화학공학소재연구정보센터
Solid State Ionics, Vol.320, 369-377, 2018
Engineering of microstructures of protonic ceramics by a novel rapid laser reactive sintering for ceramic energy conversion devices
The solid state reactive sintering (SSRS) characteristic with the assistance of sintering aids (e.g., NiO) has been proven to be an effective method for achieving high-quality proton conducting oxide electrolytes at relatively low sintering temperatures (e.g., < 1400 degrees C). In this work, instead of performing a long-term (e.g., > 10 h) SSRS in a conventional high-temperature furnace, a novel rapid laser heating process was used to perform SSRS, which was named as rapid laser reactive sintering (RLRS). This RLRS method was confirmed to be able to sinter protonic ceramics with well-engineered microstructures within a short time (e.g., < 10 s). Using the proton conducting oxides of BaCe0.7Zr0.1Y0.1Yb0.1O3-delta (BCZYYb) and BaZr0.8Y0.2Y3-delta (BZY20) as case study, the crack free protonic ceramic parts of straight strips (similar to 10 mm in length, similar to 1 mm in width, and 30-200 mu m in thickness), spiral strips (similar to 200 mm in length, similar to 1 mm in width, and 30-200 mu m in thickness), and squared films (similar to 4.5 mm in both length and width and 30-200 mu m in thickness) were successfully fabricated by RLRS method. The sintered parts usually showed fully dense large-grained and highly porous regions, which can potentially serve as electrolytes and electrode scaffolds for single cells or half-cells. The X-ray diffraction results indicated that the pure perovskite structures were obtained for both BCZYYb and BZY20 by RLRS from inexpensive carbonates and single metal oxides. The preliminary electrochemical impedance measurement for the dense strips after removal of porous regions by picosecond laser machining showed a reasonable in-plane protonic conductivities. This new RLRS method demonstrated the feasibility and promise of the rapid additive manufacturing of hierarchical ceramic energy conversion devices.