Half-peak Width Research Articles

The Characterization of Electric Field Pulses Observed in the Preliminary Breakdown Processes of Normal and Inverted Intracloud Flashes

We have studied the parameters of preliminary breakdown (PB) pulses in 395 normal and 319 inverted intracloud (IC) flashes observed in Gifu, Japan, and Ningxia, China, respectively, by using a low-frequency mapping system called fast antenna lightning mapping array (FALMA). These parameters are extracted from the first half of the PB pulses. It is found that compared to normal IC flashes, inverted IC flashes exhibited PB pulses with slower rise times (6.8 vs. 3.1 μs), wider half-peak widths (3.8 vs. 2.5 μs), longer zero-crossing times (26.2 vs. 14 μs), and extended fall times (4 vs. 3.2 μs). We further demonstrated that such discrepancies between normal and inverted IC flashes should not be caused by subjective factors, like noise threshold setting, or objective factors, like signal propagation distance. Based on this analysis, finally, we inferred that the discrepancies should be a reflection of the PB channel properties of normal and inverted IC flashes.

Synergistic effect induces self crystallization of CsPbBr3 quantum dots in Borosilicate glass matrix By LiF

Cesium lead halide perovskite (CsPbX3) quantum dots (QDs) are recognized as viable substitutes for conventional fluorescent powder color converters, which can improve the color gamut and reproducibility of liquid crystal displays (LCDs). Encapsulating QDs in glass can effectively solve the water oxygen stability of QDs, but the glass matrix impedes the nucleation of QDs and the precipitation of QDs requires secondary heating. In our research, we successfully accomplished the self-crystallization of CsPbBr3 QDs facilitated by LiF within a B2O3-SiO2-ZnO borosilicate glass matrix.The results indicate that the self crystallization of CsPbBr3 QDs induced by LiF in borosilicate glass matrix has a synergistic effect. The Li+ ions can break the glass network structure and facilitate ionic migration and transport, while F- ions have good electronegativity due to ion aggregation, and can strongly attract Cs+ and Pb2+ ions with larger atomic radii, thereby promoting the rapid nucleation and growth of CsPbBr3 QDs, ultimately synthesizing QDs with uniform particle size, narrow half peak width, good optical properties, and thermal stability.

Uniform and large-size perovskite CsPb(BrxI1-x)3 quantum dot glass for laser display application

As a new display mode, laser display is becoming popular in the industry, and it has served our lives. In addition, a new material, perovskite quantum dots(QDs) is more capable of energizing laser displays with a narrow half-peak width, tunable emission and high color purity. Here, by incorporating perovskite CsPb(BrxI1-x)3 quantum dots into the glass, we explored the performance of large-size glass in laser display. It is demonstrated that the sheet of CsPbBr3 and CsPb(Br0.25I0.75)3 glasses has good wavelength uniformity, and the phosphor wheel with the sheets yields a wide color gamut (its color gamut reaches 124.3 % of NTSC and 91.3 % of Rec.2020), which will play a significant advantage in the field of laser projection.

Stage development characteristics of oxygen-lean combustion of coal in fire zone: Leap-migration mechanism, kinetic transition mechanism, and critical oxygen concentration

Effectively preventing the re-ignition of fire zones and safely unsealing enclosed fire zones are challenging. To address these issues, a thermogravimetric analysis technique was used to explore the leap-migration mechanism of the characteristic parameters (burnout index (H), comprehensive combustion performance parameters (Cb, S, and HF), and maximum combustion mass loss rate (dWmax))/temperatures (maximum pyrolysis mass loss rate point temperature (TVmax), pyrolysis endpoint temperature (Td), thermal polycondensation endpoint temperature (Tp), maximum combustion mass loss rate point temperature (TWmax), burnout temperature (Th), and combustion half-peak width (ΔT1/2)) of low-rank coal oxygen-lean combustion under different time-scale effects (TSEs). The sensitivity of characteristic parameters/temperatures to changes in oxygen concentration under coal rank transition was analyzed. Simultaneously, the kinetic real-time transformation mechanism during the oxygen-lean combustion stage progression was investigated. The results revealed that because of the competition between oxidation and pyrolysis, the leap-migration interval of characteristic parameters/temperatures for oxygen-lean combustion of low-rank coals is in the range of 5 %–3% oxygen concentration. This feature was less affected by the coal rank but is not affected by the TSE. In the low oxygen-lean range (5 %-1%), a change of oxygen concentration was more sensitive to the coal rank, and the high sensitivity of the oxygen concentration change reduced the influence of the coal rank on coal combustion performance. In addition, the apparent activation energy (Eα) curves during the early stage of combustion were relatively concentrated with the change of oxygen concentration, but relatively dispersed during the late stage of combustion. At 3 % oxygen concentration, the Eα values of different coals began to continuously decrease with increasing conversion rate, approaching the spontaneous reaction activation energy value of 40 kJ/mol. At oxygen concentration of 1 % reflected the complete limitation of the oxidation consumption reaction. Therefore, the critical oxygen concentration of typical low-rank coal oxygen-lean combustion was determined below 3 % oxygen concentration. The results of this study can provide scientific guidance for the unsealing of fire zones, and the effective prevention and control of the formation of new fire zone disasters.

