Debye Temperature Research Articles

First-principles calculations of the elastic anisotropy, thermal conductivity, and optical properties of MAX-phase M2AlC (M = V, Nb, Ta) series carbides

Materials from the MAX phase, such as the M2AlC (M = V, Nb, Ta) series carbides, exhibit superior mechanical, electronic, and thermodynamic properties, making them highly promising for research. Density functional theory (DFT) has been employed to study the elastic anisotropy, thermal conductivity, electronic, and optical properties of these carbides. The results indicate that the formation enthalpies of the M2AlC (M = V, Nb, Ta) series are negative and the phonon spectra do not exhibit imaginary frequencies, confirming the thermodynamic and dynamic stability of these carbides. Additionally, the calculated Poisson's ratios and B/G ratios suggest that these materials are brittle and contain covalent and ionic bonds—a conclusion further corroborated by analyses of electronic structures. The elastic anisotropy is illustrated through anisotropy indices, three-dimensional (3D) surface configurations, and two-dimensional (2D) projections, with the sequence of anisotropy being: Nb2AlC > Ta2AlC > V2AlC. Further investigations into the sound velocities, Debye temperature, anisotropy of sound velocity, thermal conductivity, and optical properties of the M2AlC (M = V, Nb, Ta) series provide substantial theoretical support for the research on MAX phase M2AlC (M = V, Nb, Ta) series carbides.

A THEORETICAL STUDY OF THE PHYSICAL PROPERTIES OF HEXAGONAL GALLIUM NITRATE USING DENSITY FUNCTIONAL THEORY

First-principles calculations based on density functional theory (DFT) have been used to investigate structural, electronic, optical and thermodynamic aspects of the α-GaN crystal. Based on local density approximations (LDA), Generalized gradient approximation (GGA) and meta-generalized gradient approximation (m-GGA) functional methods, the band gap energies of α-GaN crystals have been estimated as 1.962 eV, 2.069 eV and 2.354 eV. The band gap energies that are presented in these studies are in accordance with the ones from the other experimental and theoretical studies. Besides, our findings give us knowledge about the electronic and optical properties of α-GaN crystal. The band gap energies in the α-GaN crystal are the key factors that define its electrical and optical characteristics. They are the energy range in which the electrons can be exited from the valence band to the conduction band, which in turn affects the material's conductivity and the ability of the material to absorb and emit light. The approximate of our results with the previous researches indicates the reliability of our findings and thus increases our knowledge of α-GaN's electronic and optical phenomena. The orbital characteristics of the Ga and N atoms were found by simulating the density of state and the partial density of state for α-GaN. Besides the analysis of the band structure, density of states and optical properties of the compound we also included. The results show that α-GaN has a direct bandgap, which is at the G point in the Brillouin zone. This is the reason for its great potential for the development of optoelectronic devices. Also, we use the three approximations that are given earlier to find the optical characteristics (the absorption coefficient) of the compound. In addition to that, the thermodynamic properties that can be calculated like Debye temperature, enthalpy, free energy, entropy and heat capacity enable us to understand the thermal behavior of the compound better. The heat capacity of α-GaN is detected to be 17.3 Jmole-1K-1, with a Debye temperature of 824.6K. This research will offer a detailed interpretation of α- G-N, covering all its basic properties and the possible applications in optoelectronic and electronic devices. The results of this study are very important and the new technologies that will be developed based on the α-GaN research will be very beneficial.

Low-temperature photoluminescence and Raman study of monolayer WSe2 for photocarrier dynamics and thermal conductivity

Low-temperature PL analysis reveals an intriguing temperature-dependent emission pattern in WSe2: excitonic dominance above the 150 K Debye temperature, a balance between excitonic and trionic emissions at 150 K, and trionic dominance below this threshold. At lower temperatures, both excitons and trions display linearly polarized emissions, with polarization increasing from 0% at 300 K to 23% (excitons) and 7% (trions) at 150 K, and 12% for trions at 90 K. Moreover, the synthesized monolayer of WSe2 exhibits high thermal conductivity (246 W m−1 K−1 for A1g and 185 W m−1 K−1 for E2g1 modes). This property is attributed to Se vacancies and defects at triangle edges, which redirect phonons, reducing scattering and enabling efficient heat transport along boundaries. The unveiling of these novel insights within the synthesized 2D WSe2 material holds significant promise for its potential applications in nano-optoelectronics. Its demonstrated efficiency in dissipating heat, coupled with improved thermal stability, suggests the possibility of employing it in future devices. This could facilitate compact designs and the miniaturization of advanced technological tools, showcasing the material's potential for practical implementation.

