Investigating Pb diffusion across buried interfaces in Pb(Zr0.2Ti0.8)O3 thin films via time‐of‐flight secondary ion mass spectrometry depth profiling

• Published in: Surface and interface analysis Vol. 49; no. 10; pp. 973 - 977
• Main Authors: Mangum, John S., Podowitz‐Thomas, Stephen, Nikkel, Jason, Zhou, Chuanzhen, Jones, Jacob L.
• Format: Journal Article
• Language: English
• Published: Bognor Regis Wiley Subscription Services, Inc 01.10.2017
• Subjects: Depth profiling; Diffusion layers; Heterostructures; Ions; lead diffusion; lead zirconate titanate; Lead zirconate titanates; Mass spectrometry; Polymer films; PZT; Scientific imaging; Secondary ion mass spectrometry; Silicon dioxide; Spectroscopy; Thin films; time‐of‐flight secondary ion mass spectrometry; ToF‐SIMS
• ISSN: 0142-2421; 1096-9918
• DOI: 10.1002/sia.6255

The diffusion of Pb through Pb(Zr0.2Ti0.8)O3(PZT)/Pt/Ti/SiO2/Si thin film heterostructures is studied by using time‐of‐flight secondary ion mass spectrometry depth profiling. The as‐deposited films initially contained 10 mol% Pb excess and were thermally processed at temperatures ranging from 325 to 700°C to promote Pb diffusion. The time‐of‐flight secondary ion mass spectrometry depth profiles show that increasing processing temperature promoted Pb diffusion from the PZT top film into the buried heterostructure layers. After processing at low temperatures (eg, 325°C), Pb+ counts were low in the Pt region. After processing at elevated temperatures (eg, 700°C), significant Pb+ counts were seen throughout the Pt layer and into the Ti and SiO2 layers. Intermediate processing temperatures (400, 475, and 500°C) resulted in Pb+ profiles consistent with this overall trend. Films processed at 400°C show a sharp peak in PtPb+ intensity at the PZT/Pt interface, consistent with prior reports of a Pt3Pb phase at this interface after processing at similar temperatures.