Structure Of Films Research Articles

Focusing on the corrosion resistance enhancement of HRB400 rebar by Cr addition in the marine envrionment

The corrosion resistance of Cr reinforced HRB400 rebar in the marine environment was investigated. The addition of Cr increases the amount of Cr(OH)3 and α-FeOOH in the passivate film, resulting in a denser passivate film structure. This enhanced passivation film inhibits localized corrosion. The pitting potential and critical chloride concentration (CTL) of the steel increased with the increase in chromium content, indicating improved corrosion resistance of the steel. On the other hand, an increase in the concentration of Cl- in solution leads to a decrease in the pitting potential and resistance of the steel, which reduces the corrosion resistance. At higher Cl- concentrations, the Cl- ions form an electrochemical interface with the steel surface, resulting in a sharp decrease in the Rf value. In addition, the gradual decrease in solution pH leads to a decrease in the pitting potential and CTL of HRB400 and 1.5Cr steel. The corrosion resistance was also found to be reduced, pH reduction accelerated the intrusion of chloride ions, which led to a severe breakdown of the passivation film.

Regulation of near-infrared absorbing property for the absorptive short-wave pass filter based on Ag:1st/Si3N4/SiO2/Si3N4/Ag:2nd/Si3N4/W-WOx quasi-optical microcavity

Regulation of the near-infrared absorbing property in the different spectral ranges has been a challenge for absorptive short-wave pass filters (ASPFs) to meet the increasing application demands. In this paper, the multi-layer ASPF with the film structure of substrate(quartz)/Si3N4/ Ag:1st/Si3N4/SiO2/Si3N4/Ag:2nd/Si3N4/W-WOx/SiO2 is designed and prepared by magnetron sputtering. We get an optimal spectral selectivity in that the transmissive band ranges from 380-700 nm with a peak transmittance of 72.9 %, and the absorptive band ranges from 700-1400 nm with a peak absorptance of 84.1 %. As the main part of the ASPF, the quasi-optical microcavity (QOM) is creatively constructed with the film structure of Ag:1st/Si3N4/SiO2/Si3N4/Ag:2nd/Si3N4/W-WOx, integrating the interference mechanism and surface plasmon resonance mechanism with the intrinsic spectral selectivity of the W-WOx and silver layers, achieving the good selective absorbing property. The absorptive band is widened from 700-1400 nm to 700–2500 nm by regulating the interference effect and the intrinsic property via changing the thickness of the W-WOx layer, realizing much more significant regulation. The optical property remains stable after heat treatment at 200 °C for 72 h in the air, showing better thermal stability than other ASPFs. The outdoor thermal insulation experiments show that the temperature of black paint under the ASPF is about 17 °C lower than that under quartz glass. The microscopic and optical mechanisms for regulating the optical properties have been analyzed in-depth, providing a new strategy for the development of ASPFs.

Interfacial Distortion of Sb2Te3-Sb2Se3 Multilayers via Atomic Layer Deposition for Enhanced Thermoelectric Properties.

Atomic layer deposition (ALD) is an effective technique for depositing thin films with precise control of layer thickness and functional properties. In this work, Sb2Te3-Sb2Se3 nanostructures were synthesized using thermal ALD. A decrease in the Sb2Te3 layer thickness led to the emergence of distinct peaks from the Laue rings, indicative of a highly textured film structure with optimized crystallinity. Density functional theory simulations revealed that carrier redistribution occurs at the interface to establish charge equilibrium. By carefully optimizing the layer thicknesses, we achieved an obvious enhancement in the Seebeck coefficient, reaching a peak figure of merit (zT) value of 0.38 at room temperature. These investigations not only provide strong evidence for the potential of ALD manipulation to improve the electrical performance of metal chalcogenides but also offer valuable insights into achieving high performance in two-dimensional materials.

