The free-energy profile along a geometric parameter
can be scanned by an approximate slow-growth
approach[1].
In this method, the value of
is linearly changed
from the value characteristic for the initial state (1) to that for
the final state (2) with a velocity of transformation
.
The resulting work needed to perform a transformation
can be computed as:
![{\displaystyle
w^{irrev}_{1 \rightarrow 2}=\int_{{\xi(1)}}^{{\xi(2)}} \left ( \frac{\partial {V(q)}} {\partial \xi} \right ) \cdot \dot{\xi}\, dt.
}](/wiki/index.php?title=Special:MathShowImage&hash=a4159c3a994fbee7ebfeb9edc29664f5&mode=mathml)
In the limit of infinitesimally small
, the work
corresponds to the free-energy difference between the the final and initial state.
In the general case,
is the irreversible work related
to the free energy via Jarzynski's identity[2]:
![{\displaystyle
exp^{-\frac{\Delta A_{1 \rightarrow 2}}{k_B\,T}}=
\bigg \langle exp^{-\frac{w^{irrev}_{1 \rightarrow 2}}{k_B\,T}} \bigg\rangle.
}](/wiki/index.php?title=Special:MathShowImage&hash=47e8f9d69a817273c11b2f0016f9a9ea&mode=mathml)
Note that calculation of the free-energy via this equation requires
averaging of the term
over many realizations of the
transformation.
Detailed description of the simulation protocol that employs Jarzynski's identity
can be found in reference [3].
References
- ↑ T. K. Woo, P. M. Margl, P. E. Blochl, and T. Ziegler, J. Phys. Chem. B 101, 7877 (1997).
- ↑ C. Jarzynski, Phys. Rev. Lett. 78, 2690 (1997).
- ↑ . Oberhofer, C. Dellago, and P. L. Geissler, J. Phys. Chem. B 109, 6902 (2005).