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Reorganization energies for charge transfer reactions in binary mixtures of dipolar hard sphere solvents: A Monte Carlo study

Abstract

We study the behavior of the reorganization energy for simple charge transfer reactions in mixtures of dipolar hard sphere fluids by Monte Carlo simulation. The static dielectric constants of the solvents are also obtained from the simulation. They are used as input in the reorganization energy expressions provided by the Marcus theory and the mean spherical approximation. Thus, a comparison between the values obtained from the theoretical expressions and our simulation results is possible. The dependence of the reorganization energy with the mixture composition and the influence of preferential solvation effects is also discussed.

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Reorganization energies for charge transfer reactions in binary mixtures of dipolar hard sphere solvents: A Monte Carlo study

Author: Denk, Claus; Morillo Buzón, Manuel; Sánchez Burgos, Francisco; Sánchez Murillo, Antonio
Publisher: AIP Publishing
Year: 1998
DOI: 10.1063/1.478108
Source: https://idus.us.es/bitstreams/56ac06a8-db45-4ef6-a38f-11e0aa0b4fb1/download
J. Chem. Phys. 110, 473 (1999); h ps://doi.o g/10.1063/1.478108 110, 473
© 1999 Ame ican Ins i u e o Physics.
Reo ganiza ion ene gies o cha ge ans e
eac ions in bina y mix u es o dipola ha d
sphe e sol en s: A Mon e Ca lo s udy
Ci e as: J. Chem. Phys. 110, 473 (1999); h ps://doi.o g/10.1063/1.478108
Submi ed: 07 July 1998 . Accep ed: 25 Sep embe 1998 . Published Online: 21 Decembe 1998
C. Denk, M. Mo illo, F. Sánchez-Bu gos, and An onio Sánchez
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Reo ganiza ion ene gies o cha ge ans e eac ions in bina y mix u es
o dipola ha d sphe e sol en s: A Mon e Ca lo s udy
C. Denka) and M. Mo illo
Uni e sidad de Se illa, Fı
´sica Teo
´ ica, Apa ado 1065, E-41080 Se illa, Spain
F. Sa
´nchez-Bu gos and An onio Sa
´nchez
Uni e sidad de Se illa, Quı
´mica Fı
´sica, Facul ad de Quı
´mica, C/ P o eso Ga cı
´a Gonza
´lez s/n,
E-41012 Se illa, Spain
~Recei ed 7 July 1998; accep ed 25 Sep embe 1998!
We s udy he beha io o he eo ganiza ion ene gy o simple cha ge ans e eac ions in mix u es
o dipola ha d sphe e luids by Mon e Ca lo simula ion. The s a ic dielec ic cons an s o he
sol en s a e also ob ained om he simula ion. They a e used as inpu in he eo ganiza ion ene gy
exp essions p o ided by he Ma cus heo y and he mean sphe ical app oxima ion. Thus, a
compa ison be ween he alues ob ained om he heo e ical exp essions and ou simula ion esul s
is possible. The dependence o he eo ganiza ion ene gy wi h he mix u e composi ion and he
in luence o p e e en ial sol a ion e ec s is also discussed. © 1999 Ame ican Ins i u e o Physics.
@S0021-9606~99!51401-3#
I. INTRODUCTION
Elec on ans e ~ET! eac ions in pola sol en s a e im-
po an in many biological and chemical p ocesses. Sol en
luc ua ions p o ide he ansi ion s a e con igu a ions o he
sol en –solu e sys em necessa y o he ET. Ma cus1–4 has
gi en a physical pic u e o ET eac ions, desc ibing he mul-
idimensional ee ene gy su aces o he p oduc and eac-
an s a es as pa abolic su aces in e ms o a sui able eac-
ion coo dina e. He ela ed he ac i a ion ee ene gy DG‡ o
he eac ion ee ene gy DGand he sol en eo ganiza ion
ene gy l. Ma cus also de i ed a simple exp ession o l,
based on a mac oscopic ea men o he sol en . The eo -
ganiza ion ene gy lis hen gi en in e ms o he s a ic and
op ical dielec ic cons an s o he sol en and a geome ical
ac o .
Al hough he dielec ic con inuum model ~Ma cus o -
mula!p o ides an adequa e quali a i e desc ip ion o he e-
o ganiza ion ene gy, i s quan i a i e p edic ions a e o en
imes a a iance wi h he expe imen al indings.5–7 Molecu-
la desc ip ions o he sol en a e, in p inciple, capable o
o e coming some o he di icul ies associa ed wi h a mac-
oscopic ea men o he sol en . The mean sphe ical ap-
p oxima ion ~MSA! ea men o he eo ganiza ion ene gy
ecognizes he sol en molecula i y by desc ibing he sol en
molecules as ha d sphe es wi h poin dipoles in hei cen e s.
Wi hin he MSA, an exp ession o lhas been de eloped
ha includes he ha d sphe e adius o he sol en
molecules.8,9
The need o a mic oscopic desc ip ion is o pa icula
in e es in mix u es o pola sol en s. Fo mos mix u es one
obse es a nonideal ~nonlinea !beha io o he sol a ion en-
e gy o an ionic o dipola solu e wi h espec o he mola
ac ions o he species p esen in he sol en .10 This beha -
io is usually e med as p e e en ial sol a ion. Fo ET eac-
ions in mix u es o pola sol en s, one migh also expec an
in luence o p e e en ial sol a ion e ec s on he sol en e-
o ganiza ion ene gy l. Bo h op ical11 and he mal12,13 ex-
pe imen al da a o ET eac ions in mix u es o wa e and
o ganic cosol en s show a beha io o l ha canno be ex-
plained wi h a con inuum model o he sol en . Analy ical
app oxima ions o he mic oscopic desc ip ion o he sol a-
ion ene gy in pola mix u es ha e been p esen ed in he
li e a u e.10,14
In his pape we will in es iga e he beha io o he e-
o ganiza ion ene gy lin pola sol en s by means o Mon e
Ca lo ~MC!simula ions. A quan i a i e p edic ion o expe i-
men al da a12,13 would equi e e y sophis ica ed simula ion
echniques. A his poin we a e a he in e es ed in he gen-
e al beha io o l. Fo his eason we ha e adop ed a simple
sol en model, wi h as ew adjus able pa ame e s as possible.
