Oxygen Atoms Research Articles

Study on the effect of NO2 impurity gas on the performance and local current density distribution of PEMFC

The performance of proton exchange membrane fuel cells (PEMFCs) is affected by impurities, and airborne NO2 is a potential factor in the degradation of the performance and durability of PEMFCs. Herein, the effect of 50 ppb ∼ 5 ppm NO2 on PEMFC was investigated by the poisoning strategy of increasing concentration gradient, and the effect of NO2 on the local current density distribution was explored in both galvanostatic and potentiostatic states. The results showed that 2 ppm NO2 caused a significant voltage decay accompanied by an increase in activation impedance and mass transfer impedance. NO2 was decomposed into oxygen atoms and adsorbed NO on the Pt surface, occupying active sites, impeding oxygen reduction reaction, and further hindering mass transfer. Polarization curve results showed more pronounced voltage decay at high current densities. Polarization curve testing and clean air purging were effective in restoring the poisoned PEMFC. Moreover, it was proved that the poisoning effect is more severe in the inlet region, especially in potentiostatic state. Hence, it is suggested to operate in galvanostatic state, which has a positive impact on reducing the uneven performance caused by NO2. This study provides a reference for the prevention of PEMFC poisoning and performance recovery after poisoning.

Mechanochemical and Microwave Multistep Organic Reactions

Abstract: The development of more sustainable chemical reactions and processes has been the focus of recent research activities. Advances in the field of organic synthesis have led to the emergence of new methodologies and techniques involving non-conventional energy sources. These include the applications of mechanical energy (mechanochemistry) and microwave radiation (MW) methods. This article reviews the advances in multistep organic synthesis of biologically relevant organic molecules using mechanochemistry and microwave techniques. Among them, various heterocyclic molecules (with nitrogen, oxygen, and sulphur atoms), amides, and peptides have been synthesized by multistep mechanochemical or MW reactions. Performing multiple synthetic steps using more sustainable methods shows cumulative advantages over multistep processes under conventional conditions in terms of reduced solvent use, shorter reaction times, better turnovers, and reaction yields. Simplification of protocols by carrying out two or more reaction steps in the same reaction vessel is another advantage of multistep syntheses.

Restoring the electronic properties of epitaxial graphene on SiC substrate by Ar intercalation

Thermal decomposition of 6H-SiC(0001) under an argon atmosphere is a promising technique to fabricate large-scale epitaxial graphene monolayers for electronic applications. In this manuscript, we report on the intercalation of argon, hydrogen and oxygen atoms underneath a graphene buffer layer (BL) on SiC(0001), involving bond formation between the intercalated agent and Si atoms. Density Functional Theory calculations were performed to investigate the atomic structure, stability and electronic properties of quasi free-standing monolayer graphene and bilayer graphene, accomplished by intercalation. According to our results, as the Ar intercalated atoms saturate the silicon dangling bonds in the upper SiC surface, the BL is completely detached from the substrate and transformed into free-standing graphene. Ar intercalation would be hindered by the concurrent and thermodynamically more spontaneous adsorption of Ar atop the graphene layers, resulting in a pronounced decrease of the process efficiency. High Ar-coverage regimes and low kinetic barriers for Ar intercalation might shift the intercalation/adsorption balance. These factors as well as strategies such as ion implantation could be explored to identify more favorable conditions to experimentally test Ar intercalation as a simple method to achieve control of the electronic properties of the BL and help preserve the unique characteristics of graphene.

The diffusion behavior of H3O+ in insulation systems composed of paper cellulose and modified natural ester insulating oil

The oil-paper insulation system will be affected by the synergistic effects of moisture and acids during long-term stable operation of the transformer. The moisture in the oil can be combined with the H+ionized from the acid molecules in the form of H3O+ by coordination, thus changing the proportion of acid distribution in the insulating oil and paper cellulose. Natural ester insulating oil, as a new development trend to replace mineral oil, can be significantly improved by adding nanoparticles to them. The diffusion behavior of H3O+ in paper cellulose and nano-SiO2-modified soybean oil-based natural ester insulating oil insulating system has been investigated using molecular dynamics in this article. The results indicate that the incorporation with nanoparticles is effective in mitigating the impact of temperature on the diffusion behavior of H3O+ in oil-paper insulation. Compared with the unmodified model, the nano-modified model results in a significant reduction in the concentration distribution of H3O+ in paper cellulose. The hydroxyl and ether bonds in paper cellulose will interact with H3O+ to generate hydrogen bonds and destroy its original hydrogen bonding network, while nanoparticles can inhibit diffusion by adsorbing H3O+ through hydroxyl oxygen atoms.

