TY - JOUR
T1 - Li2CO3-coated Ni particles for the inner electrodes of multilayer ceramic capacitors
T2 - Evaluation of lifetime
AU - Heidary, Damoon Sohrabi Baba
AU - Randall, Clive A.
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2017/1/11
Y1 - 2017/1/11
N2 - In previous work, it was demonstrated that using Li2CO3-coated Ni particles in the manufacturing of multilayer ceramic capacitor (MLCC) devices could improve both the permittivity and dissipation factors. However, adding Li+ ions to the system gave rise to the concern that ions could migrate under sustained electrical fields and thereby increase the degradation rates of the insulation resistance in MLCCs. In this paper, thermally stimulated depolarization current and highly accelerated lifetime testing were both utilized to evaluate the oxygen vacancy space-charge regions and migration in MLCCs. The results suggested that three parameters (the sintering schedule, Li2CO3 coatings, and oxygen flow during sintering) determine the overall resilience to the degradation. The Li+ ions did not migrate during degradation, as verified by time-of-flight secondary-ion mass spectrometry mapping; however, the Li ions enter the perovskite structure as an acceptor and, if ionically compensated for, could introduce more oxygen vacancies to the system and decrease the lifetime of the MLCCs. Nevertheless, it was demonstrated that the relative lifetimes of the newly designed MLCCs significantly improve relative to the conventional samples.
AB - In previous work, it was demonstrated that using Li2CO3-coated Ni particles in the manufacturing of multilayer ceramic capacitor (MLCC) devices could improve both the permittivity and dissipation factors. However, adding Li+ ions to the system gave rise to the concern that ions could migrate under sustained electrical fields and thereby increase the degradation rates of the insulation resistance in MLCCs. In this paper, thermally stimulated depolarization current and highly accelerated lifetime testing were both utilized to evaluate the oxygen vacancy space-charge regions and migration in MLCCs. The results suggested that three parameters (the sintering schedule, Li2CO3 coatings, and oxygen flow during sintering) determine the overall resilience to the degradation. The Li+ ions did not migrate during degradation, as verified by time-of-flight secondary-ion mass spectrometry mapping; however, the Li ions enter the perovskite structure as an acceptor and, if ionically compensated for, could introduce more oxygen vacancies to the system and decrease the lifetime of the MLCCs. Nevertheless, it was demonstrated that the relative lifetimes of the newly designed MLCCs significantly improve relative to the conventional samples.
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U2 - 10.1021/acsami.6b13526
DO - 10.1021/acsami.6b13526
M3 - Article
C2 - 27982559
AN - SCOPUS:85016288374
SN - 1944-8244
VL - 9
SP - 585
EP - 591
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 1
ER -