Organic spintronic devices and methods for making the same
An organic spintronic photovoltaic device ( 100 ) having an organic electron active layer ( 102 ) functionally associated with a pair of electrodes ( 104, 106 ). The organic electron active layer ( 102 ) can include a spin active molecular radical distributed in the active layer ( 102 ) which increases spin-lattice relaxation rates within the active layer ( 102 ). The increased spin lattice relaxation rate can also influence the efficiency of OLED and charge mobility in FET devices.
1. An organic spintronic device, comprising:
a) an organic electron active layer which is a bulk heterojunction including a donor material blended with an acceptor material, said organic electron active layer including a spin active molecular radical distributed in the organic electron active layer which increases spin-lattice relaxation rates within the organic electron active layer, wherein the acceptor material comprises a fullerene and the spin active molecular radical comprises galvinoxyl (2,6-Di-tert-butyl-α-(3,5-di-tert-butyl-4-oxo-2,5-cyclohexadien-1-ylidene)-ptolyloxy)
and
b) a pair of electrodes functionally associated with the organic electron active layer to complete a circuit which transfers electrons via the organic electron active layer.
2. The device of claim 1 , wherein the spin active molecular radical distributed in the organic electron active layer induces a spin flip in at least one of a spin ½ electron and a hole to result in a spin triplet state having an increased exciton diffusion length.
3. The device of claim 1 , wherein the organic spintronic device is an organic photovoltaic.
4. The device of claim 1 , wherein the organic electron active layer is comprised of P3HT/PCBM.
5. The device of claim 1 , wherein the spin active molecular radical is a ½ spin molecular radical.
6. The device of claim 1 , wherein the spin active molecular radical further comprises:
a) TEMPO (2,2,6,6-Tetramethylpiperidine 1-oxyl)
b) 4-Amino-TEMPO
c) 4-Hydroxy-TEMPO benzoate
d) 4 -[(1-Hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)amino]-4-oxo-2-butenoic acid
e) 1-Hydroxy-2,2,5,5-tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid
f) 4-Phenyl-2,2,5,5-tetramethyl-3-imidazolin-1-yloxy
g) 3-(3-(2-IODO-ACETAMIDO)-PROPYL-CARBAMOYL)-PROXYL
h) BDPA complex with benzene (1:1)
i) N,N-Bis(4-methoxyphenyl)hydroxylamine
j) Tris(1-hydroxy-2,2,4,6,6-pentamethyl-4-piperidinyl)phosphinetricarboxylate
k) Bis(1-hydroxy-2,2,4,6,6-pentamethyl-4-piperidinyl)oxalate
l) Trioctylphosphine oxide (TOPO);
m) M@C60, where M is Gd-157 (stable 3/2 spin nanoparticle); or
n) combinations thereof.
7. The device of claim 6 , wherein the spin active molecular radical further comprises TEMPO or TOPO.
8. The device of claim 1 , wherein the spin active molecular radical is present from 0.1 wt % to about 10 wt % of the organic electron active layer.
9. The device of claim 8 , wherein the spin active molecular radical further comprises TEMPO and is present at about 5 wt % of the organic electron active layer.
10. The device of claim 1 , wherein the organic electron active layer comprises a donor polymer and an acceptor molecule.
11. The device of claim 10 , wherein the donor polymer includes 2-methoxy-5-(2′-ethylhexyloxy)phenylene vinylene polymer (MEHPPV), 1,4-bis[(4-styryl)styryl]-2-methoxy-5-(2′-ethylhexoxy)benzene polymer, poly(2-methoxy,5-(3′,7′-dimethyloctyloxy)-1,4-phenylenevinylene (MDMOPPV), poly(2,5-(2-ethylhexyloxy)-1,4-phenylenevinylene) (BEHPPV), or regio regular poly(3-hexylthiophene).
12. The device of claim 10 , wherein the acceptor molecule includes fullerene C60, PCBM (soluble C60), modified fullerenes, C70, C84, soluble modified fullerene, or Di-PCBM.
13. The device of claim 1 , wherein the pair of electrodes include an indium tin oxide anode.
14. The device of claim 1 , wherein the pair of electrodes include a cathode which further includes a conductive metal layer and an electron transport layer, said electron transport layer located between the organic electron active layer and the conductive metal layer.