Study on the swelling of macromolecular geological organic matter with hydrocarbons and heteroatomic compounds

In this study, we conducted swelling experiments on eleven macromolecular geological organic materials using five types of organic solvents. Our primary objective was to investigate the absorption capacity of different solid organic materials in organic fluids and analyze the influence of their chemical structures. The samples utilized in this research included solid bitumen, kerogen, and coal samples from various basins. The chemical structure of the samples was assessed using solid-state 13C nuclear magnetic resonance (NMR), while X-ray diffraction (XRD) was employed to monitor any detect the structural changes during the swelling process. Our findings reveal that macromolecular geological organic compounds demonstrate a preferential expulsion of saturated hydrocarbons, followed by polycyclic aromatic hydrocarbons, upon interaction with liquid organic matter. The sulfur-containing compounds in solid organic matter demonstrated higher solubility than hydrocarbon compounds, while the solubility of oxygen-containing compounds varied based on the structure of the aliphatic chain and the proportion of oxygen atoms. This research, introduces LA [= Lac × Aac] as a new parameter to assess the combination of aliphatic chain length [Lac] and [Aac] abundance in solid organic matter. Furthermore, XRD testing revealed that the chemical structure unit of heteroatom compounds in solid organic matter consists of amorphous carbon, primarily composed of aliphatic chains. In this study, we evaluated the retention capacity of various macromolecular geological organic matter for both hydrocarbons and heteroatomic compounds. Additionally, the extent of swelling was investigated, providing theoretical support to diverse fields including organic petrology, petroleum geology, coal geology, and organic geochemistry.

Biogenic synthesis of CoO and ZnO nanoparticles using rosemary extract: Synergistic antimicrobial activity and insights from DFT simulations

Plant extracts with stabilizing and emulsifying qualities are commonly used in nanotechnology for the eco-friendly production of metallic nanoparticles. The study focused on synthesizing CoO and ZnO nanoparticles by the use of rosemary leaf extract. Quantum chemical calculations were performed using the DFT method to determine the active sites of the main chemical compounds in rosemary extract that catalyze the bi-reduction of Co+2 and Zn+2, resulting in the eco-friendly production of CoO and ZnO nanoparticles. Rosemary leaf extracts include a significant quantity of hydroxyl groups (–OH), oxygen atoms as heteroatoms, and many aromatic rings. The enhanced amount of π-electrons, resulting from aromatic rings and electron-releasing groups connected to these rings, facilitates the simultaneous reduction of Co and Zn metals. This happens because the π-electrons are more likely to interact with the vacant d-orbitals of Co and Zn. Antibacterial activity tests show that CoO and ZnO nanoparticles manufactured using green methods are effective against both gram-negative and gram-positive bacteria, as well as the fungal isolate C. albicans with superior activity of CoO nanoparticles. The MIC assay results show that the synthesized nanoparticles are more effective against gram-negative E. coli bacteria than gram-positive S. aureus bacteria and C. albicans. CoO nanoparticles showed about 1.5x - 3x fold more antibacterial activity compared to ZnO nanoparticles. The results emphasize the possibility of using green synthesis of nanoparticles as an environmentally benign and cost-efficient technique for mass manufacturing, showing potential applications in the fields of medicine and industry.

Construction of Three Novel Oxygen-containing Cage-like Frameworks and Synthesis of their Energetic Derivatives

Organic cage-like frameworks are important and versatile skeletons for developing prospective energetic compounds because of their high intrinsic density, symmetry, stability, and derivability. Herein, we show the construction of three novel cage-like frameworks including dioxaadamantane, dioxaproadamantane and dioxatwistane from 9-oxabicyclo[3.3.1]nonane-2,6-diene. In addition, their energetic derivatives were also prepared and characterized. Compared with our previous works, the introduction of more oxygen atoms into the framework gives the corresponding energetic derivative a better oxygen balance, significantly higher density and detonation properties. These results imply that the oxygen-containing framework has the potential to be used for preparing new 3D energetic compounds with superior energy performance.