Ou sol en will be modeled ei he as a pu e sol en o as a
bina y mix u e. In bo h cases we will conside dipola , non-
pola izable ha d sphe e molecules. The solu e consis s o wo
cha ged ha d sphe es. We will s udy cha ge sepa a ion and
cha ge ecombina ion p ocesses o his sys em. As he sol-
en molecules a e conside ed nonpola izable, he op ical di-
elec ic cons an will be
e
op 51 o all sol en s. In o de o
compa e he nume ical esul s o lwi h he heo e ical p e-
dic ions, we need o e alua e he s a ic dielec ic cons an .
Ex ensi e simula ions ha e been ca ied ou in o de o de-
e mine
e
0 o ou di e en sol en models.
The ou line o he pape is as ollows: In Sec. II we
desc ibe ou sol en model and e iew he mos impo an
simula ion de ails. In Sec. III we discuss he e alua ion o
he dielec ic cons an s o he sol en models used in his
wo k. In Sec. IV, he applica ion o he MC echnique o he
calcula ion o ee ene gy su aces o cha ge ans e eac-
ions is summa ized. The esul s a e p esen ed and discussed
in Sec. V. A compa ison wi h he heo e ical esul s as ob-
a!Elec onic mail: [email p o ec ed]
JOURNAL OF CHEMICAL PHYSICS VOLUME 110, NUMBER 1 1 JANUARY 1999
4730021-9606/99/110(1)/473/11/$15.00 © 1999 Ame ican Ins i u e o Physics
ained o he con inuum sol en model ~Ma cus!and he
mic oscopic desc ip ion ~MSA!is made. Finally, Sec. VI
con ains some concluding ema ks.
II. MODEL AND MC SIMULATIONS
Ou sol en is modeled as a liquid o dipola , nonpola -
izable ha d sphe e molecules. Two sol en molecules iand k
in e ac ia a long anged dipole–dipole in e ac ion:
Vi,k5
m
i–
m
k
ik
323~
m
i– ik!~
m
k– ik!
ik
5 ik>2 s~1!
and a epulsi e sho anged in e ac ion ~ he ha d sphe e po-
en ial, Vi,k5` o ik5
u
ik
u
5
u
i2 k
u
,2 s). He e, sis he
adius o he ha d sphe es,
m
iis he dipole momen and iis
he posi ion o molecule i.
In his wo k we s udy pu e sol en s and bina y mix u es
o dipola ha d sphe e luids. The adius o he sol en mol-
ecules is aken o be he same o all sol en componen s. A
packing ac ion o
h
50.417 co esponding o a dense liquid
was used in all simula ions. The pola i y o a pu e sol en
will be exp essed in e ms o he dimensionless pa ame e
y54
p
m
2
9kBT,~2!
whe e
is he densi y o he liquid. A mix u e o wo sol-
en s will be composed o wo species, he less pola species
L, cha ac e ized by i s pola i y yL, and ano he species H
wi h a highe pola i y yH. The composi ion o he mix u es
will be desc ibed by he mola ac ions o he mo e pola
species H h oughou his wo k.
Pe iodic bounda y condi ions wi h he minimum image
con en ion15,16 we e applied o a cubic simula ion box o
side leng h L. This me hod equi es he use o a cu o o
he long anged dipola in e ac ions. In o de o accoun o
he con ibu ions beyond he cu o adius c<L/2 we ha e
adop ed he gene alized eac ion ield me hod.17 We conside
he mo ing bounda y dielec ic implemen a ion, i.e., he sub-
sys em inside he cu o sphe e a ound each molecule is
hough o be imme sed in a con inuum dielec ic cha ac e -
ized by a mac oscopic s a ic dielec ic cons an
e
RF . A mol-
ecule in e ac s di ec ly wi h all molecules inside i s cu o
sphe e ia Eq. ~1!and wi h he eac ion ield. The eac ion
ield a he cen e o molecule idue o he molecules inside
he cu o sphe e su ounding i is p opo ional o he o al
dipole momen inside i s cu o sphe e16
m
i–Ei
52~
e
RF21!
2
e
RF11
1
c
3
m
i•(
ik< c
m
k5
am
i•(
ik< c
m
k,~3!
whe e we ha e de ined a sc eening cons an
a
. Summing up
all e ms con ibu ing o he o al po en ial ene gy we ob ain
E o 51
2(
kÞi, ik< c
Vi,k
dd 21
2
a
(
i
m
i
2~4!
wi h an e ec i e in e ac ion ene gy
Vi,k
dd 5
m
i–
m
k~12
a
ik
3!
ik
323~
m
i– ik!~
m
k– ik!
ik
5.~5!
The las e m in Eq. ~4!desc ibes he cons an sel -
in e ac ion o he molecules wi h hei own eac ion ields.
The o m o he e ec i e in e ac ion in Eq. ~5!is e y con-
enien o compu a ional pu poses. The inclusion o he e-
ac ion ield only equi es wo ex a loa ing poin ope a ions
o each e alua ion o he in e ac ion ene gy, which ende s
his me hod compu a ionally easible, e en o ela i ely
la ge sys ems. I has been shown ha he compu a ionally
mo e expensi e Ewald summa ion echnique yields equi a-
len esul s o he dielec ic cons an when applied o simila
sys ems.18,19 Analogous conclusions ha e been d awn o
ee ene gy calcula ions o ionic hyd a ion.20
Sys em con igu a ions we e gene a ed in he ollowing
manne : s a ing om a gi en con igu a ion, a molecule was
selec ed andomly. I was displaced om i s ini ial posi ion
in a cube o side leng h Dxwi h a uni o m dis ibu ion. Now,
a o a ional axis (x,yo z) was selec ed a andom and he
dipole o ien a ion o he molecule was o a ed by a uni o mly
dis ibu ed angle in he ange 2D
<
<D
a ound his
axis. The pa ame e s Dxand D
we e adjus ed o each an
accep ance a io o app oxima ely 30%. The implemen a ion
o he simula ion is along he lines o he s anda d Mon e
Ca lo echniques.15,16
III. DIELECTRIC CONSTANT
The applica ion o he s a is ical mechanical heo y o
he dielec ic cons an 21,22 o ini e size simula ion sys ems
wi h bounda y condi ions equi es some modi ica ions. This
issue has been lucidly add essed by Neumann.18 F om his
analysis i ollows ha he s a ic dielec ic cons an
e
0in he
eac ion ield ~RF!geome y is gi en by
e
052
e
RF~11
z
!11
112
e
RF2
z
,~6!
wi h
z
54
p
3
b
^
M2
&
L353ygK.~7!
