Copper metallization of hydroxyl-modified amorphous Si:C:H films
Thin Solid Films, ISSN: 0040-6090, Vol: 440, Issue: 1, Page: 100-108
2003
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Article Description
X-ray photoelectron spectroscopy (XPS) was used to examine the initial stages of copper deposited by Physical vapor deposition (PVD), or sputter deposition, interacting with amorphous silicon:carbon:hydrogen (a-Si:C:H) films and hydroxyl modified amorphous silicon:carbon:hydrogen (a-Si:C:H/OH) films under Ultra-high vacuum (UHV) conditions. Amorphous-Si:C:H films were formed by condensing vinyltrimethylsilane (VTMS) on a titanium substrate (temperature ≤90 K) followed by electron beam bombardment (500 eV), and annealing to 300 K in UHV. Amorphous Si:C:H/OH films were formed by condensing H 2 O on the condensed VTMS multilayer (≤90 K) followed by electron beam bombardment (500 eV) and annealing to 300 K in UHV. The stoichiometry of the unmodified and modified a-Si:C:H films was determined by XPS to be C 4.5 :Si and C 4.3 :O 0.44 :Si, respectively. XPS measurements of PVD Cu on the modified film at 300 K indicate initial conformal growth with Cu(I) and Cu(0) formation at the Cu/Si:C:H/OH film interface. At higher Cu coverages, only Cu(0) was observed. In contrast, 3-dimensional island formation (Volmer–Weber growth) of Cu(0) was observed on the unmodified film. Annealing both the modified and unmodified films up to 800 K in UHV produced no significant change in the Cu(3p)/Cu(2p 3/2 ) intensity ratio, indicating negligible Cu diffusion through the film into the titanium substrate below 800 K.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0040609003006874; http://dx.doi.org/10.1016/s0040-6090(03)00687-4; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0042622665&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S0040609003006874; http://linkinghub.elsevier.com/retrieve/pii/S0040609003006874; http://api.elsevier.com/content/article/PII:S0040609003006874?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0040609003006874?httpAccept=text/plain; http://dx.doi.org/10.1016/s0040-6090%2803%2900687-4; https://dx.doi.org/10.1016/s0040-6090%2803%2900687-4
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