Dissociative Adsorption of O2 on Ag3Au(111) Surface: A Density Functional Theory Study

The catalytic efficiency of oxygen reduction catalysts is notably influenced by the dissociative adsorption of O2. We conducted a systematic investigation into the dissociative adsorption of O2 on the Ag3Au(111) surface using ab initio density functional theory (DFT) calculations. Our computational findings indicate that adsorption the configuration designated t-b-t exhibits favorable energetics on the Ag3Au(111) surface. Regarding the dissociation of O2, we identified a reasonable dissociation pathway, which proceeds from the initial t-b-t state to the creation of two oxygen atoms that occupy a set of neighboring fcc sites. Furthermore, our analysis indicates that the adsorption of O2 on the Ag3Au(111) surface is less favored thermodynamically and more difficult to dissociate than that on the Ag(111) surface. This study furnishes a theoretical framework elucidating the prospective utilization of Ag-Au alloy in the capacity of oxygen reduction catalysts.

Thickness dependence of the room-temperature ethanol sensor properties of Cu2O polycrystalline films

This study investigates the fabrication process of copper thin films via thermal evaporation, with precise control over film thickness achieved through Z-position adjustment. Analysis of the as-fabricated copper films reveals a discernible relationship between grain size (〈D〉) and Z-position, characterized by a phenomenological equation 〈D〉XRDn(Z)=〈D〉0n1+32rZ2+158rZ4 , which is further supported by a growth exponent (n) of 0.41 obtained from the analysis. This value aligns well with findings in the literature concerning the growth of copper films, thus underlining the validity and reliability of our experimental outcomes. The resulting crystallites, ranging in size from 20 to 26 nm, exhibit a resistivity within the range of 3.3–4.6 μΩ · cm. Upon thermal annealing at 200 °C, cuprite Cu2O thin films are produced, demonstrating crystallite sizes ranging from ∼9 to ∼24 nm with increasing film thickness. The observed monotonic reduction in Cu2O crystallites relative to film thickness is attributed to a recrystallization process, indicating amorphization when oxygen atoms are introduced, followed by the nucleation and growth of newly formed copper oxide phase. Changes in the optical bandgap of the Cu2O films, ranging from 2.31 to 2.07 eV, are attributed mainly to the quantum confinement effect, particularly important in Cu2O with size close than the Bohr exciton diameter (5 nm) of the Cu2O. Additionally, correlations between refractive index and extinction coefficient with film thickness are observed, notably a linear relationship between refractive index and charge carrier density. Electrical measurements confirm the presence of a p-type semiconductor with carrier concentrations of ∼1014 cm−3, showing a slight decrease with film thickness. This phenomenon is likely attributed to escalating film roughness, which introduces supplementary scattering mechanisms for charge carriers, leading to a resistivity increase, especially as the roughness approaches or surpasses the mean free path of charge carriers (8.61 nm). Moreover, ab-initio calculations on the Cu2O crystalline phase to investigate the impact of hydrostatic strain on its electronic and optical properties was conducted. We believe that our findings provide crucial insights that support the elucidation of the experimental results. Notably, thinner cuprite films exhibit heightened sensitivity to ethanol gas at room temperature, indicating potential for highly responsive gas sensors, particularly for ethanol breath testing, with significant implications for portable device applications.

Providing a Photovoltaic Performance Enhancement Relationship from Binary to Ternary Polymer Solar Cells via Machine Learning

Ternary polymer solar cells (PSCs) are currently the simplest and most efficient way to further improve the device performance in PSCs. To find high-performance organic photovoltaic materials, the established connection between the material structure and device performance before fabrication is of great significance. Herein, firstly, a database of the photovoltaic performance in 874 experimental PSCs reported in the literature is established, and three different fingerprint expressions of a molecular structure are explored as input features; the results show that long fingerprints of 2D atom pairs can contain more effective information and improve the accuracy of the models. Through supervised learning, five machine learning (ML) models were trained to build a mapping of the photovoltaic performance improvement relationship from binary to ternary PSCs. The GBDT model had the best predictive ability and generalization. Eighteen key structural features from a non-fullerene acceptor and the third components that affect the device’s PCE were screened based on this model, including a nitrile group with lone-pair electron, a halogen atom, an oxygen atom, etc. Interestingly, the structural features for the enhanced device’s PCE were essentially increased by the Jsc or FF. More importantly, the reliability of the ML model was further verified by preparing the highly efficient PSCs. Taking the PM6:BTP-eC9:PY-IT ternary PSC as an example, the PCE prediction (18.03%) by the model was in good agreement with the experimental results (17.78%), the relative prediction error was 1.41%, and the relative error between all experimental results and predicted results was less than 5%. These results indicate that ML is a useful tool for exploring the photovoltaic performance improvement of PSCs and accelerating the design and application with highly efficient non-fullerene materials.

