化学
沸石
组态熵
多孔性
焓
熵(时间箭头)
构象熵
纳米技术
化学物理
熵产生
热力学
化学工程
晶体结构
聚合物
分子筛
作者
Mingyu Zhao,Qinming Wu,Xiao Chen,Hao Xiong,Guo Tian,Li‐Tang Yan,Feng‐Shou Xiao,Fei Wei
摘要
Entropy, stemming from the second law of thermodynamics, drives the system toward greater disorder. In zeolite design, introducing controlled disorder enhances mass transfer, yet most strategies focus on regulating structure from the perspective of energy, with few efforts devoted to entropy effect control. Here, we propose an entropy strategy by enhancing the translational and rotational confinement of large organic structure-directing agents (OSDAs), leading to an order of magnitude larger change in free energy (1.8 kJ/mol SiO2) than the enthalpy effect. This in turn promotes compensation in the configurational entropy of zeolite structures, leading to the formation of highly disordered intergrown zeolites (e.g., ITH/ITR, MFI/MEL, etc.). Our entropy strategy paves a novel perspective for the intergrowth of zeolites, holding significant guidance for the microscopic mechanisms underlying the formation of zeolite skeletons, including highly disordered porous materials.
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