Tailored detection efficiency for linear variable filter-based sensors: applying simulation models of spectral characteristics in optical design

To accurately model the specific detection characteristics of spectral sensors based on linear variable filters (LVFs) within an optical design tool, it is essential to consider crucial position-variable spectral properties, such as peak transmittance, central wavelength, half width, or slope steepness. In this context, we propose a straightforward approach, integrating a dynamic link library (DLL) containing all position-dependent spectral properties of the LVF into a commercial optical design software. Exemplary investigations are conducted for an LVF with a detection range of 450–850 nm. For ease of use, the measured position-, wavelength-, and angle-dependent transmission properties of the LVF have been described through a simple yet highly accurate model system. Moreover, to highlight the essential value of this simulation for specific applications, an efficiency-enhancing spectral module is simulated, which is an LVF-mirror arrangement characterized by a multiple-reflected beam path. The introduced optical design tool demonstrates its particular strength by enabling the optimization of the highest detection efficiency for either the short- or long-wavelength range.

Synthesis of high‑nitrogen-content doped-g-C3N4 (A new nitrogen source) diamond under high-pressure and high-temperature conditions

This study reports the successful synthesis of high‑nitrogen-content diamond (2723 ppm) within the Fe-Ni-C-N system, utilizing g-C3N4 as a new nitrogen source via the temperature gradient method under high-pressure and high-temperature (HTHP) conditions. The study investigated the role of nitrogen atoms in facilitating the growth of large diamonds with {111} plane orientation. Analysis of crystal morphology, nitrogen defect content, and nitrogen incorporation forms were conducted. As the amount of g-C3N4 increased, the crystal size decreased, the color changed from yellow to green with increasing depth, and the growth rate notably decreased. The Fourier transform microscopy infrared spectroscopy (FT-IR) characterization revealed increased nitrogen content within the crystal due to nitrogen atom introduction. Raman characterization indicated increased residual stress with higher nitrogen content, leading to shifts in Raman peak positions and broadening of half-peak widths of the diamond. Photoluminescence (PL) characterization indicated that g-C3N4 addition increased, resulting in a fading state of NV− and W8 defects. The results indicated that g-C3N4, as a new nitrogen source, exhibited superior doping efficiency within the diamond lattice compared with traditional nitrogen sources. The study offered valuable insights into the preparation and potential applications of high‑nitrogen diamond single crystals.

Long-wavelength emission room-temperature phosphorescent carbon dots activated by an ortho-carboxyl substitution strategy and employed for achieving tunable LED

While room temperature phosphorescence (RTP) associated with carbon dots (CDs) has been widely achieved, obtaining long-wavelength emission RTP, especially while mitigating the quenching effect of water or dissolved oxygen, remains a challenging yet desirable goal. We synthesized three types of phosphorescent CDs with varying luminescent properties by using three precursors with carboxyls positioned differently. The formation process of these CDs resulted in a well-ordered and compact structure, effectively inhibiting molecular vibrations and reducing non-radiative transitions. Consequently, it successfully prevented the quenching effect of dissolved oxygen on the RTP of CDs in an aqueous environment. Significantly, PA-AIBN synthesized with phthalic acid, rather than iso-phthalic acid and terephthalic acid, exhibited long-wavelength emission RTP, with the phosphorescent emission center reaching as far as 640 nm. To be specific, the ortho-substituted carboxyls played a critical role in boosting the formation of intramolecular hydrogen bonds. Simultaneously, an increase in the doping levels of both nitrogen (N) and phosphorus (P) in PA-AIBN facilitated the long-wavelength emission RTP. The increased sp2 conjugated carbon core of PA-AIBN narrowed the optical band gap, contributing to the long-wavelength emission. Taken together, these factors cooperatively promoted the long-wavelength emission of RTP. Importantly, the PA-AIBN synthesized in this study exhibited a broad half-peak width and long-wavelength emission. It was successfully used in the preparation of white-light-emitting diodes without the need for commercial phosphor powder, demonstrating its enormous potential for practical lighting devices.

