posted on 2019-02-06, 00:00authored byJacob
H. Olshansky, Matthew D. Krzyaniak, Ryan M. Young, Michael R. Wasielewski
The
ability to prepare physical qubits in specific initial quantum
states is a critical requirement for their use in quantum information
science (QIS). Subnanosecond photoinduced electron transfer in a structurally
well-defined donor–acceptor system can be used to produce an
entangled spin qubit (radical) pair in a pure initial singlet state
fulfilling this criterion. Synthetic DNA is a promising platform on
which to build spin qubit arrays with fixed spatial relationships;
therefore, we have prepared a series of DNA hairpins in which naphthalenediimide
(NDI) is the chromophore/acceptor hairpin linker, variable-length
diblock A- and G-tracts are intermediate donors, and a stilbenediether
(Sd) is the terminal donor. Photoexcitation of NDI in these DNA hairpins
generates high-yield, long-lived, entangled spin qubit pairs at 85
K, and time-resolved and pulse electron paramagnetic resonance (EPR)
spectroscopies are used to probe their spin dynamics. Specifically,
measurements of the distance-dependent dipolar coupling between the
two spins are used to obtain the average spin qubit pair distance
in the absence of the terminal Sd donor and reveal that one of the
spins is fully delocalized across up to five adjacent guanines in
a G-tract on the EPR time scale. We have recently shown that extensive
spin hopping between degenerate sites accessible to one spin of the
pair may result in spin decoherence. However, we observe a strong
out-of-phase electron spin echo envelope modulation (OOP-ESEEM) signal
from the NDI•––Sd•+ spin qubit pair in DNA hairpins showing that spin coherence is maintained
across a 2 adenine A-tract followed by a 2–4 guanine G-tract
as a result of rapid spin transport to Sd. These results demonstrate
that pulse-EPR can manipulate coherent spin states in DNA hairpins,
which is essential for quantum gate operations relevant to QIS applications.