Exploring energy harvesting potential of lithium-based halide perovskites Li2CuSbZ6 (Z=Cl, Br): First principles approach

Recent research has focused on investigating the physical characteristics of the halide perovskite combinations, Li2CuSbZ6 (Z = Cl, Br) within the context of Density Functional Theory (DFT). The optimized FCC cubic structure lattice parameters for Li2CuSbCl6 and Li2CuSbBr6 are 10.57 and 11.10 Å, respectively. We have examined the stability by evaluating the tolerance factor, formation energy, and the Born Criteria. The analysis conducted on the elastic constants identifies the ductility, anisotropy, melting, and Debye temperatures. First-principles calculations reveal that computed electronic features using the TB-mBJ approximation unveiled an indirect band gap of 1.33 and 1.04 eV, respectively. Optical analyses indicate that the studied halide perovskites exhibits significant absorption in the visible and ultraviolet regions. Boltzmann's classical theory explains the transport features and attained higher figure of merit (ZT) values for both perovskites. These research findings provide a significant potential for these materials in the absorber layer of perovskite-based solar cells as well as thermoelectric devices.

Effect of AFM ordering on thermoelectric responses of Mg3X2 (X: C, Si, Ge) monolayers : a DFT insight

Two-dimensional materials have gained a lot of attention in the last few decades due to their potential applications in thermoelectric and nano-electronic devices. This study systematically presents the mechanical, electronic and thermoelectric characteristics of two-dimensional honeycomb-kagomeMg3X2(X:C,Si,Ge) structures in the framework of density functional theory computations and by solving semiclassical Boltzmann transport equation. The geometrical stability of these structures is validated by phonon spectrum and molecular dynamics simulations. Following the elastic constants, we have inferred that all the systems are mechanically stable and brittle in nature. Lower values of Debye temperature of all structures suggest thatMg3X2monolayers should have lower values of lattice thermal conductivity compared to graphene. Electronic structure calculations indicate that these materials are semimetallic in their nonmagnetic phase. All the structures display remarkably low lattice thermal conductivity (0.9-1.5 W (mK)-1) due to a large scattering factor and higher anharmonicity. The presence of sharp density of states peaks close to the Fermi level, arising from nearly flat and dispersionless band in the antiferromagnetic (AFM) arrangement, is poised to enhance the Seebeck coefficient, thereby potentially boosting the thermoelectric performance. The estimated values of thermoelectric figure of merit (ZT) are around 0.78 and 0.67 forMg3Si2andMg3Ge2structure respectively in AFM phase atT= 700 K. These outcomes of our findings suggest thatMg3X2monolayers exhibit substantial promise for thermoelectric device application.

Unveiling the boson peaks in amorphous phase-change materials

The Boson peak is a universal phenomenon in amorphous solids. It can be observed as an anomalous contribution to the low-temperature heat capacity over the Debye model. Amorphous phase-change materials (PCMs) such as Ge-Sb-Te are a family of poor glass formers with fast crystallization kinetics, being of interest for phase-change memory applications. So far, whether Boson peaks exist in PCMs is unknown and, if they do, their relevance to PCM properties is unclear. Here, we investigate the thermodynamic properties of the pseudo-binary compositions on the tie-line between Ge15Te85and Ge15Sb85from a few Kelvins to the liquidus temperatures. Our results demonstrate the evidence of the pronounced Boson peaks in heat capacity below 10 K in the amorphous phase of all compositions. By fitting the data using the Debye model combined with a modification of the Einstein model, we can extract the characteristic parameters of the Boson peaks and attribute their origin to the excess vibrational modes of dynamic defects in the amorphous solids. We find that these parameters correlate almost linearly with the Sb-content of the alloys, despite the nonmonotonic behaviors in glass forming abilities and thermal stabilities. In a broader context, we show that the correlations of the characteristic parameters of the Boson peaks with Tg and kinetic fragility, vary according to the type of bonding. Specifically, metallic glasses and conventional covalent glasses exhibit distinct patterns of dependence, whereas PCMs manifest characteristics that lie in between. A deeper understanding of the Boson peaks in PCMs holds the promise to enable predictions of material properties at higher temperatures based on features observed in low-temperature heat capacity.

