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tweak the first flow chapter
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143
src/flow.tex
143
src/flow.tex
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@ -16,45 +16,40 @@ treated with the methods developed in here as is shown
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\cref{sec:general_obs}.
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\cref{sec:general_obs}.
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The generalization to multiple baths \cref{sec:multibath} and time
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The generalization to multiple baths \cref{sec:multibath} and time
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depend Hamiltonians \cref{sec:timedep} is straight forward.
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depend Hamiltonians \cref{sec:timedep} will present itself as straight
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forward.
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\section{Bath Energy Change of a Zero Temperature Bath}
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\section{Bath Energy Change of a Zero Temperature Bath}
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\label{sec:flow_lin}
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\label{sec:flow_lin}
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\begin{itemize}
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\item illustrate the general idea with the simplest case
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possible:
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zero T, one bath, no modulation etc, linear theory
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\item this is also the ``historical order''
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\item hint at straight forward generalizations in further sections
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\end{itemize}
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As in~\cite{Hartmann2017Dec} we choose\fixme{This section needs a lot
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In this section we demonstrate upon the example of the change of the
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of love! More Explainations etc..}
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bath energy, here defined with a negative sign as ``flow'' out of the
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bath,
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\begin{equation}
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\label{eq:heatflowdef}
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J = - \dv{\ev{H_\bath}}{t}
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\end{equation}
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how collective bath observables may be obtained from the formalism
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presented in \cref{sec:nmqsd_basics,sec:hops_basics}.
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The simplest version of the general model \cref{eq:generalmodel} is
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given by
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\begin{equation}
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\begin{equation}
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\label{eq:totalH}
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\label{eq:totalH}
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H = H_\sys + \underbrace{LB^† + L^† B}_{H_\inter} + H_\bath
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H = H_\sys + \underbrace{LB^† + L^† B}_{H_\inter} + H_\bath
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\end{equation}
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\end{equation}
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with the system hamiltonian \(H_\sys\), the bath hamiltonian
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with the system hamiltonian \(H_\sys\), the bath Hamiltonian
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\begin{equation}
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\(H_\bath = ∑_\lambda ω_\lambda a_{λ}^† a_{λ}\), the bath coupling
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\label{eq:bathh}
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system operator \(L\) and the bath coupling bath operator
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H_\bath = ∑_\lambda ω_\lambda a^† a,
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\(B=∑_{\lambda} g_{\lambda} a_{\lambda}\) which define the interaction
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\end{equation}
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Hamiltonian \(H_\inter\).
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the bath coupling system operator \(L\) and the bath coupling bath
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operator
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\begin{equation}
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\label{eq:bop}
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B=∑_{\lambda} g_{\lambda} a_{\lambda}
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\end{equation}
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which define the interaction hamiltonian \(H_\inter\).
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We define the heat flow out of the system as in~\cite{Kato2015Aug}
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We do not consider external modulation of the Hamiltonian, finite
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through
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temperatures or multiple baths, as we are interested in the essentials
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\begin{equation}
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of the procedure. With this approach we also follow the ``historical''
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\label{eq:heatflowdef}
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order of derivation.
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J = - \dv{\ev{H_\bath}}{t}.
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\end{equation}
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Working, for now, in the Schr\"odinger picture, the Ehrenfest theorem
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Working, for now, in the Schr\"odinger picture the Ehrenfest theorem
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can be employed to find
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can be employed to find
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\begin{equation}
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\begin{equation}
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\label{eq:ehrenfest}
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\label{eq:ehrenfest}
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@ -95,31 +90,24 @@ expression for \(J\) follows
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\end{equation}
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\end{equation}
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From this point on, we will assume the interaction picture and drop
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From this point on, we will assume the interaction picture and drop
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the \(I\) subscript. The two summands yield different expressions in
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the \(I\) subscript. The two summands yield different expressions when
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terms of the NMQSD. For use with HOPS with the final goal of
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evaluated in terms of the NMQSD.
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utilizing the auxiliary states the expression \(\ev{L^†∂_t B(t)}\)
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should be evaluated. When considering the complex conjugate of this
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expression, we find a formula involving the derivative of the driving
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stochastic process. This is undesirable as it does not exist for all
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bath correlation functions\footnote{Only for BCFs that are smooth at
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\(τ=0\).} and expressions involving the process directly are alleged
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to converge slower. The last fact may be explained by the fact, that
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one needs quite a lot of sample paths of the process for the mean of
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those sample paths to converge to zero. On the other hand, the first
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hierarchy states do contain an integral of-sorts of the sample paths
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and are not as sensitive to fluctuations.
