showing no significant salt crust formation after continuous operation for 24 h under 3.5 wt% brine. Especially, BCCu@FC could stably work under 21 wt% brine, and the salt crust re-dissolved within 4 h after the cessation of illumination. This facile and universal strategy was anticipated to pave the way for future designs and fabrication of diverse, more efficient, and cost-effective photothermal conversion devices.

High-Q Wireless SAW Sensors Based on AlN/Sapphire Bilayer Structure, Operating at 2.45 GHz Range for High-Temperature Applications

High-Q Wireless SAW Sensors Based on AlN/Sapphire Bilayer Structure, Operating at 2.45 GHz Range for High-Temperature Applications

Microstructural and optoelectronic properties of sputtered Al:ZnO films and Al:ZnO/Cu bilayer structures: Effects of substrate and Cu thickness

In this study, using a multi-source confocal radio frequency magnetron sputtering system, we synthesized aluminum doped zinc oxide (AZO) single layers and AZO/Cu bilayers on glass and crystalline quartz substrates with a constant AZO thickness of 65 nm and variable Cu bottom layers with a thickness of 4–13 nm. The microstructural, morphological, optical, and electrical characteristics of all samples were investigated using a variety of spectroscopic techniques. The X-ray diffraction results show that all films prepared on both substrates have a hexagonal wurtzite crystal structure and exhibit the preferred orientation along the (002) plane with some microstructural variations. The atomic force microscopy images revealed that the thickness of the Cu layer and substrate type greatly affect the films' topography and surface roughness. The transmittance spectra indicate that the single AZO layer on both substrates possess the highest average visible transmission; however, all the samples deposited on glass substrates show greater transmittance than that on quartz. Photoluminescence analysis put into evidence a decrease in ultraviolet emission with Cu thickness for both substrates, with intensities varying according to substrate type. Hall Effect measurements reveal that all samples have n-type conductivity as well as that Cu thickness has a significant impact on their electrical characteristics. Moreover, a higher value of the figure of merit is achieved with the AZO/Cu bilayer structure grown on a glass substrate with 13 nm of Cu layer thickness.

Modulation of Triton X-100 Aqueous Micelle Interface by Ionic Liquid: A Molecular Level Interaction Studied by Time-resolved Fluorescence Spectroscopy

Background: Self-assembly structure is an important area of research for understanding biological systems, owing to its resemblance to the membrane structure of the phospholipid bilayer. In a self-assembly medium, chemical reactions and chemical or physical processes are dramatically different than the bulk phase. Understanding this process in synthesizing self-assembly structures may allow us to explore various biological processes occurring in cell membranes. Objective: The study aimed to understand water dynamics in the TX-100 micellar interface via steady state and a time-resolved fluorescence spectroscopy study. The objective was also to determine the two different ionic liquids (ILs), namely 1-butyl-3-methyl imidazolium tetrafluoroborate ([bmim][BF4]) and 1-decyl-3-methyl imidazolium tetrafluoroborate ([dmim][BF4]), inducing surfactant aggregation changes at the molecular level. Also, the focus was on determining the hydration and its dynamics at the palisade layer of TX-100 micelle in the presence of two different ionic liquids. Methods: Steady state and time-resolved fluorescence spectroscopy have been used to study TX-100 micellar systems. Employing time-resolved spectroscopy, two chemical dynamic processes, solvation dynamics and rotational relaxation dynamics, have been studied to investigate structural changes in TX100 by adding ILs. Solvation dynamics was studied by measuring the time-dependent Stokes shift of the fluorescent probe. From the Stokes shift, time-resolved emission spectra were constructed to quantify the solvation dynamics. Also, using the polarization properties of light, time-resolved anisotropy was constructed to explore the rotation relaxation of the probe molecule. Results: The absorption and emission spectra of C-153 in TX-100 were red-shifted in the presence of both the ILs. Also, the C-153 experienced faster solvation dynamics and rotational relaxation with the addition of both ILs. In our previous study, we observed a significantly increased rate of solvation dynamics with the addition of [bmim][BF4] (J. Phys. Chem. B, 115, 6957-6963) [38]. However, with the addition of the same amount of [dmim][BF4], the IL rate of solvation enhancement was more pronounced than with [bmim][BF4]. The faster solvation and rotational relaxation have been found to be associated with the penetration of more free water at the TX100 micellar stern layer, leading to increased fluidity of the micellar interface. Conclusion: Upon incorporating ILs in TX100 micelle, substantially faster solvation dynamics of water as well as rotational relaxation dynamics of C-153 have been observed. By decreasing surfactant aggregations, [bmim][BF4] ILs facilitated more water molecules approaching the TX-100 micellar phase. On the other hand, [dmim][BF4] ILs comprising mixed micelles induced even more free water molecules at the palisade layer, yielding faster solvation dynamics in comparison to pure TX-100 micelle or TX100 micelle + [bmim][BF4] ILs systems. Time-resolved anisotropy study has also supported the finding and strengthened the solvation dynamics observation.

