Carbon Research Articles

The new type of heteroborospherene as a potential promising high drug-loading capacity for carmustine anticancer drug: Theoretical perspectives

Nowadays, scientists are working on creating better drug delivery systems. We got inspired by the discovery of a modern kind of nanoparticles (Phys. Chem. Chem. Phys., 21 (2019) 15541). These particles, called heteroborospherenes, were created by adding four carbon atoms to a B364- cluster (C4B32). Both the regular and lithium-doped versions of C4B32 (Li @C4B32) could be useful in delivering drugs. This study explores how nanoclusters, such as C4B32 and Li@C4B32, interact with a cancer drug called carmustine with a method called density functional theory. This study found that adding a Li atom to the C4B32 nanocluster greatly improved its ability to attract the carmustine drug. Our UV–visible results reveal that when the drug combines with nanoclusters, the electronic spectra shift towards longer wavelengths (lower energies), showing a redshift. It was found that carmustine /Li@C4B32 has strong chemical reactivity and it is important for the drug to attach to the target site effectively. This study used atoms in Molecule analysis to better understand how the analyzed systems interact with the carmustine. The research results demonstrate how carmustine and Li@C4B32 bond through electrostatic features. Hence, the study showed that Li@C4B32 could be a good way to deliver the carmustine drug.

Adaptive changes in the fatty acid composition of <i>Oxytropis scheludjakovae</i> and <i>Oxytropis strobilacea</i> under temperature fluctuations during the growth season in Central Yakutia

Although there is growing interest in understanding the mechanisms of plant adaptive resistance, there is still incomplete or missing information for many plant species. In this study, we conducted an analysis of the fatty acid composition in the vegetative and generative organs of two species belonging to the Oxytropis genus, namely O. scheludjakovae and O. strobilacea. Gas-liquid chromatography was used to analyze the qualitative and quantitative changes in fatty acids throughout the growing season. The plants were grown in the natural flora collection nursery at the Yakutsk Botanical Garden. The main fatty acids identified had carbon atoms ranging from 14 to 24. There were no significant differences in fatty acid composition between the endemic species O. scheludjakovae and the more widely distributed species O. strobilacea. The highest total fatty acid content (19.5 mg/g tissue) was observed in the leaves of O. scheludjakovae in June and in the leaves of O. strobilacea (17.0 mg/g tissue) in June and July. Palmitic acid was the primary saturated fatty acid in both species, while linolenic acid was the main unsaturated fatty acid. The adaptation of these plants to temperature changes was reflected in the variation of unsaturated fatty acid content. O. strobilacea showed higher values of fatty acid unsaturation coefficient throughout the growing season compared to O. scheludjakovae.

Xylatolides A and B, new 10-membered macrolides from the endophytic fungus Xylaria sp.

Chemical investigation of the fungal endophyte Xylaria sp. isolated from leaves of Moringa oleifera, collected in Cameroon, resulted in the previously undescribed 10-membered macrolide, and two known naturalproducts. The structures of the xylatolides A and B were unambiguously identified by their mass spectra and by extensive 1D and 2D NMR spectroscopic analysis, featuring a 10-membered lactone core structure with oxygenated substituents and an unsubstituted 10-alkyl chain presenting seven carbon atoms. Compounds were screened for their cytotoxic potential against the human HepG2 hepatocellular carcinoma cells and HCT-116 cells (human colon carcinoma cell line). Moreover, the isolated compounds were also assayed against a small panel ofsensitive strains including the bacterial species Escherichia coli, Staphylococcus aureus, and Mycobacterium tuberculosis as well as against the fungal species Candida albicans. However, no significant activities were found.

Metal factories in the early Universe

ABSTRACT We have estimated the mass of metals in the molecular gas in 13 dusty star-forming galaxies at $z \sim 4$ in which the gas, based on previous observations, lies in a cold rotating disc. We estimated the metal masses using either the submillimetre line or continuum emission from three tracers of the overall metal content – carbon atoms, carbon monoxide molecules, and dust grains – using the first simultaneous calibration of all three tracers. We obtain very similar mass estimates from the different tracers, which are similar to the entire metal content of a present-day massive early-type galaxy. We used the dynamical masses of these galaxies to estimate an upper limit on the mass of the molecular gas in each galaxy, allowing us to estimate a lower limit on the metal abundance of the gas, finding values for many of the galaxies well above the solar value. We show that the high metal masses and metal abundances are what is expected shortly after the formation of a galaxy for a top-heavy IMF. We suggest a scenario for galaxy evolution in which massive galaxies reach a high metal abundance during their formation phase, which is then gradually reduced by dry mergers with lower mass galaxies. We show that the metals in the outflows from high-redshift dusty star-forming galaxies can quantitatively explain the long-standing puzzle that such a large fraction of the metals in galaxy clusters ($\simeq$0.75) is in the intracluster gas rather than in the galaxies themselves.

