Some rigorous relations for partial conductivities in ionic liquids

Starting with the rigorous expressions, derived previously for the generalized transport coefficients of a multicomponent fluid, we obtained several exact relations for partial conductivities of ionic charge-asymmetric mixtures. For a simpler case of a charge-symmetric binary mixture such kind of re...

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Автори: Mryglod, I., Kuporov, V.
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Опубліковано: Інститут фізики конденсованих систем НАН України 2010
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Цитувати:Some rigorous relations for partial conductivities in ionic liquids / I. Mryglod, V. Kuporov // Condensed Matter Physics. — 2010. — Т. 13, № 4. — С. 43602:1-8. — Бібліогр.: 10 назв. — англ.

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author Mryglod, I.
Kuporov, V.
author_facet Mryglod, I.
Kuporov, V.
citation_txt Some rigorous relations for partial conductivities in ionic liquids / I. Mryglod, V. Kuporov // Condensed Matter Physics. — 2010. — Т. 13, № 4. — С. 43602:1-8. — Бібліогр.: 10 назв. — англ.
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container_title Condensed Matter Physics
description Starting with the rigorous expressions, derived previously for the generalized transport coefficients of a multicomponent fluid, we obtained several exact relations for partial conductivities of ionic charge-asymmetric mixtures. For a simpler case of a charge-symmetric binary mixture such kind of relations was discovered experimentally by Sundheim more than 50 years ago and is known as the “universal golden rule”. Some more complicate models, describing in particular the cases of ternary and multi-component mixtures, are considered. The general relation for partial ionic conductivities is derived for a multi-component ionic fluid. It is shown that such relations can be considered in fact as an example of a more general class of rigorous expressions valid for (k, ω)-dependent quantities.
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fulltext Condensed Matter Physics 2010, Vol. 13, No 4, 43602: 1–8 http://www.icmp.lviv.ua/journal Some rigorous relations for partial conductivities in ionic liquids I. Mryglod1,2, V. Kuporov1 1 Institute for Condensed Matter Physics of the National Academy of Sciences of Ukraine, 1 Svientsitskii Str., 79011 Lviv, Ukraine 2 Institute of Applied Mathematics and Fundamental Sciences of Lviv Polytechnic National University, 79013 Lviv, Ukraine Received November 15, 2010 Starting with the rigorous expressions, derived previously for the generalized transport coefficients of a multi- component fluid, we obtained several exact relations for partial conductivities of ionic charge-asymmetric mixtures. For a simpler case of a charge-symmetric binary mixture such kind of relations was discovered experimentally by Sundheim more than 50 years ago and is known as the “universal golden rule”. Some more complicate models, describing in particular the cases of ternary and multi-component mixtures, are considered. The general relation for partial ionic conductivities is derived for a multi-component ionic fluid. It is shown that such relations can be considered in fact as an example of a more general class of rigorous expressions valid for (k, ω)-dependent quantities. Key words: Ionic liquids, transport coefficients, mutual diffusion coefficient, ionic conductivity, molten salt PACS: 66.10.cg, 66.10.Ed, 82.45.Gj, 47.10.