Boosting thermal energy transport across the interface between phase change materials and metals via self-assembled monolayers

被引:0
|
作者
Shan, Zi-Yu [1 ,2 ]
An, Meng [3 ,4 ]
Zhang, Xing [1 ]
Zhang, Hai [2 ]
Ma, Wei-Gang [1 ]
机构
[1] Tsinghua Univ, Dept Engn Mech, Key Lab Thermal Sci & Power Engn, Minist Educ, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Dept Energy & Power Engn, Beijing 100084, Peoples R China
[3] Shaanxi Univ Sci & Technol, Coll Mech & Elect Engn, Xian 710021, Peoples R China
[4] Univ Tokyo, Grad Sch Engn, Dept Mech Engn, 7-3-1 Bunkyo Ku, Tokyo 1138656, Japan
基金
中国国家自然科学基金;
关键词
thermal energy transport; interface; phase change material; self-assembled monolayer; molecular dynamics; BINARY EUTECTIC MIXTURES; CONDUCTIVITY ENHANCEMENT; SUGAR ALCOHOLS; FOAM;
D O I
10.1088/1361-648X/ad48ef
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Thermal energy storage using phase change materials (PCMs) has great potential to reduce the weather dependency of sustainable energy sources. However, the low thermal conductivity of most PCMs is a long-standing bottleneck for large-scale practical applications. In modifications to increase the thermal conductivity of PCMs, the interfacial thermal resistance (ITR) between PCMs and discrete additives or porous networks reduces the effective thermal energy transport. In this work, we investigated the ITR between a metal (gold) and a polyol solid-liquid PCM (erythritol) at various temperatures including temperatures below the melting point (300 and 350 K), near the melting point (390, 400, 410 K, etc) and above the melting point (450 and 500 K) adopting non-equilibrium molecular dynamics. Since the gold-erythritol interfacial thermal conductance (ITC) is low regardless of whether erythritol is melted or not (<40 MW m(-2) K-1), self-assembled monolayers (SAMs) were used to boost the interfacial thermal energy transport. The SAM with carboxyl groups was found to increase the ITC most (by a factor of 7-9). As the temperature increases, the ITC significantly increases (by similar to 50 MW m(-2) K-1) below the melting point but decreases little above the melting point. Further analysis revealed that the most obvious influencing factor is the interfacial binding energy. This work could build on existing composite PCM solutions to further improve heat transfer efficiency of energy storage applications in both liquid and solid states.
引用
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页数:9
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