Physical, chemical and morphological evolution of incipient soot obtained from molecular dynamics simulation of acetylene pyrolysis

Incipient soot particles obtained from a series of reactive molecular dynamics simulations were studied to understand the evolution of physical, chemical, and morphological properties of incipient soot. Reactive molecular dynamics simulations of acetylene pyrolysis were performed using ReaxFF potential at 1350, 1500, 1650, and 1800 K. A total of 3324 incipient soot particles were extracted from the simulations at various stages of development. Features such as the number of carbon and hydrogen atoms, number of ring structures, mass, C/H ratio, radius of gyration, surface area, volume, atomic fractal dimension, and density were calculated for each particle. The calculated values of density and C/H ratio matched well with experimental values reported in the literature. Based on the calculated features, the particles were classified in two types: type 1 and type 2 particles. It was found that type 1 particles show significant morphological evolution while type 2 particles undergo chemical restructuring without any significant morphological change. The particle volume was found to be well-correlated with the number of carbon atoms in both type 1 and type 2 particles, whereas surface area was found to be correlated with the number of carbon atoms only for type 1 particles. A correlation matrix comparing the level of correlation between any two features for both type 1 and type 2 particles was created. Finally, based on the calculated statistics, a set of correlations among various physical and morphological parameters of incipient soot was proposed.

Production of high-carbon-number naphthenes for bio-aviation fuels from bio-crude prepared by fast pyrolysis of lignocellulose

Lignocellulose has been suggested as a cost-effective, environmentally sustainable substitute for paraffins, aromatics, and naphthenes in aviation fuel. However, bio-crude derived from the fast pyrolysis of lignocellulose poses challenges because of its high acidity and viscosity arising from oxygenates and water; in addition, the low-carbon-number hydrocarbons obtained from lignocellulose-derived sugars and phenols are unsuitable for aviation fuels. In this investigation, high-carbon-number hydrocarbon fuels are generated from bio-crude through condensation reactions between phenols and saturated cyclic alcohols, achieving a heavy fraction similar to that of aviation fuels. The one-pass, four-step continuous-flow reaction of bio-crude is conducted using a catalysis reactor equipped with carbon-supported palladium, titania-supported nickel–iron, hydrogen-form zeolite Y, and tungstate–zirconia-supported ruthenium. In contrast with conventional two-step hydrodeoxygenation methods yielding 1.1% dimeric cycloalkanes, the suggested multi-step reaction produced 4.5 to 4.7% yields of heavier naphthenes containing twelve or more carbon atoms.

Magic angle and STEM-EELS mapping of the sp2/sp3 hybridization in heterogeneous carbonaceous materials

Extensive research has been conducted on carbonaceous materials due to their unique combination of physical, chemical, and mechanical properties, which significantly rely on the hybridization of carbon atoms. Scanning transmission electron microscopy-electron energy loss spectroscopy is a powerful technique that enables the identification of carbon allotropes with high spatial resolution, utilizing specific spectral features. However, anisotropic materials like graphite and carbon nanotubes can exhibit variations in these spectral features based on their orientation relative to the electron beam. Optimized experimental conditions, referred to as magic angle conditions, permits overcoming this challenge. By implementing such conditions, we have successfully mapped the hybridization in a heterogeneous system containing three carbon allotropes, i.e. nanodiamonds, multi-walled carbon nanotubes, and lacey carbon. Moreover, a convolutional neural network has been created and trained to accurately identify and map these carbonaceous phases. Thus, the reported innovative approach allows nanoscale mapping of both hybridization and phase distributions for complex heterogeneous carbon systems.

