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八面沸石和ZSM-5沸石中的催化活性与吸附作用:差异稳定化和电荷离域的作用

The catalytic activity and adsorption in faujasite and ZSM-5 zeolites: the role of differential stabilization and charge delocalization.

作者信息

Nakamura Taiji, Fedorov Dmitri G

机构信息

Research Center for Computational Design of Advanced Functional Materials (CD-FMat), National Institute of Advanced Industrial Science and Technology (AIST), Central 2, Umezono 1-1-1, Tsukuba, 305-8568, Japan.

出版信息

Phys Chem Chem Phys. 2022 Mar 30;24(13):7739-7747. doi: 10.1039/d1cp05851g.

Abstract

Adsorption and chemical reactions occurring on industrially important ZSM-5 and faujasite zeolite catalysts are investigated with the quantum-mechanical fragment molecular orbital method combined with periodic boundary conditions. Suitable fragmentation patterns are devised and tested providing important case studies of computing real materials with fragmentation methods. A good accuracy is demonstrated in comparison to full calculations, and a good agreement with the available experimental data is obtained. The full production cycle of -xylene on faujasite zeolite is mapped. The catalytic role of the zeolite in the dehydration reaction, analyzed with the partition analysis, is attributed to the delocalization of the negative charge over the zeolite. On the other hand, an increase of the barrier in the Diels-Alder reaction by the zeolite is attributed to the preferential stabilization of the reactants over the transition state as demonstrated by the guest-zeolite interaction energy.

摘要

采用结合周期性边界条件的量子力学片段分子轨道方法,研究了工业上重要的ZSM - 5和八面沸石催化剂上发生的吸附和化学反应。设计并测试了合适的碎片化模式,提供了用碎片化方法计算真实材料的重要案例研究。与全计算相比,展示了良好的精度,并与现有实验数据取得了良好的一致性。绘制了八面沸石上对二甲苯的完整生产循环。用分配分析方法分析了沸石在脱水反应中的催化作用,其归因于负电荷在沸石上的离域。另一方面,如客体 - 沸石相互作用能所示,沸石使狄尔斯 - 阿尔德反应的势垒增加,这归因于反应物相对于过渡态的优先稳定化。

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