Effect of sputtering power and substrate bias on microstructure, mechanical properties and corrosion behavior of CoCrFeMnNi high entropy alloy thin films deposited by magnetron sputtering method

The CoCrFeMnNi high entropy alloy thin films with crystalline (solid solution) structure or amorphous state were fabricated by magnetron sputtering process at different target powers and different substrate bias. Effects of the target power and substrate bias on the characteristics of the CoCrFeMnNi thin films such as microstructures, morphology and surface topography, as well as mechanical properties and corrosion behavior were studied. Phase prediction was calculated by using thermodynamic and kinetic criteria under various deposition conditions. The enthalpy, entropy, δ and Ω parameters, and electronegativity differences influenced the solid solution stability of thin films. These parameters led to the formation of solid solutions with crystalline or amorphous structures under specific limits, which corresponded to the practical XRD and TEM analysis results. Using a substrate bias in the deposition of CoCrFeMnNi thin film changed the amorphous structure to a crystalline (solid solution (BCC + FCC)) at higher target powers (200 and 300 W). On the other hand, the film structure was entirely amorphous at all sputtering target powers without the substrate bias. The mechanical properties, such as hardness, Young's modulus, film strength, and fracture toughness of CoCrFeMnNi thin film, can be enhanced by using the substrate bias and increasing the sputtering power. The potentiodynamic polarization test in 3.5 wt% NaCl aqueous solution indicated that the deposition of CoCrFeMnNi thin films at different sputtering powers and without substrate bias could increase the corrosion resistance of 304 stainless steel substrate. Using the substrate bias of −100 V in the fabrication of CoCrFeMnNi thin film decreased the corrosion current density and increased its polarization resistance.

Hydrophilicity and Pore Structure Enhancement in Polyurethane/Silk Protein-Bismuth Halide Oxide Composite Films for Photocatalytic Degradation of Dye.

Polyurethane/silk protein-bismuth halide oxide composite films were fabricated using a blending-wet phase transformationin situsynthesis method. The crystal structure, micromorphology, and optical properties were conducted using XRD, SEM, and UV-Vis DRS characterize techniques. The results indicated that loaded silk protein enhanced the hydrophilicity and pore structure of the polyurethane composite films. The active species BiOX were observed to grow as nanosheets with high dispersion on the internal skeleton and silk protein surface of the polyurethane-silk protein film. The photocatalytic efficiency of BiOX/PU-SF composite films was assessed through the degradation of Rhodamine B under visible light irradiation. Among the tested films, the BiOBr/PU-SF composite exhibited the highest removal rate of RhB at 98.9%, surpassing the removal rates of 93.7% for the BiOCl/PU-SF composite and 85.6% for the BiOI/PU-SF composite. Furthermore, an active species capture test indicated that superoxide radical (•O2-) and hole (h+) species played a predominant role in the photodegradation process.

Investigation of structural, morphological and optoelectronic properties of (Ni, Co)-doped and (Ni/Co) co-doped SnO2 (110) sprayed thin films

The manuscript details the application of spray pyrolysis for the deposition of an economically viable transparent conductive oxide film comprised of (Ni/Co) co-doped SnO2 on a glass substrate. The primary objective of this research was to systematically examine the impact of Ni/Co co-doping on diverse properties of the SnO2 thin film. These properties encompassed the film's structural composition, surface morphology, optical response, and electrical behaviors. A comparison was made with pure SnO2 film, as well as SnO2 films doped with 3 %Ni and 1 %Co. The results indicate that all the samples exhibited a tetragonal structureThe introduction of Co and Ni atoms had no impact on the favored alignment of the (110) plane or the crystal structure of the SnO2 film. The crystallite size of the pure SnO2 film, as well as the (Co, Ni)-doped and (Ni/Co) co-doped SnO2 films, varied within the range of 11 to 20 nm. Scanning electron microscopy (SEM) images were employed to assess how doping and co-doping influenced the surface characteristics of the films. The presence of pores and/or roughness on the surface resulted in a hydrophilic character and a decrease in the contact angle for the doped films (Ni, Co). However, the co-doped film exhibited a hydrophobic characteristic due to the surface enhancement provided by SnO2:3 %Ni:1 %Co. The research also focused on the optical characteristics of the films, showing a positive impact with the proper incorporation of Ni and Co atoms into the SnO2 lattice. It was notably observed that the addition of Ni and Co atoms improves the optical properties of the undoped transparent SnO2 film in the visible spectrum, with a high transmittance of 87 % achieved for the Ni-doped film. Furthermore, the hydrophobic nature achieved by adding a concentration of 3 %Ni to the SnO2:1 %Co film enhances its optical transmission in the range of 300 nm to 750 nm. The SnO2 film shows an improvement in the electrical resistivity upon doping and co-doping with low resistivity value of 2.22 × 10−2 Ω.cm for the film (3 %Ni/1 %Co)-SnO2. Drawing from these insightful results, the study proposes the potential utilization of (Ni/Co) co-doped SnO2 films as transparent electrodes in optoelectronic applications, especially in the manufacturing of thin film solar cells.

