Thermal Rectification by Nanoscale Design: Overcoming Bulk Limitations

IF 3 3区 化学 Q3 CHEMISTRY, PHYSICAL
Wei-Chao Wang,Zi-Qi Lin,Shuo-Wang Yang,Jin-Cheng Zheng,Huiqiong Wang
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引用次数: 0

Abstract

Thermal rectification in bulk materials is generally weak because their thermal conductivities have similar temperature dependence. Here, we demonstrate a nanoscale design principle that overcomes the inherent efficiency limitations of bulk thermal rectifiers. By combining lattice-dynamics calculations with the Callaway transport model, we show that phonon–boundary scattering in nano crystalline silicon and diamond induces a nonmonotonic, size-dependent thermal conductivity, a behavior distinct from the monotonic dependence observed in bulk materials. Leveraging this effect, we achieve a maximum rectification ratio of 1.913 in a silicon-diamond junction, significantly exceeding the bulk value of approximately 1.044. The optimal design pairs a silicon segment with a 1000 nm grain size (d_g) with a diamond segment of 120–220 nm grain size (d_g), thereby maximizing the asymmetry in their temperature-dependent conductivities. The rectification exhibits a pronounced dependence on the operating temperature window, with the peak shifting toward lower temperatures and eventually giving way to a monotonically decreasing trend as the temperature bias increases. Extending this framework to other material combinations, we also evaluate carbon/silicon carbide (Diamond/SiC) and silicon carbide/silicon (SiC/Si) junctions in different grain size, achieving optimized rectification ratios of 1.749 and 1.296, respectively. Demonstrated by finite-difference time-domain simulations, this work establishes a general route for engineering phonon transport asymmetry via nanoscale structural design, enabling high-efficiency solid-state thermal management and phonon devices. Sensitivity analyses further show that the enhanced rectification remains robust against partial boundary specularity and a finite thermal boundary resistance, confirming that the dominant contribution arises from grain-size-induced asymmetry in the temperature-dependent thermal conductivities. This work establishes nanoscale structural engineering as a general strategy for breaking the intrinsic limitations of bulk thermal rectification, opening a new avenue for the rational design of high-performance thermal rectifiers and next-generation thermal-management technologies.
纳米级热整流设计:克服体积限制
块状材料的热整流通常较弱,因为它们的导热系数具有相似的温度依赖性。在这里,我们展示了一种纳米级设计原则,克服了体积热整流器固有的效率限制。通过将晶格动力学计算与Callaway输运模型相结合,我们发现纳米晶体硅和金刚石中的声子边界散射诱导了非单调的、与尺寸相关的导热系数,这一行为不同于在块状材料中观察到的单调依赖。利用这一效应,我们在硅-金刚石结中实现了1.913的最大整流比,大大超过了大约1.044的体积值。最佳设计将晶粒尺寸为1000 nm (d_g)的硅段与晶粒尺寸为120-220 nm (d_g)的金刚石段配对,从而最大限度地提高其随温度变化的电导率的不对称性。整流表现出明显的依赖于工作温度窗口,随着温度偏置的增加,峰值向较低的温度移动,并最终让位给单调下降的趋势。将此框架扩展到其他材料组合,我们还评估了不同晶粒尺寸的碳/碳化硅(金刚石/SiC)和碳化硅/硅(SiC/Si)结,分别获得了1.749和1.296的优化整流比。通过时域有限差分模拟证明,本研究通过纳米级结构设计建立了声子传输不对称工程的一般途径,实现了高效的固态热管理和声子器件。灵敏度分析进一步表明,增强的整流对部分边界镜面和有限的热边界阻力仍然保持稳健,证实了主要贡献来自于温度相关的热导率中晶粒尺寸引起的不对称性。这项工作确立了纳米级结构工程作为突破本体热整流固有限制的一般策略,为高性能热整流器的合理设计和下一代热管理技术开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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