He e
^
M2
&
is he con igu a ional a e age o he squa ed o al
dipole momen o he sys em and
b
51/kBT. We ha e also
indica ed he ela ion o
z
wi h he pola i y yand he Ki k-
wood g ac o gK5
^
M2
&
/N
m
2. The dielec ic cons an
e
RF
ha cha ac e izes he eac ion ield was de e mined sel -
consis en ly in he simula ions, so ha
e
RF'
e
0 o all sol-
en s.
The sol en molecules we e ini ially p epa ed in an cc
s uc u e and he sys em was hen allowed o elax du ing
53106MC con igu a ions. Mean alues we e ob ained om
NMC553108subsequen MC con igu a ions, excep whe e
o he wise s a ed. In o de o ob ain an es ima e o he s a is-
ical e o s, we calcula ed mean alues o
z
o e blocks o
106con igu a ions. We ca ied ou a ious es s o check he
con e gence o he alues o he dielec ic cons an ob ained
in ou simula ions. In Fig. 1 we show he unning a e ages o
e
0 o wo sol en s wi h y52.18 and y52.90 o wo di e -
en alues o he maximum o a ional angle D
. In he case
o he sol en wi h he highe pola i y, he alues o
e
0con-
e ge e y slowly. E en o NMC553108con igu a ions we
474 J. Chem. Phys., Vol. 110, No. 1, 1 Janua y 1999 Denk
e al.
s ill ind a de ia ion o D
e
051.6 be ween he wo simula-
ions ~ heo e ically, he simula ion esul s should be indepen-
den o D
). The s a is ical e o s es ima ed using he block
a e ages we e D
e
050.4 o simula ion ~a!and D
e
050.5 o
simula ion ~b!. This indica es ha , e en wi h 53108MC
con igu a ions, he phase space o his highly pola sys em
has no been su icien ly explo ed o ob ain p ecise alues o
e
0. The de ia ion o he wo cu es will be used as an es i-
ma e o he e o o he dielec ic cons an ~app oxima ely
3%! o sol en s wi h high pola i y. Sol en s wi h lowe mo-
lecula dipole momen s show a much as e con e gence o
e
0. Fo sol en s wi h a dielec ic cons an
e
0<30 we ound
23108MC con igu a ions o be su icien o de e mine
e
0
wi h a ela i e e o o app oxima ely 3%.
We ha e also s udied he dependency o
e
0on he sys-
em size. Simula ion ~a!o Fig. 1 was epea ed o a sys em
wi h N5864 pa icles; he esul ing alue o
e
0is shown in
Table I @simula ion ~e!#. The esul s indica e ha
e
0is inde-
penden o he size o he sys em o N>256 wi hin he e o
limi s.
As al eady men ioned, he pa ame e
e
RF was adjus ed
sel -consis en ly by epea ing each simula ion, using he e-
sul
e
0o a simula ion as an inpu pa ame e
e
RF in he nex
simula ion. In all cases, i was su icien o epea each simu-
la ion only once, as
e
0depends e y weakly on
e
RF .In
simula ion ~ !~see Table I!we ha e epea ed simula ion ~b!
wi h
e
RF558. The esul s a e p ac ically iden ical.
The dielec ic cons an
e
0was hen de e mined o a
pu e sol en o e a wide ange o alues o he molecula
pola i y y. A sys em wi h N5256 pa icles was used in hese
simula ions and he mean alues o
e
0we e ob ained a e
53108MC con igu a ions. Fo he highes pola i y, y
53.0, we inc eased he numbe o MC con igu a ions o
NMC5109 o he easons men ioned abo e. The esul s a e
shown in Fig. 2.
The heo y o liquids p o ides a ious app oxima ions
o he s uc u e o he dipola ha d sphe e luid.23 O pa -
icula in e es is he so-called MSA, as i p o ides analy ical
exp essions o he co ela ion unc ions and he dielec ic
cons an .24 We ind i ins uc i e o compa e ou simula ion
esul s wi h he MSA heo e ical p edic ions. The pai dis i-
bu ion unc ion can be expanded as23
h~1,2!5hS~R!1hD~R!D~1,2!1hD~R!D~1,2!,~8!
whe e D~1,2!is he cosine o he angle o med by he dipole
o ien a ions o wo molecules and 2D(1,2)
m
2/R3is he
dipole–dipole in e ac ion as de ined in Eq. ~1!. The MSA
p o ides he unc ions hS(R),hD(R) and hD(R) in e ms o
he adial dis ibu ion unc ion ~ d !o he Pe cus–Ye ick
~PY!solu ion o ha d sphe es a di e en densi ies.
In Fig. 3 we show he adial dis ibu ion unc ion
gS(R)5hS(R)11 o a highly pola sol en (y53.00). Sol-
en s wi h a lowe pola i y ha e a e y simila d wi h a
sligh ly lowe main peak. The MSA esul o gS(R)~also
shown in Fig. 3!is jus he PY d o ha d sphe es a densi y
and does no depend on he molecula pola i y. Al hough
he ag eemen is globally good, he e a e de ia ions be ween
he MSA and he simula ions. In he egion close o con ac ,
he MSA subes ima es he alue o gS(R), which is o p i-
ma y impo ance o many he modynamic p ope ies o he
liquid. I also p edic s a somewha slowe decay om he
peak alue o he i s minimum when compa ed wi h he
simula ions.
