Transmission Raman Spectroscopy Research Articles

Significantly improved optoelectronic performances of two-dimensional WS2(Er3+)/WSe2(Er3+) van der waals heterojunctions

Two-dimensional heterostructures with excellent properties are potential for high performance optoelectronic applications, since the ultimate thickness limit is possible to be broken with the advent of atomically thin materials. Yet the studies have also been largely constrained by the low physical doping space and absorption rates due to the atomic-thickness layers, and the efforts for high carrier concentrations and gain remain a significant challenge. Herein, high concentration of Er3+ ions are in-situ doped in WS2 and WSe2 atomic layers by chemical vapor deposition (CVD) method. The prepared layers are characterized by atomic force microscopy, transmission electron microscopy, photoluminescence (PL) spectroscopy, and Raman spectroscopy, respectively. 13–14 at% of Er3+ doping concentration in WSe2 and WS2 are examined by energy dispersive spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) with high consistency. A microregion fixed-point transfer technique is used to transfer the WS2(Er3+) monolayers onto the WSe2(Er3+) monolayers to form vertical van der Waals heterojunctions. Excellent performances are measured from the WS2(Er3+)/WSe2(Er3+) photodetector with the photoresponsivity of up to 67.4 A/W, external quantum efficiency of 13,202 %, and detectivity of 7.07 × 1011 Jones. Our results prove the effectiveness of Er3+ in-situ doping in WS2(Er3+)/WSe2(Er3+) heterojunctions for high-performance photodetectors.

Impact of crystallinity on thermal conductivity of RF magnetron sputtered MoS2 thin films

Abstract This study investigates the effects of sulfur atomic defects and crystallinity on the thermal conductivity of MoS2 thin films. Utilizing scanning transmission electron microscopy (STEM), X-ray diffraction (XRD), and Raman spectroscopy, we examined MoS2 films, several nanometers thick, deposited on Si/SiO2 substrates. These films were prepared via a combination of RF magnetron sputtering and sulfur vapor annealing (SVA) treatment. Structural analyses, including cross-sectional STEM and in-plane and out-of-plane XRD measurements, revealed an increase in the S/Mo ratio and grain size of the MoS2 films following SVA treatment. Notably, the in-plane thermal conductivity of MoS2 films treated with SVA was found to be at least an order of magnitude higher than that of films without SVA treatment. This research suggests that the in-plane thermal conductivity of MoS2 thin films can be significantly enhanced through crystallinity improvement via SVA treatment.

Aminosilane assisted deposition of gold nanoparticles on Zn(OH)2 nanosheets and their application in electrochemical sensor

A facile and efficient method for systematical deposition of gold nanoparticles (AuNPs) on Zn(OH)2 nanosheets (NS) with different Zn and Au ratios was established in the presence of N-[3-(trimethoxysilyl)propyl]diethylenetriamine (TPDT silane), without adding any external reducing agents, at room temperature. Here, TPDT silane behaves as both a stabilizing and reducing agent. UV-vis absorption spectroscopy, transmission electron microscopy, high-angle annular dark-field scanning transmission electron microscopy-energy dispersive X-ray spectroscopy, X-ray diffraction, Raman spectroscopy, and X-ray photoelectron spectroscopy were used to confirm the formation of AuNPs on Zn(OH)2 NS. As the concentration of AuNPs increased, a proportional increase in both the number and size of deposited AuNPs on Zn(OH)2 NS was observed. To understand how the variation in the number and size of AuNPs affects their catalytic activity, the electrocatalytic activity of different composition ratios of Zn(OH)2-Au NS toward nitrite ions was studied using cyclic voltammetry and amperometric technique. The TPDT-stabilized Zn(OH)2-Au NS showed high electrocatalytic activity, attributed to the effective electron transfer from Zn(OH)2 NS to AuNPs, creating a synergistic effect that enhances the overall activity. The optimal Zn(OH)2-Au NS modified electrode showed an amperometric sensitivity of 5.72nA/µM and a limit of detection of 1.2µM for nitrite ions in water sample well below the guideline value of WHO. This demonstrates the practical applicability of this method for real-world water analysis.