Enhanced spin pumping in heterostructures of coupled ferrimagnetic garnets

Spin pumping has significant implications for spintronics, providing a mechanism to manipulate and transport spins for information processing. Understanding and harnessing spin currents through spin pumping is critical for the development of efficient spintronic devices. The use of a magnetic insulator with low damping enhances the signal-to-noise ratio in crucial experiments such as spin-torque ferromagnetic resonance (FMR) and spin pumping. A magnetic insulator coupled with a heavy metal or quantum material offers a more straightforward model system, especially when investigating spin-charge interconversion processes to greater accuracy. This simplicity arises from the absence of unwanted effects caused by conduction electrons unlike in ferromagnetic metals. Here, we investigate the spin pumping in coupled ferrimagnetic (FiM) Y3Fe5O12 (YIG)/Tm3Fe5O12 (TmIG) bilayers combined with heavy-metal (Pt) using the inverse spin Hall effect. It is observed that magnon transmission occurs at both of the FiMs FMR positions. The enhancement of spin pumping voltage (Vsp) in the FiM garnet heterostructures is observed. The plausible reason might be the interfacial exchange coupling between FiMs. The modulation of Vsp is achieved by tuning the bilayer structure. Further, the spin mixing conductance for these coupled systems is found to be ≈1018 m−2. Our findings describe a coupled FiM system for the investigation of magnon coupling providing opportunities for magnonic devices.

Streamlining Skin Regeneration: A Ready-To-Use Silk Bilayer Wound Dressing.

Silk proteins have been highlighted in the past decade for tissue engineering (TE) and skin regeneration due to their biocompatibility, biodegradability, and exceptional mechanical properties. While silk fibroin (SF) has high structural and mechanical stability with high potential as an external protective layer, traditionally discarded sericin (SS) has shown great potential as a natural-based hydrogel, promoting cell-cell interactions, making it an ideal material for direct wound contact. In this context, the present study proposes a new wound dressing approach by developing an SS/SF bilayer construct for full-thickness exudative wounds. The processing methodology implemented included an innovation element and the cryopreservation of the SS intrinsic secondary structure, followed by rehydration to produce a hydrogel layer, which was integrated with a salt-leached SF scaffold to produce a bilayer structure. In addition, a sterilization protocol was developed using supercritical technology (sCO2) to allow an industrial scale-up. The resulting bilayer material presented high porosity (>85%) and interconnectivity while promoting cell adhesion, proliferation, and infiltration of human dermal fibroblasts (HDFs). SS and SF exhibit distinct secondary structures, pore sizes, and swelling properties, opening new possibilities for dual-phased systems that accommodate the different needs of a wound during the healing process. The innovative SS hydrogel layer highlights the transformative potential of the proposed bilayer system for biomedical therapeutics and TE, offering insights into novel wound dressing fabrication.

Influence of additional intermediate thick Al layers on the reaction propagation and heat flow of Al/Ni reactive multilayers

This study investigates the effects of sputtering and electron beam evaporation (e‐beam) on the microstructure and reactive properties of Al/Ni reactive multilayers (RML). The intermixing zone, a critical factor influencing reaction kinetics, was characterized using high‐resolution transmission electron microscopy and found to be consistently 3 nm for both fabrication methods. Differential scanning calorimetry revealed that e‐beam samples, with thicker Al layers, exhibited slightly higher total molar enthalpy and maintained high reaction temperatures despite reduced reaction velocities in comparison to sputtered samples. X‐ray diffraction confirmed the formation of both Al3Ni2 and AlNi phases in the e‐beam samples. These findings indicate that while thicker bilayer structures reduce reaction velocity, they keep thermal output and mitigate the impact of intermixing zones, leading to similar total molar enthalpy. This analysis underscores the significance of deposition technique and bilayer thickness in optimizing the performance of Al/Ni RML, offering the possibility to establish different phase formations in thicker RML. It advances the control over the reactive properties of reactive multilayers in their applications, for example reactive bonding.This article is protected by copyright. All rights reserved.

