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In many applications, one assumes (often for simplicity) a linear coupling to the bath,
![$\displaystyle H_B[x]+H_{SB}[xq]$](img894.png) |
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![$\displaystyle \sum_{\alpha=1}^N \left[
\frac{p_\alpha^2}{2M_\alpha}+ \frac{1}{2...
...ha^2 \left(x_\alpha -
\frac{c_\alpha}{M_\alpha\Omega_\alpha^2}q\right)^2\right]$](img895.png) |
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![$\displaystyle \sum_{\alpha=1}^N \left[
\frac{p_\alpha^2}{2M_\alpha}+ \frac{1}{2...
...pha q x_\alpha
+\frac{1}{2}\frac{c_\alpha^2}{M_\alpha\Omega_\alpha^2}q^2\right]$](img896.png) |
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![$\displaystyle {\cal F}[q_{t'},q'_{t'}]$](img821.png) |
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Influence Functional |
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![$\displaystyle \Phi[q_{t'},q'_{t'}]$](img823.png) |
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(208) |
Here, the kernel
and the spectral density
are
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(209) |
Note that in this form, an additional term appears in
as a potential
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(210) |
Since the action
appears as
in the path integral for
and
in the path integral for
, we could absorb the counter term into
the influence phase as
Note that the entire information on the coupling to the bath is now
contained in the spectral density
, which we have defined following the
notation of Weiss, `Quantum Dissipative Systems'.
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Up: Applications: Linear Coupling, Damped
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Tobias Brandes
2004-02-18