Quantum Dot-Organic Molecule Conjugates as Hosts for Photogenerated Spin Qubit Pairs

被引:8
作者
Lee, Autumn Y. [1 ]
Colleran, Troy A. [1 ]
Jain, Amisha [1 ]
Niklas, Jens [2 ]
Rugg, Brandon K. [3 ]
Mani, Tomoyasu [4 ]
Poluektov, Oleg G. [2 ]
Olshansky, Jacob H. [1 ]
机构
[1] Amherst Coll, Dept Chem, Amherst, MA 01002 USA
[2] Argonne Natl Lab, Chem Sci & Engn Div, Lemont, IL 60439 USA
[3] Natl Renewable Energy Lab, Chem & Nanosci Ctr, Golden, CO 80401 USA
[4] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
基金
美国国家科学基金会;
关键词
CORRELATED RADICAL PAIRS; CHARGE-SEPARATED STATE; ELECTRON-SPIN; EPR-SPECTRA; POLARIZATION; SIZE; RELAXATION; MECHANISMS; COMPLEXES; COHERENCE;
D O I
10.1021/jacs.2c11952
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:4372 / 4377
页数:6
相关论文
共 58 条
[1]   ZnO-Based Dye-Sensitized Solar Cells [J].
Anta, Juan A. ;
Guillen, Elena ;
Tena-Zaera, Ramon .
JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (21) :11413-11425
[2]   High-Frequency EPR and ENDOR Spectroscopy on Semiconductor Quantum Dots [J].
Baranov, Pavel G. ;
Orlinskii, Sergei B. ;
Donega, Celso de Mello ;
Schmidt, Jan .
APPLIED MAGNETIC RESONANCE, 2010, 39 (1-2) :151-183
[3]   ELECTRON-SPIN-RESONANCE OF SPIN-CORRELATED RADICAL PAIRS [J].
BUCKLEY, CD ;
HUNTER, DA ;
HORE, PJ ;
MCLAUCHLAN, KA .
CHEMICAL PHYSICS LETTERS, 1987, 135 (03) :307-312
[4]   Evidence for photo-induced charge separation between dye molecules adsorbed to aluminium oxide surfaces [J].
Cappel, Ute B. ;
Moia, Davide ;
Bruno, Annalisa ;
Vaissier, Valerie ;
Haque, Saif A. ;
Barnes, Piers R. F. .
SCIENTIFIC REPORTS, 2016, 6
[5]   EPR investigation of photoinduced radical pair formation and decay to a triplet state in a carotene-porphyrin-fullerene triad [J].
Carbonera, D ;
Di Valentin, M ;
Corvaja, C ;
Agostini, G ;
Giacometti, G ;
Liddell, PA ;
Kuciauskas, D ;
Moore, AL ;
Moore, TA ;
Gust, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (18) :4398-4405
[6]   Photoselective DNA Hairpin Spin Switches [J].
Carmieli, Raanan ;
Thazhathveetil, Arun K. ;
Lewis, Frederick D. ;
Wasielewski, Michael R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (30) :10970-10973
[7]   SPIN-POLARIZED ELECTRON-PARAMAGNETIC RESONANCE-SPECTRA OF RADICAL PAIRS IN MICELLES - OBSERVATION OF ELECTRON-SPIN SPIN INTERACTIONS [J].
CLOSS, GL ;
FORBES, MDE ;
NORRIS, JR .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (13) :3592-3599
[8]  
DiMagno T. J., 2013, PHOTOSYNTHETIC REACT, P105
[9]  
DiVincenzo DP, 2000, FORTSCHR PHYS, V48, P771, DOI 10.1002/1521-3978(200009)48:9/11<771::AID-PROP771>3.0.CO
[10]  
2-E