Quantum chemical modeling of alkane 2D monolayer formation on graphene

The paper presents a quantum chemical approach for assessment of the thermodynamic parameters of association for alkanes CnH2n+2 (n = 6–14) and polyaromatic hydrocarbons (PAH) of the coronene series as model structures of the graphene surface within the framework of semiempirical methods. The enthalpy, entropy and Gibbs energy of formation and binding for alkanes with PAH were calculated using the PM3 and PM6-DH2 methods. It is shown that an adequate description of the interactions in the regarded complexes requires the use of PM6-DH2 method, since it contains corrections for dispersion interactions and hydrogen bonds. The parallel orientation of the alkane molecule relative to the coronene plane is proved to be more energetically preferable than perpendicular one, which is consistent with experimental data.Intermolecular C–H/π interactions are revealed to be crucial in the 2D film formation of alkanes on graphene/graphite. While interactions between alkane molecules make a destabilizing contribution due to the implementation of energetically unfavorable types of intermolecular CH/HC interactions. This stipulates a threshold chain length of alkanes capable of film formation on the graphene/graphite surface at standard temperature: 14 and 19 carbon atoms for parallel and perpendicular oriented alkanes, respectively. The obtained threshold values of the alkane chain length, as well as the geometric parameters of their orientation in 2D monolayers on the graphene/graphite surface are consistent with available experimental data.

Computational Insights into the Intramolecular Aromatic C-C Coupling Catalyzed by the Cytochrome P450 Enzyme CYP121 from Mycobacterium tuberculosis.

CYP121 is a P450 enzyme that catalyzes the intramolecular C-C coupling of its native substrate, dicyclotyrosine (cYY). According to previous suggestions, when the cosubstrate peracetic acid was used to generate Cpd I, the substrate cYY was suggested to participate in the cleavage of the O-O bond; however, whether cYY is involved in the formation of Cpd I and how two distant aromatic carbon atoms are activated are still unclear. Here, we constructed computational models and performed QM/MM calculations to clarify the reaction mechanism. On the basis of our calculation results, cYY is not involved in the formation of Cpd I, and the C-C coupling reaction starts from hydrogen abstraction. In the second stage, the substrate should first undergo a complex conformational change, leading to two phenolic hydroxyls of cYY close to each other. In the subsequent reaction, the resultant Cpd II again abstracts a hydrogen atom from the proximal tyrosine to generate the diradical intermediate. In addition, the C-C coupling occurs in the active site, but the final aromatization may be a nonenzymatic reaction. In general, the intramolecular C-C coupling requires two basic conditions, including the active site having good flexibility and the substrate itself having a suitable and rotatable skeleton.

STRUCTURAL CHANGES DURING THERMAL STRENGTHENING OF THE RAILWAY WHEEL

Purpose. Justification of mechanism of the structure transformations in the carbon steel of the railway wheel during disk thermal strengthening. Research methods. The material for the study was carbon steel of a railway wheel with a content of 0.57 % C, 0.65 % Si, 0.45 % Mn, 0.0029 % S, 0.014 % P and 0.11 % Cr. The railway wheel was heated to temperatures higher than Ac3, kept at this temperature to complete austenite homogenization process, and disk was rapidly cooled to the specified temperature. Degree defectiveness structure of the metal after accelerated cooling was assessed using technique of X-ray structural analysis. Strength stress, yield stress and relative elongation of the carbon steel were determined at stretching at rate of deformation 10-3 s-1. Results. At accelerated cooling of the carbon steel, the sources of strengthening are the processes of blocking mobile dislocations due to the condensation of carbon atoms on them and dispersion strengthening from the formed particles of the carbide phase. At temperatures of termination of forced cooling of carbon steel above 300…350 °C, the reduction rate of strength properties is determined by the excess of total effect of softening from decomposition of the solid solution, acceleration of spheroidization and coalescence of cementite particles over the blocking of dislocations by carbon atoms and dispersion hardening. Scientific novelty. The level of strength and plasticity characteristics of carbon steel of the railway wheel disc, depending on the temperature end forced cooling, is determined by the ratio of the influence of degree super saturation of the solid solution and the dispersion strengthening by carbide phase. Practical value. For temperatures termination of accelerated cooling of 200…300 °C, degree of super saturation of the solid solution is the main factor that determines the level of strength and plasticity characteristics. When manufacturing an all-rolled railway wheel, the strength limit of the disc metal can be increased by accelerated cooling to the middle range of temperature.