The dielec ic p ope ies o he sol en a e ela ed o
hD(R), which desc ibes he angula co ela ion o wo mol-
ecules a a gi en dis ance R. The dielec ic cons an
e
0is
FIG. 1. Running a e ages o
e
0 o ~a!,~b!y52.90 and ~c!,~d!y52.18. The
sys ems we e simula ed wi h wo di e en alues o he maximum o a ional
angle D
5
p
/2 ~a!and ~c!and D
51.0 ~b!and ~d!.
FIG. 2. The s a ic dielec ic cons an
e
0 o a pu e sol en . The e o ba s o
he simula ion esul s indica e he es ima ed ela i e e o o 3% ~see main
ex !. The solid line is a ou h deg ee in e pola ion polynomial. The do ed
line co esponds o he heo e ical esul as ob ained om he MSA.
TABLE I. Dielec ic cons an s ob ained o sol en s wi h y52.90
~a!,~b!,~e!,~ !and y52.18 ~c!,~d!
e
0NMC ND
e
RF
~a!59.68 53108256
p
/2 70
~b!58.05 53108256 1.0 70
~c!28.29 53108256
p
/2 30
~d!29.05 53108256 1.0 30
~e!58.41 23108864
p
/2 70
~ !58.78 53108256 1.0 58
475J. Chem. Phys., Vol. 110, No. 1, 1 Janua y 1999 Denk
e al.
de e mined by he pola i y yand he Ki kwood g ac o gK
@see Eq. ~6!#. The Ki kwood g ac o gKcan be ob ained
om hD(R) by in eg a ion
gK5114
p
3
E
0
`hD~R!R2dR.~9!
In Fig. 4 we show hD(R) o a highly pola sol en (y
53.0) as ob ained om ou simula ions and he co espond-
ing MSA esul . The MSA does no p o ide a good app oxi-
ma ion o hD(R) as i unde es ima es he angula co ela ion.
This esul s in an unde es ima ion o gKand hus
e
0. This
de ia ion is mo e p onounced o sol en s wi h a high pola -
i y ~see Fig. 2!. Bu , e en o sol en s wi h he lowes pola -
i y unde conside a ion in his wo k, he MSA esul o
hD(R) does no ag ee wi h he simula ion da a. The dielec ic
cons an as ob ained by he MSA gi es a good app oxima-
ion o
e
0only o sol en s wi h gK'1. These limi a ions o
he MSA a e well known and mo e sophis ica ed heo ies
based on he hype ne ed chain ~HNC!app oxima ion p o-
ide much be e angula co ela ion unc ions and dielec ic
cons an s o dipola ha d sphe e luids. Compa isons o he
MSA and o he heo ies can be ound in he li e a u e.23,25–33
Le us now conside he case o bina y sol en mix u es.
We s udy wo di e en ypes o mix u es: ~A!mix u es wi h
wo componen s o simila pola i ies (yH53.0 and yL
52.18), and ~B!mix u es whose componen s a e o a he
di e en pola i y (yH53.0 and yL50.75). Fo each ype o
mix u e, he dielec ic p ope ies will only depend on i s mo-
la composi ion ~de ined by he mola ac ion o species H,
H), i he empe a u e is held ixed. This gi es us he pos-
sibili y o s udying wo qui e di e en mix u es, spanning a
wide ange o dielec ic cons an s. The simula ion p ocedu e
is he same as o pu e sol en s, and he dielec ic cons an is
e alua ed by using Eqs. ~6!and ~7!.
In Fig. 5 we show he dielec ic cons an s as ob ained o
he simula ed composi ions o mix u es o ype ~A!and ~B!.
The alues o
e
0 o he pu e sol en s ( H50 and H51)
we e aken om he simula ions desc ibed abo e ~see Fig.
2!. Fo bo h mix u es we obse e an almos quad a ic depen-
dence o he s a ic dielec ic cons an on he mola ac ion
H. This beha io can be unde s ood by no icing ha in he
case o a bina y mix u e,
^
M2
&
/Nis o a good app oxima ion
a quad a ic unc ion o he mola ac ion H. Fo
e
0
'
e
RF , i ollows om Eq. ~6! ha he dielec ic cons an is
essen ially a linea unc ion o
z
, which in u ns is p opo -
ional o
^
M2
&
/Nas can be seen in Eq. ~7!.
IV. REORGANIZATION ENERGIES
A. Calcula ion o he eo ganiza ion ene gy
om molecula simula ions
In Sec. III we ha e analyzed he dielec ic beha io o
dipola ha d sphe e sol en s. We will now s udy he si ua ion
when a solu e is imme sed in he sol en . Ou aim he e is o
s udy he ene ge ics o he mal cha ge ans e eac ions be-
ween wo solu e molecules in he p esence o a pola sol-
en . We ha e adop ed a simple model o he solu e: The
solu e consis s o wo ha d sphe e molecules ~dono and ac-
cep o !wi h gi en adii dand asepa a ed by a ixed dis-
FIG. 3. The adial dis ibu ion unc ion gS(R)(R5 /2 s) o a sol en wi h
y53.00 ~ illed ci cles!. The do ed line ep esen s gS(R) as ob ained om
he MSA.
FIG. 4. The angula co ela ion unc ion hD(R) o a highly pola sol en
(y53.0, illed ci cles!. The do ed line co esponds o hD(R) as p o ided by
he MSA.
FIG. 5. S a ic dielec ic cons an
e
0 o bina y mix u es o dipola ha d
sphe es wi h yL52.18 @mix u e ~A!, ci cles#and yL50.75 @mix u e ~B!,
squa es#in e ms o he mola ac ion H. In bo h cases yH53.0. The solid
lines ep esen quad a ic in e pola ion polynomials.
476 J. Chem. Phys., Vol. 110, No. 1, 1 Janua y 1999 Denk
e al.