Effect of the Addition of WO3 on the Structure and Luminescent Properties of ZnO-B2O3:Eu3+ Glass

Glasses with the compositions in mol % of 50ZnO:(50 − x)B2O3:0.5Eu2O3:xWO3, x = 0, 1, 3, 5 and 10 were obtained by applying the melt-quenching method and investigated by Raman spectroscopy, DSC analysis and photoluminescence (PL) spectroscopy. Raman spectra revealed that tungstate ions incorporate into the base zinc borate glass as tetrahedral [WO4]2− groups, and octahedral [WØ4O2]2− species with four bridging and two non-bridging oxygen atoms. There are also metaborate, [BØ2O]− and pyroborate units, [B2O5]4−, in the glass networks. The glasses are characterized by good transmission in the visible region, at about 80%. Photoluminescence (PL) spectra evidenced that WO3 is an appropriate constituent for the modification of zinc borate glass structure and for enhancing the Eu3+ luminescent intensity. The most intense luminescence peak observed, at 612 nm, suggests that the glasses are potential materials for red emission.

Oxygen‐Bridged Quasi‐Planar para‐Phenylenediamine and its Oxidized States

AbstractA quasi‐planar N, N, N’,N’‐tetraphenyl‐para‐phenylenediamine, where all the phenyl rings are tethered by four oxygen atoms to embed quasi‐planar triphenylamine moieties into the molecular skeleton, was prepared and characterized to evaluate the impact by incorporating the structural rigidity. The monocationic and dicationic species could be selectively generated, depending on the type of oxidizing agents used. Spectroscopic and X‐ray diffraction analyses revealed the radical cation was in a unique charge/spin delocalized class III mixed‐valence state due to an exquisite balance between the electronic effect by the oxygen‐bridges and the rigidity of molecular framework.

Origin of the Activity of Electrochemical Ozone Production over Rutile PbO2 Surfaces.

Ozonation water treatment technology has attracted increasing attention due to its environmental benign and high efficiency. Rutile PbO2 is a promising anode material for electrochemical ozone production (EOP). However, the reaction mechanism underlying ozone production catalyzed by PbO2 was rarely studied and not well-understood, which was in part due to the overlook of the electrochemistry-driven formation of oxygen vacancy (OV) of PbO2. Herein, we unrevealed the origin of the EOP activity of PbO2 starting from the electrochemical surface state analysis using density functional theory (DFT) calculations, activity analysis, and catalytic volcano modeling. Interestingly, we found that under experimental EOP potential (i.e., a potential around 2.2 V vs. reversible hydrogen electrode), OV can still be generated easily on PbO2 surfaces. Our subsequent kinetic and thermodynamic analyses show that these OV sites on PbO2 surfaces are highly active for the EOP reaction through an interesting atomic oxygen (O*)-O2 coupled mechanism. In particular, rutile PbO2(101) with the "in-situ" generated OV exhibited superior EOP activities, outperforming (111) and(110). Finally, by catalytic modeling, we found that PbO2 is close to the theoretical optimum of the reaction, suggesting a superior EOP performance of rutile PbO2. All these analyses are in good agreement with experimental observations.

Synthesis, structural characterization, in vitro biological activity, and DFT calculations of Cu(II) complex

Using a diazonium combination of aniline and 1,3‐diphenylpropane‐1,3‐dione, the Japp‐Klingemann reaction yielded the 1,3‐diphenyl‐2‐(2‐phenylhydrazono)propane‐1,3‐dione ligand (HL). The copper (II) complex has been made using copper (II) acetate salt. The geometry of HL and its Cu (II) chelate were described through CHN analyses, FTIR, UV–Visible, XRD, TGA, and magnetic susceptibility tests. According to the spectral data, the ligand exhibits monobasic bidentate behavior by connecting through the N atom of hydrazone moiety (=N − NH−) by deprotonating beside the oxygen atom of the carbonyl (C=O) group forming octahedral geometry. Density functional theory (DFT) calculations were done by molecular studio software to examine the optimal geometry of HL and its complexity. MCF‐7 and HepG‐2 cell lines demonstrated anticancer action in response to the HL and its copper (II) complex. Additionally, inhibition zone diameter was used to assess the in vitro antibacterial action of HL and particular complex toward Gram +ve bacteria Staphylococcus aureus and Gram‐ve bacteria Escherichia coli (E. coli). Both viscosity and absorption spectra of Calf‐thymus DNA binding experimentations were used to examine the compounds.

Organoselenium compounds in medicinal chemistry.

