We introduce a top-ranked cycle flux ranking scheme of network analysis to assess the performance of molecular junction solar cells. By mapping the Lindblad master equation to the quantum-transition network, we propose a microscopic Hamiltonian description underpinning the rate equations commonly used to characterize molecular photocells. Our approach elucidates the paramount significance of edge flux and unveils two pertinent electron transfer pathways that play equally important roles in robust photocurrent generation. Furthermore, we demonstrate that nonradiative loss processes impede the maximum power efficiency of photocells, which may otherwise be above the Curzon-Ahlborn limit. These findings shed light on the intricate functionalities that govern molecular photovoltaics and offer a comprehensive approach to address them in a systematic way. Link 

We introduce a simplified model for a three-terminal quantum thermocouple consisting of two strongly coupled quantum dots. To elucidate spin-dependent Seebeck and Peltier effects, we employ a microscopic Hamiltonian and map the Lindblad master equation onto a quantum transition network, capturing the key working principles for both reciprocal effects. Our analysis reveals quantum thermodynamic networks encompassing both Coulomb interaction and spin-flipping processes, lead to the emergence of spin-thermolectric effects. Using algebraic graph theory, we recover the phenomenological law of irreversible thermodynamics from the stochastic version of the entropy production rate expressed in terms of cycle flux and cycle forces. Remarkably, Onsager reciprocity and Kelvin relation for transport coefficients find their premises in the properties of cycle flux trajectories within the quantum transition network. This underscores the universal generality of thermodynamic principles across classical and quantum realms, despite their fundamentally different basis from classical laws of irreversible thermodynamics relying on local equilibrium assumptions. Link