Effect of transition metals (Fe, Ru and Os) on the elastic, thermodynamic, electronic, magnetic and thermoelectric properties of three Nd-filled arsenide skutterudites based on first-principles computations

Elastic, electronic, magnetic, thermodynamic, and thermoelectric properties of three neodymium-filled skutterudites NdT4As12 (T = Fe, Ru and Os) have been investigated using density functional theory. The bulk moduli increase with the atomic numbers of the transition metals. All materials are stiff, while the Os compound is the stiffest. A considerable ionic contribution is seen in their inter-atomic bonding. The Fe compound possesses the highest Debye temperature, while the Os compound has the highest melting temperature. GGA+U formalism predicts the semimetallic nature of all the compounds, but their total DOS differs near the Fermi level in both spin channels. The contributions of the Nd-f and T-d electrons differ in the three compounds and two methods. GGA+U predicts the highest magnetic moment in the Fe compound, followed by the Ru and Os compounds. The thermoelectric figure of merit shows no systematic variation with z of the transition metals and in the high temperature region it increases with temperature pretty fast. The highest value of ZT is 0.32 in the Ru compound in the spin-down channel while it is 0.24 in the spin-up channel in the Fe compound, both at 1000 K.

Analyzing the structural, optoelectronic, and thermoelectric properties of InGeX3 (X = Br) perovskites via DFT computations

The Electronic and optical properties of InGeX3(X = Cl, Br) were examined by adopting the density functional theory (DFT) approach. We applied the GGA + Trans-Blaha modified Becke–Johnson (TB-mBJ) technique to acquire the precise bandgap of 1.52 and 0.98 eV of the compounds InGeX3(X = Cl, Br) respectively which suggests the direct bandgap at (M-M). The stability of the material is confirmed by the formation energy (– 2.83 = Cl; – 2.35 = Br) and Mechanical stability. Primarily elastic constants were extracted for each of the materials under scrutiny, and these values then served to gauge all of the materials’ mechanical properties. The assessed Poisson’s and Pugh’s ratios for the materials InGeCl3 and InGeBr3 were verified to identify the degree of ductility. The quasi-harmonic Debye model additionally covers the temperature and pressure dependence on thermodynamic parameters, particularly volume, specific heat capacity (Cv) at constant volume, and the Gruneisen parameter (γ) in the range of 0–800 K and 0–5 GPa. It is anticipated that InGeCl3 and InGeBr3 will have static dielectric constants of 4.01 and 5.74, respectively. InGeX3(X = Cl, Br) also reveals significant absorption in the high UV spectrum. The thermoelectric properties have also been calculated vdata-element-id="9QNfR3VHbcMHX_W0fJCYp" data-element-type="html" style="display: initial; visibility: initial; opacity: initial; clip-path: initial; position: relative; float: left; top: 0px; left: 0px; z-index: 1 !important; pointer-events: none;" />ia boltztrap2 code using a k mesh of around 1,50,000 points.

First-Principles Linear Combination of Atomic Orbitals Calculations of K2SiF6 Crystal: Structural, Electronic, Elastic, Vibrational and Dielectric Properties.

The results of first-principles calculations of the structural, electronic, elastic, vibrational, dielectric and optical properties, as well as the Raman and infrared (IR) spectra, of potassium hexafluorosilicate (K2SiF6; KSF) crystal are discussed. KSF doped with manganese atoms (KSF:Mn4+) is known for its ability to function as a phosphor in white LED applications due to the efficient red emission from Mn⁴⁺ activator ions. The simulations were performed using the CRYSTAL23 computer code within the linear combination of atomic orbitals (LCAO) approximation of the density functional theory (DFT). For the study of KSF, we have applied and compared several DFT functionals (with emphasis on hybrid functionals) in combination with Gaussian-type basis sets. In order to determine the optimal combination for computation, two types of basis sets and four different functionals (three advanced hybrid-B3LYP, B1WC, and PBE0-and one LDA functional) were used, and the obtained results were compared with available experimental data. For the selected basis set and functional, the above-mentioned properties of KSF were calculated. In particular, the B1WC functional provides us with a band gap of 9.73 eV. The dependencies of structural, electronic and elastic parameters, as well as the Debye temperature, on external pressure (0-20 GPa) were also evaluated and compared with previous calculations. A comprehensive analysis of vibrational properties was performed for the first time, and the influence of isotopic substitution on the vibrational frequencies was analyzed. IR and Raman spectra were simulated, and the calculated Raman spectrum is in excellent agreement with the experimental one.

