Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0169-4332(00)00896-5
DC FieldValue
dc.titleAdsorption and reaction of NH3 on Ti/Si(1 0 0)
dc.contributor.authorSiew, H.L.
dc.contributor.authorQiao, M.H.
dc.contributor.authorChew, C.H.
dc.contributor.authorMok, K.F.
dc.contributor.authorChan, L.
dc.contributor.authorXu, G.Q.
dc.date.accessioned2014-10-16T08:19:49Z
dc.date.available2014-10-16T08:19:49Z
dc.date.issued2001-03-22
dc.identifier.citationSiew, H.L., Qiao, M.H., Chew, C.H., Mok, K.F., Chan, L., Xu, G.Q. (2001-03-22). Adsorption and reaction of NH3 on Ti/Si(1 0 0). Applied Surface Science 173 (1-2) : 95-102. ScholarBank@NUS Repository. https://doi.org/10.1016/S0169-4332(00)00896-5
dc.identifier.issn01694332
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93052
dc.description.abstractThe nitridation of ultra-thin Ti films on Si(1 0 0) have been studied using X-ray photoelectron spectroscopy (XPS) in a temperature range of 120-1000 K. Upon ammonia exposure to the multilayer Ti thin films at 120 K, three N 1s peaks at 397.8-398.1, 400.5-400.8 and 402.2-402.6 eV were observed, attributable to NHx (x = 1 or 2), molecular NH3 and NH4 δ+, respectively. Annealing of the NH3 saturated Ti/Si(1 0 0) surfaces results in the conversion of the NHx species. This species undergo two different pathways between 300 and 800 K, i.e. further dissociation to N(a) and H(a), and recombing with H(a) to form NH3(g). The atomic N reacts with Ti to yield a stable TiN film that retards significantly the interdiffusion at the Ti/Si interface.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0169-4332(00)00896-5
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/S0169-4332(00)00896-5
dc.description.sourcetitleApplied Surface Science
dc.description.volume173
dc.description.issue1-2
dc.description.page95-102
dc.description.codenASUSE
dc.identifier.isiut000167345800014
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