The inherent spin polarization present in photogenerated spin-correlated radical pairs makes them promising candidates for quantum computing and quantum sensing applications. The spin states of these systems can be probed and manipulated with microwave pulses using electron paramagnetic resonance spectrometers. However, to date, there are no reports on magnetic resonance-based spin measurements of photogenerated spin-correlated radical pairs hosted on quantum dots. In the current work, we prepare dye molecule-inorganic quantum dot conjugates and show that they can produce photogenerated spin-polarized states. The dye molecule, D131, is chosen for its ability to undergo efficient charge separation, and the nanoparticle materials, ZnO quantum dots, are chosen for their promising spin properties. Transient and steady state optical spectroscopy performed on ZnO quantum dot-D131 conjugates shows that reversible photogenerated charge separation is occurring. Transient and pulsed electron paramagnetic resonance experiments are then performed on the photogenerated radical pair, which demonstrate that (1) the radical pair is polarized at moderate temperatures and well modeled by existing theories and (2) the spin states can be accessed and manipulated with microwave pulses. This work opens the door to a new class of promising qubit materials that can be photogenerated in polarized states and hosted by highly tailorable inorganic nanoparticles.
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http://dx.doi.org/10.1021/jacs.2c11952 | DOI Listing |
J Phys Chem A
October 2024
Department of Chemistry, Center for Molecular Quantum Transduction, and Paula M. Trienens Institute for Sustainability and Energy, Northwestern University, Evanston, Illinois 60208-3113, United States.
We report on new donor-chromophore-acceptor triads and where the BDX donor is 2,2,6,6-tetramethylbenzo[1,2-;4,5-]bis[1,3]dioxole, the ANI chromophore is 4-(-piperidinyl)naphthalene-1,8-dicarboximide, the NDI acceptor is naphthalene-1,8:4,5-bis(dicarboximide), and xy is a 2,5-xylyl spacer. The results on these compounds are compared to the analogous derivatives having a -methoxyaniline (MeOAn) as the donor. BDX has no nitrogen atoms and only a single hydrogen atom coupled to its unpaired electron spin, and therefore has significantly decreased hyperfine interactions compared to MeOAn.
View Article and Find Full Text PDFJ Am Chem Soc
July 2023
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, United States.
Quantum sensing affords the possibility of using quantum entanglement to probe electromagnetic fields with exquisite sensitivity. In this work, we show that a photogenerated spin-correlated radical ion pair (SCRP) can be used to sense an electric field change created at one radical ion of the pair using molecular recognition. The SCRP is generated within a covalent donor-chromophore-acceptor system PXX-PMI-NDI, , where PXX = -xanthenoxanthene, PMI = 1,6-bis(--butylphenoxy)perylene-3,4-dicarboximide, and NDI = naphthalene-1,8:4,5-bis(dicarboximide).
View Article and Find Full Text PDFJ Chem Phys
May 2023
Department of Chemical Physics, University of Science and Technology of China, Hefei, Anhui 230026, China.
Singlet fission (SF) is a spin-allowed exciton multiplication process, in which a photogenerated singlet separates efficiently into two free triplets. Herein, we report an experimental study on the solution-phase intermolecular SF (xSF) in a prototype radical dianion system of PTCDA2-, which is produced from its neutral precursor PTCDA (i.e.
View Article and Find Full Text PDFJ Am Chem Soc
March 2023
Department of Chemistry, Amherst College, Amherst, Massachusetts 01002, United States.
The inherent spin polarization present in photogenerated spin-correlated radical pairs makes them promising candidates for quantum computing and quantum sensing applications. The spin states of these systems can be probed and manipulated with microwave pulses using electron paramagnetic resonance spectrometers. However, to date, there are no reports on magnetic resonance-based spin measurements of photogenerated spin-correlated radical pairs hosted on quantum dots.
View Article and Find Full Text PDFJ Am Chem Soc
September 2021
Department of Chemistry, Center for Molecular Quantum Transduction, and Institute for Sustainability and Energy at Northwestern, Northwestern University, Evanston, Illinois 60208-3113, United States.
More than a half century ago, the NMR spectra of diamagnetic products resulting from radical pair reactions were observed to have strongly enhanced absorptive and emissive resonances. At the same time, photogenerated radical pairs were discovered to exhibit unusual electron paramagnetic resonance spectra that also had such resonances. These non-Boltzmann, spin-polarized spectra were observed in both chemical systems as well as in photosynthetic reaction center proteins following photodriven charge separation.
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