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For use with HOPS with the final goal of utilizing the auxiliary
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states the expression \(\ev{L^†∂_t B(t)}\) should be evaluated.
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We calculate
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We calculate
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\begin{equation}
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\begin{equation}
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\label{eq:interactev}
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\label{eq:interactev}
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\ev{L^†∂_t B(t)}=\ev{L^†∂_t B(t)}{\psi(t)} =
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\ev{L^†∂_t B(t)}=\ev{L^†∂_t B(t)}{\psi(t)} =
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∫ \braket{\psi(t)}{z}\mel{z}{L^†∂_tB(t)}{\psi(t)}\frac{\dd[2]{z}}{\pi^N},
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∫ \braket{\psi(t)}{\vb{z}}\mel{\vb{z}}{L^†∂_tB(t)}{\psi(t)}\frac{\dd[2]{\vb{z}}}{\pi^N},
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\end{equation}
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\end{equation}
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where \(N\) is the total number of environment oscillators and
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where \(N\) is the total number of environment oscillators and
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\(z=\qty(z_{\lambda_1}, z_{\lambda_2}, \ldots)\). Using
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\(\vb{z}=\qty(z_{\lambda_1}, z_{\lambda_2}, \ldots)\).
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\(\mel{z}{a_λ}{ψ}= ∂_{z^\ast_λ}\braket{z}{ψ}=
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∂_{z^\ast_λ}\ket{ψ(z^\ast,t)}\) and
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Using
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\(\mel{z}{a_λ^\dag}{ψ}= z_λ^\ast\braket{z}{ψ}\) we find,
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\(\mel{\vb{z}}{a_λ}{ψ}= ∂_{z^\ast_λ}\braket{\vb{z}}{ψ}=
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∂_{z^\ast_λ}\ket{ψ(\vb{z}^\ast,t)}\) and
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\(\mel{\vb{z}}{a_λ^\dag}{ψ}= z_λ^\ast\ket{ψ(\vb{z}^\ast,t)}\) we find
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\begin{equation}
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\begin{equation}
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\label{eq:nmqsdficate}
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\label{eq:nmqsdficate}
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\begin{aligned}
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\begin{aligned}
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@ -129,18 +117,21 @@ where \(N\) is the total number of environment oscillators and
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&= ∫_0^t ∑_\lambda g_\lambda
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&= ∫_0^t ∑_\lambda g_\lambda
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\qty(∂_t \eu^{-\iω_\lambda
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\qty(∂_t \eu^{-\iω_\lambda
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t})\pdv{η_s^\ast}{z^\ast_\lambda}\fdv{\ket{\psi(z^\ast,t)}}{η^\ast_s}\dd{s}\\
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t})\pdv{η_s^\ast}{z^\ast_\lambda}\fdv{\ket{\psi(z^\ast,t)}}{η^\ast_s}\dd{s}\\
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&= -\i∫_0^t\dot{\alpha}(t-s)\fdv{\ket{\psi(η^\ast,t)}}{η^\ast_s}\dd{s},
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&= -\i∫_0^t\dot{\alpha}(t-s)\fdv{\ket{\psi(η^\ast_{t},t)}}{η^\ast_s}\dd{s},
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\end{aligned}
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\end{aligned}
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\end{equation}
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\end{equation}
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where
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where
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\(η^\ast_t\equiv -\i ∑_\lambda g^\ast_\lambda z^\ast_\lambda
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\(η^\ast_t\equiv -\i ∑_\lambda g^\ast_\lambda z^\ast_\lambda
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\eu^{\iω_\lambda t}\) which led to the chain rule
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\eu^{\iω_\lambda t}\) which led to the chain rule
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\(∂_{z^\ast_λ}=∫\dd{s}\pdv{η_s^\ast}{z^\ast_λ}\fdv{}{η_s^\ast}\). With
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\(∂_{z^\ast_λ}=∫\dd{s}\pdv{η_s^\ast}{z^\ast_λ}\fdv{}{η_s^\ast}\)
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this we obtain
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exactly corresponding to the procedure in
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\cref{sec:nmqsd_basics}.
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With this we obtain
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\begin{equation}
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\begin{equation}
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\label{eq:steptoproc}
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\label{eq:steptoproc}
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\ev{L^†∂_t B(t)} = -\i \mathcal{M}_{η^\ast}\bra{\psi(η,
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\ev{L^†∂_t B(t)} = -\i \mathcal{M}_{η^\ast}\bra{\psi(η_{t},
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t)}L^†∫_0^t\dd{s} \dot{\alpha}(t-s)\fdv{η^\ast_s} \ket{\psi(η^\ast,t)}.
