研究生: |
蕭羽婷 Hsiao, Yu Ting |
---|---|
論文名稱: |
單元至多元銅合金膜鍍製與固溶合金元素分離偏析之研究 Deposition of Unitary to Multi-component Copper Alloy Films and Segregation of Alloyed Solute Elements |
指導教授: |
張守一
Chang, Shou Yi |
口試委員: |
陳育良
蔡哲瑋 |
學位類別: |
碩士 Master |
系所名稱: |
工學院 - 材料科學工程學系 Materials Science and Engineering |
論文出版年: | 2016 |
畢業學年度: | 104 |
語文別: | 中文 |
論文頁數: | 94 |
中文關鍵詞: | 單元至多元銅合金 、薄膜 、擴散阻障層 |
外文關鍵詞: | Unitary to Multi-component Copper Alloy, thin film, diffusion barrier |
相關次數: | 點閱:3 下載:0 |
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隨半導體製程技術快速發展,銅導線之寬度及間距亦不斷縮小,為防止銅原子擴散進入矽元件中造成元件特性退化,因此須在銅導線與介電層之間加入一擴散阻障層。擴散阻障層材料發展中,使用二元以上過渡金屬化合物、疊層結構或高熵合金作為擴散阻障層材料皆已有許多良好的研究成果;但隨銅製程進入20 nm以下,擴散阻障層厚度亦須降至3 nm以下,然均勻鍍覆超薄擴散阻障層具有難度,因此近年研究指出,透過自形成法製作擴散阻障層,再經由極短時間低溫熱處理後,少量元素自銅膜分離偏析至銅與介電材料界面處,即可自形成奈米等級超薄膜之優點,但迄今仍未有文獻探討固溶合金元素分離偏析行為。本研究利用磁控濺鍍法製備單元至多元合金與銅合金薄膜,分析合金與銅合金膜性質,再經低溫退火處理單元至多元銅合金薄膜,以釐清固溶合金元素分離偏析之行為。研究結果顯示,單元至多元銅合金薄膜經由熱處理,元素添加數目不同,固溶合金元素分離偏析之行為不同;由能量觀點來探討固溶合金元素數目不同對於合金元素分離偏析之行為影響。
With the rapid development of copper metallization technology, the line spacing of integrated circuits is drastically reduced. To prevent rapid Cu diffusion and silicide formation in interconnect structures, diffusion barriers are strongly demanded. In recent years, more stable and diffusion-resistant barriers have been intensively studied, including those of ternary components, of layered structures and of multi-principal components (high-entropy materials and their stacking structures). Due to the difficulty in uniform depositions of ultrathin barrier layers in nanoscale trenches, self-forming diffusion barriers (barrierless metallization) have further been developed in the past few years. The segregation of minor alloying elements in Cu films to Cu/dielectric interfaces under thermal annealing will self-form an ultrathin barrier layer. Thus in this study, Cu alloy films were deposited on Si substrates by magnetron sputtering, and alloyed solute elements would segregate during thermal annealing. Experimental results indicated that, in the six Cu alloy films, different solute segregation behaviors were observed under the competition of mixing enthalpy and mixing entropy. For the Cu(V) alloy film, the solute segregated to the Cu/Si interface, dominated by the large positive mixing enthalpy of V and Cu. For the Cu(V,Nb), the Cu(V,Nb,Mo) and the Cu(V,Nb,Mo,Ta) alloy films, the solutes formed intermetallic compounds due to the negative mixing enthalpies and the low-to-medium mixing entropies of the solute elements. For the Cu(V,Nb,Mo,Ta,Cr) alloy film, the solutes again segregated to the Cu/Si interface owing to the high mixing entropy of the solute elements.
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