Exploration of the Existence Forms and Patterns of Dissolved Oxygen Molecules in Water

HighlightsA clear negative correlation between the size of water clusters and theconcentration of dissolved oxygen was observed. This implied that smaller clusters water exhibits higher concentrations of dissolved oxygen.Oxygen molecules are primarily existed at the surfaces or interfaces of waterclusters and can rapidly traverse the gas liquid interface.A semi empirical formula relating the average number of water molecules in acluster to 17O NMR half peak width was derived, demonstrating an approximatelin ear relationship.

Luminescent Perovskite-Cross-Linked Polymer with Low Shrinkage and Excellent Stability.

When organic cross-linked polymers are combined with metal halide perovskite nanocrystals (PNCs) for realizing luminescent perovskite-polymer display materials, the stability of PNCs is enhanced and their shrinkage is suppressed. This work presents a feasible strategy for preparing CsPbBr3 nanocrystals (NCs) within a polydicyclopentadiene (PDCPD) thermosetting cross-linked resin matrix simultaneously via a one-step reaction. The obtained PDCPD@PNCs composite exhibits narrow peak half-widths (15-20 nm), high light transmittance (80%), low curing volume shrinkage (1.4%), tunable tensile properties, excellent stability, and a photoluminescence quantum yield (PLQY) of 44.3%. The composite material exhibits long-term stability in water, acid, and base solutions for over 90 days, with the PL intensity being maintained at over 90%. Furthermore, the composite is highly resistant to polar organic solvents owing to the insolubility imparted by cross-linking. White LEDs (WLED) fabricated using the as-prepared composite demonstrate excellent potential as light sources in optical devices.

Ultrabroad distribution of multiple anelasticities in O-doped refractory multiprincipal element alloys

The Snoek anelastic internal friction (IF) peak due to stress-induced dipole ordering associated with interstitial atoms was well observed in IF curves of single-principal element alloys (SPEAs) as early as in the 1950s, however, its behavior remains elusive in multi-principal element alloys (MPEAs) to date. Here the temperature-dependent IF spectra of NbTiV0.5Zr refractory MPEAs with varying O contents were presented, and the analysis of these data indicates that for O-doped NbTiV0.5Zr MPEAs, the O addition triggers two anelastic IF peaks (the PO1 and PO2), corresponding to the O-Snoek-type relaxation in random solid solution (RSS) and local chemical ordering (LCO) structures, respectively. The half-peak width of the PO1 is 2–3 times broader than that for SPEAs, associated with the wide O migration energy barrier distribution in MPEAs. These phenomena show a striking contrast to the single and narrow Snoek-type peak observed for SPEAs. Our analysis further reveals an approximate linear correlation between the half-peak width of the Snoek-type peak and the mixing entropy. The introduction of O also shifts grain boundary relaxation peaks (PG) towards higher temperatures. Interestingly, high-temperature anomalous modulus changes were observed for the first time in TiV-based lightweight refractory MPEAs, which is suggested to be originated from the order reduction of the body-centered cubic (bcc) structure at elevated temperatures. Moreover, the 1 at.%O doped NbTiV0.5Zr MPEA with a favorable balance between the peak heights of the PO2 and PG, exhibits outstanding specific yield stress (SYS) among refractory MPEAs while maintaining an elongation as high as 20 %. This work provides not only a bridge between the anelastic behavior of SPEAs and MPEAs for upcoming studies and theories concerning bcc MPEAs with interstitial atoms, but contributes to the holistic design of bcc MPEAs with high strength and excellent ductility.

Temperature-Driven Structural Evolution during Preparation of MCM-41 Mesoporous Silica.