ance d. The dono and accep o in he eac an s a e ca y a
cha ge qdand qa, espec i ely; a nega i e ne cha ge ans-
e s om he dono o he accep o . We will conside he
eac ion coo dina e o his p ocess in e ms o a cha ging
pa ame e
j
, so ha
qd~
j
!5qd1
j
e,~10!
qa~
j
!5qa2
j
e.~11!
He e, eis he elemen a y cha ge ~ ha we will ake as posi-
i e!. The eac an s a e o he solu e is gi en by
j
50, while
he p oduc s a e is ob ained by se ing
j
51. In his wo k we
ha e s udied wo ypical ans e eac ions: ~i!a cha ge e-
combina ion ~CR!p ocess qd52eand qa51eand ~ii! he
in e se p ocess, a cha ge sepa a ion ~CS!p ocess (qd5qa
50). The a es o hese p ocesses a e go e ned by an ac i-
a ion ee ene gy law. Ma cus1–4 ob ained o he nonadia-
ba ic elec on ans e a e
ke 5
k
A
4
p
l/
b
exp~2
b
DG‡!,~12!
whe e he ac i a ion ee ene gy DG‡is de ined as
DG‡5~DG1l!2
4l.~13!
He e,
k
is a ma ix elemen desc ibing he elec onic cou-
pling be ween eac an and p oduc s a e, and DGand l
deno e he ee-ene gy change o he eac ion and he eo -
ganiza ion ene gy, espec i ely. Equa ion ~12!was de i ed
unde he assump ion o a classical sol en ha esponds
linea ly o a edis ibu ion o cha ges.
The p ocedu e used o he e alua ion o eo ganiza ion
ene gies in cha ge ans e eac ions om simula ions is well
documen ed.34–36 He e we will b ie ly indica e he main
poin s. Le H
j
deno e he sol en –solu e in e ac ion ene gy
o a solu e s a e cha ac e ized by he cha ging pa ame e
j
and a ce ain ixed sol en con igu a ion. The ene gy gap
DV5H12H0desc ibes he ene gy di e ence be ween p od-
uc s and eac an s o a gi en con igu a ion o he sol en .
An elec on ans e will ake place only o sol en con igu-
a ions ha ul ill he condi ion DV52Ei~F ank–Condon
p inciple!, whe e Eiis he in insic ene gy di e ence
be ween he gas phase elec onic s uc u es o he ini ial
and inal s a e o he solu e. Le us de ine he andom a i-
able D5DV, wi h a p obabili y law gi en by p
j
(D)
5
^
d
(D2DV)
&
j
, whe e he angula b acke s indica e an
equilib ium a e age aken wi h a canonical dis ibu ion de-
sc ibing a sys em a empe a u e Tand Hamil onian H
j
. The
a e o he ET p ocess is p opo ional o he p obabili y den-
si y p0(2Ei) o he ene gy gap DVha ing a alue 2Ei.
This p obabili y dis ibu ion co esponds o a sol en in he -
modynamical equilib ium wi h he eac an s a e o he sol-
u e,
j
50.
The main p oblem in simula ions lies in he cons uc ion
o his p obabili y densi y as he en i e phase space o he
sol en deg ees o eedom has o be explo ed. This is an
imp ac ical ask, and one eso s o a ee ene gy pe u ba ion
me hod,34 which is based on he ollowing. Fo a gi en alue
o he ac ional cha ge pa ame e
j
,DVis sampled a ound
a alue D
j
wi h a dis ibu ion ha is app oxima ed e y well
by a Gaussian
p
j
~D!51
A
2
ps
j
2e2~D2D
j
!2/2
s
j
2.~14!
Va ious s a es
j
o he solu e a e simula ed, each simula ion
p o iding a p obabili y dis ibu ion p
j
(D) a ound D
j
. These
dis ibu ions can be pieced oge he 34 o yield he dis ibu ion
p0(D) o e a wide ange o alues D. Zhou and Szabo35
ha e p oposed a simpli ied me hod ha pe mi s ob aining
p0(D) by simula ing only wo s a es o he solu e:
j
50 and
j
51. In hei wo k, he eo ganiza ion ene gy is gi en by
l5D02DG10 ,~15!
wi h he ee-ene gy di e ence be ween s a e
j
and he eac-
an s a e o he solu e
DG
j
05
E
0
j
d
j
8D
j
8.~16!
The mean alue o he ene gy gap D
j
o a ce ain alue o
he cha ging pa ame e
j
can be ob ained by a cubic in e -
pola ion polynomial in
j
, whe e all coe icien s a e de e -
mined by he mean alues D0and D1and he dispe sions
b
s
0
2and
b
s
1
2in he eac an and p oduc s a e, espec i ely.
Inse ing he polynomial exp ession o Zhou and Szabo in
Eqs. ~15!and ~16!leads o
lCR51
2~D02D1!11
12 ~
b
s
0
22
b
s
1
2!,~17!
lCS51
2~D02D1!21
12 ~
b
s
0
22
b
s
1
2!.~18!
As poin ed ou by Zhou and Szabo, he accu acy o he in-
e pola ion polynomial app oxima ion o D
j
can be checked
by ca ying ou an addi ional simula ion o
j
51/2. The
alue o he ene gy gap D1/2 ob ained is hen compa ed o he
alue p o ided by he in e pola ion o mula. We ound a
de ia ion o less han 1% o all cases conside ed he e. F om
he in e pola ion polynomial, he p obabili y densi y p0(D)
can also be cons uc ed.35
B. Simula ion de ails
The inclusion o he cha ged solu e pa icles in he simu-
la ion in oduces a di icul y when dealing wi h sys ems o
ini e size: The o ien a ion o he dipole momen s o he sol-
en molecules is aniso opic and he pe iodic eplica ion o
he cen al simula ion cell does no ep esen a physical pic-
u e o he sol en . This issue has been widely discussed in
he li e a u e37 and a ious me hods ha e been de eloped o
a oid pe iodic bounda y condi ions ~pbc! o such sys ems.