Chiral Supramolecular Self-Assembly Catalysts with Enhanced Metal Ion Interaction for Higher Enantioselectivity.

Understanding the interaction between metal ions as catalytic centers and supramolecular scaffolds as chiral substrates plays an important role in developing chiral supramolecular catalysts with high enantioselectivity. Herein, we found that compared with l-norleucine chiral amphiphile (l-NorC16), l-methionine chiral amphiphile (l-MetC16) with the only heteroatom of S site difference in the hydrophilic group can form a similar supramolecular chiral nanoribbon (NR) with the bilayer structure through the self-assembly approach; yet, the interaction between the Cu(II) ion catalytic centers and supramolecular scaffolds is reinforced, favoring the chirality transfer and therefore enhancing their catalytic enantioselectivity of Diels-Alder reaction from 23% [l-NorC16-NR-Cu(II)] to 78% [l-MetC16-NR-Cu(II)]. Our work demonstrates a new strategy from the perspective of strengthening the metal ion-supramolecular scaffold interaction for the preparation of chiral supramolecular catalysts with good catalytic enantioselectivity.

Chiral versus achiral crystal structures of 4-benzyl-1H-pyrazole and its 3,5-di-amino derivative.

The crystal structures of 4-benzyl-1H-pyrazole (C10H10N2, 1) and 3,5-di-amino-4-benzyl-1H-pyrazole (C10H12N4, 2) were measured at 150 K. Although its different conformers and atropenanti-omers easily inter-convert in solution by annular tautomerism and/or rotation of the benzyl substituent around the C(pyrazole)-C(CH2) single bond (as revealed by 1H NMR spectroscopy), 1 crystallizes in the non-centrosymmetric space group P21. Within its crystal structure, the pyrazole and phenyl aromatic moieties are organized into alternating bilayers. Both pyrazole and phenyl layers consist of aromatic rings stacked into columns in two orthogonal directions. Within the pyrazole layer, the pyrazole rings form parallel catemers by N-H⋯N hydrogen bonding. Compound 2 adopts a similar bilayer structure, albeit in the centrosymmetric space group P21/c, with pyrazole N-H protons as donors in N-H⋯π hydrogen bonds with neighboring pyrazole rings, and NH2 protons as donors in N-H⋯N hydrogen bonds with adjacent pyrazoles and other NH2 moieties. The crystal structures and supra-molecular features of 1 and 2 are contrasted with the two known structures of their analogs, 3,5-dimethyl-4-benzyl-1H-pyrazole and 3,5-diphenyl-4-benzyl-1H-pyrazole.

Bilayer Solar Steam Generator by Co-Gelation Method

The interfacial solar steam generator presents a viable and environmentally conscious solution for generating fresh water from seawater. The interfacial solar steam generator is accomplished through the integration of a photothermal material with a supporting material, resulting in a bilayer structure. In general, the efficiency of achieving a bilayer structure by the coating of a photothermal material on the surface of a substrate is limited. This is due to the potential for separation and variations in coating thickness, which can result in a drop in the rate of evaporation. In this study, a bilayer structure was successfully obtained through the implementation of a co-gelation technique utilizing a biomass-derived substrate, aerogel cellulose, and magnetite (Fe3O4) as photothermal materials. Additionally, we investigate the impact of magnetic fields on the evaporation rate of photothermal materials. The bilayer solar steam generator obtained demonstrates a notable evaporation rate of 1.87 kg.m-2h-1, which is sufficient to meet the daily water requirements of individuals.