This study explores the influence of micelles on the evolution of MCM-41's pore structure via 24 h hydrothermal treatments in a range of temperatures from 100 °C to 200 °C. MCM-41 was characterized using BET, SAXD, FTIR, TEM, and TG-DSC. The findings demonstrate that with temperature elevation from 100 °C to 160 °C, the micelles undergo expansion, leading to an enhanced lattice constant from 4.50 nm to 4.96 nm and an increase in pore diameter from 3.17 nm to 3.45 nm, while maintaining the structural orderliness of the pore channels. Upon cooling, the reversible contraction of micelles and the strategic addition of water glass contribute to a reduction in pore size. However, at a threshold of 180 °C, the SAXD (100) peak's half-peak width surges by approximately 40% relative to that at 160 °C, illustrating a progressive disruption of the hexagonal configuration of MCM-41. Coupled with elevated silica dissolution at higher temperatures in an alkaline solution, a total disintegration of the ordered pore structure at 200 °C results in a drastic reduction in the specific surface area to 307 m2/g. These results are beneficial to developing structural transformation mechanisms of MCM-41 materials and designing mesoporous materials via temperature modulation innovatively.

Investigating a defect width identification based on half-peak width for LDC-based eddy current testing

ABSTRACT The eddy current testing (ECT) technology based on the Inductance-to-Digital Converter (LDC) has the advantages of low power consumption and simple signal conditioning circuitry, which contributes to the miniaturisation of the instrument and low power consumption design. Existing defect identification methods primarily focus on the conventional Analog-to-Digital Converter (ADC)-based ECT. These methods rely on complex analytical models to analyze the phase and amplitude information of voltage signal. However, these approaches do not apply to the LDC-based ECT. The paper proposes a method to identify defects employing the R p -Inductance 2D plane, and use the half-peak width of the inductance signal to evaluate the defect width for symmetric slots. Using finite element simulation and experimental verification, the half-peak widths of the inductive signal wave crests at the defects are the same for the four slots with 1 mm width and different depths on the aluminum specimen; for four wire-cut slots with 4 mm depth and different widths, the half-peak widths are positively correlated with the defect widths. These experimental results demonstrate that the relationship between crack width, wave crest, and half-peak width can serve as the foundation for width identification and classification. This also offers a fresh perspective for further quantifying crack widths.

Growth, optical and thermal properties of YbxHo1-xCa4O(BO3)3 crystals

YbxHo1-xCa4O(BO3)3 (Yb:HoCOB, x = 0, 0.1, 0.2, 0.3) crystals were grown by the Bridgman method for the first time. The crystal structure, rocking curve, transmission spectra, absorption spectra, band structure and thermal properties of Yb:HoCOB were characterized in detail. The maximum half peak width (FMHW) of Yb0.1Ho0.9COB and Yb0.2Ho0.8COB is 26.7″ and 23.8″, respectively, and the effective segregation coefficient is greater than 0.9. In addition, the transmittance of Yb:HoCOB is 88 %. New absorption peaks are introduced by doping Yb3+ at 850–1000 nm. The UV absorption cut-off edge of Yb:HoCOB is red-shifted with increasing Yb3+ doping. The thermal diffusivity and thermal conductivity of Yb:HoCOB decrease with increasing temperature. The specific heat increases with the increasing temperature and finally approaches a constant value. The specific heat of Yb:HoCOB crystal are above 0.670 J/gK at room temperature. Yb:HoCOB with good crystallization quality, high transmittance and high specific heat has the application potential in laser frequency and QPCPA. This work provides a useful exploration for the study of nonlinear optical materials in solid state lasers.

Strategy of Charge Compensation for High-Performance Ni2+-Activated MgAl2O4 Spinel Near-Infrared Phosphor Synthesis via the Sol-Gel Combustion Method.

Near-infrared (NIR) phosphor conversion light-emitting diodes (pc-LEDs) have great application potential as NIR light sources in many fields such as food analysis, night vision illumination, and bioimaging for noninvasive medical diagnosis. In general, phosphors synthesized by a high-temperature solid-phase method have large particle sizes and have to be processed to fine powders by a grinding process, which may introduce surface defects and lower the luminous efficiency. Here, we report a sol-gel sintering method with ammonium nitrate and citric acid as the sacrificing agents to synthesize high purity, nanosized (less than 50 nm) Zr4+/Ni2+ codoped MgAl2O4 spinel NIR phosphors, in which MgAl2O4 spinel is the matrix, Ni2+ is the luminous center, and Zr4+ acts as the charge compensator. We systematically characterized the crystal structures and NIR luminescence properties of the Ni2+-doped MgAl2O4 and the Zr4+/Ni2+ codoped MgAl2O4. Under 390 nm light excitation, the emission spectrum of the Ni2+-doped MgAl2O4 phosphor covers 900-1600 nm, the half-peak width is 251 nm, and the peak position is located at 1230 nm. We demonstrated that by incorporating small amounts of Zr4+ as the charge compensator, the NIR emission intensity of the Zr4+/Ni2+ codoped MgAl2O4 nanosized phosphor was doubled over that of the Ni2+-doped MgAl2O4 phosphor. The optimal content of the charge compensator was 2 mol %. More importantly, the inclusion of Zr4+ led to a NIR phosphor with improved thermal stability in luminous properties, and the luminous intensity measured at 100 °C was 33.83% of that measured at room temperature (20 °C). This study demonstrates that NIR phosphor nanomaterials with high-purity and enhanced optical properties can be designed and synthesized through the charge compensation strategy by a sol-gel sintering method.

