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Title: A molecular quantum spin network controlled by a single qubit. Author: Schlipf L, Oeckinghaus T, Xu K, Dasari DBR, Zappe A, de Oliveira FF, Kern B, Azarkh M, Drescher M, Ternes M, Kern K, Wrachtrup J, Finkler A. Journal: Sci Adv; 2017 Aug; 3(8):e1701116. PubMed ID: 28819646. Abstract: Scalable quantum technologies require an unprecedented combination of precision and complexity for designing stable structures of well-controllable quantum systems on the nanoscale. It is a challenging task to find a suitable elementary building block, of which a quantum network can be comprised in a scalable way. We present the working principle of such a basic unit, engineered using molecular chemistry, whose collective control and readout are executed using a nitrogen vacancy (NV) center in diamond. The basic unit we investigate is a synthetic polyproline with electron spins localized on attached molecular side groups separated by a few nanometers. We demonstrate the collective readout and coherent manipulation of very few (≤ 6) of these S = 1/2 electronic spin systems and access their direct dipolar coupling tensor. Our results show that it is feasible to use spin-labeled peptides as a resource for a molecular qubit-based network, while at the same time providing simple optical readout of single quantum states through NV magnetometry. This work lays the foundation for building arbitrary quantum networks using well-established chemistry methods, which has many applications ranging from mapping distances in single molecules to quantum information processing.[Abstract] [Full Text] [Related] [New Search]