Effect of lipid composition on the characteristics of liposomes prepared using the polyol dilution method

Polyol dilution (PD) is a liposome preparation method suitable for mass production in the cosmetics industry. For PD-liposomes, lecithin is the primary material of choice because of its cost advantage. However, despite the importance of understanding the effect of lipid composition on the physicochemical properties of PD-liposomes in terms of formulation design, this has not yet been elucidated. In this study, PD-liposomes were prepared using hydrogenated egg yolk lecithin (EL) and its main components, 1,2-distearoyl-glycero-3-phosphocholine (DSPC), 1,2-dipalmitoyl-glycero-3-phosphocholine (DPPC), and 1,2-distearoyl-glycero-3-phosphoethanolamine (DSPE). The compound 1,3-butylene glycol (BG), which is widely used in the cosmetics industry, was used as a representative polyol. Herein, we aimed to clarify the effect of lipid composition on PD-liposomes. The results showed that the particle size, dispersion stability, shape, and phase state of the lipid bilayer in PD-liposomes could be controlled by changing the composition of the hydrophilic and hydrophobic groups of the lipids. In particular, when PE was added to a system consisting of PC molecules, a significant decrease in particle size, improvement in dispersion stability, and shape changes were observed, indicating a significant effect on the physicochemical properties of the PD-liposomes. In addition, adding BG induced the formation of an interdigitated structure in the lipid bilayer when PC was the only hydrophilic group component; adding even a small amount of PE suppressed the formation of this structure. Furthermore, we confirmed that premixing BG and lipids enhanced the miscibility of different types of lipid molecules. The findings of this study are expected to contribute to the design of highly functional PD-liposomes by enabling the selection and design of appropriate lipid compositions for practical applications.

Modulating lipid bilayer permeability and structure: Impact of hydrophobic chain length, C-3 hydroxyl group, and double bond in sphingosine

Sphingosine, an amphiphilic molecule, plays a pivotal role as the core structure of sphingolipids, essential constituents of cell membranes. Its unique capability to enhance the permeability of lipid membranes profoundly influences crucial life processes. The molecular structure of sphingosine dictates its mode of entry into lipid bilayers and governs its interactions with lipids, thereby determining membrane permeability. However, the incomplete elucidation of the relationship between the molecular structure of sphingosine and the permeability of lipid membranes persists due to challenges associated with synthesizing sphingosine molecules. A series of sphingosine-derived molecules, featuring diverse hydrophobic chain lengths and distinct headgroup structure, were meticulously designed and successfully synthesized. These molecules were employed to investigate the permeability of large unilamellar vesicles, functioning as model lipid bilayers. With a decrease in the hydrophobic chain length of sphingosine from C15 to C11, the transient leakage ratio of vesicle contents escalated from ∼ 13 % to ∼ 28 %. Although the presence of double bond did not exert a pronounced influence on transient leakage, it significantly affected the continuous leakage ratio. Conversely, modifying the chirality of the C-3 hydroxyl group gives the opposite result. Notably, methylation at the C-3 hydroxyl significantly elevates transient leakage while suppressing the continuous leakage ratio. Additionally, sphingosines that significantly affect vesicle permeability tend to have a more pronounced impact on cell viability. Throughout this leakage process, the charge state of sphingosine-derived molecule aggregates in the solution emerged as a pivotal factor influencing vesicle permeability. Fluorescence lifetime experiments further revealed discernible variations in the effect of sphingosine molecular structure on the mobility of hydrophobic regions within lipid bilayers. These observed distinctions emphasize the impact of molecular structure on intermolecular interactions, extending to the microscopic architecture of membranes, and underscore the significance of subtle alterations in molecular structure and their associated aggregation behaviors in governing membrane permeability.

Quadrupolar and dipolar excitons in symmetric trilayer heterostructures: insights from first principles theory

Excitons in van der Waals heterostructures come in many different forms. In bilayer structures, the electron and hole may be localized on the same layer or they may be separated forming an interlayer (IL) exciton with a finite out-of-plane dipole moment. Using first principles calculations, we investigate the excitons in a symmetric WS2/MoS2/WS2 heterostructure in the presence of a vertical electric field. The excitons exhibit a quadratic Stark shift for low field strengths and a linear Stark shift for stronger fields. This behavior is traced to the coupling of IL excitons with opposite dipole moments, which lead to the formation of quadrupolar excitons at small fields. The formation of quadrupolar excitons is determined by the relative size of the electric field-induced splitting of the dipolar excitons and the coupling between them given by the hole tunneling across the MoS2 layer. For the inverted structure, MoS2/WS2/MoS2, the dipolar excitons are coupled by electron tunneling across the WS2 layer. Because this effect is much weaker, the resulting quadrupolar excitons are more fragile and break at a weaker electric field.

