Landau–de Gennes theory

In physics, Landau–de Gennes theory describes the NI transition, i.e., phase transition between nematic liquid crystals and isotropic liquids, which is based on the classical Landau's theory and was developed by Pierre-Gilles de Gennes in 1969.[1][2] The phenomonological theory uses the Q {\displaystyle \mathbf {Q} } tensor as an order parameter in expandiing the free energy density.[3][4]

Mathematical description

The NI transition is a first-order phase transition, albeit it is very weak. The order parameter is the Q {\displaystyle \mathbf {Q} } tensor, which is symmetric, traceless, second-order tensor and vanishes in the isotripic liquid phase. We shall consider a uniaxial Q {\displaystyle \mathbf {Q} } tensor, which is defined by

Q = S ( n n 1 3 I ) {\displaystyle \mathbf {Q} =S\left(\mathbf {n} \mathbf {n} -{\frac {1}{3}}\mathbf {I} \right)}

where S = S ( T ) {\displaystyle S=S(T)} is the scalar order parameter and n {\displaystyle \mathbf {n} } is the director. The Q {\displaystyle \mathbf {Q} } tensor is zero in the isotropic liquid phase since the scalar order parameter S {\displaystyle S} is zero, but becomes non-zero in the nematic phase.

Near the NI transition, the (Helmholtz or Gibbs) free energy density F {\displaystyle {\mathcal {F}}} is expanded about as

F = F 0 + 1 2 A ( T ) Q i j Q j i 1 3 B ( T ) Q i j Q j k Q k i + 1 4 C ( T ) ( Q i j Q i j ) 2 {\displaystyle {\mathcal {F}}={\mathcal {F}}_{0}+{\frac {1}{2}}A(T)Q_{ij}Q_{ji}-{\frac {1}{3}}B(T)Q_{ij}Q_{jk}Q_{ki}+{\frac {1}{4}}C(T)(Q_{ij}Q_{ij})^{2}}

or more compactly

F = F 0 + 1 2 A ( T ) t r ( Q 2 ) 1 3 B ( T ) t r ( Q 3 ) + + 1 4 C ( T ) [ t r ( Q 2 ) ] 2 . {\displaystyle {\mathcal {F}}={\mathcal {F}}_{0}+{\frac {1}{2}}A(T)\mathrm {tr} (\mathbf {Q} ^{2})-{\frac {1}{3}}B(T)\mathrm {tr} (\mathbf {Q} ^{3})++{\frac {1}{4}}C(T)[\mathrm {tr} (\mathbf {Q} ^{2})]^{2}.}

Further, we can expand A ( T ) = a ( T T ) + {\displaystyle A(T)=a(T-T_{*})+\cdots } , B ( T ) = b + {\displaystyle B(T)=b+\cdots } and C ( T ) = c + {\displaystyle C(T)=c+\cdots } with ( a , b , c ) {\displaystyle (a,b,c)} being three positive constants. Now substituting the Q {\displaystyle \mathbf {Q} } tensor results in[5]

F F 0 = a 3 ( T T ) S 2 2 b 27 S 3 + c 9 S 4 . {\displaystyle {\mathcal {F}}-{\mathcal {F}}_{0}={\frac {a}{3}}(T-T_{*})S^{2}-{\frac {2b}{27}}S^{3}+{\frac {c}{9}}S^{4}.}

This is minimized when

3 a ( T T ) b S 2 + 2 c S 3 = 0. {\displaystyle 3a(T-T_{*})-bS^{2}+2cS^{3}=0.}

The two required solutions of this equation are

Isotropic: S I = 0 , Nematic: S N = b 4 c [ 1 + 1 24 a c b 2 ( T T ) ] > 0. {\displaystyle {\begin{aligned}{\text{Isotropic:}}&\,\,S_{I}=0,\\{\text{Nematic:}}&\,\,S_{N}={\frac {b}{4c}}\left[1+{\sqrt {1-{\frac {24ac}{b^{2}}}(T-T_{*})}}\,\right]>0.\end{aligned}}}

The NI transition temperature T N I {\displaystyle T_{NI}} is not simply equal to T {\displaystyle T_{*}} (which would be the case in second-order phase transition), but is given by

T N I = T + b 2 27 a c , S N I = b 3 c {\displaystyle T_{NI}=T_{*}+{\frac {b^{2}}{27ac}},\quad S_{NI}={\frac {b}{3c}}}

S N I {\displaystyle S_{NI}} is the scalar order parameter at the transition.

References

  1. ^ De Gennes, P. G. (1969). Phenomenology of short-range-order effects in the isotropic phase of nematic materials. Physics Letters A , 30 (8), 454-455.
  2. ^ De Gennes, P. (1971). Short range order effects in the isotropic phase of nematics and cholesterics. Molecular Crystals and Liquid Crystals, 12(3), 193-214.
  3. ^ De Gennes, P. G., & Prost, J. (1993). The physics of liquid crystals (No. 83). Oxford university press.
  4. ^ Mottram, N. J., & Newton, C. J. (2014). Introduction to Q-tensor theory. arXiv preprint arXiv:1409.3542.
  5. ^ Kleman, M., & Lavrentovich, O. D. (Eds.). (2003). Soft matter physics: an introduction. New York, NY: Springer New York.