The chemical and biological interest in this element and the molecules bearing selenium has been exponentially growing over the years. Selenium, formerly designated as a toxin, becomes a vital trace element for life that appears as selenocysteine and its dimeric form, selenocystine, in the active sites of selenoproteins, which catalyze a wide variety of reactions, including the detoxification of reactive oxygen species and modulation of redox activities. From the point of view of drug developments, organoselenium drugs are isosteres of sulfur-containing and oxygen-containing drugs with the advantage that the presence of the selenium atom confers antioxidant properties and high lipophilicity, which would increase cell membrane permeation leading to better oral bioavailability. This statement is the paramount relevance considering the big number of clinically employed compounds bearing sulfur or oxygen atoms if their structures including nucleosides and carbohydrates. Thus, in this article we have focused on the relevant features of the application of selenium in medicinal chemistry. With the increasing interest in selenium chemistry, we have attempted to highlight the most significant published data on this subject, mainly concentrating the analysis on the last years. In consequence, the recent advances of relevant pharmacological organoselenium compounds are discussed.

Main Group SnN4O Single Sites with Optimized Charge Distribution for Boosting the Oxygen Reduction Reaction.

Transition metal single-atom catalysts (SACs) have been regarded as possible alternatives to platinum-based materials due to their satisfactory performance of the oxygen reduction reaction (ORR). By contrast, main-group metal elements are rarely studied due to their unfavorable surface and electronic states. Herein, a main-group Sn-based SAC with penta-coordinated and asymmetric first-shell ligands is reported as an efficient and robust ORR catalyst. The introduction of the vertical oxygen atom breaks the symmetric charge balance, modulating the binding strength to oxygen intermediates and decreasing the energy barrier for the ORR process. As expected, the prepared Sn SAC exhibits outstanding ORR activity with a high half-wave potential of 0.912 V (vs RHE) and an excellent mass activity of 13.1 A mgSn-1 at 0.850 V (vs RHE), which surpasses that of commercial Pt/C and most reported transition-metal-based SACs. Additionally, the reported Sn SAC shows excellent ORR stability due to the strong interaction between Sn sites and the carbon support with oxygen atom as the bridge. The excellent ORR performance of Sn SAC was also proven by both liquid- and solid-state zinc-air battery (ZAB) measurements, indicating its great potential in practical applications.

Synthesis, Optical Performance Characterization, and Durability of Electrospun PTFE-PEO Materials for Space Applications.

Passive heat management is crucial in space, especially for extended missions involving protection from sunlight. Thermal coatings with desirable optical properties can drastically reduce the power consumed by active cooling systems, thereby reserving more resources for other critical systems onboard. Specifically, materials with wavelength-dependent reflectance and emittance are desirable for managing incident sunlight and self-cooling by thermal emission. This study demonstrates the use of polymer nanofibers, specifically poly(tetrafluoroethylene) (PTFE), for passive temperature control in space applications. This study describes the electrospinning fabrication process to create nanofibers and how process parameters can be varied to control the fiber geometry. We combine poly(tetrafluoroethylene) (PTFE) and poly(ethylene oxide) (PEO) polymers to fabricate highly reflective thermal control materials by electrospinning. To understand the role of material and fiber geometry, we measure spectral reflectance, absorptance, and transmittance using spectrophotometers interfaced with integrating spheres. We control the materials' fiber geometry and solar reflectance by modifying the solution properties, flow rate, rotating collector speed, and fabrication time. With 220-1560 μm thick electrospun nanofiber materials, we demonstrate an average solar reflectance of 94.73-99.75%, with values approaching 99.9% for thicker samples, which is among the highest for space applications. Meanwhile, a thermal emittance of 81.4% was observed at 300 K for a 3360 μm thick sample. The durability of these samples was also tested under ultraviolet light and atomic oxygen. Compared to the state-of-the-art materials, the electrospun PTFE-PEO fibers present a new paradigm for passive thermal management in space applications.

Unraveling the dynamic slowdown in supercooled water: The role of dynamic disorder in jump motions.

