ABSTRACT
In pulse power systems, multilayer ceramic capacitors (MLCCs) encounter significant challenges due to the heightened loading electric field (E), which can lead to fatigue damage and ultrasonic concussion caused by electrostrictive strain. To address these issues, an innovative strategy focused on achieving an ultra-weak polarization-strain coupling effect is proposed, which effectively reduces strain in MLCCs. Remarkably, an ultra-low electrostrictive coefficient (Q33) of 0.012 m4 C-2 is achieved in the composition 0.55(Bi0.5Na0.5)TiO3-0.45Pb(Mg1/3Nb2/3)O3, resulting in a significantly reduced strain of 0.118% at 330 kV cm-1. At the atomic scale, the local structural heterogeneity leads to an expanded and loose lattice structure, providing ample space for large ionic displacement polarization instead of lattice stretching when subjected to the applied E. This unique behavior not only promotes energy storage performance (ESP) but also accounts for the observed ultra-low Q33 and strain. Consequently, the MLCC device exhibits an impressive energy storage density of 14.6 J cm-3 and an ultrahigh efficiency of 93% at 720 kV cm-1. Furthermore, the superior ESP of the MLCC demonstrates excellent fatigue resistance and temperature stability, making it a promising solution for practical applications. Overall, this pivotal strategy offers a cost-effective solution for state-of-the-art MLCCs with ultra-low strain-vibration in pulse power systems.
ABSTRACT
BaBiNb5O15 (BBN) based oxide-ion conductors have great potential for application in intermediate-temperature solid oxide fuel cells. In this work, electrical property enhancement is achieved by Sr2+ ion doping and sintering process improvement. The BaBi1-xSrxNb5O15-δ samples are prepared by the traditional solid-state reaction to investigate their electrical properties and oxygen relaxation behavior. Upon increasing the Sr2+ doping amount, the bulk conductivity of BaBi1-xSrxNb5O15-δ compounds increases first and then gradually decreases, and the bulk conductivity of the sample is the best when the doping concentration is 2 mol%. With the increase of Sr2+ doping, the activation energy shows a first decreasing and then increasing trend. Compared with the traditional sintering method, the total conductivity of the BaBi0.98Sr0.02Nb5O15-δ sample prepared by the two-step sintering method is greatly improved. These results have great implications for improving the electrical performances of BBN-based oxide conductors and studying their sintering process.
ABSTRACT
A short discussion on the structure of H2TiO3 presented in the article entitled Lithium recovery from salt lake brine by H2TiO3 (R. Chitrakar, Y. Makita, K. Ooi and A. Sonoda, Dalton Trans., 2014, 43, 8933) is presented. In our opinion, it is not correct to identify the phase of H2TiO3 as monoclinic. The XRD pattern of H2TiO3 differs substantially from that of Li2TiO3. XRD pattern simulation shows that the peak (1[combining macron]33) and the peak (2[combining macron]06) cannot be fully collapsed or substantially decrease in intensity by substitution of Li(+) with H(+) if H2TiO3 shares a similar space group and lattice parameters with Li2TiO3. A direct verification of a similar structure by N. V. Tarakina and co-workers may aid the confirmation of the structure. The layered double hydroxide type with the 3R1 sequence of oxygen layers is more reasonable for H2TiO3 and can be described as a stacking of charge-neutral metal oxyhydroxide slabs [(OH)2OTi2O(OH)2].