具有低全球变暖潜力的C2H2F4/CF4O对SiNx作为CHF3替代品的蚀刻的影响
Kyung Lim Kim1,2, Jong Woo Hong3, Young Woo Jeon4
1Department of Semiconductor and Display Engineering, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Scientific reports
|November 18, 2025
概括
像C2H2F4和CF4O这样的新型环保气体显著改善了用于半导体制造的化 (SiNx) 蚀刻. 与传统的CHF3.3相比,这些替代品提供更高的蚀刻率和选择性,同时减少温室气体排放.
科学领域:
- 半导体制造业 半导体制造业
- 材料科学 材料科学 材料科学
- 环境化学环境化学
背景情况:
- 半导体制造中的双重图案工艺需要化 (SiNx) 蚀刻,其蚀刻速率高,并且比二氧化 (SiOx) 有选择性.
- 传统的蚀刻气体,如CHF3/CF4,具有包括低选择性和高全球变暖潜力 (GWP) 的局限性.
研究的目的:
- 研究CHF3的替代气体,用于二重模式的SiNx蚀刻.
- 评估C2H2F4和CF4O对蚀刻特性和环境足迹的影响.
主要方法:
- 使用C2H2F4和C2H2F4 + CF4O混合物的SiNx蚀刻的实验研究.
- 对蚀刻速率,蚀刻选择性,沟,临界维度 (CD) 变化和聚合物形成的分析.
- 温室气体排放的测量 (MMTCE) 与CHF进行比较3.
主要成果:
- C2H2F4提高了蚀刻速率和选择性,但导致了沟和CD增加.
- 将CF4O添加到C2H2F4中进一步提高了蚀刻速度和选择性,消除了沟.
- 与CHF3.3相比,替代气体表明温室气体排放明显减少.
结论:
- C2H2F4 + CF4O为SiNx蚀刻提供了一个卓越的环保替代品,平衡性能和环境影响.
- 这些先进的蚀刻工艺适用于下一代半导体设备,如FinFET和3D NAND.
- 该研究强调了半导体行业可持续蚀刻解决方案的发展.
相关概念视频
Radical Halogenation: Thermodynamics
4.5K
The thermodynamic favorability of a reaction is determined by the change in Gibbs free energy (ΔG). ΔG has two components- enthalpy (ΔH) and entropy (ΔS). The entropy component is negligible for alkane halogenation because the number of reactants and product molecules are equal. In this case, the ΔG is governed only by the enthalpy component. The most crucial factor that determines ΔH is the strength of the bonds. ΔH can be determined by comparing the energy...
4.5K
Acid Halides to Ketones: Gilman Reagent
3.8K
Lithium dialkyl cuprate, also known as Gilman reagents, selectively reduces acid halides to ketones. The acid chloride is treated with Gilman reagent at −78 °C in the presence of ether solution to produce a ketone in good yield.
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
3.8K
Acid Halides to Carboxylic Acids: Hydrolysis
3.5K
Hydrolysis of acid halides is a nucleophilic acyl substitution reaction in which acid halides react with water to give carboxylic acids. The reaction occurs readily and does not require acid or a base catalyst.
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
3.5K
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
7.3K
Bromination and chlorination of aromatic rings by electrophilic aromatic substitution reactions are easily achieved, but fluorination and iodination are difficult to achieve. Fluorine is so reactive that its reaction with benzene is difficult to control, resulting in poor yields of monofluoroaromatic products. To address this, Selectfluor reagent is used as a fluorine source in which a fluorine atom is bonded to a positively charged nitrogen.
7.3K
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
9.7K
In the presence of heat or light, alkanes react with molecular halogens to form alkyl halides by a substitution reaction called radical halogenation. This reaction has three steps: initiation, propagation, and termination, as seen in the radical chlorination of methane to produce methyl chloride.
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
9.7K
Alkyl Halides
19.5K
Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
19.5K


