学术文献库

Excited states of molecules lie in the heart of photochemistry and chemical reactions. The recent development in quantum computational chemistry leads to inventions of a variety of algorithms that calculate the excited states of molecules on near-term quantum computers, but they require more computational burdens than the algorithms for calculating the ground states. In this study, we propose a scheme of supervised quantum machine learning which predicts the excited-state properties of molecules only from their ground state wavefunction resulting in reducing the computational cost for calculating the excited states. Our model is comprised of a quantum reservoir and a classical machine learning unit which processes the measurement results of single-qubit Pauli operators with the output state from the reservoir. The quantum reservoir effectively transforms the single-qubit operators into complicated multi-qubit ones which contain essential information of the system, so that the classical machine learning unit may decode them appropriately. The number of runs for quantum computers is saved by training only the classical machine learning unit, and the whole model requires modest resources of quantum hardware that may be implemented in current experiments. We illustrate the predictive ability of our model by numerical simulations for small molecules with and without noise inevitable in near-term quantum computers. The results show that our scheme well reproduces the first and second excitation energies as well as the transition dipole moment between the ground states and excited states only from the ground state as an input. We expect our contribution will enhance the applications of quantum computers in the study of quantum chemistry and quantum materials.