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t)}L^†∫_0^t\dd{s} \dot{\alpha}(t-s)\fdv{η^\ast_s} \ket{\psi(η^\ast_{t},t)}.
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\end{equation}
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\end{equation}
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Defining
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Defining
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\begin{equation}
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\begin{equation}
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@ -169,32 +160,23 @@ Interestingly one finds that
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\ev{L∂_t B^†(t)} = \i∫\frac{\dd[2]{z}}{\pi^N}
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\ev{L∂_t B^†(t)} = \i∫\frac{\dd[2]{z}}{\pi^N}
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\dot{η}_t^\ast \mel{\psi(η,t)}{L}{\psi(η^\ast,t)}.
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\dot{η}_t^\ast \mel{\psi(η,t)}{L}{\psi(η^\ast,t)}.
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\end{equation}
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\end{equation}
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However, this approach becomes more complicated in the nonlinear
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This expression is undesirable as it does not exist for all bath
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method.
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correlation functions\footnote{Only for BCFs that are smooth at
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The previous expression has the advantage
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\(τ=0\).} and expressions involving the process directly are alleged
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that we utilize the first hierarchy states that are already being
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to converge slower. Furthermore, this approach becomes more
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calculated as a byproduct.
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complicated in the nonlinear method. We will briefly return to this
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issue in \cref{sec:general_obs}.
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In the language of~\cite{Hartmann2021Aug} we can generalize to
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In the language of \cref{sec:hops_basics} we can generalize to
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\(\alpha(t) = ∑_i G_i \eu^{-W_i t}\) and thus
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\(\alpha(t) = ∑_i G_i \eu^{-W_i t}\) obtaining
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\begin{equation}
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\label{eq:hopsflowrich}
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J(t) = ∑_\mu\frac{G_\mu W_\mu}{\bar{g}_\mu} \i\mathcal{M}_{η^\ast}\bra{\psi^{(0)}(η,
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t)}L^†\ket{\psi^{\vb{e}_\mu}(η^\ast,t)} + \cc,
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\end{equation}
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where \(\psi^{\vb{e}_\mu}\) is the \(\mu\)-th state of the first
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hierarchy and \(\bar{g}_\mu\) is an arbitrary scaling introduced in
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the definition of the hierarchy in~\cite{Hartmann2021Aug} to help with
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the scaling of the norm.
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With the new ``fock-space'' normalization (see \cref{eq:dops_full})
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however the expression becomes
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\begin{equation}
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\begin{equation}
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\label{eq:hopsflowfock}
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\label{eq:hopsflowfock}
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J(t) = - ∑_\mu\sqrt{G_\mu}W_\mu
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J(t) = - ∑_\mu\sqrt{G_\mu}W_\mu
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\mathcal{M}_{η^\ast}\bra{\psi^{(0)}(η,
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\mathcal{M}_{η^\ast}\bra{\psi^{(0)}(η,
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t)}L^†\ket{\psi^{\vb{e}_\mu}(η^\ast,t)} + \cc.
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t)}L^†\ket{\psi^{\vb{e}_\mu}(η^\ast,t)} + \cc,
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\end{equation}
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\end{equation}
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where \(\ket{\psi^{\vb{e}_\mu}(η^\ast,t)}\) are the first hierarchy
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states.
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\section{Generalization to the Nonlinear Theory}
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\section{Generalization to the Nonlinear Theory}
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\label{sec:nonlin_flow}
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\label{sec:nonlin_flow}
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@ -519,12 +501,17 @@ the form
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The corresponding version of~\cref{eq:f_ex_zero} would only depend on
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The corresponding version of~\cref{eq:f_ex_zero} would only depend on
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the zeroth order state and the stochastic processes. It has been
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the zeroth order state and the stochastic processes. It has been
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observed that expressions involving the stochastic process directly
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observed that expressions involving the stochastic process directly
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tend to converge slower. However this statement comes without
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tend to converge slower. However, this statement comes without
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empirical proof and its verification may be left to future
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empirical proof and its verification may be left to future study. An
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study. Also, this alternative method could be used convergence and
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explanation may be that the first hierarchy states fluctuate about
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their average dynamics whereas the stochastic process fluctuates
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around zero and does not contain much information about the actual
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dynamics.
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Also, this alternative method could be used convergence and
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consistency check, as expressions of the form~\cref{eq:with_process}
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consistency check, as expressions of the form~\cref{eq:with_process}
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only involve the hierarchy cutoff and the exponential expansion of the BCF
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only involve the hierarchy cutoff and the exponential expansion of the
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in an indirect manner.
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BCF in an indirect manner.
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\subsection{Interaction Energy}
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\subsection{Interaction Energy}
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\label{sec:intener}
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\label{sec:intener}
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