A Feasible Dual Modification Strategy of Internal Anion Redox Chemistry and Surface Engineering on P2 Layer-Structured Cathodes in Sodium-Ion Batteries.

Boosting the anion redox reaction opens up a possibility of further capacity enhancement on transition-metal-ion redox-only layer-structured cathodes for sodium-ion batteries. To mitigate the deteriorating impact on the internal and surface structure of the cathode caused by the inevitable increase in the operation voltage, probing a solution to promote the bulk-phase crystal structure stability and surface chemistry environment to further facilitate the electrochemical performance enhancement is a key issue. A dual modification strategy of establishing an anion redox hybrid activation trigger agent inside the crystal structure in combination with surface oxide coating is successfully developed.

Effective and Low-Cost In Situ Surface Engineering Strategy to Enhance the Interface Stability of an Ultrahigh Ni-Rich NCMA Cathode.

Ultrahigh Ni-rich quaternary layered oxides LiNiCoMnAlO (1 - - - ≥ 0.9) are regarded as some of the most promising cathode candidates for lithium-ion batteries (LIBs) because of their high energy density and low cost. However, poor rate capacity and cycling performance severely limit their further commercial applications.

Synergistic Effect of Microstructure Engineering and Local Crystal Structure Tuning to Improve the Cycling Stability of Ni-Rich Cathodes.

Ultrahigh Ni-rich layered oxides have been regarded as one of the most promising cathode candidates. However, cycling instability induced by interfacial reactions and irreversible H2-H3 lattice distortion is yet to be demonstrated by an effective strategy that could construct a stable grain interface and microstructure. Here, Ni-rich cathode LiNiCoMnO is modified by B and Ti to realize the synchronous regulation of a microstructure and the oxygen framework robustness.

Multiphase Engineered BNT-Based Ceramics with Simultaneous High Polarization and Superior Breakdown Strength for Energy Storage Applications.

Dielectric ceramics are crucial for high-temperature, pulse-power energy storage applications. However, the mutual restriction between the polarization and breakdown strength has been a significant challenge. Here, multiphase engineering controlled by the two-step sintering heating rate is adopted to simultaneously obtain a high polarization and breakdown strength in 0.

Phase-field modeling of the coupled domain structure and dielectric breakdown evolution in a ferroelectric single crystal.

The study of domain switching and dielectric breakdown behavior of ferroelectrics together with their relations is crucial for understanding the essence of ferroelectric physics and exploring their applications. In this work, a phase-field method is developed to reveal the coupled domain structure and dielectric breakdown evolution in a ferroelectric single crystal (FSC) by employing the Ginzburg-Landau kinetic equation and Griffith type energy criterion. Results show that the domain switching mobility, symbolizing the speed of polarization evolution, has a significant influence on ferroelectric properties, namely coercive field, dielectric breakdown strength (DBS), discharge energy density (DED), and energy storage efficiency (ESE).