Vibrational anharmonicity of A-band related optical center and its temperature dependence studied by femtosecond laser excitation in bulk natural diamond

Unusual A-band spectra with well-resolved quasi-periodical phonon progressions of multiple peaks (N\(\sim \)9) were excited in a natural diamond by 515-nm, 300-fs laser pulses at variable pre-heating temperatures of 24-200oC. The non-radiative multi-phonon part of the relaxation path was comparable with the total relaxation energy (zero-phonon line energy), pointing out some extended defects (e.g., dislocations) as the recombination center of the A-band emission. The derived temperature dependences of the peak intensities, separations and half-widths of the separate spectral peaks in the A-band phonon progressions indicate the different trends for vibration-free zero-phonon transition and vibration-related lower-energy transitions to high vibrational levels of the bottom state – lower thermal damping and more softened phonon for the zero-phonon transition, also implying the extended defect origin of the A-band photoluminescence.

Ion transfer mediated by TEMPO in ionophore-doped thin films for multi-ion sensing by cyclic voltammetry

We report here on the development of thin-layer ion-selective membranes containing lipophilic TEMPO as a phase-transfer redox mediator for the simultaneous detection of non-redoxactive ions. This redox probe was recently introduced by our group and provides ideal ion-transfer waves when the membrane is interrogated by cyclic voltammetry. To perform multianalyte detection in the same sensing film, plasticized PVC-based membranes were doped with lithium and potassium ionophores in addition to a lipophilic cation-exchanger. The ionophores allow for ion discrimination owing to the different ionophore-cation complexation constants and the oxidation of TEMPO to the oxoammonium form results in the selective transfer of lithium and potassium at different potentials. The resulting voltammograms have half-peak widths of 100 and 102 mV, and the peak separation between anodic and cathodic scans is 8 and 9 mV for lithium and potassium, respectively, close to theoretical expectations. High peak resolution was observed, and the ion-transfer waves are still distinguishable when the ion activities differ by three orders of magnitude. These parameters are remarkably better than those obtained with other redox probes, which is important for multianalyte detection in the same voltammetric scan. Optimized membranes showed independent Nernstian shifts (slopes of 59.23 mV and 54.8 mV for K+ and Li+, respectively) of the peak position for increasing ion concentrations. An idealized model for two ionophore-based membranes combining redox and phase-boundary potentials was applied to the proposed system with excellent correlation. Potassium and lithium ions were simultaneously detected in undiluted human serum samples with good accuracy and precision.

Highly efficient GPCR immobilization with enhanced fouling resistance, salt tolerance, and chromatographic performance

The feasibility of immobilized protein-based biodetection relies critically on the activity of the immobilized proteins as well as the biocompatibility of the protein surface. Although many protein immobilization strategies have been developed with satisfied detection readout signals. Non-specific interactions caused by the protein-coating surface are still of great concern since they often interfere with or affect the reliability of detection. Herein, we developed a highly efficient G protein-coupled receptor (GPCR) immobilization method by the combination of polyethylene glycol (PEG) with a self-labeling enzyme-catalyzed reaction. The immobilization relies on the covalent interaction between the fusion tag of a target GPCR (kinase domain of epidermal growth factor receptor, EGFR) and its covalent inhibitor ibrutinib, which is modified on PEGylated silica gels. Two types of GPCRs, N-methyl-D-aspartate 2 A receptor (NMDAR2A) and endothelin A receptor (ETAR), were used as examples to realize protein immobilization. The GPCR modified gels and the affinity columns packed with them have been extensively characterized, in terms of non-specific adsorptions, retention factor (k′), half peak width (W1/2), tailing factor (Tf), theoretical plates (N), and association and dissociation constants of the ligands with the receptors. The immobilized GPCRs with reduced non-specific interactions and enhanced fouling resistance, salt tolerance, and chromatographic performance were clearly observed. We believe it is the first work to introduce PEGylation in GPCR immobilization and provide comprehensive proof-of-concept studies to illustrate the improved antifouling property, salt tolerance, and chromatographic performance. This method could be generally applicable in other immobilized protein-based technology for reliable biodetection.