Plasmon-driven creation of magnetic topological structures

We demonstrate the creation and control of magnetic topological textures in thin film structures by plasmonic effects. From electromagnetic and photothermal models, the heat and absorption were determined, then the results were implemented in micromagnetic formalism to study the dynamics of magnetization under various conditions. The laser pulse duration and the contact area between nanoparticles and the magnetic layer are key parameters in the formation of topological textures. It is possible to generate a single skyrmion, multiple skyrmions, and skyrmioniums in the range of picoseconds. These results highlight the possibility of manipulating magnetic textures by using plasmonic effects, which presents significant opportunities for spintronics and non-conventional computer applications.

Comparative Study of Plasma-Enhanced-Atomic-Layer-Deposited Al2O3/HfO2/SiO2 and HfO2/Al2O3/SiO2 Trilayers for Ultraviolet Laser Applications.

High-performance thin films combining large optical bandgap Al2O3 and high refractive index HfO2 are excellent components for constructing the next generation of laser systems with enhanced output power. However, the growth of low-defect plasma-enhanced-atomic-layer-deposited (PEALD) Al2O3 for high-power laser applications and its combination with HfO2 and SiO2 materials commonly used in high-power laser thin films still face challenges, such as how to minimize defects, especially interface defects. In this work, substrate-layer interface defects in Al2O3 single-layer thin films, layer-layer interface defects in Al2O3-based bilayer and trilayer thin films, and their effects on the laser-induced damage threshold (LIDT) were investigated via capacitance-voltage (C-V) measurements. The experimental results show that by optimizing the deposition parameters, specifically the deposition temperature, precursor exposure time, and plasma oxygen exposure time, Al2O3 thin films with low defect density and high LIDT can be obtained. Two trilayer anti-reflection (AR) thin film structures, Al2O3/HfO2/SiO2 and HfO2/Al2O3/SiO2, were then prepared and compared. The trilayer AR thin film with Al2O3/HfO2/SiO2 structure exhibits a lower interface defect density, better interface bonding performance, and an increase in LIDT by approximately 2.8 times. We believe these results provide guidance for the control of interface defects and the design of thin film structures and will benefit many thin film optics for laser applications.

Nonequilibrium molecular dynamics investigation on friction behavior of organic friction modifiers under dynamic load

The evolution of lubricating oil containing additives under dynamic conditions is very significant, since its oil film structure, velocity distribution, and adsorption characteristic have an obvious impact on friction and wear. In this work, a boundary lubrication (BL) and elastohydrodynamic lubrication (EHL) models under sinusoidal load were carried out by nonequilibrium molecular dynamics (NEMD), using iron oxide as the substrate, hexadecane, and stearic acid molecules as lubricants. It was discovered that the friction in the BL regime is positively correlated with the degree of additive’s solidification. The greater the solidification degree of additive layers, the less the interlacing between them, making the relative motion between them easier and reducing compression oscillation within them, thus diminishing friction in the BL regime. The degree of liquefaction of base oil and additive regions, as well as the velocity difference within their interlacing zones, are connected to the friction force in the EHL regime. At high frequencies as well as large amplitudes, the oil film has a very high degree of liquefaction, which facilitates internal shear in it, and there is essentially no relative motion between the base oil and additives, resulting in low friction.

Influence of annealing times for W films on the structure and electrochromic properties of anodized WO\(_{3}\) films

WO3 films were prepared from annealed W films by anodization and annealing at 450℃ for 1 h. The sputtered W films were annealed before anodization at different times for 0.5 h to 2 h, followed by immediate removal from the furnace (quenching) or slow cooling (cool-down). The WO3 films exhibited a different preferred orientation between the (200) and (222) planes. The morphological structure of the WO3 films depended on the annealing time and cooling features of the W films. The WO3 films for the cool-down condition had smaller grains and more pores than the quenching condition. The WO3 films prepared from annealed W for 1.5 h with cool-down showed maximum transmittance change of 48.20% with the diffusion coefficient of 3.533 x 10-7 cm2∙s‒1. The quenching condition can be improved durability of WO3 films. Therefore, annealing time and cooling conditions can be used to design film properties that are suitable for the electrochromic application.

