High performance rechargeable aluminium ion batteries enabled by full utilization and understanding of polyaniline cathodes

As a renowned conductive polymer, polyaniline (PANI) shows remarkable potential in organic cathode materials for rechargeable aluminium ion batteries (RAIBs). However, existing research has not given sufficient understanding and explanation of the structure and states of PANI but failed to achieve ideal electrochemical performance. In this study, we differentiate and investigate for the first time its primary-doped (PANI-1), re-doped (PANI-Re), secondary-doped (PANI-2), and emeraldine based (PANI-EB) forms, meanwhile attempt to enhance the conductivity of PANI-EB using multi-walled carbon nanotubes (PANI-EB@C). Among them, the high-doped PANI-2 and non-doped PANI-EB exhibit theoretical capacity utilization far superior to lower doped PANI-1 and PANI-Re, with both specific capacities reaching approximately 225 mAh/g (full capacity utilization rate of 76.53 %) at a current density of 1 A/g, while maintaining capacity retention rates of 92.89 % after 2000 cycles and 92.44 % after 5000 cycles, respectively. Furthermore, the high-conductivity PANI-EB@C displays a discharge specific capacity of 284 mAh/g (full capacity utilization rate of 96.59 %), with a capacity retention rate of 91.19 % after 5000 cycles. Electrochemical analysis, Gaussian theoretical calculations, ex-situ characterization collectively indicate that the electrochemical performance of doped PANI is positively correlated with the degree of doping-induced conductivity changes, while the unique internal redox process of PANI-EB enhances the release of performance and could be further optimized by the assistant of conductivity medium. This work advances the classification of the electrochemical performance and structural understanding of PANI cathode materials to an extremely high stage, towards the practical application of a low-cost, high-performance, sustainable, and green cathode material in large-scale energy storage devices.Chemical Engineering Journa

Influence of impregnation-vacuum filtration conditions on Ni dispersion and activity of Ni-cordierite for hydrogenation

The influence of the preparation conditions of the impregnation-vacuum filtration method was investigated systematically on the Ni dispersion and the activity of Ni-cordierite structured catalysts in hydrogenation of m-dinitrobenzene to m-phenylenediamine. H2-TPD measurement showed that the Ni dispersion has close relationship with the impregnation solution concentration of nickel nitrate, the impregnation time, the vacuum degree, the vacuum filtration time and the calcination temperature. The hydrogenation activity test and nitrogen physisorption investigation showed that the catalytic performance of Ni-cordierite is dependent upon the Ni dispersion and the chemisorption mode of m-dinitrobenzene on Ni particles

Insight of a Phase Compatible Surface Coating for Long-Durable Li-Rich Layered Oxide Cathode

Li-rich layered oxides (LLOs) can deliver almost double the capacity of conventional electrode materials such as LiCoO2 and LiMn2O4; however, voltage fade and capacity degradation are major obstacles to the practical implementation of LLOs in high-energy lithium-ion batteries. Herein, hexagonal La0.8Sr0.2MnO3−y (LSM) is used as a protective and phase-compatible surface layer to stabilize the Li-rich layered Li1.2Ni0.13Co0.13Mn0.54O2 (LM) cathode material. The LSM is MnOMbonded at the LSM/LM interface and functions by preventing the migration of metal ions in the LM associated with capacity degradation as well as enhancing the electrical transfer and ionic conductivity at the interface. The LSM-coated LM delivers an enhanced reversible capacity of 202 mAh g−1at 1 C (260 mA g−1) with excellent cycling stability and rate capability (94% capacity retention after 200 cycles and 144 mAh g−1 at 5 C). This work demonstrates that interfacial bonding between coating and bulk material is a successful strategy for the modification of LLO electrodes for the next-generation of high-energy Li-ion batteries

Insight of a Phase Compatible Surface Coating for Long-Durable Li-Rich Layered Oxide Cathode

Li-rich layered oxides (LLOs) can deliver almost double the capacity of conventional electrode materials such as LiCoO2 and LiMn2O4; however, voltage fade and capacity degradation are major obstacles to the practical implementation of LLOs in high-energy lithium-ion batteries. Herein, hexagonal La0.8Sr0.2MnO3−y (LSM) is used as a protective and phase-compatible surface layer to stabilize the Li-rich layered Li1.2Ni0.13Co0.13Mn0.54O2 (LM) cathode material. The LSM is MnOMbonded at the LSM/LM interface and functions by preventing the migration of metal ions in the LM associated with capacity degradation as well as enhancing the electrical transfer and ionic conductivity at the interface. The LSM-coated LM delivers an enhanced reversible capacity of 202 mAh g−1at 1 C (260 mA g−1) with excellent cycling stability and rate capability (94% capacity retention after 200 cycles and 144 mAh g−1 at 5 C). This work demonstrates that interfacial bonding between coating and bulk material is a successful strategy for the modification of LLO electrodes for the next-generation of high-energy Li-ion batteries

Hierarchical and lamellar porous carbon as interconnected sulfur host and polysulfide-proof interlayer for Li–S batteries

A robust three-dimensional (3D) interconnected sulfur host and a polysulfide-proof interlayer are key components in high-performance Li–S batteries. Herein, cellulose-based 3D hierarchical porous carbon (HPC) and two-dimensional (2D) lamellar porous carbon (LPC) are employed as the sulfur host and polysulfide-proof interlayer, respectively, for a Li–S battery. The 3D HPC displays a cross-linked macroporous structure, which allows high sulfur loading and restriction capability and provides unobstructed electrolyte diffusion channels. With a stackable carbon sheet of 2D LPC that has a large plane view size and is ultrathin and porous, the LPC-coated separator effectively inhibits polysulfides. An optimized combination of the HPC and LPC yields an electrode structure that effectively protects the lithium anode against corrosion by polysulfides, giving the cell a high capacity of 1339.4 mAh g−1 and high stability, with a capacity decay rate of 0.021% per cycle at 0.2C. This work provides a new understanding of biomaterials and offers a novel strategy to improve the performance of Li–S batteries for practical applications

Three-Dimension Hierarchical Al₂O₃ Nanosheets Wrapped LiMn₂O₄ with Enhanced Cycling Stability as Cathode Material for Lithium Ion Batteries

A three dimensional (3D) Al₂O₃ coating layer was synthesized by a facile approach including stripping and in situ self-assembly of γ-AlOOH. The uniform flower-like Al₂O₃ nanosheets with high specific area largely sequesters acidic species produced by side reaction between electrode and electrolyte. The inner coating layer wrapping spinel LiMn₂O₄ effectively inhibits the dissolution of Mn by suppressing directive contact with electrolyte to enhance cycling stability. The rate performance is improved because of the better electrolyte storage of the assembled hierarchical architecture of the 3D coating layer affording unimpeded Li⁺ diffusion from electrode to electrolyte. The electrochemical results reveal the as-prepared coated LiMn₂O₄ sample with the amount of Al₂O₃ at 1 wt % exhibits superior cycle stability under room temperature even at elevated temperature. The initial specific discharge capacity is 128.5 mAh g^–1 at 0.1 C and retains 89.8% of the initial capacity after 800 cycles at 1 C rate. When cycling at 55 °C, the composite shows 93.6% capacity retention after 500 cycles. This facile surface modification and effective structure of coating layer can be adopted to enhance the cycling performance and thermal stability of other electrode materials for which Al₂O₃ plays its role