Effect of temperature on the friction behavior and mechanism of DLC film in CO2 foam fracturing environment

Diamond-like carbon (DLC) film is considered to be an attractive candidate material for reducing friction and wear in oil and gas equipment due to its low friction and high wear resistance. This study investigated the evolution of friction interfaces and tribochemical reaction at three different temperatures through reactive molecular dynamics simulations. The results reveal that the synergistic effect of atomic transfer layer and chemical passivation of DLC film leads to the decrease of friction force with increasing ambient temperature. The cumulative atomic transfer layer with increasing ambient temperature also contributes to the increase of wear amount, while the atomic lattice transition dominates friction temperatures. More importantly, the phenomenon of increased sp3 carbon atoms in DLC film is also temperature dependent.

Impact of deodorisation time and temperature on the removal of different MOAH structures: a lab-scale study on spiked coconut oil

Vegetable fats and oils are prone to contamination by mineral oil hydrocarbons due to the lipophilic and ubiquitous character of the latter. As the aromatic fraction of these hydrocarbons, MOAH, is associated with carcinogenicity, mutagenicity, and detrimental effects on foetal development, finding strategies to limit or reduce their contamination is highly relevant. Deodorisation (i.e. a refining step) has shown the ability to remove MOAH < C25 in vegetable fats and oils, but there is little information about the structures removed. Therefore, the present study investigated the impact of deodorisation conditions on the removal of different structures of MOAH in spiked coconut oil. An inscribed central composite design was built with time and temperature as variables (0.5-4h, 150-240 °C), while pressure (3 mbar) and steam flow (1 g water/g oil per hour) were kept constant. The analysis of MOAH in the oil was performed using a fully automated liquid chromatography coupled with two parallel comprehensive two-dimensional gas chromatography systems with flame ionisation and time-of-flight mass spectrometric detection. Response surfaces plotting the MOAH loss according to time and temperature were built for different MOAH fractions. The latter were defined based on the number of aromatic rings (>3 or ≤3) and the number of carbon atoms present (C16-C20, C20-C24, C24-C35, C35-C40). It was found that at 200 °C, compounds < C24, including weakly alkylated triaromatics, could be reduced to below the limit of quantification, while at 230 °C, it was possible to remove >60% of the C24-C35 fraction, including pentaromatics of low alkylation.

Study of the Spectroscopic Analysis, Electronic Structure and Thermodynamic Properties of Ethyl benzene Using First-Principles Density Functional Theory

This study describes the optimized molecular structure, spectroscopic analysis, electronic structure and thermodynamics properties of the ethylbenzene molecule using first-principles DFT/B3LYP method with 6-311++G(d,p) basis set. The C-H in-plane bending vibration is observed between 1400 and 1050 cm-1, while the C-H out-of-plane bending vibration is observed between 1000 and 675 cm-1. The benzene ring has the most negative potential that corresponds to the attraction of proton due to concentrated electron density while the moderate positive potential is localized closed to the hydrogen atom. Analysis of the HOMO and LUMO in ethylbenzene anticipates an energy disparity of 6.3028 eV, a value closely matching the energy gap derived from DOS calculations. Mulliken charge analysis of the ethylbenzene molecules gives the information that all the hydrogen atom corresponds to the positive charges while all the carbon atom except C3 corresponds to the negative charge and the values of the global parameters such as hardness, chemical potential, electronegativity, electrophilicity index, softness are found to be 3.1514 eV, -3.5979 eV, 3.5979 eV, 2.0538 eV and 0.3173 eV-1 respectively. Various thermodynamic parameters such as heat capacity at constant volume, heat capacity at constant pressure, total internal energy, enthalpy and entropy, exhibit a rising trend with increasing temperature whereas Gibbs free energy shows an inverse relationship with temperature variation.