High performance antimony-rich RexSb3Te for phase-change random access memory applications

Phase-change random access memory (PCRAM) demands for high-performance phase change materials, including operation speed, data retention, resistance drift etc. In this work, a high performance PCRAM device based on antimony-rich RexSb3Te material was put forward and studied. Excellent data retention, fast operation speed, low resistance drift, low power consumption and good cycle characteristics were achieved. The lattice information, bonding properties and surface morphology of the films were characterized by transmission electron microscopy, Raman spectroscopy and atomic force microscopy. Density functional theory calculations show that the Re dopant is more inclined to replace Sb and forms chemical bonds with Te, and the Re-Te bonds are more stable than the previous Sb-Te bonds, which is conducive to the formation of stable precursors to accelerate nucleation. The research shows that the antimony-rich Re0.18Sb3Te material has good overall performance, which provides a strategy for developing high-performance memory.

Revolutionizing Glucose Monitoring: Enzyme-Free 2D-MoS2 Nanostructures for Ultra-Sensitive Glucose Sensors with Real-Time Health-Monitoring Capabilities.

The growing requirement for real-time monitoring of health factors such as heart rate, temperature, and blood glucose levels has resulted in an increase in demand for electrochemical sensors. This study focuses on enzyme-free glucose sensors based on 2D-MoS2 nanostructures explored by simple hydrothermal route. The 2D-MoS2 nanostructures were characterized by powder X-ray diffraction, energy-dispersive X-ray spectroscopy, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and XPS techniques and were immobilized at GCE to obtain MoS2-GCE interface. The fabricated interface was characterized by electrochemical impedance spectroscopy which shows less charge transfer resistance and demonstrated superior electrocatalytic properties of the modified surface. The sensing interface was applied for the detection of glucose using amperometry. The MoS2-GCE-sensing interface responded effectively as a nonenzymatic glucose sensor (NEGS) over a linearity range of 0.01-0.20 μM with a very low detection limit of 22.08 ng mL-1. This study demonstrates an easy method for developing a MoS2-GCE interface, providing a potential option for the construction of flexible and disposable nonenzymatic glucose sensors (NEGS). Moreover, the fabricated MoS2-GCE electrode precisely detected glucose molecules in real blood serum and urine samples of diabetic and nondiabetic persons. These findings suggest that 2D-MoS2 nanostructured materials show considerable promise as a possible option for hyperglycemia detection and therapy. Furthermore, the development of NEGS might create new prospects in the glucometer industry.

Vanadium Metal Doping of Monolayer MoS2 for p-Type Transistors and Fast-Speed Phototransistors.

Modulating the electrical properties of two-dimensional (2D) materials is a fundamental prerequisite for their development to advanced electronic and optoelectronic devices. Substitutional doping has been demonstrated as an effective method for tuning the band structure in monolayer 2D materials. Here, we demonstrate a facile selective-area growth of vanadium-doped molybdenum disulfide (V-doped MoS2) flakes via pre-patterned vanadium-metal-assisted chemical vapor deposition (CVD). Optical microscopy characterization revealed the presence of flake arrays. Transmission electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy were employed to identify the chemical composition and crystalline structure of as-grown flakes. Electrical measurements indicated a light p-type conduction behavior in monolayer V-doped MoS2. Furthermore, the response time of phototransistors based on V-doped MoS2 monolayers exhibited a remarkable capability of 3 ms, representing approximately 3 orders of magnitude faster response than that observed in pure MoS2 phototransistors. This work hereby provides a feasible approach to doping of 2D materials, promising a scalable pathway for the integration of these materials into emerging electronic and optoelectronic devices.

Superior room temperature ammonia gas sensing of copper selenide nanoflowers

Facile wet chemical synthesis was utilized to synthesize nanoflowers of copper selenide (CuSe) that exhibited exceptional room temperature ammonia (NH3) gas sensing capability. Observations of surface morphology revealed the presence of petal-like structures arranged in a flower-like pattern. The layered materials have been analyzed for their crystalline structure, phase, composition, and band gap by utilizing X-ray diffraction, Transmission Electron Microscopy, Raman spectroscopy, and energy-dispersive X-ray spectroscopy, UV-Vis, respectively. At ambient conditions, CuSe nanoflowers-based sensor demonstrated exceptional sensitivity, reaching up to 79% (200 ppm NH3) with short response and recovery time of 12.9 s and 6.3 s, respectively, at 5 ppm gas concentration. The sensor exhibited rapid response and recovery times, a broad concentration range, long-term stability over extended periods, exceptional specificity towards NH3, and good repeatability owing to its distinct flower-shaped structures assembled in thin layers. Density Functional Theory simulations were conducted to investigate the interactions between NH3 and CuSe. Our findings revealed an increase in the adsorption energy of NH3 on CuSe, indicating a stronger binding affinity. We observed a higher charge transfer from CuSe to NH3, which suggests an increase in conductivity. This increase in conductivity enhances the superior sensing capability observed in the experimental results.