Tuning the emission half-peak width of CaMgSi2O6:Cr3+ from 138 nm to 393 nm by controlling the Cr3+ concentration

Broadband near-infrared (NIR) phosphors play a crucial role in the development of next-generation smart NIR light sources based on blue light-emitting diodes (LEDs). The emission bandwidth is an important parameter for evaluating the performance of these phosphors. Herein, an ultra-broadband NIR phosphor CaMgSi2O6:Cr3+ (CMSO:Cr), with a tunable emission band and a full width at half maximum (FWHM) ranging from 138 nm to 393 nm, is obtained by adjusting the doping concentration of Cr3+. In the low-concentration doped sample, a single emission peak at 785 nm is observed. When the concentration of Cr3+ exceeds 1.0 at%, emissions at both 785 nm and 980 nm are detected. The emission peak at 785 nm originates from the [MgO6](Ⅰ) octahedron within the CMSO structure. On the other hand, the emission peak at 980 nm is attributed to the presence of a twisted octahedron [MgO6](Ⅱ), which is caused by defects and vacancies resulting from the charge imbalance when Mg2+ ions are replaced by Cr3+ ions. The Cr3+ ion primarily occupies the [MgO6](Ⅰ) site in the lower-concentration doped sample, which explains the photoluminescence peak at 785 nm. With the increase in the concentration of Cr3+ ions, more and more Cr3+ ions preferentially occupy the [MgO6](Ⅱ) octahedral sites, leading to the broad emission at 980 nm. A novel NIR phosphor light source was fabricated by combining a blue chip with CMSO:Cr phosphor. Driven by a current of 60 mA, the NIR light output power of 5.89 mW and 0.76 mW is achieved by using CMSO:0.015Cr and CMSO:0.04Cr, respectively. This work demonstrates that new luminescent centers can be generated by substituting heterovalent ions, resulting in broadened emission spectra.

Radial basis function neural network optimization algorithm based on dynamic inertial weight particle swarm optimization for separating overlapping peaks in ion mobility spectrometry.

Ion mobility spectrometry (IMS), as a promising analytical tool, has been widely employed in the structural characterization of biomolecules. Nevertheless, the inherent limitation in the structural resolution of IMS frequently results in peak overlap during the analysis of isomers exhibiting comparable structures. The radial basis function (RBF) neural network optimization algorithm based on dynamic inertial weight particle swarm optimization (DIWPSO) was proposed for separating overlapping peaks in IMS. The RBF network structure and parameters were optimized using the DIWPSO algorithm. By extensively training using a large dataset, an adaptive model was developed to effectively separate overlapping peaks in IMS data. This approach successfully overcomes issues related to local optima, ensuring efficient and precise separation of overlapping peaks. The method's performance was evaluated using experimental validation and analysis of overlapping peaks in the IMS spectra of two sets of isomers: 3'/6'-sialyllactose; fructose-6-phosphate, glucose-1-phosphate, and glucose-6-phosphate. A comparative analysis was conducted using other algorithms, including the sparrow search algorithm, DIWPSO algorithm, and multi-objective dynamic teaching-learning-based optimization algorithm. The comparison results show that the DIWPSO-RBF algorithm achieved remarkably low maximum relative errors of only 0.42%, 0.092%, and 0.41% for ion height, mobility, and half peak width, respectively. These error rates are significantly lower than those obtained using the other three algorithms. The experimental results convincingly demonstrate that this method can adaptively, rapidly, and accurately separate overlapping peaks of multiple components, improving the structural resolution of IMS.

The effect of SiC on the growth habit of Fe-Ni-C system Ib gem grade diamond crystals

This article investigates the influence of different silicon carbide contents on the morphology and quality of diamond single crystals synthesized in the Fe-Ni-C-Si system under high temperature and pressure environments. It was found that silicon successfully entered the diamond lattice through bonding. As the doping concentration increases, the growth rate of diamond crystals decreases and defects appear on the crystal surface. The increase in internal stress in the lattice reduces the quality of diamond, as evidenced by the shift in Raman peak and half peak width of the diamond. Moreover, the infrared characterization results showed that the nitrogen element in the crystal exists as a single atom (C-center) in the diamond crystal, and the nitrogen content decreases with the increase of SiC content. This work provides insights for understanding the growth mechanism of natural diamonds and enriching the application of silicon doped diamond single crystals.