Transcriptomic re-analyses of human hepatocyte spheroids treated with PFAS reveals chain length and dose-dependent modes of action

To identify pathway perturbations and examine biological modes of action (MOAs) for various perfluoroalkyl substances, we re-analyzed published in vitro gene expression studies from human primary liver spheroids. With treatment times ranging from 10 to 14 days, shorter-chain PFAS (those with 6 or fewer fluorinated carbon atoms in the alkyl chain) showed enrichment for pathways of fatty acid metabolism and fatty acid beta-oxidation with upregulated genes. Longer-chain PFAS compounds, specifically PFOS (perfluorooctane sulfonate), PFDS (perfluorodecane sulfonate), and higher doses of PFOA (perfluorooctanoic acid), had enrichment for pathways involved in steroid metabolism, fatty acid metabolism, and biological oxidation for downregulated genes. Although PFNA (perfluorononanoic acid), PFDA (perfluorodecanoic acid), and PFUnDA (perfluoroundecanoic acid) were more toxic and could only be examined after a 1-day treatment, all three had enrichment patterns similar to those observed with PFOS. With PFOA there were dose-dependent changes in pathway enrichment, shifting from upregulation of fatty acid metabolism and downregulation of steroid metabolism to downregulation of both at higher doses. The response to PFHpS (perfluoroheptanesulfonic acid) was similar to the PFOA pattern at the lower treatment dose. Based on results of transcription factor binding sites analyses, we propose that downregulation of pathways of lipid metabolism by longer chain PFAS may be due to inhibitory interactions of PPARD on genes controlled by PPARA and PPARG. In conclusion, our transcriptomic analysis indicates that the biological MOAs of PFAS compounds differ according to chain length and dose, and that risk assessments for PFAS should consider these differences in biological MOAs when evaluating mixtures of these compounds.

Effects of post-deposition annealing on structure and mechanical properties of multilayer Ti/DLC films

The multilayer (Ti/DLC) × 3 films were deposited using a DC arc evaporator with a titanium cathode and a pulsed cathode-spark evaporator with a graphite cathode. Following the deposition of the films, a heat treatment process was performed in air and Ar atmosphere at temperatures of 200 °C and 400 °C. The investigation of the films involved the examination of their structure, surface morphology, and chemical composition using AFM, SEM, XPS and Raman. Additionally, the mechanical properties of the films were assessed by nanoindentation, sclerometry and wear test. Changes in the structure, RMS roughness, С-sp2/С-sp3 ratio of carbon atoms in the film and the formation of Ti-C carbide were determined in relation to the heat treatment conditions. Studies have demonstrated that subjecting materials to heat treatment at temperatures of 400 °C results in a decrease in friction coefficient and an increase in hardness. The deposition of films on the working surfaces of microdrills with subsequent heat treatment leads to a reduction in wear, an extension of their service life, and an improvement in drilling accuracy as compared to microdrills without films. Furthermore, microdrills with (Ti/DLC) × 3 films annealed in air at 400 °C exhibit negligible size reduction and better drilling accuracy.

Regio- and stereoselective access to highly substituted vinylphosphine oxides via metal-free electrophilic phosphonoiodination of alkynes

In general, the P-centered ring-opening of quaternary phosphirenium salts (QPrS) predominantly leads to hydrophosphorylated products, while the C-centered ring-opening is primarily confined to intramolecular nucleophilic reactions, resulting in the formation of phosphorus-containing cyclization products instead of difunctionalized products generated through intermolecular nucleophilic processes. Here, through the promotion of ring-opening of three-member rings by iodine anions and the quenching of electronegative carbon atoms by iodine cations, we successfully synthesize β-functionalized vinylphosphine oxides by the P-addition of QPrS intermediates generated in situ. Multiple β-iodo-substituted vinylphosphine oxides can be obtained with exceptional regio- and stereo-selectivity by reacting secondary phosphine oxides with unactivated alkynes. In addition, a variety of β-functionalized vinylphosphine oxides converted from C-I bonds, especially the rapid construction of benzo[b]phospholes oxides, demonstrates the significance of this strategy.

Thermodynamical stability of carbon-based defects in α boron from first principles

We report an exhaustive study of the formation enthalpy and charge states of carbon-based defects in rhombohedral α boron within the density functional theory (DFT) that enables us to derive rules about the formation of complex carbon defects. We have accounted for one and two interstitial carbon atoms, eventually combined with one substitutional carbon atom and/or one interstitial boron atom and varied several geometric parameters. We find that when positioned in the plane perpendicular to the [111] rhombohedral axis, two carbon atoms turn out to preferentially form a graphite-like hexagon with four boron atoms. When positioned instead along the [111] axis, the distance between them strongly affects the defect thermodynamic stability, and we find in particular that additional negative charges strongly stabilize the diatomic carbon–carbon chains.