Sphe ical simula ion cells in conjunc ion wi h a sui able
me hod o a oid sel -pola iza ion on he su ace o he cell
a e usually employed.38
We ha e conside ed simula ions wi h pe iodic bounda y
condi ions and wi hin a sphe ical geome y. In he pbc simu-
la ions, he cha ge–dipole in e ac ions can be desc ibed ia
an e ec i e in e ac ion po en ial ha includes he eac ion
ield in a simila manne o Eq. ~5!:
477J. Chem. Phys., Vol. 110, No. 1, 1 Janua y 1999 Denk
e al.
Vi,j
qd5qi
S
2
ij
2
a
D
m
j– ij,~19!
whe e
a
is he sc eening cons an as de ined in Eq. ~3!. The
solu e cha ges in e ac wi h all dipoles inside hei co e-
sponding cu o sphe es. The cu o adius o he cha ge–
dipole in e ac ions was se o be he same as o he dipole–
dipole in e ac ions.
In he sphe ical model, he simula ion cell is a sphe ical
essel wi h he solu e si ua ed a he cen e o he essel.
Each molecule in e ac s wi h all molecules inside he essel
and elec os a ic in e ac ions a e aken ully in o accoun @se
a
50 in Eqs. ~5!and ~19!#. The simula ion sphe e is di ided
in o wo egions: an inne sphe e, whe e he molecules a e
allowed o mo e and o a e and an ou e shell, whe e he
molecules a e kep ixed du ing he simula ion. The mol-
ecules cons i u ing he ou e shell a e si ua ed ini ially in a
cc s uc u e wi h andomly dis ibu ed dipole momen s. The
ixed dipoles in he ou e shell p e en an unphysical pola -
iza ion o he dipoles close o he su ace o he essel. A
co ec ion o he ene gy gap D0has o be applied in he case
o he sphe ical model. Con ibu ions om he sol en ou -
side he sphe e can be pa ially aken in o accoun by con-
side ing he sphe e o be imme sed in a con inuous dielec ic
medium wi h dielec ic cons an
e
ou . The in luence o his
dielec ic medium is no aken in o accoun du ing he simu-
la ion ~as i would equi e he ull solu ion o he Laplace
equa ion inside he sphe e o each con igu a ion!, bu i s
e ec on D0may be es ima ed by elec os a ic conside -
a ions. Fo a CR p ocess, he con ibu ions o D0 om ou -
side he simula ion cell wi h adius Ra e
D0
ou 52~
e
ou 21!
2
e
ou 11
~ed!2
R3,~20!
whe e dis he dis ance be ween he solu e cha ges.
We s udied he dependency o D0on he size o he
sys em o bo h models. A highly pola sol en (y52.90)
was used o sol a e wo solu e ions wi h equal adii d5 a
5a51.44Å, cha ges qd52e,qa51eand sepa a ed by a
dis ance o d56 Å. The sol en adius was se o be he
same as he solu e adius and a packing ac ion o
h
50.417 was used.
In he case o he pbc geome y we simula ed sys ems
wi h N5246 490 854 sol en molecules. The cu o adius
o he dipole–dipole and cha ge–dipole in e ac ions was se
o c5min(L/2,8 s) o each sys em, whe e Lis he side-
leng h o he cubic simula ion cell. Fo he sys em wi h N
5854 sol en molecules we conduc ed a simula ion wi h he
ull cu o c5L/2 in o de o check he in luence o he
educed cu o on D0.
In he sphe ical geome y we simula ed he same sys em
wi h a o al o N o 5673 sol en molecules. In his case, he
adius o he inne sphe e ~whe e he molecules a e allowed
o mo e!was a ied. The esul s a e combined in Table II.
Fo small sys em sizes, he wo geome ies p oduce qui e
di e en alues o he ene gy gap D0. The pbc simula ions
o e es ima e D0, whe eas he sphe ical model esul s in oo
small alues o he gap. As he sys em size inc eases, bo h
models yield simila esul s. As he size o he ou e shell in
he sphe ical model dec eases ~las alue in Table II!, he
pola iza ion o he cell su ace esul s in lowe alues o
D0. The educed cu o c58 s511.52Å o he pbc sys em
wi h N5854 sol en molecules gi es p ac ically he same
alue o D0as he sys em wi h c5L/2514.75Å.
Al hough he sphe ical geome y pe mi s he usage o
smalle sys em sizes, we ha e op ed o he pbc geome y
wi h N5854 sol en molecules and a educed cu o c
58 s o ou simula ions. Ou choice is based on he ac
ha he sphe ical model was no able o ep oduce he dielec-
ic cons an o he sol en . Thus he usage o a single ge-
ome y o he de e mina ion o bo h he dielec ic cons an
and he eo ganiza ion ene gy is clea ly p e e able. The pbc
geome y also allows us o calcula e he sol en adial dis i-
bu ion unc ions. Wi h ou choice o he sys em size and he
cu o adius, a molecule close o he simula ion cell bound-
a y only in e ac s wi h a small ac ion o he pe iodic im-
ages o he sol en molecules in he i s sol a ion shell.
When applying he con en ional Mon e Ca lo me hod
o c ea ing sys em con igu a ions ~ ansla ion and o a ion o
a molecule!in he case o mix u es, we no iced a e y slow
elaxa ion o he sys em. I a cha ged solu e is p esen , he
ini ial cc s uc u e o he sol en elaxes apidly o a si ua-
ion whe e he solu e is sol a ed by he molecules ha a e
ini ially in he icini y o he solu e. Thus, he mola compo-
si ion o he i s sol a ion shells depends on he ini ial po-
si ions o he wo species wi hin he cc g id. The high den-
si y o sol en molecules close o he solu e now ende s a
es uc u e o he sol a ion shell ex emely di icul . I he
wo componen s o he mix u e a e equally sized, one can
adop a much mo e e icien me hod o c ea ing con igu a-
ions: The con en ional ‘‘mo e’’ is al e na ed wi h a
‘‘swap’’ o molecules: wo molecules o di e en species a e
selec ed andomly. Now, he iden i ies o he molecules a e
in e changed, i.e., he dipole momen o he wo molecules is
changed. We only change he absolu e alues o he dipole
momen s; he dipole o ien a ions a e no al e ed. Each new
con igu a ion is gene a ed ei he by a mo e o by a swap and
he p obabili y o a swap was se o 10%.