Detection of Multi-Layered Bond Delamination Defects Based on Full Waveform Inversion.

This study aimed to address the challenges encountered in traditional bulk wave delamination detection methods characterized by low detection efficiency. Additionally, the limitations of guided wave delamination detection methods were addressed, particularly those utilizing reflected waves, which are susceptible to edge reflections, thus complicating effective defect extraction. Leveraging the full waveform inversion algorithm, an innovative approach was established for detecting delamination defects in multi-layered structures using ultrasonic guided wave arrays. First, finite element modeling was employed to simulate guided wave data acquisition by a circular array within an aluminum-epoxy bilayer structure with embedded delamination defects. Subsequently, the full waveform inversion algorithm was applied to reconstruct both regular and irregular delamination defects. Analysis results indicated the efficacy of the proposed approach in accurately identifying delamination defects of varying shapes. Furthermore, an experimental platform for guided wave delamination defect detection was established, and experiments were conducted on a steel-cement bilayer structure containing an irregular delamination defect. The experimental results validated the exceptional imaging precision of our proposed technique for identifying delamination defects in multi-layered boards. In summary, the proposed method can accurately determine both the positions and sizes of defects with higher detection efficiency than traditional pulse-echo delamination detection methods.

Research on efficient braille recognition based on the pair-U-shaped micro-nano optical fiber fingerprint-like tactile sensors

Tactile sensors are essential for capturing touch information, yet existing sensors struggle to accurately mimic human pressure and motion perception. This study introduces a novel design resembling a fingerprint, featuring a pair-U-shaped flexible optical fiber tactile sensor, and assesses its efficacy in braille input interactions. Constructed from 3D-printed elastomeric resin, the sensor incorporates a bilayer structure that mirrors a fingerprint pattern, with interlocking microstructures and encapsulated pair-U-shaped micro-nano-optical fibers (MNF) within a polydimethylsiloxane (PDMS) layer. These design elements allow these two MNF sensing channels to achieve synchronization, enhancing durability and sensitivity (66.08 % N−1 and 65.59 %N−1), quickening response (84.17/17.49 ms) and recovery time (58.31/10.02 ms) for detecting braille surfaces. Utilizing the Long Short-Term Memory (LSTM) algorithm significantly boosts the accuracy of braille character recognition. Post-training, the sensor achieved a 97.10 % recognition rate for 26 English letters under varying speeds and pressures. Moreover, the recognition rate for letters with similar features (B/K, F/M, G/X, H/U) improved to 98.58 %, underscoring the sensor’s effectiveness in braille recognition. This innovative approach holds potential for applications in braille reading, surface sensing, and related areas.

Harnessing exosomes and plant-derived exosomes as nanocarriers for the efficient delivery of plant bioactives.

Exosomes, a category of extracellular vesicle (EV), are phospholipid bilayer structures ranging from 30 to 150nm, produced by various organisms through the endosomal pathway. Recent studies have established the utilization of exosomes as nanocarriers for drug distribution across various therapeutic areas including cancer, acute liver injury, neuroprotection, oxidative stress, inflammation, etc. The importance of plant-derived exosomes and exosome vesicles derived from mammalian cells or milk, loaded with potent plant bioactives for various therapeutic indications are discussed along with insights into future perspectives. Moreover, this review provides a detailed understanding of exosome biogenesis, their composition, classification, stability of different types of exosomes, and different routes of administration along with the standard techniques used for isolating, purifying, and characterizing exosomes.

Widening the Gamut of Structural Colors of Gold via Insulator–Metal Bilayer Coatings

Tuning the color of Au has been a longstanding problem in the luxury industry. Conventional approaches, involving Au alloying, compromise purity and demand distinct alloy compositions for each hue. This study demonstrates a lithography‐free method for generating structural colors on a gold surface by adjusting the thickness of titanium dioxide, a high‐index dielectric. While color tuneability is limited if TiO2 is coated directly on the Au surface, a range of vivid colors can be generated if a 50−100 nm thick AuAl2 underlayer is used. AuAl2, an accepted alloy for purple gold, broadens the color gamut, providing a protective coating without diminishing gold purity. The reflectance dip of the bilayer structure exhibits a significant red shift with increasing thickness of the TiO2 layer, allowing diverse colors by TiO2 insulator tuning. Simulation studies corroborate experimental results, affirming that coating a TiO2 layer on the AuAl2 underlayer yields a wide range of colors. This method, based on thin‐film interference, shows promise for widespread use, offering a broad spectrum of structural colors in an industry striving for diverse Au color representation.