Correlation of Structural Changes and Hydrogen Diffusion in Polycrystalline WO3 Thin Films by Combining In Situ Transmission Measurements and Raman Spectroscopy

AbstractDiffusion in polycrystalline tungsten trioxide (WO3) thin films is studied in a lateral geometry to better understand the impact of hydrogen‐induced structural phase transitions on the diffusion. WO3 thin films are coated with polymethylmethacrylate layer (PMMA). The latter is microstructured in such a way that a narrow stripe‐like gap occurs in the PMMA layer exposing the surface of the WO3 thin film. This stripe serves as the contact to the electrolyte in the intercalation experiment with hydrogen. After intercalation, the lateral diffusion of hydrogen inside WO3 below the PMMA layer can be observed, increasing the analyzable path and time scale by several orders of magnitude compared to the film thickness, thus, significantly improving spatial and temporal resolution of in situ transmission and Raman measurements. Spatially resolved transmission measurements in the wavelength range of 633±55 nm show that the diffusion process is dependent on hydrogen concentration and exhibits two regimes describable by different diffusion coefficients. Time‐resolved Raman spectroscopic measurements at different distances from the electrolyte contact area show that the switching between the two diffusion coefficients occurs at the phase transition from the orthorhombic to the tetragonal phase. The results are further supported by a simulation. The measurement approach is universally applicable for electrochromic films or multilayers.

Study on Crystal Structure, Surface Area, and Energy Gap Behaviors of Nanotitania Polymorphs Prepared Using Monoethanolamine

Polymorphous nanotitania samples were prepared from titanium butoxide (TTB) as a precursor using sol-gel processing in ethanol as a solvent, without and with monoethanolamine (MEA). The experiments used 5.25 mL TTB and MEA with varied volumes of 0.5, 1.0, 1.5, and 2.0 mL. The sample without MEA was specified as sample A, and the samples produced using MEA were specified as samples B, C, D, and E, respectively. All samples were calcined at 500 °C for 4 h and then collected data by X-ray Diffraction (XRD), the Brunauer-Emmett-Teller (BET) method used to analyze Surface Area Analyzer (SAA), Transmission Electron Microscopy (TEM), Raman Spectroscopy, and UV-Visible Diffuse Reflectance Spectroscopy (UV-Vis DRS). The results of XRD characterization indicate that samples A and B form anatase phase, while samples C and D are composed of anatase, brookite, and rutile phases, and sample E is consisted of anatase and brookite phases with weight percentages of (94.53 ± 1.72) % and (5.47 ± 0.36) %, respectively. The presence of the three phases of titania is also confirmed by Raman spectroscopy analysis, which showed anatase peaks at 146, 197, 398, and 513 cm-1, brookite peaks at 245 and 402 cm-1, and rutile peaks at 319, 436, and 612 cm-1. According to XRD, the samples have the particle size in the range of 14-19 nm. A representative sample (sample C) was also characterized using TEM, revealing a particle size of 16.0 ± 0.3 nm. This representative sample revealed the largest surface area of 172.2 m2/g, as seen by BET, and the lowest energy gap of 3.03 eV.

Synthesis of multi-layer graphene oxide from HCl-treated coke and Brazilian coals by sulfuric acid thermal exfoliation and ozone oxidation

This study involved the synthesis and characterization of graphene oxide (GO) from mineral coke and bituminous coal. HCl treated and non-HCl treated ultrafine powder obtained from both precursors were treated with H2SO4, followed by thermal treatment, and oxidation with ozone and ultra-sonication for GO production. The synthesized materials were characterized using Fourier transform infrared spectroscopy (FTIR), zeta potential (ZP), particle size distribution (PSD), transmission electron microscopy (TEM), X-ray diffraction (XRD) and Raman spectroscopy. The results confirmed the exfoliation of the material primarily at the edges of its structure and the formation of multilayer graphene oxide (GO) from mineral coke and bituminous coal. Furthermore, it was found that carbonaceous materials with graphitic morphology are easier to exfoliate and oxidize, leading to the production of higher quality graphene oxide. Therefore, the GO synthesized from mineral coke exhibited the best quality in this study. The methodology used proposes an innovative approach, offering a faster, more economical, and environmentally friendly synthesis compared to the traditional Hummers method, thereby adding value to other raw materials that can be utilized in this process, such as Brazilian coke and coal.