When a liquid is rapidly cooled below its melting point without inducing crystallization, its dynamics slow down significantly without noticeable structural changes. Elucidating the origin of this slowdown has been a long-standing challenge. Here, we report a theoretical investigation into the mechanism of the dynamic slowdown in supercooled water, a ubiquitous yet extraordinary substance characterized by various anomalous properties arising from local density fluctuations. Using molecular dynamics simulations, we found that the jump dynamics, which are elementary structural change processes, deviate from Poisson statistics with decreasing temperature. This deviation is attributed to slow variables competing with the jump motions, i.e., dynamic disorder. The present analysis of the dynamic disorder showed that the primary slow variable is the displacement of the fourth nearest oxygen atom of a jumping molecule, which occurs in an environment created by the fluctuations of molecules outside the first hydration shell. As the temperature decreases, the jump dynamics become slow and intermittent. These intermittent dynamics are attributed to the prolonged trapping of jumping molecules within extended and stable low-density domains. As the temperature continues to decrease, the number of slow variables increases due to the increased cooperative motions. Consequently, the jump dynamics proceed in a higher-dimensional space consisting of multiple slow variables, becoming slower and more intermittent. It is then conceivable that with further decreasing temperature, the slowing and intermittency of the jump dynamics intensify, eventually culminating in a glass transition.

Nitrate Chemodenitrification by Iron Sulfides to Ammonium under Mild Conditions and Transformation Mechanism.

Autotrophic denitrification utilizing iron sulfides as electron donors has been well studied, but the occurrence and mechanism of abiotic nitrate (NO3-) chemodenitrification by iron sulfides have not yet been thoroughly investigated. In this study, NO3- chemodenitrification by three types of iron sulfides (FeS, FeS2, and pyrrhotite) at pH 6.37 and ambient temperature of 30 °C was investigated. FeS chemically reduced NO3- to ammonium (NH4+), with a high reduction efficiency of 97.5% and NH4+ formation selectivity of 82.6%, but FeS2 and pyrrhotite did not reduce NO3- abiotically. Electrochemical Tafel characterization confirmed that the electron release rate from FeS was higher than that from FeS2 and pyrrhotite. Quenching experiments and density functional theory calculations further elucidated the heterogeneous chemodenitrification mechanism of NO3- by FeS. Fe(II) on the FeS surface was the primary site for NO3- reduction. FeS possessing sulfur vacancies can selectively adsorb oxygen atoms from NO3- and water molecules and promote water dissociation to form adsorbed hydrogen, thereby forming NH4+. Collectively, these findings suggest that the NO3- chemodenitrification by iron sulfides cannot be ignored, which has great implications for the nitrogen, sulfur, and iron cycles in soil and water ecosystems.

Synergistic corrosion inhibition of rubber seed extract with KI on cold rolled steel in sulfuric acid solution

BackgroundPlant-based inhibitor has emerged an important topic owing to the combing merits of eco-friendly, low cost, rich natural resources as well as easy preparation. Rubber seed is the agricultural waste, and is mainly composed of oil and fatty acids those contain many polar oxygen atoms, and so it can be extracted to prepare the potential corrosion inhibitor. MethodsRubber seed extract (RSE) is prepared using reflux extraction method with the extracting solvent of ethanol aqueous solution. The synergistic inhibition effect of RSE and potassium iodide (KI) on the corrosion of cold rolled steel (CRS) in 0.50 M H2SO4 solution is firstly studied by weight loss, potentiodynamic polarization (PDP) curves and electrochemical impedance spectroscopy (EIS) methods. CRS surface was thoroughly characterized using metallographic microscope, scanning electron microscope (SEM), atomic force microscope (AFM), X-ray photoelectron spectroscopy (XPS) and contact angle measurements. FTIR, UV–vis and liquid chromatography mass spectrometry (LC-MS) compositional analysis of RSE were used to analyze the efficient components in RSE. Significant findingsThe results indicate that individual RSE or KI cannot function as a successful inhibitor to prevent CRS corrosion, but the mixture of RSE/KI performs better at inhibiting, with a maximal inhibition efficacy of up to 96.4% of 200 mg L−1 RSE/100 mg L−1 KI. The synergistic coefficient of the mixture is larger than 1, indicating that a true synergism. RSE/KI can drastically retard both cathodic and anodic processes, and interfacial capacitance falls as the charge transfer resistance of CRS/solution rises. It exhibits remarkable inhibition properties when the capacitor arc grows. There is only a small corrosion response in the inhibited media, as evidenced by the variations in electrical conductivity and ultraviolet spectrum before and after immersion. The hydrophilicity and surface roughness of CRS surface is dropped as a result of the introduction of RSE/KI. A series of metallurgical microscopy, AFM, SEM or contact angle tests indicate a synergistic inhibition effect is more pronounced for RSE/KI. XPS results clearly demonstrate that elements including Fe, S, N, and I are bonded to the surface of CRS. The primary ingredients of oleic acid, polyphenols, phenylpropanoids can also produce a strong synergism with KI.