PARASITIC CHANNEL INDUCED BY SPIN-ON-GLASS IN A DOUBLE-LEVEL METALLIZATION COMPLIMENTARY METAL-OXIDE-SEMICONDUCTOR PROCESS - ITS FORMATION AND METHOD OF SUPPRESSION

被引:15
作者
MURATA, M
YAMAUCHI, K
KOJIMA, H
YOKOYAMA, A
INOUE, T
IWAMORI, T
机构
[1] Fuji Xerox Company, Limited Electronic Imaging and Devices Research Laboratory, Ebina
关键词
D O I
10.1149/1.2220821
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We studied the degradation mechanism and the supression method for parasitic channel formation by inorganic spin-on-glass (SOG) in complimentary metal oxide semiconductor (CMOS) devices with double-level metallization using test structures and a high frequency C-V technique. The positive charge induced near the Si/SiO2 interface in the field isolation region caused the parasitic channel. We propose a new mechanism that atomic hydrogen created by the SOG film diffuses to The Si/SiO2 interfacial region and generates the positive charge. There are two distinct mechanisms for the creation of the atomic hydrogen by the SOG films with different cap oxide. In p-SiO cap which is nondoped silicon oxide deposited by PECVD, Si-OH bonds in the SOG film are broken during the cap p-SiO deposition and create the atomic hydrogen. In nondoped silicate glass (NSG) cap which is nondoped silicate glass deposited by atmospheric pressure chemical vapor deposition (APCVD), water desorbed from the SOG film reacts with the aluminum electrode and creates the atomic hydrogen. Furthermore, p-SiO film with higher dangling bond density exhibited a capability to reduce the density of the SOG-related positive charge. Especially, the bottom p-SiO film under the SOG film was more effective for reducing the positive charge density compared with the cap p-SiO film on the SOG film. The improvement is attributed to trapping of SOG-related atomic hydrogen by the dangling bond in the p-SiO film. These experimental results are qualitatively explained well with the trapping model introducing the dangling bond as the trap center in the cap and bottom p-SiO films.
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收藏
页码:2346 / 2356
页数:11
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