Interfacing a Potential Purely Organic Molecular Quantum Bit with a Real-Life Surface
Source abstract
Abstract
By using a multidisciplinary and multitechnique approach, we have addressed the issue of attaching a molecular quantum bit to a real surface. First, we demonstrate that an organic derivative of the pyrene-Blatter radical is a potential molecular quantum bit. Our study of the interface of the pyrene-Blatter radical with a copper-based surface reveals that the spin of the interface layer is not canceled by the interaction with the surface and that the Blatter radical is resistant in presence of molecular water. Although the measured pyrene-Blatter derivative quantum coherence time is not the highest value known, this molecule is known as a "super stable" radical. Conversely, other potential qubits show poor thin film stability upon air exposure. Therefore, we discuss strategies to make molecular systems candidates as qubits competitive, bridging the gap between potential and real applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Molecular Junctions and Nanostructures · Quantum and electron transport phenomena · Organic Light-Emitting Diodes Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Physical and Theoretical Chemistry, University of Tübingen, 72076 Tübingen, Germany
CNR-NANO Istituto Nanoscienze, Centro S3, 41125 Modena, Italy
Institute of Physical Chemistry, University of Stuttgart, 70569 Stuttgart, Germany
Central European Institute of Technology, CEITEC BUT, Purkyňova 656/123, 61600 Brno, Czech Republic
Department of Chemistry, University of Nebraska−Lincoln, Lincoln, Nebraska 68588-0304, United States
Funding
Deutsche Forschungsgemeinschaft · Verband der Chemischen Industrie
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