Anomalous size effects of ultra-small graphene sheets on the thermal properties of macroscopic films

Graphene films assembled from graphene nanosheets have achieved a wide range of applications in thermal management due to their ultra-high thermal conductivity. Although it is well established in the micron range that increasing the lateral size of graphene sheets enhances the thermal conductivity of graphene films. However, the preparation of large-size graphene sheets and their assembly into ordered film structures remain challenging, which impedes the development of high-performance thermally conductive graphene films. Herein, by unifying the properties of graphene sheets and preparation processes, we correlate the thermal conductivity of graphene films and the lateral size of starting sheets ranging from 0.32 to 20.32 μm and probe the underlying mechanism from the perspectives of macroscopic and microscopic structural defects. Surprisingly, decreasing lateral size to 0.32 μm achieved as high in-plane thermal conductivity (K//, 1550.06 ± 12.99 W/mK) and significantly higher through-plane thermal conductivity (K⊥, 8.11 ± 0.08 W/mK) of graphene films as the case of 20.32 μm. Besides, the commonly overlooked size effect of K⊥ shows an unexpected negative correlation, and the size effect of K// is also not monotonically increasing. These phenomena are correlated with micro-structure defects and lattice defects. Mechanism analysis reveals that thermally induced gas generation and the complex gas-sheet interactions during micro-structure evolution play a critical role in the size effect and may explain the unexpected negative size effect in the sub-micro range. These findings in size effects provide theoretical guidance for the selection of raw materials in fabricating highly thermally conductive graphene films.

A mechanistic approach to determine the relationship between film structure, electronic properties, and photocatalytic activity of ALD ZnO thin films on glass gibers

Atomic layer deposition (ALD), a high-conformality thin-film deposition technique, offers the opportunity to immobilize photocatalytic materials on high surface area substrates. Textile substrates are inexpensive, easily accessible materials with a fibrous nature, making them high surface area scaffolds for photocatalytic applications. This study applied ZnO thin-film coatings to fabric structures with different numbers of ALD cycles. The effect of coating thickness on the surface and electronic properties of the films and their photocatalytic properties were investigated. SEM, XRD, PL, and UV–Vis were used to examine the surface morphology, crystal structure, defects, and optical properties of the ZnO thin films. As the film thickness increased, the crystal sizes and the number of defects in the structure increased. Contact angle and Hall Effect measurements revealed that these structural defects are present on the surface of the films. Optimum wettability, mobility, and photocatalytic efficiency values were observed in the 15-nm coated samples, resulting in the highest photocatalytic activity and a turning point.

Microstructures and tribological properties of MoS2/Mo2N multilayer gradient films deposited by reactive magnetron sputtering

In order to compare the microstructures and tribological properties of films, pure Mo2N, pure MoS2, 3-layer and 13-layer MoS2/Mo2N gradient films were deposited by reactive magnetron sputtering. The crystalline structure, surface and cross-section morphologies, 3D surface topography, binding energy, hardness and tribological properties of films were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), atom force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), nanoindenter, and wear tester, respectively. The results indicate that the preferred orientation of MoS2 in gradient films has changed. The surface and cross-section structures of gradient films become denser with increasing the number of gradient layers. Average surface roughness (Ra) of pure MoS2 film is the highest, and Ra of 13-layer film is the lowest. The binding energy of MoS2 in the composite layer of gradient film has changed. The hardness of gradient film is higher than that of MoS2 and lower than that of Mo2N. The wear resistance of gradient films is much better than that of pure MoS2, and this phenomenon is more obvious under high load conditions. The improvement in the wear resistance of gradient films is attributed to the increase of dense, hardness, H/E and H3/E2. In the initial stage of friction, the 3-layer gradient film can maintain low friction coefficient (≤0.15), which is attributed to the thick MoS2 surface layer. The wear resistance of 13-layer is much better than that of 3-layer gradient film, because it has higher hardness, higher H/E and H3/E2 than 3-layer gradient film.