-g Introduction About 50 years ago a phenomenological “universal golden rule” for the ratio of partial conduc- tivities of ions in molten salts was proposed by Sundheim [1] from the analysis of experimental data. This rule is expressed in a very simple form σ+ σ− = m− m+ . (1) Recently, there were made several theoretical attempts [2] to derive this relation using the equations of motion, the Langevin equation as well as molecular dynamics studies for the model of binary charge symmetrical molten salts. A few years later using similar approaches such relation was also obtained for pseudo-binary molten salt KCl–NaCl [3]. Our goal is to consider this problem in a more general framework. We start with the rigorous relations derived by us previously for generalized transport coefficients of a multi-component fluid [4, 5]. We obtain the “universal golden rule” for (k, ω)-dependent partial conductivities of an ionic charge-asymmetric binary mixture as well as the relations for the partial ionic conductivities in some cases of ternary and four-component ionic liquids. 1. Theoretical framework Let us start with some introductory remarks and consider the general framework that can be used for the description of both kinds of multi-component mixtures, in particular mixtures of neutral particles as well as mixtures containing charged particles. In general case we deal with a ν-component fluid in the volume V , containing Nα particles in the αth species (α = 1, 2, . . . , ν). To derive hydrodynamic equations one has to define the microscopic basic set of the slowest (hy- drodynamic) variables [5], which for a multi-component mixture may be introduced as follows c© I. Mryglod, V. Kuporov 43602-1 http://www.icmp.lviv.ua/journal I. Mryglod, V. Kuporov P̂ hyd k = {N̂k, Ĵk, Êk}, where N̂k = {N̂k,α} is a column-vector with the components N̂k,α = Nα ∑ i=1 exp{ikRα i }, (2) being the number density of particles in the α-th species; Ĵk is the density of the total current, Ĵk = ∑ α Ĵk,α , Ĵk,α = Nα ∑ i=1 pα i exp{ikRα i }, (3) with Ĵk,α being the current densities of particles in the α-th species, and Êk = ∑ α Êk,α = ∑ α Nα ∑ i=1 eαi exp{ikRα i } (4) is the total energy density, where the one-particle energy eαj can be expressed via the sum of kinetic energy and potential energy of pair interactions: eαj = [pα j ] 2 2mα + ∑ l 6=j,β V βα jl . The set of dynamic variables P̂ hyd k = {N̂k, Ĵk, Êk} includes the densities of all the additive integrals of motion for a mixture. In the case of longitudinal dynamics, as it follows from the sym- metrical properties, the scalar densities n̂k,α and Êk interact only with the longitudinal component of Ĵk, namely ĴL k , that is the projection of Ĵk onto the direction of wave-vector k. Hence, the total number of longitudinal hydrodynamic variables for ν-component mixture is equal to ν+2, namely P̂L k = {P̂ ι k } with ι = 1, 2, . . . , ν + 2. In practical applications it may be more convenient [4, 5] to use the set of orthogonalized dynamic variables possessing the following properties (P̂ ι k , P̂ κ −k ) = δικ (P̂ ι k , P̂ κ −k ). Such an orthog- onalized set of longitudinal hydrodynamical variables can be defined as follows P̂L k = {N̂k, Ĵ L k , Ĥk} (5) where Ĥk = Êk − (Êk, N̂ + k )(N̂k, N̂ + k )−1N̂k = (1− PN )Êk is the so-called enthalpy density, the Mori-like projection operator denotes as PN . . . = (. . . ,N+ k )(N̂k, N̂ + k )−1N̂ = ∑ αγ (. . . , N̂−k,α) (N̂k, N̂ + k )−1 αγ N̂k,γ , (6) and the notation (. . . , . . .) is used for the definition of an equilibrium correlation function (A,B) = 〈(A− 〈A〉)(B − 〈B〉)〉 with 〈. . .〉 denoting the equilibrium averaging. The generalized hydrodynamic fluxes Id k,ι can be defined in the standard way: ikId k,ι = (1− PH)iLN P̂ ι k , (7) where PH is the Mori-like projection operator, constructed on the set of all hydrodynamic variables (5), and iLN is the Liouville operator. Thus, for the number density flux one can easily obtain ikIdk,α = ik mα ( ĴL k,α − mαcα m̄ ĴL k ) , (8) 43602-2 Some rigorous relations for partial conductivities in ionic liquids where mα is the particle mass in the α-th species, cα = Nα/N = nα/n denotes concentrations, and m̄ = ∑ α cαmα is the mean mass per particle. The generalized (k, z)-dependent transport coefficients