Chemically Amplified Resist Polymer for Lithography Sensitivity

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current chemically amplified resist compositions for semiconductor microfabrication face challenges in achieving high resolution and good pattern profile, particularly in sensitivity and heat resistance, despite advancements in resin structures and acid generators.

Innovation Solution

A novel polymer with specific structural units, including acid-labile groups and alicyclic hydrocarbon groups, is developed, combined with an acid generator to enhance the chemically amplified resist composition's sensitivity and heat resistance, and improve line width roughness and adhesiveness.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional resin structures and acid generators are used in chemically amplified resist compositions, then the basic resist function is maintained, but sensitivity and heat resistance are insufficient for high resolution patterning

Engineering Contradiction:
Improvesensitivity and heat resistanceVSAvoidpattern profile quality
Core Design Contradiction:
ReliabilityVSManufacturing precision

Solution Approach 1:

The patent employs composite polymer structures combining multiple functional units: adamantane-derived acid-labile groups for sensitivity enhancement, alicyclic hydrocarbon groups for heat resistance and mechanical strength, and carboxyl-containing groups for adhesion control. This composite approach allows simultaneous optimization of sensitivity and thermal properties that cannot be achieved with conventional single-structure resins.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The resist polymer is designed with specific local structural characteristics: adamantane groups positioned to provide acid-labile functionality for sensitivity, alicyclic groups distributed to enhance heat resistance and line width control, and carboxyl groups strategically placed to control adhesion and pattern profile. Each local region of the polymer chain contributes specific properties to resolve the contradiction.

Inventive Principle:
Principle #3Local quality

2Measurement precision

If polymer structures are optimized for sensitivity, then acid-labile groups enhance detection, but heat resistance and line width roughness deteriorate

Engineering Contradiction:
ImprovesensitivityVSAvoidheat resistance
Core Design Contradiction:
Measurement precisionVSTemperature

Solution Approach 1:

The polymer is segmented into distinct functional units with specific roles: adamantane-derived acid-labile groups (20-80 mol%) for sensitivity and acid generation, alicyclic hydrocarbon groups (10-60 mol%) for heat resistance and mechanical stability, and carboxyl-containing groups (5-30 mol%) for adhesion control. This segmentation allows each component to optimize its function without compromising overall performance.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent systematically varies the molar ratios of different structural units to optimize the balance between sensitivity and heat resistance. By adjusting the content of acid-labile groups versus thermally stable alicyclic groups, the composition achieves optimal sensitivity while maintaining sufficient heat resistance for high resolution patterning processes.

Inventive Principle:
Principle #35Parameter changes

3Measurement precision

If acid-labile groups are increased to improve sensitivity, then pattern detection enhances, but pattern profile and adhesiveness deteriorate

Engineering Contradiction:
ImprovesensitivityVSAvoidpattern profile
Core Design Contradiction:
Measurement precisionVSShape

Solution Approach 1:

The patent optimizes the molar ratio of acid-labile groups to alicyclic groups and carboxyl groups to achieve the desired pattern profile. By controlling the concentration of acid-labile groups within 20-80 mol% and balancing with thermally stable and adhesive groups, the composition achieves high sensitivity while maintaining good pattern profile and adhesiveness.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The resist composition uses a composite polymer system where adamantane-derived acid-labile groups provide sensitivity, alicyclic hydrocarbon groups maintain pattern profile and mechanical strength, and carboxyl-containing groups control adhesion. This composite structure resolves the contradiction between sensitivity enhancement and pattern profile maintenance.

Inventive Principle:
Principle #40Composite materials

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The novel polymer composition achieves improved sensitivity, heat resistance, and line width roughness, making it suitable for advanced lithography techniques like ArF excimer laser lithography, KrF excimer laser lithography, and ArF immersion lithography.

Implementation Method 1

a chemically amplified resist composition used for semiconductor microfabrication employing a lithography process contains an acid generator comprising a compound generating an acid by irradiation

Methodology Applied
Scientific EffectPhotochemical reaction: Photopolymerisation

Data Source

PatentUS8048612B2Polymer and chemically amplified resist composition comprising the same
Publication Date: 2011.11.01 SUMITOMO CHEM CO LTD
  • US8048612B2 patent drawing
  • US8048612B2 patent drawing
  • US8048612B2 patent drawing

AI summary

A polymer comprising a structural unit represented by the formula (Ia) or (Ib):wherein R1 represents a hydrogen atom etc., R2 represents a linear, branched chain or cyclic C1-C8 alkyl group, R3 represents a methyl group, n represents an integer of 0 to 14, Z1 represents a single bond etc., k represents an integer of 1 to 4, R4 and R5 each independently represents a hydrogen atom etc., and m represents an integer of 1 to 3, a structural unit represented by the formula (II):wherein R6 and R7 each independently represents a hydrogen atom etc., R8 represents a methyl group, R9 represents a hydrogen atom etc., n′ represents an integer of 0 to 12, Z2 represents a single bond etc., k′ represents an integer of 1 to 4, R21 and R22 each independently represents a hydrogen atom etc., and R23 represents a C1-C30 monovalent hydrocarbon group, andat least one structural unit selected from the group consisting of structural units represented by the formulae (IIIa), (IIIb), (IIIc), (IIId) and (IIIf)wherein R10 represents a hydrogen atom etc., R11 represents a methyl group, R12 is independently in each occurrence a carboxyl group etc., j represents an integer of 0 to 3, a represents an integer of 0 to 5, b represents an integer of 0 to 3, c represents an integer of 0 to (2j+2), Z3 represents a single bond etc., and k″ represents an integer of 1 to 4.