Design and Implementation of a Low-Power Device for Non-Invasive Blood Glucose

Glucose is a simple sugar molecule. The chemical formula of this sugar molecule is C6H12O6. This means that the glucose molecule contains six carbon atoms (C), twelve hydrogen atoms (H), and six oxygen atoms (O). In human blood, the molecule glucose circulates as blood sugar. Normally, after eating or drinking, our bodies break down the sugars in food and use them to obtain energy for our cells. To execute this process, our pancreas produces insulin. Insulin “pulls” sugar from the blood and puts it into the cells for use. If someone has diabetes, their pancreas cannot produce enough insulin. As a result, the level of glucose in their blood rises. This can lead to many potential complications, including blindness, disease, nerve damage, amputation, stroke, heart attack, damage to blood vessels, etc. In this study, a non-invasive and therefore easily usable method for monitoring blood glucose was developed. With the experiment carried out, it was possible to measure glucose levels continuously, thus eliminating the disadvantages of invasive systems. Near-IR sensors (optical sensors) were used to estimate the concentration of glucose in blood; these sensors have a wavelength of 940 nm. The sensor was placed on a small black parallelepiped-shaped box on the tip of the finger and the output of the optical sensor was then connected to a microcontroller at the analogue input. Another sensor used, but only to provide more medical information, was the heartbeat sensor, inserted into an armband (along with the microprocessor). After processing and linear regression analysis, the glucose level was predicted, and data were sent via the Bluetooth network to a developed APP. The results of the implemented device were compared with available invasive methods (commercial products). The hardware consisted of a microcontroller, a near-IR optical sensor, a heartbeat sensor, and a Bluetooth module. Another objective of this experiment using low-cost and low-power hardware was to not carry out complex processing of data from the sensors. Our practical laboratory experiment resulted in an error of 2.86 per cent when compared to a commercial product, with a hardware cost of EUR 8 and a consumption of 50 mA.

Micro-nanobubble-assisted As(III) removal from water by Ni-doped MOF materials.

Micro-nanobubbles (MNBs) can form reactive oxygen species (ROS) with high oxidizing potential. In this study, nickel-doped metal-organic framework materials (MOFs) capable of activating molecular oxygen were synthesized using trivalent arsenic (As(III)) as a target pollutant and combined with peroxymonosulfate (PMS) to construct a MOF/MNB/PMS system. The results included the rapid oxidation of As(III), the successful absorption of oxidized As(V), and finally the efficient removal of As. The effects of pH, amount of PMS used, and preparation time of MNBs on the As removal performance of the MOF/MNB/PMS system were investigated experimentally. The changes in the properties of the materials before and after the reaction were analyzed by XPS, and it was found that the main active sites on the surface of the MOFs were the metal elements and the pyridine nitrogen near the carbon atom. The regular morphology and elemental composition of the MOFs were determined by TEM scanning and EDS test, which indicated the presence of nickel. XRD tests before and after the reaction showed that the MOFs were structurally stable. The results of the free radical burst experiments show that the single linear oxygen (1O2) is the main active substance in the system, and that the MNBs are key factors by which the system achieves efficient oxidation performance. In addition to providing a sustainable supply of molecular oxygen to the MOFs during the reaction process, coupling the MNBs with PMS was found to improve the oxidation capacity of the system. The results of this study thus provide a new concept for As removal and advanced oxidation in water bodies.

Selective removal of single-layer graphene over double-layer graphene on SiO2 by remote oxygen plasma irradiation

Graphene sheet transferred onto the SiO2 substrate has various types at different regions such as single-layer graphene (SLG), double-layer graphene (DLG), and multi-layer graphene (MLG). These layers were identified by Raman analysis of 2D band position around 2700 cm−1 and full width at half maximum (FWHM). The transferred graphene sheets on SiO2 were remotely irradiated by oxygen plasma without energetic ions at a room temperature. At the beginning of the oxygen plasma irradiation, the carbons on the surface of the graphene sheets were oxidized and the 2D-FWHMs were broadened due to an increase of defects on the basal plane. By controlling the plasma irradiation time up to 120 min, selectively stripping away the SLG regions on the SiO2 surface was observed while leaving the other DLG and MLG regions. The difference in attractive forces resulted in favorable desorption of carbon atoms occurred in the oxidized SLG regions on SiO2 surface by the remote oxygen plasma irradiation.