are defined via the generalized fluxes Id k,ι as follows [4, 5] Lικ(k, z) = β V ∞ ∫ 0 dt exp{−zt} ( Idk,ι, exp{−(1− PH)iLN t}Id−k,κ ) . (9) Note that the expression (9) has the structure of the well-known Green-Kubo formulas [6], but the evolution operator is more complicated and additionally involves the projection operator PH. However, in the hydrodynamic limit (k, z) → 0 one gets the expression Lικ = lim k,z→0 Lικ(k, z) = β V ∞ ∫ 0 dt ( Idι , exp{−iLNt}Idκ ) , (10) that is commonplace in numerous textbooks (e.g. [7]) and has been routinely employed in computer simulations. In the context of this paper we are mainly interested in the behavior of the generalized mutual diffusion coefficients Dαγ(k, z) that are simply related to the corresponding transport coefficients Lαγ(k, z). Namely, one has Lαγ(k, z) = ncαcγDαγ(k, z)/kBT, (11) where n = N/V . The explicit frequency dependence in (9) can be found by taking into account that z = iω + ε and ε → +0. In general for a ν-component mixture the matrix of mutual diffusion coefficients D(k, ω) = ‖Dαγ(k, ω)‖ has ν × ν elements. Due to the symmetry properties Dαγ(k, ω) = Dγα(k, ω) this number is reduced to the ν(ν + 1)/2 independent elements. However, there are still additional ν explicit relations that follow from the total momentum conversation law. Namely, taking into account that ν ∑ α=1 mαI d k,α = ν ∑ α=1 ( ĴL k,α − mαcα m̄ ĴL k ) ≡ 0 (12) and using the definition (9), the set of new useful relations for generalized transport coefficients, that involve the processes caused by number densities fluctuations, can be easily derived. In particular, one gets ν ∑ α=1 mαcαDαγ(k, ω) = ν ∑ γ=1 Dαγ(k, ω)cγmγ ≡ 0. (13) Hence, taking into account the relations (13) one can conclude that the total number of independent matrix elements in the matrix D(k, ω) = ‖Dαγ(k, ω)‖ is equal to ν(ν − 1)/2. In a particular case of binary mixture (ν = 2) we have ν(ν − 1)/2 = 1 and D11(k, ω) D12(k, ω) = − m2 m1 c2 c1 , D11(k, ω) D22(k, ω) = m2 2 m2 1 c22 c21 . (14) These relations directly follow from the identity (13). Being valid for an arbitrary binary mixture, they are of rather general character. 2. Binary mixture of charged particles Let us now consider the case of a binary mixture composed of oppositely charged particles with charges q+ and q−, massesm+ and m−, and densities n+, n−. The total electroneutrality condition is satisfied, so that q+n+ + q−n− = 0. 43602-3 I. Mryglod, V. Kuporov The electrical conductivity can be calculated by means of the Green-Kubo formula [8, 9] σ = β V ∞ ∫ 0 dt〈Iq(t)Iq(0)〉, (15) where Iq(t) = ∑ α Iqα(t) with Iqα(t) = qαnα Nα ∑ i=1 vα i being the partial ionic electrical current (α = +,−). Ionic conductivity is also connected with the mutual diffusion coefficients [9]: σ = n kBT ∑ α,β qαqβcαcβDαβ , (16) where mutual diffusion coefficients are defined as follows Dαβ = N NαNβ Nα,Nβ ∑ i,j=1 ∞ ∫ 0 dt 〈 vα i (t)v β j (0) 〉 with α, β = +,−. In the center of mass reference frame the expression (16) can be easily derived from (15) with the help of equations (8), (9) and (11). For generalized (k, ω)-dependent ionic conductivity one can use the definition σ(k, ω) = n kBT ∑ α,β qαqβcαcβDαβ(k, ω). (17) It is seen from (17) that the total ionic conductivity can be presented as the sum of partial ionic conductivity σ = σ+ + σ−, where σα ∼ qαcα ∑ β qβcβDαβ , so that for the ratio of partial ionic conductivity one gets σ+ σ− = q2+c 2 +D++ + q+c+q−c−D+− q2−c 2 −D−− + q+c+q−c−D+− . (18) This expression can be significantly simplified if we use the relations that follow from (14), namely: D++/D−− = (m2 −/m 2 +)(c 2 −/c 2 +), D++/D+− = −(m−/m+)(c−/c+), D−−/D−+ = −(m+/m−)(c+/c−), D+− = D−+. Taking into account the electroneutrality condition q+c+ + q−c− = 0, one gets σ+(k, ω) σ−(k, ω) = − q+ q− m− m+ . (19) In the case of charge-symmetric systems with q− = −q+ (in particular, for molten salts NaCl, KCl, NaF, KF, RbBr) we obtain σ+(k, ω) σ−(k, ω) = m− m+ . (20) In fact, the expression (20) represents the generalized version of the so-called “universal golden rule” (1) valid for binary charge-symmetric ionic liquids with arbitrary values (k, ω). In a more general form (19) such a relation is derived for a charge-asymmetric binary mixture by means of the rigorous expressions (13) obtained for the generalized mutual diffusion coefficients of a multi- component fluid. 