V. RESULTS AND DISCUSSION
The eo ganiza ion ene gies lCR and lCS o a cha ge
ecombina ion and a cha ge sepa a ion p ocess ha e been
TABLE II. Values o D0 o pbc and he sphe ical model. The sol en and
solu e pa ame e s a e speci ied in he main ex . Fo he sphe ical model N
e e s o he numbe o molecules ha a e allowed o mo e. In his geome y
he o al numbe o molecules was held ixed a N o 5673.
ND0~kcal/mol! cGeome y
246 226.9 c5L/2 pbc
490 223.1 c58 spbc
854 221.9 c58 spbc
854 222.1 c5L/2 pbc
239 217.9 ¯sphe ical
371 222.4 ¯sphe ical
521 223.5 ¯sphe ical
593 218.6 ¯sphe ical
478 J. Chem. Phys., Vol. 110, No. 1, 1 Janua y 1999 Denk
e al.
calcula ed o a ious sol en s using he me hods desc ibed
abo e. The solu e consis s o wo ha d sphe es wi h adius
d5 a5a51.44Å and dis ance d56Å.
A. Pu e sol en s
We i s s udy he case o ET eac ions in pu e sol en s.
We ha e conside ed sol en s wi h pola i ies yin he ange o
0.75<y<3.0. The sol en adius was chosen o be he same
as he solu e adius. A packing ac ion o
h
50.417 and a
empe a u e o T5300K was used in all simula ions.
We will compa e ou simula ion da a wi h he eo gani-
za ion ene gy exp essions p o ided by he Ma cus heo y
and he MSA. In he Ma cus con inuum desc ip ion, he e-
o ganiza ion ene gy o a cha ge ans e o an elemen a y
cha ge be ween wo equally sized solu e molecules o adius
aa a dis ance din a nonpola izable sol en wi h s a ic di-
elec ic cons an
e
0is gi en by
l5e2
S
121
e
0
DS
1
a21
d
D
.~21!
The MSA heo y akes in o accoun he molecula aspec o
he sol en . In he case o in ini ely sepa a ed cha ge cen e s
(d→`), he eo ganiza ion ene gy is jus he sum o he
sol a ion ee ene gies o he wo ions8,9
l5e2
S
121
e
0
D
1
a~11
d
!.~22!
He e,
d
is a co ec ion o he sol a ed ion adius, which o a
e y good app oxima ion is gi en by39
d
53 s/a~1081/3
e
0
1/622!21.~23!
I he dis ance be ween he ions is no in ini e, he inclusion
o he ion–ion in e ac ion in Eq. ~22!wi hin he amewo k
o he MSA would equi e he knowledge o he mean ion–
ion po en ial. We will app oxima e his e m by he sc eened
in e ac ion in a con inuum dielec ic medium, as i has been
done by o he s.36 The inclusion o his e m in Eq. ~22! e-
sul s in
lMSA5e2
S
121
e
0
DS
1
a~11
d
!21
d
D
.~24!
We should keep in mind ha his app oxima e lMSA does no
eme ge om a pu ely mic oscopic pic u e o he sol en , as
i s in luence on he ion–ion in e ac ion is aken in o accoun
by a con inuum desc ip ion. This is expec ed o be a good
app oxima ion, as long as he dis ance o he ions is su i-
cien ly la ge.
When e alua ing Eqs. ~24!and ~23!, we ha e o p o ide
he solu e adius a, he ion dis ance d, he sol en adius s
and he s a ic dielec ic cons an o he sol en
e
0. The la e
may be ob ained di ec ly om he MSA, using he ollowing
ela ions:23
3y5~114
j
!2
~122
j
!42~122
j
!2
~11
j
!4,
~25!
e
05~114
j
!2~11
j
!4
~122
j
!6.
Fo compa ison wi h expe imen al da a i is o en mo e con-
enien o use he expe imen al alue o
e
0in Eqs. ~24!and
~23!.
We will hus compa e h ee heo e ical exp essions wi h
ou simula ion da a: ~a! he Ma cus exp ession Eq. ~21!,~b!
he ‘‘consis en ’’ MSA esul as gi en by Eq. ~24!using he
sol en pola i y yin o de o de e mine
e
0 om he MSA and
~c! he ‘‘expe imen al’’ MSA esul lMSA
ex , using he dielec-
ic cons an s as ob ained om he simula ions in Eq. ~24!.
The esul s a e shown in Fig. 6, whe e we ep esen he e-
o ganiza ion ene gy e sus he Peka ac o 121/
e
0. In his
ep esen a ion, he Ma cus esul @Eq. ~21!# is a s aigh line.
We ind ha lCS.lCR o all simula ed pu e sol en s.
Simila esul s ha e been ob ained by o he au ho s o com-
pa able sys ems.36 This is due o he combina ion o wo
e ec s:34,40 Fi s , he ee ene gy su aces a e no s ic ly
pa abolic, as i would be equi ed by linea esponse heo y.
Second, e en i he de ia ions om pa abolic su aces a e
small, he cu a u e o he pa abolas may be di e en in he
eac an and p oduc s a es. Bo h ea u es gi e ise o a di -
e en eo ganiza ion ene gy o he cha ge sepa a ion and
cha ge ecombina ion p ocesses.
The Ma cus exp ession o l esul s in an o e es ima ion
o he eo ganiza ion ene gy. Equa ion ~21!gi es l(y
53.0)5172.6 kcal/mole o he sol en wi h he highes po-
la i y. In he plo we ha e scaled he co esponding cu e o
coincide wi h lMSA
ex a his pola i y. This is equi alen o
using an e ec i e ion adius o a52.0Å in Eq. ~21!. When
he geome ic ac o is adjus ed in his way, he con inuum
desc ip ion s ill does no desc ibe well he o e all beha io
FIG. 6. Reo ganiza ion ene gies o a pu e sol en . The squa es ep esen
lCS, he ci cles co espond o lCR as ob ained om he simula ions. The
dashed line is he esul as ob ained by he con inuum desc ip ion ~Ma cus!
scaled o coincide wi h lMSA
ex o he highes pola i y. The do ed line co -
esponds o he heo e ical MSA esul o he simula ed sys em. The MSA
esul lMSA
ex , using
e
0as ob ained om he simula ions as an inpu pa am-
e e , is ep esen ed by he solid line.