In-situ grown ZnO-nanorods of slippery liquid-injected porous surface coating on Mg alloy with hydrophobic, durable, and anti-corrosion properties

In this work, an in-situ self-grown nano-ZnO/epoxy-based slippery lubricant liquid-injected porous surface (SLIPS) coating with a unique bilayer structure is reported to achieve robustness, hydrophobicity, and anti-corrosion properties. Dense epoxy coated ZnO nanoparticles are used as the anti-corrosion barrier layer. Self-grown ZnO nanorods provide a robust micro- and nano-rough porous structure. The lubricant perfluoropolyether (PFPE) is strongly locked into the porous structure via low surface energy material pretreatment and capillary effect. This SLIPS coating has a high water contact angle (WCA) value and has excellent repellency to various liquids. The SLIPS surface maintains a high contact angle of more than 115° even after 20 days of immersion in corrosive solutions and withstand the erosion of corrosive solutions with pH = 3. It also has a very low corrosion current density of 8.97 × 10−12 A/cm2 and the Rct (the charge transfer resistance) of optimum SLIPS remained 1.41 × 108 ohm cm2 after 70 days immersion in 3.5 wt% NaCl solution, which is in the same order of magnitude as the initial value. The SLIPS coating with excellent mechanical stability, super-hydrophobicity, anti-fouling, chemical stability, and long-term corrosion resistance performance possesses tremendous application potential in long-term corrosion protection of Mg alloys.

An ultra high-endurance memristor using back-end-of-line amorphous SiC

Integrating resistive memory or neuromorphic memristors into mainstream silicon technology can be substantially facilitated if the memories are built in the back-end-of-line (BEOL) and stacked directly above the logic circuitries. Here we report a promising memristor employing a plasma-enhanced chemical vapour deposition (PECVD) bilayer of amorphous SiC/Si as device layer and Cu as an active electrode. Its endurance exceeds one billion cycles with an ON/OFF ratio of ca. two orders of magnitude. Resistance drift is observed in the first 200 million cycles, after which the devices settle with a coefficient of variation of ca. 10% for both the low and high resistance states. Ohmic conduction in the low resistance state is attributed to the formation of Cu conductive filaments inside the bilayer structure, where the nanoscale grain boundaries in the Si layer provide the pre-defined pathway for Cu ion migration. Rupture of the conductive filament leads to current conduction dominated by reverse bias Schottky emission. Multistate switching is achieved by precisely controlling the pulse conditions for potential neuromorphic computing applications. The PECVD deposition method employed here has been frequently used to deposit typical BEOL SiOC low-k interlayer dielectrics. This makes it a unique memristor system with great potential for integration.

Nanosecond laser-induced crystallization of SiOx/Au bilayers in air and vacuum

High-quality polycrystalline silicon films on low-cost and low-temperature substrates have attracted much attention as promising materials for high-speed thin-film transistors and thin-film solar cells fabrication. To obtain poly-Si films on low temperature substrates, several concepts have been proposed. Usually the amorphous material undergoes crystallization which can be achieved by various methods including solid-phase crystallization, metal-induced crystallization or liquid-phase crystallization. In this work, we tried to combine the advantages of metal-induced crystallization and liquid-phase crystallization. To achieve this we explored the nanosecond laser crystallization of a bilayer structure consisting of Au and SiO0.1 layers with thicknesses of 30 nm and 130 nm, respectively. The study reveals that when exposed to 532 nm wavelength radiation leads to its destruction due to rupture. On the other hand, when subjected to 1064 nm wavelength radiation, no similar material behavior is observed, and the measured modification threshold is 0.15 J/cm2, representing a 40 % reduction compared to SiO0.1 film without gold. It is demonstrated that at laser fluences of 0.35 J/cm2 and higher, the treatedsurfaceinair becomes enriched with silicon dioxidenanoporous coating, attributed to the return of evaporation products to the target surface. Theoretical modeling, assuming thermal evaporation of the coating, suggests that the undesirable nanoporous layer formation can be avoided.