Tunable annealing temperature for the structural, magnetic, optical, and dielectric characteristics of Mn0.5Zn0.5Ni0.5Fe1.5O4 nano-ferrite

The as-prepared Mn0.5Zn0.5Ni0.5Fe1.5O4 ferrite was prepared by the co-precipitation process and annealed at 300, 500, 900, and 1100 °C. The single-phase cubic spinel structure was confirmed by XRD patterns, Rietveld fitting, TEM imaging and several structural parameters, including crystalline size and lattice constant have been examined. The FTIR spectrum confirmed the main two absorption bands of tetrahedral and octahedral sites in ferrite, where the elastic parameters such as force constants and Debye temperature have been investigated. The saturation magnetization increases with the annealing temperature, while the energy band gap decreases with the annealing temperature, and also the ac conductivity decreases with annealing temperature.

First-principles calculations to investigate physical properties of oxide perovskites LaBO3 (B[dbnd]Mn, Fe) for thermo-spintronic devices

Oxide perovskite LaBO3 was extensively examined using first principles computations with density functional theory. Various exchange-correlation functionals were applied to investigate several of its physical properties. The compound's stability was validated through energy optimization in both ferromagnetic and non-magnetic phases, revealing that the ferromagnetic phase is more energetically stable. With the optimized lattice parameter, we explored various electronic, mechanical, magnetic, and thermodynamic properties. According to the GGA + U approximation, LaMnO3 and LaFeO3 exhibit half-metallic and semiconductor characteristics, respectively. The elastic constants, along with the elastic moduli (Y, B, and G) and Vickers hardness (Hv) number, were calculated to assess the mechanical properties of both compounds. Our simulation confirmed the ductile nature of the material by analyzing the Cauchy pressure, Poisson's ratio, and Pugh ratio. Additionally, thermodynamic parameters, including thermal expansion, specific heat capacity, and Debye temperature, were computed using the quasi-harmonic Debye model. The study's findings suggest that these materials are suitable for thermo-spintronic devices.

Employing Young's modulus and Debye temperature to calculate the elastic, thermodynamic and thermophysical properties of titanium oxynitrides.

The values of the shear v s and longitudinal v l wave velocities were calculated for 14 selected titanium oxynitrides TiN x O y using the known values of Young's modulus and Debye temperature. The errors Δ of the calculations did not exceed ±0.01%. It turned out that some TiN x O y samples are able to compete with artificial diamonds in terms of v l values and can potentially be used in acoustic resonators for intelligent chemical and biochemical sensors. A number of elastic, thermodynamic and thermophysical quantities were calculated, and graphical dependencies between them were plotted. The established correlations were used to develop two algorithms for predicting the properties of TiN x O y alloys based on a single experimental parameter, namely the X-ray coefficient of thermal expansion or pycnometric density. The highest accuracy was shown by the method based on the experimental density, which allowed to estimate, with acceptable errors, the values of the shear v s and mean v m wave velocities (Δ = ±(1-5)%), the minimum thermal conductivity λ min within the framework of the Cahill‒Pohl model (Δ = ±(0-3)%), the isobaric C p and isochoric C V heat capacities (Δ < 1%); while the known experimental methods and alternative models for determining these quantities are characterized by wider error intervals: Δ(v s) = ±(1-10)%, Δ(λ) = ±(1-10)% and Δ(C p) = ±(1-3)%.

Physical, Structural and Elastic Properties of New Oxyfluoride Borate Glasses

New mixed alkali/alkaline oxyfluoride borate glasses with composition xCaF2–(50-x)LiF–50B2O3 (x = 0, 5, 10, 15 and 20 mol%) were prepared by the conventional melt-quenching technique. X-ray diffraction (XRD) patterns confirmed the amorphous nature of the prepared samples, while energy dispersive X-ray (EDX) analysis confirmed the presence of the constituent elements B, O, F, and Ca. Fourier transform infrared (FTIR) spectra revealed the formation of BO3, BO2F, BO4 and BOF3 structural groups, as well as non-bridging oxygen/fluorine atoms in the glass network. The concentrations of these structural groups were found to vary with CaF2 concentration. The measured density and the calculated molar volume were found to increase over the entire range of composition. The increase in ultrasonic velocity, elastic moduli, micro-hardness and Debye temperature with the addition of CaF2 was discussed in terms of competition between the above-mentioned borate groups. Fraction of four-coordinated boron atoms, average boron–boron separation, fluorine molar volume, total packing density, dissociation energy per unit volume and average cross-link density were estimated. A close correlation is achieved between these quantities and elastic properties. Excellent agreement is found between the experimentally determined values and the theoretically calculated values of elastic properties from Makishima–Mackenzie's theory.

