Converting ceria polyhedral nanoparticles into single-crystal nanospheres

被引:575
作者
Feng, Xiangdong
Sayle, Dean C.
Wang, Zhong Lin
Paras, M. Sharon
Santora, Brian
Sutorik, Anthony C.
Sayle, Thi X. T.
Yang, Yi
Ding, Yong
Wang, Xudong
Her, Yie-Shein
机构
[1] Cranfield Univ, Def Acad United Kingdom, Swindon SN6 8LA, Wilts, England
[2] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[3] Peking Univ, Dept Adv Mat & Nanotechnol, Coll Engn, Beijing 100871, Peoples R China
[4] Natl Ctr Nanosci & Technol, Beijing 100080, Peoples R China
[5] Nanocerox Inc, Ann Arbor, MI 48108 USA
[6] Ferro Corp, Independence, OH 44131 USA
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1126/science.1125767
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ceria nanoparticles are one of the key abrasive materials for chemical-mechanical planarization of advanced integrated circuits. However, ceria nanoparticles synthesized by existing techniques are irregularly faceted, and they scratch the silicon wafers and increase defect concentrations. We developed an approach for large-scale synthesis of single-crystal ceria nanospheres that can reduce the polishing defects by 80% and increase the silica removal rate by 50%, facilitating precise and reliable mass-manufacturing of chips for nanoelectronics. We doped the ceria system with titanium, using flame temperatures that facilitate crystallization of the ceria yet retain the titania in a molten state. In conjunction with molecular dynamics simulation, we show that under these conditions, the inner ceria core evolves in a single-crystal spherical shape without faceting, because throughout the crystallization it is completely encapsulated by a molten 1- to 2-nanometer shell of titania that, in liquid state, minimizes the surface energy. The principle demonstrated here could be applied to other oxide systems.
引用
收藏
页码:1504 / 1508
页数:5
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