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arXiv 2603.15519cond-mat.stat-mechcond-mat.dis-nncond-mat.soft
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二维无晶格粒子模型中的玻璃与阻塞转变

Glass and jamming transitions in a random organization model

Università di Trieste(的里雅斯特大学);ESPCI Paris, PSL Research University(巴黎物理化工国立高等学院,巴黎文理研究大学)

Leonardo Galliano, Ludovic Berthier

AI总结:

研究二维无晶格粒子模型,探讨其在驱动非布朗运动悬浮液中的吸收相变。通过数值分析(ϕ,ε)相图,发现大ϕ时存在非平衡玻璃转变,影响临界吸收转变位置,且阻塞转变不唯一定义随机密实度。

摘要:

我们研究了一个二维无晶格粒子模型,用于描述驱动非布朗悬浮液中的吸收相变。我们数值研究了(ϕ,ε)相图,其中ϕ是填充分数,ε控制粒子跳跃幅度。我们使用二元混合物抑制结晶,从而分离模型在非晶态之间的不同相变。在大ϕ时,发现吸收转变前存在非平衡玻璃转变至非扩散非晶态。这种动态停滞使临界吸收转变的位置依赖于协议。ε→0终点定义了阻塞转变,其位置连续依赖于准备协议,不能作为随机密实度的唯一定义。接近阻塞时,我们观察到复杂景观和边缘稳定性,类似于热玻璃中的Gardner相。临界指数与基于能量最小化的其他方法和平均场复制理论的解析预测一致。我们分析了流体和玻璃相中的超均匀性,发现其具有质不同特征,并表明随机组织动力学不影响阻塞packing中观察到的超均匀性,后者被发现是非通用的。我们的结果表明,随机组织模型与热软粒子系统经历玻璃和阻塞转变有深刻的物理相似性,微观动力学的非平衡性质对涌现的物理性质影响较小。

英文摘要:

We study a two-dimensional, off-lattice particle model introduced to describe absorbing phase transitions in driven non-Brownian suspensions. We numerically explore the $(ϕ,ε)$ phase diagram, where $ϕ$ is the packing fraction and $ε$ controls the amplitude of particle jumps. We use a binary mixture to suppress crystallization, which allows us to disentangle the model's distinct phase transitions between amorphous states. At large $ϕ$, we find that the approach to the absorbing transition is preceded by a non-equilibrium glass transition to a non-diffusive amorphous state. This dynamic arrest makes the location of the critical absorbing transition protocol-dependent. The $ε\to 0$ end-point of the transition line defines a jamming transition whose location is shown to vary continuously with the preparation protocol, and cannot serve as a unique definition of random close packing. Near jamming, we observe a complex landscape and marginal stability, reminiscent of Gardner phases found in thermal glasses. The critical exponents characterizing packings at the jamming transition numerically agree with alternative approaches based on energy minimization, and with analytic predictions from mean-field replica theory. We analyze hyperuniformity of large-scale density fluctuations in fluid and glass phases, where it emerges with qualitatively distinct signatures, and show that random organization dynamics does not determine the hyperuniformity observed in jammed packings, which is found to be non-universal. Our results show that random organization models share deep physical similarities with thermal soft-particle systems undergoing glass and jamming transitions, with little impact of the non-equilibrium nature of the microscopic dynamics on emerging physical properties.

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