皮肤超固态影响水滴的性能和功能

Droplet Pub Date : 2024-08-24 DOI:10.1002/dro2.139
Chang Q. Sun, Yong Zhou, Hengxin Fang, Biao Wang
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引用次数: 0

摘要

与母体相比,水滴更令人着迷,它具有非凡的催化和水电能力、弹性适应性、疏水性、灵敏性、热稳定性等,但其内在机理仍然难以捉摸。我们在此强调,H-O 键遵循普遍的键序-长度-强度相关性和非键电子极化调控,氢键合作性和极化性概念调控耦合氢键(O:H-O)的性能。计算和光谱证据一致表明,分子配位不足会使分子内 H-O 键缩短多达 10%,同时使分子间 O:H 非键延长 20%,并与电子极化相关联,从而使 0.3 纳米厚的液滴表皮形成超固相自电化。超固相表皮决定了液滴在化学、介电、电学、机械、光学和热学特性以及电子和声子传输动力学方面的性能和功能。这些发现的扩展可以加深我们对气泡和分子团簇等欠配位水系统的了解,并促进水和冰的深度工程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Skin supersolidity matters the performance and functionality of water droplets

Skin supersolidity matters the performance and functionality of water droplets

Even more fascinating than its bulk parent, a water droplet possesses extraordinary catalytic and hydro-voltaic capability, elastic adaptivity, hydrophobicity, sensitivity, thermal stability, etc., but the underlying mechanism is still elusive. We emphasize herewith that the H‒O bond follows the universal bond order‒length‒strength correlation and nonbonding electron polarization regulation and the hydrogen bond cooperativity and polarizability notion regulates the performance of the coupling hydrogen bond (O:H‒O). Computational and spectrometric evidence consistently shows that molecular undercoordination shortens the intramolecular H‒O bond by up to 10% while lengthening the intermolecular O:H nonbond by 20% cooperatively with an association of electron polarization, making the 0.3-nm thick droplet skin of a supersolid phase of self-electrification. The supersolid skin dictates the performance and functionality of the droplet in chemical, dielectric, electrical, mechanical, optical, and thermal properties as well as the transport dynamics of electrons and phonons. The amplification of these findings could deepen our insight into the undercoordinated aqueous systems, including bubbles and molecular clusters, and promote deep engineering of water and ice.

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