材料科学
解耦(概率)
润湿
复合数
热的
密度泛函理论
表面能
功率密度
化学物理
复合材料
热能
纳米技术
可扩展性
图像拼接
储能
分子动力学
声子
化学工程
光电子学
热能储存
能量(信号处理)
热稳定性
热导率
科技与社会
聚合物
降级(电信)
作者
Yifei Zhu,Tiansheng Wang,Yanfei Zhu,Guangmin Zhou
摘要
Composite phase-change materials offer a scalable route for thermal energy storage, yet breaking the inherent trade-off between energy and power densities is constrained by fundamental mismatches at the skeleton-storage-medium interface. Conventional interface engineering remains trapped in empirical trial-and-error, struggling to distinguish the typically entangled variables of interfacial wettability and heat-transport behavior. Here, we present a machine learning-assisted design paradigm based on functional group deconstruction. By resolving surface functional groups into independent elemental and structural dimensions, we achieve programmable control over skeleton-molten salt interfacial behaviors. We reveal an intrinsic property decoupling: interfacial wettability is governed by bonding interactions derived from elemental composition, whereas heat transport is dictated by low-frequency phonon spectral matching rooted in geometric topology. Guided by this predictive atlas, we synthesized targeted carbon-molten salt composites. Compared to unmodified baselines, the engineered composite achieves 1.6-fold higher mass loading and 3.6-fold enhanced thermal conductivity. Crucially, after 350 thermal cycles, it retains ∼90% mass and ∼80% conductivity, decisively suppressing the degradation of pristine hosts (∼60% and ∼25% retention). Device-level finite-difference method simulations indicate this dual-property optimization effectively overcomes the inherent energy-power trade-off-sustaining triple the energy density of unmodified baselines under extreme 10C constant-power loads.
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