43602-4 Some rigorous relations for partial conductivities in ionic liquids 3. Ternary mixtures 3.1. Charged particles in solvent Let us consider a more complicated model of a ternary mixture that is composed of oppositely charged particles in neutral solvent with the particle charges q+ and q−, the particle masses m+, m−, and m0, and concentrations c+, c−, c0 (c++c−+c0 = 1). The total electro-neutrality condition can be written in the form: q+c+ + q−c− = 0. From the relations (13) one obtains the equations m+c+D++(k, ω) +m−c−D−+(k, ω) +m0c0D0+(k, ω) ≡ 0, m+c+D+−(k, ω) +m−c−D−−(k, ω) +m0c0D0−(k, ω) ≡ 0, m+c+D+0(k, ω) +m−c−D−0(k, ω) +m0c0D00(k, ω) ≡ 0, (21) where Dαβ = Dβα. The electroneutrality condition enables us to express the concentrations of charged particles via c0, namely: c+ = (1 − c0)q−/(q− − q+), c− = (1 − c0)q+/(q+ − q−). It is obvious that q2+c 2 + = q2−c 2 − = (1 − c0) 2 q2+q 2 − (q+ − q−)2 ≡ Q2, q+c+q−c− = −(1− c0) 2 q2+q 2 − (q+ − q−)2 ≡ −Q2. Therefore, one gets σ+ = Q2(D++−D+−) and σ− = Q2(D−−−D+−), so that the expression (18) for the ratio of partial ionic conductivities can be rewritten in the form σ+(k, ω) σ−(k, ω) = D++(k, ω)−D+−(k, ω) D−−(k, ω)−D+−(k, ω) . (22) Combining the first two equations in (21), one can obtain: m+c+(D++ −D+−)−m−c−(D−− −D+−) +m0c0(D0+ −D0−) ≡ 0 (23) or m+c+σ+ −m−c−σ− +m0c0∆ = 0, (24) where the quantity ∆ ≡ Q2(D0+ −D0−) is expressed in terms of the mutual diffusion coefficients for ions in solvent. The relation (24) could be considered as the generalization of “universal golden rule” for solutions of electrolytes. Note that in the limit c0 → 0 the expression (22) can be easily recovered from (22). 3.2. Pseudo-binary molten salts A special class of ternary ionic liquids is formed by the so-called pseudo-binary molten salts, for instance KCl−NaCl. In this case we deal with a ternary mixture of ions. In particular, for KCl−NaCl in the system with the elementary charge e = 1 the ionic charges are qNa = qK = 1 and qCl = −1 with the electro-neutrality condition cNa + cK = cCl, where cNa + cK + cCl = 1. For the mutual diffusion coefficients from (13) one has: m1c1D11(k, ω) +m2c2D21(k, ω) +m3c3D31(k, ω) ≡ 0, m1c1D12(k, ω) +m2c2D22(k, ω) +m3c3D32(k, ω) ≡ 0, m1c1D13(k, ω) +m2c2D23(k, ω) +m3c3D33(k, ω) ≡ 0, (25) where {K,Na,Cl} ↔ {1, 2, 3}. Using the definition for partial ionic conductivities σα(k, ω), σα(k, ω) = qαcα ∑ β qβcβDαβ(k, ω), (26) 43602-5 I. Mryglod, V. Kuporov we obtain the expressions: σK(k, ω) ≡ σ1(k, ω) = c1 [c1D11(k, ω) + c2D12(k, ω)− c3D13(k, ω)], σNa(k, ω) ≡ σ2(k, ω) = c2 [c1D21(k, ω) + c2D22(k, ω)− c3D23(k, ω)], σCl(k, ω) ≡ σ3(k, ω) = −c3 [c1D31(k, ω) + c2D32(k, ω)− c3D33(k, ω)]. (27) If we multiply each equation in (27) by m1, m2 and (-m3), respectively, add them and use the identities (25), it is easy to obtain the following relation m1σ1(k, ω) +m2σ2(k, ω) = m3σ3(k, ω), (28) or mKσK(k, ω) +mNaσNa(k, ω) = mClσCl(k, ω). (29) In the hydrodynamic limit when (k, ω) → 0 this result was obtained in [3] by means of the Langevin equation and confirmed directly by molecular dynamics simulations. We note that relation (29)is valid for arbitrary (k, ω). Using (28) one can write mAσA(k, ω) +mBσB(k, ω) = mIσI(k, ω), (30) for a pseudo-binary electrolyte AI− BI with ion charges qA = qB = −qI. 4. Multi-component mixture of charged particles Let us now consider the model of a multi-component fluid composed of Nα ions with charges