Phillips 66 Company

Joseph Bullock

Brian J Worfolk

Hualong Pan

Kathy Woody

Taeshik Earmme

Nneka Uguru Eboagwu

A process of reacting (SnO)ZnOand a fullerene dopant to produce an electron transport layer. (SnO)ZnOis produced from reacting an organic Zn precursor in the amounts of (1-); an organic Sn precursor in the amounts of y; and a base in the amount of (1-) to 1.

Formation of films for organic photovoltaics

An organic photovoltaic device comprising an electron transport layer disposed between an anode and a polymer layer. In this organic photovoltaic device the polymer layer can also be disposed between the electron transport layer and a cathode. The electron transport layer comprises (AO)BOwith an optional fullerene dopant. The polymer comprises a molecular complex comprising wherein X1 and X2 are independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, ester, ketone, amide and aryl groups; R1, R2, R1' and R2&#x2032; are side chains independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, alkylthio, ester, ketone and aryl groups; R3 are selected from the group consisting of alkyl group, alkoxy group, aryl groups and combinations thereof; G is an aryl group; and wherein the thiophene groups are unsymmetrical.

Unsymmetrical benzothiadiazole-based molecular complexes in organic photovoltaic devices

A process of dissolving in a solvent to produce a first mixture. To the first mixture a reagent is added to produce a second mixture. A H&#x2014;N&#x2014;R'&#x2014;R&#x2033; is then added to the second mixture to produce a third mixture. The third mixture is then refluxed to produce 

Process of manufacturing an electron transport material

A process of dissolving in a solvent to produce a first mixture. To the first mixture a reagent is added to produce a second mixture. A H&#x2014;R'&#x2014;R&#x2033; is then added to the second mixture to produce a third mixture. The third mixture is then refluxed to produce 

A process of dissolving [6,6]-phenyl-C-butyric-N-2-dimethylaminoethyl ester in a solvent to produce a first mixture. A reagent is added to the first mixture to produce a second mixture. The second mixture is then refluxed to produce [6,6]-phenyl-C-butyric-N-2-trimethylammonium ethyl ester iodide.

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Bartlesville, OK, United States of America

Joseph Bullock