Proportional correlation between heat capacity and thermal expansion of atomic, molecular crystals and carbon nanostructures

IF 0.9 4区 物理与天体物理 Q4 PHYSICS, CONDENSED MATTER
M. Barabashko, A. I. Krivchikov, R. Basnukaeva, O. A. Korolyuk, A. Jeżowski
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引用次数: 0

Abstract

Correlation between thermal expansions β(T) and heat capacity C(T) of atomic and molecular crystals, amorphous materials with a structural disorder, carbon nanomaterials (fullerite C60, bundles SWCNTs of single-walled carbon nanotubes) was analyzed. The influence of the contribution to the coefficient of linear thermal expansion αXe(T) of Xe atoms adsorbed on the SWCNTs bundles is considered. The proportional correlation was found between the contribution to the coefficient of linear thermal expansion αXe(T) and the normalized to the gas constant heat capacity C Xe(T)/R of Xe atoms adsorbed on the SWCNTs bundles. The proportional correlation (β/β*) ∼ (CV/R) with the parameter β* for the bulk thermal expansion coefficient for cryocrystals is proposed. In the case of atomic crystals such as Xe and Ar, the proportional correlation (β/β*) ∼ (CV/R) is observed in the temperature range from the lowest experimental to temperatures where CV/R ≈ 2.3. The correlation is not observed in the temperatures where 2.3 < C V/R < 3 (classical Dulong-Petit law). It was found that the universal proportional correlation is also observed for molecular crystals with linear symmetry, such as CO2, CO, and N2O if the normalized heat capacity below the values CV/R ≈ 3 ÷ 3.5. It indicates that the proportional correlation between thermal expansions (β/β*) and heat capacity (CV/R) is related not only to the translational, but also to the rotational degrees of freedom of the molecule in the crystal. In the case of the C0, molecular crystal with translational and rotational degrees of freedom and intramolecular vibrations, the discussed above correlation occurs below the values of normalized heat capacity CV/R ≈ 7.5. In strongly anisotropic systems, such as systems of compacted bundles of single-walled carbon nanotubes and SWCNTs bundles with adsorbed Xe atoms, this universal dependence appears in a limited temperature range that does not include the lowest temperatures. A qualitative explanation of the observed correlation is proposed.
原子、分子晶体和碳纳米结构的热膨胀与热容的比例关系
分析了原子晶体和分子晶体、结构无序的非晶态材料、碳纳米材料(富勒石C60、单壁碳纳米管束状SWCNTs)的热膨胀β(T)与热容C(T)的相关性。考虑了吸附在SWCNTs束上的Xe原子对线性热膨胀系数αXe(T)的贡献。发现对线性热膨胀系数αXe(T)的贡献与被吸附在SWCNTs束上的Xe原子对气体恒热容C Xe(T)/R的归一化呈正比关系。提出了晶体体热膨胀系数与参数β*之间的比例关系(β/β*) ~ (CV/R)。在原子晶体如Xe和Ar的情况下,在从最低实验温度到CV/R≈2.3的温度范围内观察到比例相关(β/β*) ~ (CV/R)。在2.3 < C V/R < 3(经典的Dulong-Petit定律)的温度下,没有观察到相关。当归一化热容小于CV/R≈3 ÷ 3.5时,对于线性对称的分子晶体,如CO2、CO和N2O,也存在普遍的比例相关关系。结果表明,晶体中分子的热膨胀(β/β*)与热容(CV/R)之间的正比关系不仅与分子的平移自由度有关,还与分子的旋转自由度有关。对于具有平移自由度和旋转自由度以及分子内振动的C0分子晶体,上述相关性发生在归一化热容CV/R≈7.5值以下。在强各向异性体系中,如单壁碳纳米管致密束体系和吸附Xe原子的SWCNTs束体系,这种普遍依赖关系出现在有限的温度范围内,不包括最低温度。对观察到的相关性提出了定性解释。
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来源期刊
Condensed Matter Physics
Condensed Matter Physics 物理-物理:凝聚态物理
CiteScore
1.10
自引率
16.70%
发文量
17
审稿时长
1 months
期刊介绍: Condensed Matter Physics contains original and review articles in the field of statistical mechanics and thermodynamics of equilibrium and nonequilibrium processes, relativistic mechanics of interacting particle systems.The main attention is paid to physics of solid, liquid and amorphous systems, phase equilibria and phase transitions, thermal, structural, electric, magnetic and optical properties of condensed matter. Condensed Matter Physics is published quarterly.
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