Planarization over topography with molecular glass materials
AssigneeInternational Business Machines Corporation
InventorsRobert D. Allen, Mark W. Hart, Ratnam Sooriyakumaran
Life of this patent
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Abstract
Molecular glass based planarizing compositions for lithographic processing are disclosed. The processes generally include casting the planarizing composition onto a surface comprised of lithographic features, the planarizing composition comprising at least one molecular glass and at least one solvent; and heating the planarizing composition to a temperature greater than a glass transition temperature of the at least one molecular glass. Exemplary molecular glasses include polyhedral oligomeric silsesquioxane derivatives, calixarenes, cyclodextrin derivatives, and other non-polymeric large molecules.
Claims21
A lithographic process comprising:
- casting a planarizing composition onto a surface comprised of lithographic features, the planarizing composition comprising at least one molecular glass and at least one solvent;
- and
- heating the planarizing composition to a temperature greater than a glass transition temperature of the at least one molecular glass.
A process of lithographically patterning a layer comprised of topographical features, comprising:
- casting a planarizing composition onto the patterned layer, the planarizing composition comprising at least one molecular glass and at least one solvent;
- post apply baking the planarizing composition at a temperature greater than a glass transition temperature of the molecular glass;
- selectively etching a portion of the planarizing composition to expose a top surface of the topographical features defined by the patterned layer surface;
- and
- selectively etching the exposed patterned layer with respect to the planarizing composition.
A planarizing composition, comprising:
- a polyhedral oligomeric silsesquioxane selected from the group consisting of formulas (I)-(VI):
- wherein formula (I) is denoted by the formula T8R3, where T represents R3SiO3/2;
- wherein formula (II) is denoted by the formula Q8M8R1,R2,R3 where Q represents SiO4/2 and MR1,R2,R3 represents R1, R2, R3SiO1/2;
- wherein formula (III) is denoted by the formula T10R3, where T represents R3SiO3/2;
- wherein formula (IV) is denoted by the formula Q10M10R1,R2,R3 where Q represents SiO4/2 and MR1,R2,R3 represents R1, R2, R3SiO1/2;
- wherein formula (V) is denoted by the formula T12R3, where T represents R3SiO3/2;
- wherein formula (VI) is denoted by the formula Q12M12R1,R2,R3 where Q represents SiO4/2 and MR1,R2,R3 represents R1, R2, R3SiO1/2;
- wherein R1 and R2 are independently selected from the group consisting of hydrogen, a linear alkyl group having 1-6 carbon atoms, a branched alkyl group having 2-12 carbon atoms, a cycloalkyl group having 3-17 carbon atoms, a fluorinated linear alkyl group having 2-12 carbon atoms, a fluorinated branched alkyl group having 2-12 carbon atoms, a fluorinated cycloalkyl group having 3-17 carbon atoms, a cycloalkyl substituted alkyl group having 4-23 carbon atoms and an alkyl substituted cycloalkyl group having 4-23 carbon atoms;
- wherein R3 is selected from the group consisting of a linear alkyl group having 1-6 carbon atoms, a branched alkyl group having 2-12 carbon atoms, a cycloalkyl group having 3-17 carbon atoms, a fluorinated linear alkyl group having 2-12 carbon atoms, a fluorinated branched alkyl group having 2-12 carbon atoms, a fluorinated cycloalkyl group having 3-17 carbon atoms, a cycloalkyl substituted alkyl group having 4-23 carbon atoms and an alkyl substituted cycloalkyl group having 4-23 carbon atoms, a cycloaliphatic alcohol, a cycloaliphatic acid, a cycloaliphatic ester, a phenol, an aliphatic alcohol, an aliphatic acid, an aliphatic ester, a fluorocarbon alcohol, an amine, an amide, a vinyl ether, and an epoxide;
- and
- at least one solvent.
A planarizing composition, comprising:
- a polyhedral oligomeric silsesquioxane selected from the group consisting of formulas (I)-(VI):
- wherein formula (I) is denoted by the formula T8R3, where T represents R3SiO3/2;
- wherein formula (II) is denoted by the formula Q8M8R1,R2,R3 where Q represents SiO4/2 and MR1,R2,R3 represents R1, R2, R3SiO1/2;
- wherein formula (III) is denoted by the formula T10R3, where T represents R3SiO3/2;
- wherein formula (IV) is denoted by the formula Q10M10R1,R2,R3 where Q represents SiO4/2 and MR1,R2,R3 represents R1, R2, R3SiO1/2;
- wherein formula (V) is denoted by the formula T12R3, where T represents R3SiO3/2;
- wherein formula (VI) is denoted by the formula Q12M12R1,R2,R3 where Q represents SiO4/2 and MR1,R2,R3 represents R1, R2, R3SiO1/2;
- wherein R1 and R2 are independently selected from the group consisting of hydrogen, a linear alkyl group having 1-6 carbon atoms, a branched alkyl group having 2-12 carbon atoms, a cycloalkyl group having 3-17 carbon atoms, a fluorinated linear alkyl group having 2-12 carbon atoms, a fluorinated branched alkyl group having 2-12 carbon atoms, a fluorinated cycloalkyl group having 3-17 carbon atoms, a cycloalkyl substituted alkyl group having 4-23 carbon atoms and an alkyl substituted cycloalkyl group having 4-23 carbon atoms;
- wherein R3 is selected from the group consisting of a linear alkyl group having 1-6 carbon atoms, a branched alkyl group having 2-12 carbon atoms, a cycloalkyl group having 3-17 carbon atoms, a fluorinated linear alkyl group having 2-12 carbon atoms, a fluorinated branched alkyl group having 2-12 carbon atoms, a fluorinated cycloalkyl group having 3-17 carbon atoms, a cycloalkyl substituted alkyl group having 4-23 carbon atoms and an alkyl substituted cycloalkyl group having 4-23 carbon atoms, a cycloaliphatic alcohol, a cycloaliphatic acid, a cycloaliphatic ester, a phenol, an aliphatic alcohol, an aliphatic acid, an aliphatic ester, a fluorocarbon alcohol, an amine, an amide, a vinyl ether, and an epoxide.
- a crosslinking component;
- a thermal acid generator;
- and
- at least one solvent.
Dependencies are inferred from the claim text.