Nb2O5 film optical properties and laser-induced damage by phase-change-driven tuning

Niobium oxide (Nb2O5) is widely used in optical and electrical fields because of its high refractive index, wide band gap, high laser-induced damage threshold (LIDT) and high transparency in the ultraviolet to middle-infrared-wavelength range (0.35–7 μm). In this study, Nb2O5 films with different crystalline phases were successfully prepared on BK7 and Si substrates through electron beam evaporation (EB) and post-annealing. Based on the results of X-ray diffraction (XRD) and Raman spectroscopy analysis, the impact of the post-annealing technique on the structure, and optical and physical properties of Nb2O5 films was thoroughly discussed at the molecular level. The crystal phase of an Nb2O5 film and its molecular bonds considerably affect its properties. The Nb2O5(-12 1 2) film prepared in this study exhibited a higher LIDT (17.72 J/cm2) and a higher RMS (0.447 nm) than the corresponding films prepared in previous studies. Following the post-annealing process, the band gap and refractive index of the prepared films were significantly higher than those of the as-deposited film. Thus, this study has significant guiding implications for Nb2O5 film applications and the development costs of the films.

Corrosion behavior of Cr/RE alloyed rebar in carbonated simulated concrete pore solutions with chloride ions

Corrosion behavior of Cr/RE alloyed rebar in carbonated simulated concrete pore solutions with chloride ions

The role of Cu and film thickness on the photocatalytic activity of mesoporous spin coated TiO2 films

Most practical applications of photocatalysts will involve coatings on an inert support; here we have examined how copper doping of spin coated porous TiO2 films affects their physical characteristics and photocatalytic activity. The photocatalytic degradation of stearic acid was used as a measure of photocatalytic activity for catalysts spin coated from a sol-gel onto glass with 0, 0.1, 0.5, 1, 2.5 and 5 wt% copper introduced into the catalyst lattice before gelation. The effects of spin coating speed on film thickness, structure and band gap were studied and the nature of the copper incorporated into the films examined with XPS and XANES measurements. Increased spin coating speeds reduces the thickness of the deposited films from ∼ 50 μm to ∼ 20 μm until a spin speed of ∼ 3000 rpm at which point non-Newtonian behaviour of the gels prevents further reductions in film thickness. A larger effect on film thickness is the presence of the added copper nitrate which results in thinner films. After calcining, XANES shows the bulk of the copper to be in a Cu(II) state but at the surface of the thinnest, most active films XPS shows only Cu(I). Photocatalytic activity is much more strongly affected by the presence of the copper than the thickness of the films with 0.1 wt% Cu catalysts as much as 10 times more active than the undoped catalysts. Increasing the copper content, however, reduces activity until at ∼ 5 wt% activity is lower than for the pure TiO2 films.

Multi-Component Lithiophilic Alloy Film Modified Cu Current Collector for Long-Life Lithium Metal Batteries by a Novel FCVA Co-Deposition System.

Surface modification of Cu current collectors (CCs) is proven to be an effective method for protecting lithium metal anodes. However, few studies have focused on the quality and efficiency of modification layers. Herein, a novel home-made filtered cathode vacuum arc (FCVA) co-deposition system with high modification efficiency, good repeatability and environmental friendliness is proposed to realize the wide range regulation of film composition, structure and performance. Through this system, ZnMgTiAl quaternary alloy films, which have good affinity with Li are successfully constructed on Cu CCs, and the fully enhanced electrochemical performances are achieved. Symmetrical cells constructed with modified CCs maintained a fairly low voltage hysteresis of only 13mV after 2100h at a current density of 1mA cm-2. In addition, the capacity retention rate is as high as 75.0% after 100 cycles in the full cells. The influence of alloy films on the dynamic evolution process of constructing stable artificial solid electrolyte interphase (SEI) layer is revealed by in situ infrared (IR) spectroscopy. This work provides a promising route for designing various feasible modification films for LMBs, and it displays better industrial application prospects than the traditional chemical methods owing to the remarkable controllability and scale-up capacity.

Large Area Film of Highly Crystalline, Cleavable, and Transferable Semi-Conducting 2D-Imine Covalent Organic Framework on Dielectric Glass Substrate.

