Novel Polymer Resist for ArF Lithography Resolution

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Solution Overview

Problem

Current lithography techniques face challenges in developing materials that can handle increasingly shorter exposure light wavelengths and higher resolution requirements for semiconductor and liquid crystal display element production, particularly with the need for novel resist materials that offer improved sensitivity and pattern miniaturization.

Innovation Solution

A novel polymer compound with a specific structural unit, represented by general formula (a0-1), is introduced, which includes a resin component and an acid-generator component. This compound forms a resist composition that, upon exposure, undergoes solubility changes in an alkali developing solution, enabling the formation of precise resist patterns.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If conventional ultraviolet radiation (g-line and i-line) is used for lithography, then existing resist materials can be used, but pattern miniaturization and resolution are limited

Engineering Contradiction:
Improvepattern resolutionVSAvoidcompatibility with short wavelength exposure
Core Design Contradiction:
Manufacturing precisionVSAdaptability or versatility

Solution Approach 1:

The patent changes the chemical parameters of the resist material by introducing a novel polymer compound with specific structural units (formula a0-1) containing carboxyl groups and ester groups. This chemical parameter change enables the resist to be sensitive to shorter wavelength exposure (ArF excimer laser at 193 nm) while maintaining manufacturability and pattern resolution

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite resist system by combining the novel polymer compound (base resin) with an acid generator. This composite material approach allows the resist to function effectively with ArF excimer laser exposure, achieving both short wavelength compatibility and high pattern resolution through the synergistic interaction between the polymer compound and acid generator

Inventive Principle:
Principle #40Composite materials

2Productivity

If KrF or ArF excimer lasers are used for lithography, then pattern miniaturization is achieved, but novel resist materials with improved sensitivity are required

Engineering Contradiction:
Improvelithography efficiencyVSAvoidresist material performance
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent modifies the chemical structure parameters of the base resin by incorporating specific structural units with carboxyl and ester groups that exhibit high sensitivity to ArF excimer laser exposure. This parameter optimization enhances both the reliability of the resist material and the productivity of the lithography process by reducing exposure dose requirements

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces localized functional groups (carboxyl and ester groups in formula a0-1) within the polymer structure that specifically respond to acid generation upon exposure. This local quality enhancement ensures reliable resist performance by creating distinct exposed and unexposed regions with different solubility characteristics, improving pattern fidelity

Inventive Principle:
Principle #3Local quality

3Illumination intensity

If (meth)acrylic acid-based resins are used for ArF lithography, then transparency at 193 nm is achieved, but novel structural features are needed for improved performance

Engineering Contradiction:
Improvetransparency at 193 nmVSAvoidmolecular structure complexity
Core Design Contradiction:
Illumination intensityVSDevice complexity

Solution Approach 1:

The patent introduces specific local structural features (formula a0-1) within the polymer chain that provide both transparency at 193 nm and improved resist performance. The structural unit contains R1 (hydrogen, alkyl, or fluorinated alkyl), R2 and R3 (hydrogen, alkyl, or alkoxy), and R4 and R5 (hydrogen, alkyl with oxygen, cycloalkyl with oxygen, or alkoxycarbonyl), creating localized functional regions that enhance performance without excessive molecular complexity

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent optimizes the molecular structure parameters by controlling the types and positions of substituents in the (meth)acrylic acid-based polymer. By selecting appropriate R groups and their configurations, the patent achieves the desired balance between transparency at 193 nm and resist performance while maintaining manageable molecular complexity for manufacturing

Inventive Principle:
Principle #35Parameter changes

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 compound and resist composition provide enhanced sensitivity and resolution capabilities, allowing for the formation of precise patterns suitable for advanced lithography applications, particularly in ArF excimer laser lithography, with improved transparency and alkali solubility properties.

Implementation Method 1

an acid generator that generates acid upon exposure

Methodology Applied
Scientific EffectPhotoacid generation: Photopolymerisation

Implementation Method 2

a base resin that exhibits a changed solubility in an alkali developing solution under action of acid

Methodology Applied
Scientific EffectChemically amplified solubility change: Chemical Bonding

Data Source

PatentUS8021824B2Polymer compound, resist composition and method of forming resist pattern
Publication Date: 2011.09.20 TOKYO OHKA KOGYO CO LTD
  • US8021824B2 patent drawing
  • US8021824B2 patent drawing
  • US8021824B2 patent drawing

AI summary

A polymer compound including a structural unit (a0) represented by general formula (a0-1) shown below:wherein R1 represents a hydrogen atom, an alkyl group of 1 to 5 carbon atoms or a fluorinated alkyl group of 1 to 5 carbon atoms; R2 and R3 each independently represents a hydrogen atom, an alkyl group or an alkoxy group, or R2 and R3 may be bonded together to form an alkylene group that may include an oxygen atom or sulfur atom at an arbitrary position, —O— or —S—; R4 and R5 each independently represents a hydrogen atom, an alkyl group that may include an oxygen atom at an arbitrary position, a cycloalkyl group that may include an oxygen atom at an arbitrary position or an alkoxycarbonyl group.