首页> 外文期刊>The Journal of Chemical Physics >Increase in local crystalline order across the limit of stability leads to cubic-hexagonal stacking in supercooled monatomic (mW) water
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Increase in local crystalline order across the limit of stability leads to cubic-hexagonal stacking in supercooled monatomic (mW) water

机译:跨稳定性极限增加局部结晶顺序导致超级冷却单体(MW)水中的立方六边形堆叠

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At the limit of stability of a supercooled tetrahedral liquid modeled by monatomic (mW) water potential, it was recently shown that relaxation occurs across a unique value of per particle potential energy (phi(mid)), which corresponds to a dynamical (non-stationary) condition of Gibbs free energy function G(T, P, N, phi): [partial derivative(2) (G/N)/partial derivative phi(2) = 0] and [partial derivative(G/N)/partial derivative phi not equal 0]. In this work, we explore the inherent structures responsible for the formation of the amorphous states through such a mechanism of relaxation of mW liquid. We first identify 6-member boat and chair shaped rings using a criterion based on the internal dihedral angles. We then consider the stacking of the cubic diamond (10-atom cluster with 4 chair shaped rings) and hexagonal wurtzite (12-atom cluster with 3 boat and 2 chair shaped rings) units through a shared chair ring. We find that the local crystalline (tetrahedral) order is exhibited by the eclipsed bond particles of the laterally connected wurtzite units which are stacked from both sides with the diamond units (DWD stacking). Increasingly longer range crystalline order is obtained as the number of stacked wurtzite layers increases: the particles shared by the stacked (laterally connected) wurtzite layers in DWWD show a longer range crystalline order. An even longer range crystalline order is exhibited by the eclipsed bond particles of the middle (laterally connected) wurtzite layer of DWWWD stacking. We find that cubic-hexagonal stacking occurs primarily in the form of DWD layers across the limit of stability. The local tetrahedral order of the purely cubic (diamond) network particles (which are not shared with wurtzite units) deviates significantly from that of the hexagonal crystal. Nonetheless, the average length of the bonds in the purely cubic network approaches that in the hexagonal crystal very closely. Thus a large increase in the purely cubic ice across the ins
机译:在由单妥泡(MW)水势建模的过冷四面液体的稳定性极限下,最近据表明,弛豫发生在每粒子势能(PHI(中间))的独特价值上,这对应于动态(非静止)Gibbs自由能功能G(t,p,n,phi):[部分衍生物(2)(g / n)/部分衍生物phi(2)= 0]和[部分导数(g / n)/部分衍生PHI不等于0]。在这项工作中,我们探讨了负责通过MW液体的松弛机制形成非晶态的固有结构。我们首先使用基于内部二面角的标准来识别6个成员船和椅子形环。然后,我们考虑立方体金刚石(10个原子簇用4个椅子形圆环)和六边形湿度(12原子簇,3艘船和2个椅子形圆圈)通过共用椅环。我们发现局部结晶(四面体)序列由横向连接的张力钛单元的果实键合颗粒呈现,其与金刚石单元(DWD堆叠)从两侧堆叠。获得越来越多的范围晶体阶,因为堆叠的紫立岩层的数量增加:由堆叠(横向连接)的粒子共享DWWD中的颗粒显示较长的晶级。通过DWWWD堆叠的中间(横向连接)张全层的eMlipsed键颗粒展示了均匀的晶莹阶。我们发现立方 - 六边形堆叠主要以稳定性极限的DWD层的形式发生。纯度立方(金刚石)网络颗粒的局部四面体顺序(不与紫立岩单位共用)显着地从六边形晶体的偏差。尽管如此,纯度立方体网络中的键的平均长度非常接近六边形晶体。因此,对纯粹立方冰的大幅增加

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