Diffusion in a binary mixture of molecules adsorbed on a multisite two-dimensional lattice

被引:2
作者
Tarasenko, Alexander [1 ]
机构
[1] AS CR, Inst Phys, Na Slovance 1999-2, Prague 18221, Czech Republic
关键词
Multicomponent diffusion; Lattice gas systems; Fick?s law; Onsager phenomenological coefficients; SELF-DIFFUSION; IRREVERSIBLE-PROCESSES; RECIPROCAL RELATIONS; MONTE-CARLO; MEAN-FIELD; DIFFUSIVITIES; SIMULATION; DYNAMICS; DEPENDENCE; TRANSPORT;
D O I
10.1016/j.seppur.2022.121984
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The diffusion in a binary mixture of species coadsorbed on a multisite square lattice is investigated by a theoretical approach (Chumak and Tarasenko, 1980) based on the non-equilibrium statistical operator method proposed by Zubarev (1961). The investigated lattice gas system is rather complex. There is a mixture of two types of particles (atoms, and/or molecules) adsorbed on a multisite lattice which consists of the three types of adsorption sites. This lattice can be subdivided onto three homogeneous square sublattices composed of the sites of the same type. As the binding energies for the molecules of distinct types adsorbed on the nonidentical sublattices are different, there are six average occupancies (coverages) describing the molecule distribution over the sublattices. A system of the balance equations, which controls the exchange of the molecules between the sublattices on the atomistic level is reduced to the diffusion equations describing the evolution of small hydrodynamic fluctuations of these coverages on the macroscopic level. The diffusion equations are written in the Onsager representation, when the driving forces are gradients of the chemical potentials and in the Fickian representation, when the driving forces are the gradients of coverages. The derivation of these equations results in the analytical expressions for the Fickian diffusivities and Onsager phenomenological coefficients. Despite the complex process of derivation, the final results are simple. The kinetic coefficients, which describe the non-equilibrium state of the molecule system, are expressed via the thermodynamic quantities calculated in the equilibrium state of the system: the chemical potentials (or activities), pair correlation functions and the isothermal susceptibilities. These expressions are derived with account of the lateral interactions between the nearest neighbor molecules. The matrix of the Fickian diffusivities has the ordinary classical form. The diffusivity is a non-symmetric 2 x 2 matrix. The Onsager coefficients are represented by a diagonal 2 x 2 matrix, where the cross terms are absent.
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页数:10
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共 28 条
[1]   Theory and simulation of jump dynamics, diffusion and phase equilibrium in nanopores [J].
Auerbach, SM .
INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 2000, 19 (02) :155-198
[2]   SIMULATION OF TRANSPORT AND SELF-DIFFUSION IN ZEOLITES WITH THE MONTE-CARLO METHOD [J].
AUST, E ;
DAHLKE, K ;
EMIG, G .
JOURNAL OF CATALYSIS, 1989, 115 (01) :86-97
[3]   Diffusion and separation of CO2 and CH4 in silicalite, C168 schwarzite,and IRMOF-1:: A comparative study from molecular dynamics simulation [J].
Babarao, Ravichandar ;
Jiang, Jianwen .
LANGMUIR, 2008, 24 (10) :5474-5484
[4]   Dependence of the self-diffusion coefficient on the sorbate concentration: A two-dimensional lattice gas model with and without confinement [J].
Bhide, SY ;
Yashonath, S .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (04) :1658-1667
[5]   Applications of molecular modeling in heterogeneous catalysis research [J].
Broadbelt, LJ ;
Snurr, RQ .
APPLIED CATALYSIS A-GENERAL, 2000, 200 (1-2) :23-46
[6]   DIFFUSION AND DENSITY-FLUCTUATIONS OF ATOMS ADSORBED ON SOLID-SURFACES [J].
CHUMAK, AA ;
TARASENKO, AA .
SURFACE SCIENCE, 1980, 91 (2-3) :694-706
[7]   Dynamic Monte-Carlo and mean-field study of the effect of strong adsorption sites on self-diffusion in zeolites [J].
Coppens, MO ;
Bell, AT ;
Chakraborty, AK .
CHEMICAL ENGINEERING SCIENCE, 1999, 54 (15-16) :3455-3463
[8]   Some applications of the transition state method to the calculation of reaction velocities, especially in solution. [J].
Evans, MG ;
Polanyi, M .
TRANSACTIONS OF THE FARADAY SOCIETY, 1935, 31 (01) :0875-0893
[9]   The activated complex in chemical reactions [J].
Eyring, H .
JOURNAL OF CHEMICAL PHYSICS, 1935, 3 (02) :107-115
[10]   Real-Time Ab Initio KMC Simulation of the Self-Assembly and Sintering of Bimetallic Epitaxial Nanoclusters: Au + Ag on Ag(100) [J].
Han, Yong ;
Liu, Da-Jiang ;
Evans, James W. .
NANO LETTERS, 2014, 14 (08) :4646-4652