qα in the αth species (α = 1, 2, . . . , ν). Mutual diffusion coefficients Dαβ(k, ω) of the system should satisfy the relations (13). For partial ionic conductivities one has the definition (26), so that if we multiply σα(k, ω) by mα/qα one can write ∑ α mα qα σα(k, ω) = ∑ α mαcα   ∑ β qβcβDαβ(k, ω)   = ∑ β qβcβ [ ∑ α mαcαDαβ(k, ω) ] . (31) Taking into account (13) we finally obtain ∑ α mα qα σα(k, ω) ≡ 0. (32) This is a rather general result that includes, as a particular case, the relation (30), derived above. For example, using (32) it is easy to obtain the relation for partial ionic conductivities for pseudo- binary four-component mixture AnIl − BkYj with different charges of ions. A more complicated case corresponds to the model of a (ν+ν̄)-component fluid that is composed of Nα ions with charges qα (α = 1, 2, . . . , ν) and Nᾱ neutral particles belonging to the ᾱth species (ᾱ = 1, 2, . . . , ν̄). In this case the equation (31) should be rewritten in the form ν ∑ α=1 mα qα σα(k, ω) = ν ∑ β=1 qβcβ [ ν ∑ α=1 mαcαDαβ(k, ω) ] = − ν ∑ β=1 qβcβ [ ν̄ ∑ ᾱ=1 mᾱcᾱDᾱβ(k, ω) ] , (33) where the relations (13) have been used. Note that the index ᾱ denotes the neutral particles. Therefore, on the right hand side of (33) the effects of mutual diffusion of all the ions in solvent are included. It is obvious that in particular case of a ternary mixture of charged particles in neutral solvent, the expression (24) can be easily recovered from (33). 43602-6 Some rigorous relations for partial conductivities in ionic liquids The expression (33) can be further simplified if we introduce two new densities, namely the mass density of solvent M̂k (formed by neutral particles only) and the charge density Q̂k: M̂k = ν̄ ∑ ᾱ=1 mᾱcᾱN̂k,ᾱ , Q̂k = ν ∑ α=1 qαcαN̂k,α . (34) Now we can rewrite (34) in the form ν ∑ α=1 mα qα σα(k, ω) = −DMQ(k, ω), (35) where the generalized transport coefficient DMQ(k, ω) = ν̄ ∑ ᾱ=1 ν ∑ β=1 mᾱcᾱ Dᾱβ(k, ω) qβcβ describes the diffusive ion-solvent cross-correlations. The relation (35) yields, in fact, the most general form of identity valid for partial ionic conductivities of classical systems of charged particles at arbitrary (k, ω). 5. Conclusions It is shown that the general relations, that link partial ionic conductivities in a binary mixture of charged particles, three- and four-component pseudo-binary molten salts as well as in multi- component classical fluids of charged particles, can be derived by means of rigorous expressions, obtained previously for the mutual diffusion coefficients of multi-component liquids. Some of these relations generalize the results known in the literature (see, for instance, [2]), but most of them are new. Moreover, all of these relations are valid for (k, ω)-dependent quantities and this, in particular, explains the results of molecular dynamic simulations of the frequency-dependent partial conductivities carried out [10] for molten NaCl and NaI. References 1. Sundheim B.R., J. Phys. Chem., 1956, 60, 1381. 2. Koishi T., Kawase S., Tamaki S., J. Chem. Phys., 2002, 116, 3018; Koishi T., Tamaki S., J. Chem. Phys., 2004, 121, 333. 3. Matsunaga S., Koishi T., Tamaki S., Proc. of the AIP Conference, 2008, 982, 399. 4. Mryglod I., Condens. Matter Phys., 1997, 10, 115. 5. Mryglod I., Bryk T., Kuporov V., Collective dynamics in ionic liquids: A comparative study with non- Coulombic fluids. – In: NATO Science Series II, Eds. D. Henderson, M. Holovko, A. Trokhymchuk, Vol. 206, 2005, p. 109. 6. Kubo R.J., Phys. Soc. Jpn., 1957, 12, 570. 7. Zubarev D.N., Morozov V.G., Röpke G., Statistical mechanics of nonequilibrium processes, Vol. 2: Relazation and hydrodynamic processes. Akademie Verlag, Berlin, 1997. 8. Hansen J.P., McDonald I.R., Phys. Rev. A, 1975, 11, 2111. 9. Trullas J., Padro J.A., J. Chem. Phys., 1993, 99(5), 3983. 10. Koishi T., Tamaki S., J. Phys. Soc. Jpn., 1999, 68, 964. 