The phase-controlled synthesis of metallic and ambient-stable 2D MX 2 (M is Mo or W; X is S) with 1T octahedral coordination will endow these materials with superior performance compared with their semiconducting 2H coordination counterparts. We report a clean and facile route to prepare 1T-MoS 2 and 1T-WS 2 through hydrothermal processing under high magnetic fields. We reveal that the as-synthesized 1T-MoS 2 and 1T-WS 2 are ambient-stable for more than 1 year. Electrochemical measurements show that 1T-MoS 2 performs much better than 2H-MoS 2 as the anode for sodium ion batteries. These results can provide a clean and facile method to prepare ambientstable 1T-phase MX 2 .
Transparent conducting oxides (TCOs), combining the mutually exclusive functionalities of high electrical conductivity and high optical transparency, lie at the center of a wide range of technological applications. The current design strategy for n-type TCOs, making wide bandgap oxides conducting through degenerately doping, obtains successful achievements. However, the performances of p-type TCOs lag far behind the n-type counterparts, primarily owing to the localized nature of the O 2p-derived valence band (VB). Modulation of the VB to reduce the localization is a key issue to explore p-type TCOs. This Perspective provides a brief overview of recent progress in the field of design strategy for p-type TCOs. First, the introduction to principle physics of TCOs is presented. Second, the design strategy for n-type TCOs is introduced. Then, the design strategy based on the concept of chemical modulation of the valence band for p-type TCOs is described. Finally, through the introduction of electron correlation in strongly correlated oxides for exploring p-type TCOs, the performance of p-type TCOs can be remarkably improved. The design strategy of electron correlation for p-type TCOs could be regarded as a promising material design approach toward the comparable performance of n-type TCOs.
Environmentally benign Bi3.25La0.75Ti3O12 (BLTO) thin film capacitors were prepared by a cost effective chemical solution deposition method for high energy density storage device applications. Low annealing temperature annealed BLTO thin films showed very slim hysteresis loops with high maximum and small remnant polarization values. Increasing the applied electric field to 2040 kV/cm, the optimized BLTO thin films show a high recoverable energy density of 44.7 J/cm3 and an energy efficiency of 78.4% at room temperature. Additionally, the BLTO thin film capacitors exhibited excellent fatigue endurance after 4 × 108 cycles and a good thermal stability up to 140 °C, proving their strong potential for high energy density storage and conversion applications.
Bismuth ferrite (BiFeO3) has recently become interesting as a room‐temperature multiferroic material, and a variety of prototype devices have been designed based on its thin films. A low‐cost and simple processing technique for large‐area and high‐quality BiFeO3 thin films that is compatible with current semiconductor technologies is therefore urgently needed. Development of BiFeO3 thin films is summarized with a specific focus on the chemical solution route. By a systematic analysis of the recent progress in chemical‐route‐derived BiFeO3 thin films, the challenges of these films are highlighted. An all‐solution chemical‐solution deposition (AS‐CSD) for BiFeO3 thin films with different orientation epitaxial on various oxide bottom electrodes is introduced and a comprehensive study of the growth, structure, and ferroelectric properties of these films is provided. A facile low‐cost route to prepare large‐area high‐quality epitaxial BFO thin films with a comprehensive understanding of the film thickness, stoichiometry, crystal orientation, ferroelectric properties, and bottom electrode effects on evolutions of microstructures is provided. This work paves the way for the fabrication of devices based on BiFeO3 thin films.
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Thin film ferroelectric capacitors (TFFCs) with excellent energy storage have attracted increasing attention due to the electronic devices toward miniaturization and integration. BiFeO3 (BF)/Bi3.25La0.75Ti3O12 (BL) based thin films are prepared by chemical solution deposition for energy storage. Ultrahigh energy storage with a recoverable energy density Ure of 54.9 J/cm3 and an efficiency η of 74.4% is observed in the bilayered BF/BL thin films. Further improvement of energy storage is realized in trilayered BL/BF/BL thin films with a Ure of 65.5 J/cm3 and an efficiency η of 74.2% at an electric field of 2753 kV/cm as well as excellent fatigue endurance up to 109 cycles. The results suggest that BF/BL based thin films can be used as lead-free TFFCs in energy storage applications.
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