Relaxation behaviour, conductive grains and resistive boundaries of bismuth-based double perovskite Bi2-xLaₓFeGaO₆

The successful synthesis of the ceramic Bi2-xLaxFeGaO6 powder ceramic sample with varying La content (x = 0.01, 0.03, 0.07, 0.10) were synthesized via the solid-state method. Analysis using X-ray diffraction at room temperature was carried out to examine its structure, revealing a crystallite size of approximately 22.07–50.84 nm. This size indicates the potential applications in microwave technology due to its small grain size, which has the capability to enhance microwave absorption properties. The dielectric constant of the material shows an increase with the frequency applied, in accordance with the behaviour anticipated by the dielectric HN model and Debye model. This model proposes that the material's dielectric response can be manipulated by modifying the applied frequency, making it a valuable tool in the material design for specific purposes. The full width at half maximum (FWHM) curve of the electrical modulus displayed variability, suggesting the existence of a non-Debye relaxation mechanism in the material. This indicates that the material could possess distinct electrical properties that might be beneficial for certain applications. The outcomes demonstrated a negative temperature coefficient resistance (NTCR), indicating a decrease in the material's resistance with increasing temperature. Such behaviour can be advantageous in situations where temperature variations require monitoring or regulation. The Cole-Cole plot illustrated that the grains exhibit conductive behaviour at lower frequencies, a crucial insight for comprehending the material's electrical properties. In conclusion, these results indicate that the ceramic Bi2-xLaxFeGaO6 for x = 0.01, 0.03, 0.07, 0.1) showcases promising attributes for various applications, particularly in microwave technology and electrical conductivity.

Drug-amino acid interaction: Molecular dynamics in aqueous medium using time domain reflectometry

Present work reports dielectric response of the non-steroidal anti-inflammatory drug (NSAID) aceclofenac in aqueous valine solutions at various concentrations and temperatures (278.15 K–298.15 K) in the frequency range of 0.01 GHz to 30 GHz using Time-domain reflectometry (TDR) technique. The frequency dependent complex dielectric permittivity has been analyzed by Harviliak-Negami equation. Debye model is used for the description of complex dielectric permittivity spectra ε*(ν). The structural and dynamical properties of water has been investigated at different concentrations of valine and aceclofenac using dielectric as well as thermodynamic parameters that includes static dielectric constant (ε0), relaxation time (τ0), Kirkwood correlation factor (g), free energy of activation (ΔF), entropy of activation (ΔS), and enthalpy of activation (ΔH). Towards the measured low temperature and high concentrations of Valine and Aceclofenac (ACF), static dielectric constant (ε0) was found to be increasing. This could be due to increased effective dipole-dipole parallel alignment and can be confirmed by the increasing values of correlation factor (g > 1). The dipole-dipole interaction between Drug-Amino acid resulted in increased dielectric relaxation time (τ0) of system due to increased steric hindrance for the rotation of dipoles. The free energy of activation was found to be in the range of 2.22 and 2.58 Kcal mol-1. The entropy is more negative at high concentration suggesting more ordered structure. The slope of log (Tτ0) vs. 1000/T gives the value of enthalpy (ΔH).

Growth, first-principles calculations and optical properties of a novel near-infrared Ho: NLGW laser crystal

A rigid structure was constructed using an isotopic doping strategy, and a novel near-infrared 1 at% Ho3+: NaLa0.93Gd0.06(WO4)2 (Ho: NLGW) laser crystal with a size of Φ 18 mm × 30 mm was successfully grown by the Czochralski method. X-ray rocking curves and Rietveld refinement indicate that the grown crystal possesses high crystalline quality and crystallizes in the I41/a space group with lattice parameters: a = b = 5.3518 Å, c = 11.6438 Å and V = 333.5051 Å3. The Ho: NLGW crystal exhibits a low coefficient of thermal expansion (8.472 × 10−6 K−1), and the c-axis thermal conductivity increases from 1.235 W/(m × K) to 1.404 W/(m × K). The thermal properties of the Ho: NLGW crystal surpass those of other Ho3+-doped tungstate series and mainstream near-infrared laser crystals, suggesting that it is easier to obtain excellent laser gain. For revealing the excellent thermal properties, the elastic moduli of the NLW and NLGW crystals have been calculated by first principles. With the introduction of Gd3+, the structural stiffness of the NLW as a whole has been increased to optimize the mechanical properties in each axial direction and to obtain the reason for the larger Debye temperature. Finally, the transmission, absorption and near-infrared emission spectra of the Ho: NLGW crystal were investigated. The crystal exhibits a high transmittance of 88.5 % and an emission cross-section of 0.84 × 10−20 cm2 calculated according to the J-O theory. Experimental results indicate that the grown Ho: NLGW crystal can achieve large laser output more easily and are expected to be an excellent medium for 2 μm solid-state lasers.

