Viability of all-solid-state lithium metal battery coupled with oxide solid-state electrolyte and high-capacity cathode

Owing to the utilization of lithium metal as anode with the ultrahigh theoretical capacity density of 3860 mA h g^(-1)and oxide-based ceramic solid-state electrolytes(SE),e.g.,garnet-type Li7La_(3)Zr_(2)O_(12)(LLZO),all-state-state lithium metal batteries(ASLMBs)have been widely accepted as the promising alternatives for providing the satisfactory energy density and safety.However,its applications are still challenged by plenty of technical and scientific issues.In this contribution,the co-sintering temperature at 500℃is proved as a compromise method to fabricate the composite cathode with structural integrity and declined capacity fading of LiNi_(0.5)Co_(0.2)Mn_(0.3)O_(2)(NCM).On the other hand,it tends to form weaker grain boundary(GB)inside polycrystalline LLZO at inadequate sintering temperature for LLZO,which can induce the intergranular failure of SE during the growth of Li filament inside the unavoidable defect on the interface of SE.Therefore,increasing the strength of GB,refining the grain to 0.4μm,and precluding the interfacial defect are suggested to postpone the electro-chemo-mechanical failure of SE with weak GB.Moreover,the advanced sintering techniques to lower the co-sintering temperature for both NCM-LLZO composite cathode and LLZO SE can be posted out to realize the viability of state-of-the-art ASLMBs with higher energy density as well as the guaranteed safety.

Development of Co-Sintering Process for Effective Fabrication of Direct-Write Planer Waveguide

We propose a co-sintering process for effective fabrication of three-layered structure for direct-write planar waveguide. Processing parameters and optical properties of the waveguide was investigated.

Improvement of luminescent stability from carbon nanotube field emission display based on printed CNT film

Aiming at the influences of poor contact at carbon nanotube (CNT)/electrode interface on luminescence stability in printed CNT film, a new co-sintering process for cathode fabrication was presented to improve the luminescent stability of fully printed CNT-FED. By co-sintering the printed silver and CNT layers, CNTs geometrically matched with Ag surface and/or embedded into Ag layer at the bottom of the co-sintered film, large CNTs block and bulk silver nested each other at the top of the co-sintered film. All these structures increased the contact area at CNT/Ag interface, which could increase the probability of forming ohmic contact at CNT/Ag interface. The luminescent stability of printed CNT-FED with co-sintered cathode could be improved as 5.6 times high as that of common devices.

Densification behavior of yttria-stabilized zirconia powders for solid oxide fuel cell electrolytes

Yttria-stabilized zirconia(YSZ) is the most common electrolyte material for solid oxide fuel cells. Herein, we conducted a comparative study on the densification behavior of three different kinds of commercial 8 mol% YSZ powders:(i) TZ-8Y(Tosoh, Japan),(ii) MELox 8Y(MEL Chemicals, UK), and(iii) YSZ-HT(Huatsing Power, China). The comparison was made on both the selfsupporting pellets and thin-film electrolytes coated onto a NiO–YSZ anode support. For the pellets, MELox 8Y showed the highest densification at lower sintering temperatures with 93% and 96% of the theoretical density at 1250 and 1300 ℃, respectively. Although YSZ-HT showed a higher sintering rate than TZ-8Y, a sintering temperature of 1350 ℃ was required for both the powders to reach 95% of the theoretical density. For the thin-film electrolytes, on the other hand, YSZ-HT showed the highest sintering rate with a dense microstructure at a co-sintering temperature of 1250 ℃. Our results indicate that besides the average particle size, other factors such as particle size distribution and post-processing play a significant role in determining the sintering rate and densification behavior of the YSZ powders. Additionally, a close match in the sintering shrinkage of the electrolyte and anode support is important for facilitating the densification of the thin-film electrolytes.