Two dimensional (2D) imine-based covalent organic framework (COF), 2D-COF, is a newly emerging molecular 2D polymer with potential applications in thin film electronics, sensing, and catalysis. It is considered an ideal candidate due to its robust 2D nature and precise tunability of the electronic and functional properties. Herein, we report a scalable facile synthesis of 2D imine-COF with control over film thickness (ranging from 100 nm to a few monolayers) and film dimension reaching up to 2 cm on a dielectric (glass) substrate. Highly crystalline 2D imine polymer films are formed by maintaining a quasi-equilibrium (very slow, ∼15 h) in Schiff base condensation reaction between p-phenylenediamine (PDA) and benzene-1,3,5-tricarboxaldehyde (TCA) molecules. Free-standing thin and ultrathin films of imine-COF are obtained using sonication exfoliation of 2D-COF polymer. Insights into the microstructure of thin/ultrathin imine-COF are obtained using scanning and transmission electron microscopy (SEM and TEM) and atomic force microscopy (AFM), which shows high crystallinity and 2D layered structure in both thin and ultrathin films. The chemical nature of the 2D polymer was established using X-ray photoelectron spectroscopy (XPS). Optical band gap measurements also reveal a semiconducting gap. This is further established by electronic structure calculation using density functional theory (DFT), which reveals a semiconductor-like band structure with strong dispersion in bands near conduction and valence band edges. The structural characteristics (layered morphology and microscopic structure) of 2D imine-COF show significant potential for its application in thin film device fabrication. In addition, the electronic structure shows strong dispersion in the frontier bands, making it a potential semiconducting material for charge carrier transportation in electronic devices.

Effects ofAs8structure formation on the surface morphology and internal microstructure of GaAs thin films.

Gallium arsenide (GaAs) materials have the advantages of high electron mobility, electron saturation drift rate, and other irreplaceable semiconducting properties. They play an important role in the electronics, solar and other fields. However, during GaAs film sedimentary growth, As atoms can undergo segregation to formAs8clusters because of the influence of external factors, which affect the surface morphology and internal structure of these films. In this study, a series of investigations on the deposition and growth of GaAs crystal films were performed. Additionally, the deposition and growth of GaAs thin films were simulated using molecular dynamics. The influence of As8clusters on the surface morphology and internal structure of GaAs films at different incidence angles, velocities and substrate temperatures was studied by using 'defect analysis technology' and 'diamond structure identification' in open source software, along with surface roughness and radial distribution function. Results show that with increasing incident angle, the number ofAs8clusters decreases and film density increases. Increasing incident velocity increases the irregular movement ofAs8clusters in air, and their deposition on the film surface affects the morphology of the film, and the surface roughness increases first and then decreases. Additionally, we investigated the effect of different substrate temperatures on the film surface. Results show that at a substrate temperature of 1173 K, the number ofAs8clusters in the film decreases or the As8clusters disappear, heterogeneous nucleation occurs in the film, and the crystallization rate increases. Although the dislocation line associated with nucleation may affect the mechanical and optical properties of the film, it considerably reduces the annealing effort after the deposition and growth.

Uniform monolayer of branched silver nanoplates-assembled nanoparticles for sensitive and reproducible SERS detection of harmful molecules

Surface-enhanced Raman scattering (SERS) technique can offer the fingerprint information of trace substances, and thus has wide potential applications in many fields. There is still a requirement to develop new and effective methods to construct high-performance SERS substrates. Here, a facile electrodeposition method is presented for fabricating large-scale uniform films assembled by branched silver (Ag) nanoplates. The morphology and structure of such film are highly uniform over a large area, which can ensure good spectral uniformity and reproducibility. There are dense sub-10 nm gaps between neighboring Ag nanoplates and between neighboring branches, forming plenty of hot spots. Therefore, the Ag nanoparticle monolayer exhibits high SERS activity along with excellent spectral repeatability. It is found that the limits of detection (LODs) towards rhodamine 6G and 4-aminothiophenol can reach 0.387 pM and 49.0 pM, respectively, showing high sensitivity of the designed SERS substrate. The enhancement factor of the prepared roughened Ag nanoparticle monolayer is computed to be as large as 2.37 × 108. Then, the highly roughened nanoparticle monolayer is used to detect cationic dye and fungicide (methylene blue, MB) and a synthetic cytokinin (6-benzylaminopurine, 6-BAP), and the corresponding LODs are determined down to 1.1 nM and 28.8 pM, respectively. Such LODs are much lower than the tolerance for MB and 6-BAP residues established by some authoritative regulations. Sensitive monitoring of 6-BAP residue on vegetables and fruits can also be achieved using such SERS substrate, indicating its promising application in environment monitoring and food safety supervision.