scispace - formally typeset
Search or ask a question

Why phase transformation and solid solution behaviour showing in different compositions of LiMnFePO4? 


Best insight from top research papers

Phase transformation and solid solution behavior in different compositions of LiMnFePO4 are influenced by factors such as lithiation mechanisms, electrochemical properties, and kinetic responses. The phase transformation pathway significantly impacts the electrochemical kinetics, with solid-solution phases exhibiting faster current decay and lower polarization compared to two-phase transformations. Studies on LiFePO4 and its derivatives reveal the existence of solid solutions and binary lithiated/delithiated states, affecting rate capability and performance. Additionally, the introduction of elements like Mg in LiMnFePO4 alters the reaction mechanism, leading to one-phase reactions and changes in redox potentials. Understanding these transformations is crucial for optimizing battery performance and energy storage devices.

Answers from top 5 papers

More filters
Papers (5)Insight
Phase transformation and solid solution behavior in different compositions of LiMnFePO4 are due to the addition of Mg, altering the redox couple voltages, leading to single-phase lithiation/delithiation mechanisms.
Phase transformation and solid solution behavior in LiMnFePO4 are influenced by small elastic misfits between phases, leading to extended solid solutions and coherent transformations, enhancing performance.
Phase transformation pathways in LiFePO4 nanoparticles affect electrochemical properties. Solid-solution behavior leads to faster kinetics, reduced nucleation, and improved electrochemical responses compared to typical two-phase transformations.
Phase transformation and solid solution behavior in LiFePO₄/FePO₄ compositions vary due to lithium-ion diffusion, observed to be time-dependent at higher charging currents, affecting capacity in LiFePO₄ electrodes.
Phase transformation and solid solution behavior in different LiMnFePO4 compositions are influenced by the enthalpic interactions and stoichiometry, affecting voltage hysteresis and phase separation during lithiation.

Related Questions

How storage time effect phosphogypsum properties?5 answersThe storage time significantly affects phosphogypsum properties. Studies show that the calcination time of phosphogypsum (PG) impacts the compressive strength of phosphogypsum-based composite cementitious materials (PGCMs). Additionally, the utilization of phosphogypsum in cement production demonstrates alterations in clinkerization temperature and compressive strength based on the amount of phosphogypsum added and the firing schedule. Furthermore, the substitution of natural gypsum by phosphogypsum in slag cement influences the hydration rate and enhances the mechanical properties of the mixes. Moreover, the behavior and mechanical properties of mixtures containing phosphogypsum and red clay are influenced by the mass ratios and cement content, affecting the unconfined compressive strength, expansion, and shrinkage rates. Overall, the storage time of phosphogypsum plays a crucial role in determining its properties and subsequent applications.
How can the phase transformation affect on the materials inside the accelerators?4 answersPhase transformations can significantly impact materials inside accelerators. For instance, in the context of partially stabilized zirconia (PSZ) irradiated with electrons, phase transition from tetragonal to monoclinic phase occurred due to low-temperature degradation, affecting oxygen ion positions. Similarly, in the case of Ti-Ni shape memory alloy irradiated with protons, the parent phase was stabilized, altering transformation temperatures due to local stress fields induced by irradiation. Moreover, in the study of high-speed impacts, projectile austenite phase transformation was observed, affecting projectile performance at critical impact velocities. These findings highlight how phase transformations induced by various factors like radiation and impact can alter material properties, potentially influencing the performance and longevity of materials used in accelerator systems.
What are the differences in the crystal structure and magnetic properties of NiFe and NiFe2O4?5 answersNiFe and NiFe2O4 exhibit distinct differences in crystal structure and magnetic properties. NiFe2O4 nanoparticles typically display a cubic spinel structure, while NiFe can have additional Fe2O3 phases. NiFe2O4 shows ferromagnetic behavior at room temperature, whereas NiFe's magnetic behavior may vary based on the specific composition. The lattice parameters and magnetic moments of NiFe2O4 can be influenced by W-doping. Additionally, the strain in NiFe2O4 thin films grown on different substrates affects their crystal structure and anisotropy. Overall, NiFe2O4 demonstrates a well-defined crystal structure and consistent magnetic behavior, while NiFe may exhibit variations in structure and magnetic properties based on synthesis methods and compositions.
How does the phase of Fe3O4 change with temperature?5 answersThe phase of Fe3O4 undergoes a change with temperature. At low temperatures, a low temperature phase of magnetite is observed, which undergoes an abrupt change in line shape at around 26 K. This change is attributed to the changing electron ordering structure in the magnetic domain walls, resulting in a reconstruction of the magnetic domain structure.
How do the phase transitions in MHyPbBr3 change with temperature?5 answersThe phase transitions in MHyPbBr3 change with temperature. At higher temperatures, MHyPbBr3 undergoes a sequence of phase changes from orthorhombic to tetragonal to cubic structures. The orthorhombic phase (Pbnm) transforms into a tetragonal polymorph (I4/mcm) in the temperature range of 1373 - 1423 K, followed by a transformation to the cubic aristotype. In the lowest temperature phase, below 200 K, coexistence of a tetragonal and a nonoclinic form is observed. The ferroelectric phase of MHyPbBr3 possesses a rhombohedral sub-cell with an acute angle α. The phase transitions in MHyPbBr3 are influenced by the temperature-dependent superlattice intensities, cell parameters, and anionic mobility of the oxygen sub-lattice. The temperature changes in MHyPbBr3 are also associated with changes in the properties of collective ion vibrations.
What are the properties of lithium iron phosphate?5 answersLithium iron phosphate (LiFePO4) is a positive electrode material for Li-ion batteries. It has been recognized for its low cost, small toxicity, high security, and long life. The material can be prepared with carbon-coated particles free of any impurity phase, ensuring structural stability and electrochemical performance. However, it has some disadvantages such as poor electrical conductivity and low ion mobility. To overcome these limitations, significant modifications and processes can be applied to improve the performance and cost of the material. Additionally, the material can be prepared with a unique hollow porous sphere-like structure, which increases the contact area with the electrolyte, reduces ion diffusion resistance, and improves low-temperature performance. The lithium iron phosphate also has advantages such as low internal resistance, good high-temperature cycle performance, good safety quality, high charging speed, improved design capacity, and capability of meeting high-quality performance safety requirements.