@article{Shen2017,
abstract = {In classical computational chemistry, the coupled-cluster ansatz is one of the most commonly used ab initio methods, which is critically limited by its nonunitary nature. The unitary modification as an ideal solution to the problem is, however, extremely inefficient in classical conventional computation. Here, we provide experimental evidence that indeed the unitary version of the coupled-cluster ansatz can be reliably performed in a physical quantum system, a trapped-ion system. We perform a simulation on the electronic structure of a molecular ion (HeH+), where the ground-state energy surface curve is probed, the energies of the excited states are studied, and bond dissociation is simulated nonperturbatively. Our simulation takes advantages from quantum computation to overcome the intrinsic limitations in classical computation, and our experimental results indicate that the method is promising for preparing molecular ground states for quantum simulations.},
archivePrefix = {arXiv},
arxivId = {1506.00443},
author = {Shen, Yangchao and Zhang, Xiang and Zhang, Shuaining and Zhang, Jing Ning and Yung, Man Hong and Kim, Kihwan},
doi = {10.1103/PhysRevA.95.020501},
eprint = {1506.00443},
issn = {24699934},
journal = {Physical Review A},
number = {2},
title = {{Quantum implementation of the unitary coupled cluster for simulating molecular electronic structure}},
volume = {95},
year = {2017}
}

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