479J. Chem. Phys., Vol. 110, No. 1, 1 Janua y 1999 Denk
e al.
o he eo ganiza ion ene gy. This ea u e is expec ed. The
exp ession o lin he con inuum desc ip ion, Eq. ~21!, in-
dica es ha he eo ganiza ion ene gy depends only on
e
0 o
ixed adii and sepa a ion dis ance and his dependence is
e y weak.
Fo he MSA esul s, we ind a much be e ag eemen
be ween he heo e ical exp essions and he simula ion da a.
The heo e ical MSA esul ~b!gi es good ag eemen o
small pola i ies, bu unde es ima es he eo ganiza ion en-
e gy o high pola i ies. This is no su p ising, as i is well
known ha he MSA unde es ima es he dielec ic cons an
o high sol en pola i ies. This esul s in an unde es ima ion
o he Peka ac o 121/
e
0on one hand and o he geome ic
ac o 1/a(11
d
) on he o he .
The MSA exp ession lMSA
ex wi h
e
0 aken om he simu-
la ion da a yields eo ganiza ion ene gies which a e close o
he simula ion esul s o he cha ge ecombina ion p ocess.
By cons uc ion, he MSA does no dis inguish be ween he
cha ge ecombina ion and cha ge sepa a ion p ocesses,
which as shown by he simula ion esul s, ha e di e en e-
o ganiza ion ene gies. Thus, he good ag eemen o lMSA
ex
wi h he esul s o he cha ge ecombina ion p ocess in he
case p esen ed is p obably o ui ous. Howe e , his exp es-
sion desc ibes he o e all shape o bo h cu es much be e
han he Ma cus app oxima ion. The heo e ical exp ession
o lwi hin he amewo k o MSA includes he geome ic
ac o 1/a(11
d
) which depends on
e
0 ia Eq. ~23!. The
abili y o lMSA
ex o ep oduce he end o he simula ion da a
o bo h p ocesses sugges s ha he inclusion o his geome -
ic ac o is an impo an co ec ion o he Ma cus exp ession
o he eo ganiza ion ene gy, Eq. ~21!. The geome ic ac o ,
as gi en by he MSA, can be in e p e ed as an e ec i e
solu e adius a(11
d
) and is a consequence o he sol en
molecula i y in he MSA pic u e. This emphasizes he need
o a molecula desc ip ion o he sol en , e en in he case o
pu e sol en s.
F om hese esul s one may be emp ed o conclude ha
he MSA is able o p edic he sol en s uc u e a ound he
solu es. We a e cu en ly examining his ques ion o single
ions in solu ion. P elimina y esul s indica e ha he pola -
iza ion densi y o he sol en a ound an ion is no e y well
ep esen ed by he MSA exp ession. Howe e , he ee en-
e gy o sol a ion, gi en as an in eg al o e he pola iza ion
densi y, is p edic ed qui e well by he MSA exp ession.
B. Mix u es
We will now p oceed o he case o bina y mix u es o
pola sol en s. We ha e calcula ed he eo ganiza ion ene gy
o he wo mix u es s udied in he p e ious sec ion @mix u e
~A!wi h simila pola i ies o he wo componen s: yH53.0
and yL52.18 and mix u e ~B!wi h a he di e en pola i ies
o he wo componen s: yH53.0 and yL50.75#. The esul s
o mix u e ~A!a e shown in Fig. 7 and o mix u e ~B!in
Fig. 8.
When he solu e is no p e e en ially sol a ed by one o
he wo componen s o he mix u e, one would expec a lin-
ea beha io o he sol a ion ene gy, as he mola ac ion o
he componen s is a ied.10 Fo nonpola izable sol en s, he
heo e ical exp essions o he eo ganiza ion ene gy educe
o a sol a ion ene gy in he limi d→`. Thus, a linea ~o
close o linea !dependence o lon he mola ac ion H
would indica e ha no p e e en ial sol a ion is p esen in he
p ocess. Fo bo h mix u es we obse e de ia ions om a
linea beha io in he eo ganiza ion ene gy. In mix u e ~A!
we obse e an almos linea beha io o lCS, while all al-
ues o lCR o he mix u es lie abo e a s aigh line connec -
ing he esul s o he pu e sol en s. Fo mix u e ~B! his
beha io is much mo e p onounced. When adding a small
mola ac ion o he componen wi h he highe pola i y, he
eo ganiza ion ene gy shows a d as ic inc ease, and e y
quickly he eo ganiza ion ene gy l eaches a alue close o
ha o he pu e sol en ( H51). As i was al eady obse ed
o mix u e ~A!, he eo ganiza ion ene gy o he cha ge
ecombina ion p ocess lCR de ia es mo e om he linea
FIG. 7. Reo ganiza ion ene gies o mix u e ~A!(yH53.0 and yL52.18).
The squa es ep esen lCS, he ci cles co espond o lCR. The linea depen-
dence, as expec ed in he limi d→` o ideal sol a ion, is ep esen ed as a
dashed line o each case. The xsymbols ep esen he MSA esul s lMSA
ex .
FIG. 8. Reo ganiza ion ene gies o mix u e ~B!(yH53.0 and yL50.75).
The squa es ep esen lCR, he ci cles co espond o lCS. The solid lines
connec ing he da a poin s ha e been ob ained by spline in e pola ion. The
linea dependence, as expec ed in he limi d→` o ideal sol a ion, is
ep esen ed as a dashed line o each case. The xsymbols ep esen he
MSA esul s lMSA
ex .
480 J. Chem. Phys., Vol. 110, No. 1, 1 Janua y 1999 Denk
e al.