论文标题
玻璃理论：耦合电子对的地面和激发态
Glass theory: ground and excited states of coupled electron pairs
论文作者
论文摘要
由于发现严格的二阶 - 矢量（磁矩）（SODV）GENNES n = 0理论，理论界一直在寻找可以从复杂玻璃状态演变为生物分子系统的SODV。在纠缠聚合物融化的异常粘度的理论研究中，我们意外地发现了SODV。它是一种同步的抗对称耦合电子对（CEP）激发态，它在两个稍微重叠的相邻硬球分子（HSM）之间产生动态界面。这两个HSM突然以相反的方向获得了相同的新自旋，因此在玻璃模型中发现了DE Gennes预测的二维软基质。与电子激发态不同，CEP激发态的能量比电子激发态的能量小三个数量级，并且它们以纳米级动力学模型的形式出现。这种新的数学物理制度几乎可以直接解释所有玻璃和玻璃过渡现象。在本文中，给出了两个具有N = 0的范例，并讨论了其广泛的应用前景。
Since the discovery of the strict second-order-delta-vector (magnetic moment) (SODV) theory of Gennes n = 0, the theoretical community has been searching for SODVs that can evolve from complex glass states to biomolecular systems. In the theoretical study of the abnormal viscosity of entangled polymer melts, we unexpectedly found an SODV. It is a synchronous-antisymmetric coupled electron pair (CEP) excited state that creates a dynamic interface between two slightly overlapping adjacent hard-sphere molecules (HSMs). The two HSMs suddenly acquired the identical new spin in opposite directions, so the two-dimensional soft matrix predicted by de Gennes was found in the glass model. Unlike electronic excited states, the energy of CEP excited states is three orders of magnitude smaller than that of electronic excited states, and they appear in the form of a nano-scale dynamic Ising models. This new mathematical physics regime can directly explain almost all glass and glass transition phenomena. In this paper, two paradigms with n = 0 are given, and discussed its wide application prospects.