Improved piezo-photocatalysis for aquatic multi-pollutant removal via BiOBr/BaTiO3 heterojunction construction

Piezo-catalysis is a green and effective method for degrading rich and obstinate molecules in wastewater. Yet, the piezo-catalytic performance of frequently-used barium titanate (BTO) is still limited for practical applications, thus it is crucial to construct high-efficiency BTO-based catalysts. Herein, BiOBr/BTO heterojunction-based piezo-photocatalysts were successfully prepared using the chemical precipitation method, and an internal electric field was established via ultrasound to promote the separation of photogenerated electron-hole pairs through the synergistic effect of piezocatalysis and photocatalysis. Transmission electron microscopy, Raman spectroscopy and X-ray photoelectron spectroscopy were utilized to characterize the heterojunction. The degradation performance of Rhodamine B (RhB) by BiOBr/BTO is the best among various pollutants, giving a reaction rate constant up to 20.839 × 10−2 min−1, exceeding numerous previously reported catalysts. In addition, the piezo-photocatalytic reaction rate of BiOBr/BTO for Methyl Orange was 9.298 × 10−2 min−1, ≈ 3.3 times than those of pure BTO (2.806 × 10−2 min−1), and also ≈ 15.9 times and 3.3 times than those of single photocatalysis (0.585 × 10−2 min−1) or piezocatalysis (2.848 × 10−2 min−1). Importantly, the BiOBr/BTO heterojunction demonstrates excellent catalytic degradation performance for a broad range of pollutants (e.g., dyes and antibiotics) and their mixtures, as well as favorable cycling stability and repeatability with changed environmental conditions, displaying applicability in actual wastewater treatment. The possible degradation pathways of RhB were analyzed by liquid chromatography-mass spectrometry. The present work supplies a feasible strategy for the preparation of high-efficiency piezo-photocatalytic BTO-based heterojunctions, which can guide other composites for environmental remediation.

Box-Behnken Design for Photocatalytic Degradation of Sudan Black B by Catalyst-Embedded Multiwalled Carbon Nanotubes

This research employs a Box Behnken design-based technique for photocatalytic use of Multiwalled Carbon Nanotubes (MWCNTs) derived from spray pyrolysis. This procedure was used for photocatalytic degradation applications on Sudan black dye using Citrus limonum oil as a carbon precursor and Fe/Co/Mo supported on silica as a catalyst. The influence of initial dye concentration was compared to the effects of H2O2, catalyst concentration and solar light intensity. The Response Surface Methodology was used to optimize growth parameters for higher yield and graphitization. The as-grown CNTs were exemplified using scanning and transmission electron microscopy and Raman spectroscopy. This work resulted in the identification of the optimal set of spray pyrolysis turning parameters for achieving high CNT yield and effective decolorization of Sudan black B dye by employing MWCNTs as catalyst. The degree of decolorization of Sudan black B dye increases upto a certain level with an increase in initial H2O2 concentration and subsequently declines as excess H2O2 hydroxyl radicals formed serve as scavengers, resulting in less dye decolonization.

Evaluating Noise Reduction Methods for Raman Spectroscopy in Transmission and Reflection Configurations

This work involved comparing Raman signals obtained from two different Raman spectroscopy configurations, using two distinct noise reduction methods. The excitation light source was a laser diode with a wavelength of 532 nm. A long-pass filter and focusing lens were utilized to block the excited light from the source and concentrate the Raman signals due to their weaker nature compared to the excited light signals. Light of 532 nm wavelength was blocked during green laser diode illumination using a long-pass filter. Two configurations were studied: transmission Raman spectroscopy (TRS) and reflection Raman spectroscopy (RRS). Raman signals from both configurations were compared, and the boxcar averaging and Vancouver Raman algorithm (VRA) noise reduction methods were investigated and compared. The results showed that Raman signals from the transmission configuration were higher than those from the reflection configuration, and noise signals were effectively reduced using both the boxcar averaging and VRA methods.

