Revealing the role of liquid preordering in crystallisation of supercooled liquids

被引:45
作者
Hu, Yuan-Chao [1 ]
Tanaka, Hajime [1 ,2 ]
机构
[1] Univ Tokyo, Dept Fundamental Engn, Inst Ind Sci, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
[2] Univ Tokyo, Res Ctr Adv Sci & Technol, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
关键词
CRYSTAL-NUCLEATION; GLASS-FORMATION; SOLIDIFICATION; SURFACE; ALLOYS; GROWTH; ORDER; BCC; CU;
D O I
10.1038/s41467-022-32241-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The recent discovery of non-classical crystal nucleation pathways has revealed the role of fluctuations in the liquid structural order, not considered in classical nucleation theory. On the other hand, classical crystal growth theory states that crystal growth is independent of interfacial energy, but this is questionable. Here we elucidate the role of liquid structural ordering in crystal nucleation and growth using computer simulations of supercooled liquids. We find that suppressing the crystal-like structural order in the supercooled liquid through a new order-killing strategy can reduce the crystallisation rate by several orders of magnitude. This indicates that crystal-like liquid preordering and the associated interfacial energy reduction play an essential role in nucleation and growth processes, forcing critical modifications of the classical crystal growth theory. Furthermore, we evaluate the importance of this additional factor for different types of liquids. These findings shed new light on the fundamental understanding of crystal growth kinetics. In classical nucleation theory, structural order in the liquid phase is not considered. But simulations of supercooled liquids now show that crystal-like liquid preordering play an essential role in nucleation and growth processes - calling for extensions of the classical theory.
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页数:12
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共 63 条
  • [1] Quantitative parameter-free prediction of simulated crystal-nucleation times
    Aga, Rachel S.
    Morris, James R.
    Hoyt, Jeffrey J.
    Mendelev, Mikhail
    [J]. PHYSICAL REVIEW LETTERS, 2006, 96 (24)
  • [2] SHOULD ALL CRYSTALS BE BCC - LANDAU THEORY OF SOLIDIFICATION AND CRYSTAL NUCLEATION
    ALEXANDER, S
    MCTAGUE, J
    [J]. PHYSICAL REVIEW LETTERS, 1978, 41 (10) : 702 - 705
  • [3] Arai S, 2017, NAT PHYS, V13, P503, DOI [10.1038/NPHYS4034, 10.1038/nphys4034]
  • [4] Prediction of absolute crystal-nucleation rate in hard-sphere colloids
    Auer, S
    Frenkel, D
    [J]. NATURE, 2001, 409 (6823) : 1020 - 1023
  • [5] Unsupervised topological learning for identification of atomic structures
    Becker, Sebastien
    Devijver, Emilie
    Molinier, Remi
    Jakse, Noel
    [J]. PHYSICAL REVIEW E, 2022, 105 (04)
  • [6] Atomic-level structure and structure-property relationship in metallic glasses
    Cheng, Y. Q.
    Ma, E.
    [J]. PROGRESS IN MATERIALS SCIENCE, 2011, 56 (04) : 379 - 473
  • [7] Crystallization by particle attachment in synthetic, biogenic, and geologic environments
    De Yoreo, James J.
    Gilbert, Pupa U. P. A.
    Sommerdijk, Nico A. J. M.
    Penn, R. Lee
    Whitelam, Stephen
    Joester, Derk
    Zhang, Hengzhong
    Rimer, Jeffrey D.
    Navrotsky, Alexandra
    Banfield, Jillian F.
    Wallace, Adam F.
    Michel, F. Marc
    Meldrum, Fiona C.
    Coelfen, Helmut
    Dove, Patricia M.
    [J]. SCIENCE, 2015, 349 (6247)
  • [8] Can Ordered Precursors Promote the Nucleation of Solid Solutions?
    Desgranges, Caroline
    Delhornmelle, Jerome
    [J]. PHYSICAL REVIEW LETTERS, 2019, 123 (19)
  • [9] Unusual Crystallization Behavior Close to the Glass Transition
    Desgranges, Caroline
    Delhommelle, Jerome
    [J]. PHYSICAL REVIEW LETTERS, 2018, 120 (11)
  • [10] Unraveling the Coupling between Demixing and Crystallization in Mixtures
    Desgranges, Caroline
    Delhommelle, Jerome
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (23) : 8145 - 8148