43602-7 I. Mryglod, V. Kuporov Деякi строгi спiввiдношення для парцiальних провiдностей в iонних рiдинах I. Мриглод1,2, В. Купоров2 1 Iнститут фiзики конденсованих систем НАН України, 79011 Львiв, вул. Свєнцiцького, 1 2 Iнститут прикладної математики i фундаментальних наук Нацiонального унiверситету “Львiвська полiтехнiка”, 79013 Львiв, Україна Стартуючи з точних спiввiдношень, що були виведенi нами нещодавно для узагальнених коефiцiєнтiв переносу в багатокомпонентних плинах, ми отримали кiлька строгих спiввiдношень для парцiальних провiдностей в iонних зарядово-асиметричних сумiшах. Для найпростiшого випадку зарядово- симетричної бiнарної системи таке спiввiдношення було виявлене експериментально Сундхеймом бiльш нiж 50 рокiв тому i вiдоме як “унiверсальне золоте правило”. Розглянуто також деякi бiльш складнi моделi, що описують, зокрема, випадки потрiйних та багатокомпонентних сумiшей. Виведено загальне спiввiдношення для парцiальних iонних провiдностей багатокомпонентного iонного плину. Показано, що такого типу спiввiдношення є фактично лише одним з прикладiв бiльш широкого класу виразiв, що дiйснi для (k, ω)-залежних величин. Ключовi слова: iоннi рiдини, коефiцiєнти переносу, коефiцiєнти взаємної дифузiї, iонна провiднiсть, розплави солей 43602-8 Theoretical framework Binary mixture of charged particles Ternary mixtures Charged particles in solvent Pseudo-binary molten salts Multi-component mixture of charged particles Conclusions
id nasplib_isofts_kiev_ua-123456789-32129
institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
issn 1607-324X
language English
last_indexed 2025-12-07T17:15:02Z
publishDate 2010
publisher Інститут фізики конденсованих систем НАН України
record_format dspace
spelling Mryglod, I.
Kuporov, V.
2012-04-09T21:22:06Z
2012-04-09T21:22:06Z
2010
Some rigorous relations for partial conductivities in ionic liquids / I. Mryglod, V. Kuporov // Condensed Matter Physics. — 2010. — Т. 13, № 4. — С. 43602:1-8. — Бібліогр.: 10 назв. — англ.
1607-324X
PACS: 66.10.cg, 66.10.Ed, 82.45.Gj, 47.10.-g
https://nasplib.isofts.kiev.ua/handle/123456789/32129
Starting with the rigorous expressions, derived previously for the generalized transport coefficients of a multicomponent fluid, we obtained several exact relations for partial conductivities of ionic charge-asymmetric mixtures. For a simpler case of a charge-symmetric binary mixture such kind of relations was discovered experimentally by Sundheim more than 50 years ago and is known as the “universal golden rule”. Some more complicate models, describing in particular the cases of ternary and multi-component mixtures, are considered. The general relation for partial ionic conductivities is derived for a multi-component ionic fluid. It is shown that such relations can be considered in fact as an example of a more general class of rigorous expressions valid for (k, ω)-dependent quantities.
en
Інститут фізики конденсованих систем НАН України
Condensed Matter Physics
Some rigorous relations for partial conductivities in ionic liquids
Деякі строгі співвідношення для парціальних провідностей в іонних рідинах
Article
published earlier
spellingShingle Some rigorous relations for partial conductivities in ionic liquids
Mryglod, I.
Kuporov, V.
title Some rigorous relations for partial conductivities in ionic liquids
title_alt Деякі строгі співвідношення для парціальних провідностей в іонних рідинах
title_full Some rigorous relations for partial conductivities in ionic liquids
title_fullStr Some rigorous relations for partial conductivities in ionic liquids
title_full_unstemmed Some rigorous relations for partial conductivities in ionic liquids
title_short Some rigorous relations for partial conductivities in ionic liquids
title_sort some rigorous relations for partial conductivities in ionic liquids
url https://nasplib.isofts.kiev.ua/handle/123456789/32129
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