High-pressure study of synthesized α-Bi2O3/NiBi3 nanostructured composite: In-situ synchrotron XRD measurements, DFT calculations and PDF approach

We investigated a nanostructured composite of α-Bi2O3/NiBi3, which was synthesized through high-energy milling, under high-pressure conditions of up to 30 GPa. To track its structural changes, we employed in-situ synchrotron angle-dispersive X-ray diffraction measurements in conjunction with density functional theory calculations. Crystallographic information was derived using the Rietveld method and DFT computations. Additionally, we examined the chemical short-range order using pair distribution functions and determined the compressibility parameters through the Birch-Murnaghan equation of state.We explored the high-pressure behavior of a nanostructured composite of α-Bi2O3/NiBi3, applying pressures up to 30 GPa. The composite sample, synthesized by mechanical alloying, underwent thorough structural characterization by X-ray diffraction, high-resolution transmission electron microscopy and Raman spectroscopy. The sample's response to applied pressure was studied by analyzing crystallographic data obtained from in-situ synchrotron angle-dispersive X-ray diffraction measurements and density functional theory calculations. Crystallographic information from experiments was refined using the Rietveld method. Additionally, chemical short-range order was examined using pair distribution functions, and compressibility parameters were determined via the Birch-Murnaghan equation of state. This investigation into the high-pressure behavior of NiBi3 provides valuable insights for future studies and potential applications of similar materials in extreme pressure environments.

Cobalt Ferrite Nanorods Synthesized with a Facile "Green" Method in a Magnetic Field.

We report a new facile method for the synthesis of prolate cobalt ferrite nanoparticles without additional stabilizers, which involves a co-precipitation reaction of Fe3+ and Co2+ ions in a static magnetic field. The magnetic field is demonstrated to be a key factor for the 1D growth of cobalt ferrite nanocrystals in the synthesis. Transmission electron microscopy (TEM), X-ray diffraction (XRD), and Raman spectroscopy are applied to characterize the morphology and structure of the obtained nanoparticles. According to TEM, they represent nanorods with a mean length of 25 nm and a diameter of 3.4 nm that have a monocrystalline structure with characteristic plane spacing of 2.9 Å. XRD and Raman spectroscopy confirm the spinel CoFe2O4 structure of the nanorods. After aging, the synthesized nanorods exhibit maximum saturation magnetization and coercivity equal to 30 emu/g and 0.3 kOe, respectively. Thus, the suggested method is a simple and "green" way to prepare CoFe2O4 nanorods with high aspect ratios and pronounced magnetic properties, which are important for various practical applications, including biomedicine, energy storage, and the preparation of anisotropic magnetic nanocomposites.

Investigation of long-term stability of a transmission Raman calibration model using orthogonal projection methods

Transmission Raman Spectroscopy (TRS) was implemented as an ‘Extended’ Content Uniformity (ECU) method for un-coated tablets for a commercial pharmaceutical product. By sampling un-coated tablets throughout the duration of the tablet compression stage, it can be demonstrated that the material from the preceding blend step was of uniform composition, and therefore the blend and compression unit-operations were in a state of control. TRS was selected as a rapid, non-destructive measurement that can be automated through the use of a sample tray that can hold many tablets. In this work, the performance of a multivariate calibration model (PLS) deployed to two Transmission Raman Spectrometers co-located within the same QC laboratory was studied using data obtained over a 3-year period. The aim of the investigation was to assess the impact of various annual instrument maintenance events, and to evaluate several chemometric methods for reducing or eliminating the spectral effects that led to deterioration of a models performance. Linear orthogonal projection approaches such as Transfer by Orthogonal Projection (TOP), Dynamic Orthogonal Projection (DOP) and Unsupervised Dynamic Orthogonal Projection (uDOP) were applied, along with a more recent, non-linear method called Transfer Component Analysis-Orthogonal Projection (TCA-OP). This works shows that each method has merits, depending on the nature of the spectral/model correction required. In most cases, the model performance could be fully restored, or significantly improved. This work also highlights how these various methods can be useful tools to better understand the root-cause for a deterioration in model performance.

Nanocomposite materials based on amorphous SiC-containing DLC structures modified with rhodium nanoparticles

From the 1980s to the present, interest in carbon has remained very high. The variety of polytypic forms of carbon is expected to have a large number of possible applications. The creation of electronic and optical devices based on them is a promising direction. One of the most interesting carbon materials could be amorphous diamond-like carbon (DLC) films. This work considers nanocomposite materials based on DLC with nanostructures of SiC components. Thin composite DLC:Si films modified with Rhodium nanoparticles (Rh NPs) were synthesized by magnetron sputtering. The structure of the films has been studied by transmission electron microscopy, Raman and X-ray photoelectron spectroscopy (XPS). It is shown that a diamond-like carbon matrix with inclusions of SiC nanostructures and Rh nanocrystals is formed. Significant influence of Rh NPs on the structures of the carbon matrix and SiC during the formation of the DLC: Si matrix is revealed. In addition, X-ray photoelectron spectroscopy shows a considerable effect of Rh NPs on the edge of the valence zone and the density of localized states. The significant effect of rhodium nanoparticles on the electronic component of the valence band of DLC:Si films can be used in the development of new optoelectronic devices.