Novel Parameter Identification Method of Extended Debye Model for Long-Length Submarine Cables

Novel Parameter Identification Method of Extended Debye Model for Long-Length Submarine Cables

Machine-learning assistant DFT study of half-metallic full-Heusler alloy N2CaNa: Structural, electronic, mechanical, and thermodynamics properties

We studied the structural, electronic, mechanical, and thermodynamic properties of N2CaNa full Heusler alloys using density functional theory (DFT). Results for the structural analysis establish structural stability with a minimum formation energy of 29.9 eV. The compound is brittle and mechanically stable, having checked out with the Pugh criteria. The B/G ratio of bulk modulus B to shear modulus G for N2CaNa is 4.766, hence the material is ductile. N2CaNa alloy is ductile in nature. The Debye model correctly predicts the low-temperature dependence of heat capacity, which is proportional to Debye’s T3 law. Just like the Einstein model, it also recovers the Dulong–Petit law at high temperatures, suggesting the thermodynamic stability of the compounds at moderate temperatures. The results demonstrate potential N2CaNa for applications in spintronics, structural engineering, and other fields requiring materials with tailored properties.

An Examination of the Electronic, Optical, and Thermodynamic Properties of Β-Gan

The current work involves the systematic examination of the features of Gallium Nitride (GaN) including the electronic, optical, structural, and thermodynamic features, depending on first principles calculation. This is according to approximations, (LDA), (GGA), and (m-GGA). The bandgap energies of Gallium nitride are (1.85 eV, 1.93 eV, and 2.179 eV), respectively. Furthermore, our study also reveals that GaN has a direct bandgap and is highly stable. Finally, our results indicate that the m-GGA method accurately predicts the bandgap energy of GaN. The m-GGA method outperforms both LDA and GGA methods in accuracy to predict the bandgap energy of GaN, as evidenced by its closest approximation to the experimental value. To determine the orbital nature of the Gallium and Nitrogen atoms, the state density and state partial density of Gallium nitride were simulated. The absorption coefficient of Gallium nitride is computed and analyzed in depth for the optical transitions. The absorption coefficient of Gallium nitride is affected by various factors, including the material's band structure, temperature, doping level, and the energy of the incident photons. In addition to that, the thermodynamic properties that can be calculated like enthalpy, entropy, heat capacity, free energy, and Debye temperature enable us to understand the thermal behavior of the compound better. The heat capacity of α-GaN is detected to be (39.9, 25.5, and 32.4) Jmole-1K-1, and a Debye temperature of 807 K, 1134 K, and 866 K for LDA, GGA, and m-GGA, respectively. This research will offer a detailed interpretation of β-GaN, covering all its basic properties and possible applications in electronic devices and optoelectronic devices. The results of this study are very important and the new technologies that will be developed based on the Cubic phase - GaN research will be very beneficial.

Room-temperature superconductivity in carbons – a mini review

The search for room-temperature superconductivity in carbons is gathering momentum because it has a long history, impressive track record, clear advancement route, and theoretical backup. The report of a suspected Josephson current in Al-C-Al sandwiches at room temperature, published in Nature 50 years ago, led to the report of a voltage in nano-graphite films believed to mark the reverse Josephson effect. The report on oxygen-doped diamonds led to full-blown superconductivity in boron-doped diamonds. The reports on highly oriented pyrolytic graphite (HOPG) and water-treated graphite powder led to the claim of a current running by itself for 50 days in a ring of HOPG soaked with alkane at room temperature. It also led to a claim of a current running for 1,000 seconds in a ring of graphene soaked in hexane. The carbons are amicable to intercalation chemistry, electrostatic carrier doping, and surface-proving techniques to promote an increase in carrier density, metallization, and applicability of the Ashcroft proposal. Consequently, the high Debye temperatures (1,670, 2,230 and 2,500 K in graphene, diamond and HOPG) may be sufficient to underwrite superconductivity at T∼300 K in carbons, provided the phonon-exchange factor, λ, is around 3 to mark strong enough interactions between electrons and phonons.