Characteristics of 4-inch (100) oriented Mg-doped β-Ga2O3 bulk single crystals grown by a casting method

In this Letter, 4-inch diameter (100) magnesium-doped monoclinic gallium oxide (Mg:β-Ga2O3) bulk single crystals were grown by a casting method. The crystallographic structure, electrical, optical properties, and defects of Mg-doped β-Ga2O3 was thoroughly investigated by XRD rocking curves, AFM, non-contact resistivity measurements, XPS, optical transmission spectra, Raman spectroscopy, and defect-selective chemical etching processes. Comparing to the UID samples, the larger bandgap of 4.75 eV and high resistivity of 3.50×1012 Ω∙cm indicated Mg a proper dopant for fabricating semi-insulating β-Ga2O3 substrates which could be preferred for power devices. XPS spectra exhibited the ability of Mg2+ to inhibit the formation of oxygen vacancy defects in the crystals. Meanwhile, the high crystalline quality and low density of defects demonstrated the advantages of casting method in achieving large-size and high-quality β-Ga2O3 bulk single crystals with changeable resistivity. This result indicates a high potential to achieve high-quality and low-cost substrates which satisfy the requirement of high-performance power electronic devices.

Enhanced electrochemical properties of multiwalled carbon nanotubes modified with silver nanoparticles for energy storage application

This work reports an easy, straightforward, and cost-effective method to synthesize a composite material using multiwalled carbon nanotubes (MWCNTs) and silver nanoparticles (Ag NPs) for application as an electrode in supercapacitors. The objective of this work was to enhance the charge transfer mechanism in supercapacitor cells by introducing the conductive particles in the MWCNT framework. The pivotal studies, like scanning (SEM), and transmission (TEM) electron microscopy, X-ray diffraction (XRD), Raman, and X-ray photoelectron (XPS) spectroscopy confirmed the formation of the composite as well as a successful deposition of Ag NPs on MWCNT. The surface area of the composite was evaluated by using the N2 adsorption-desorption studies and it was found to be of the order of 358 m2 g−1. Electrochemical studies were performed using a two-electrode system. Magnesium ion-based polymer gel electrolyte was used as an electrolyte material. The single electrode-specific capacitance was observed to be ∼31.9 F g−1 with power density and energy density values of ∼4.4 kW kg−1 and 1.2 Wh kg−1, respectively, at a current density of 0.46 A g−1. The cell was stable up to ∼5000 charge-discharge cycles with ∼96% of capacitance retention at the end of 5000 cycles.

Effects of polyoxymethylene dimethyl ethers (PODEn) on soot characteristics in isooctane inverse diffusion flames

Polyoxymethylene dimethyl ethers (PODEn, n = 1–3) such as dimethoxymethane (DMM) and PODE3 are considered highly promising alternative fuels due to their lack of C–C bonds and significant oxygen contents. Particularly, PODE3-blends with diesel have been proven to substantially reduce soot emissions and fuel consumption rates under optimized engine conditions, although the impact on soot nanostructure properties remains unclear. This study explored the effects of DMM and PODE3 on soot characteristics in isooctane (i-octane) inverse diffusion flames, focusing on soot morphology, soot nanostructure, soot nanocrystallite, and soot spectral features. To compare soot particles behavior, DMM and PODE3 blended as the isooctane substitute (by 20% and 40% volumetric fractions) were examined with various diagnostic techniques, including high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS).The results showed that DMM and PODE3 contributed to a reduction in sooting tendency from i-octane flames, whereas the average soot mass decreased significantly as the PODE3 ratio increased, consistent with a higher oxygen concentration. Therefore, 20% PODE3/i-octane exhibited growing disorganized arrangements of soot particles with shorter fringes, smaller crystallite sizes, and a relatively lower degree of graphitization than 20% and 40% DMM additions. However, XPS analysis indicated that soot produced from PODE3/i-octane mixtures had less oxygen atoms because PODE3 has multiple –CH2O- chain groups that can convert oxygen into carbon monoxide with little soot production. Moreover, HRTEM, XRD, and Raman spectra analyses of 40% PODE3-doped flames confirmed an exceptional correlation with turbostratic soot structure, as manifested by the shortest fringe length, longest fringe tortuosity, more amorphous soot with the smallest crystallite dimensions, and least degree of graphitization.