Surface Reconstruction Enhanced Li-Rich Cathode Materials for Durable Lithium-Ion Batteries.

Regulating the distribution of surface elements in lithium-rich cathode materials can effectively change the electrochemical performance of cathode materials. Considering that the enrichment of Mn element on the surface is the main reason for the irreversible phase transition and dissolution of its surface structure, which in turn is the main reason for performance degradation. Based on the molten salt-assisted sintering method, a lithium rich cathode material with surface rich Ni and Co is designed and prepared.

Interface Engineering via Manipulating Solvation Chemistry for Liquid Lithium-Ion Batteries Operated≥100 °C.

High-performance and temperature-resistant lithium-ion batteries (LIBs), which are able to operate at elevated temperatures (i.e., >60 °C) are highly demanded in various fields, especially in military or aerospace exploration.

Enhancing Orbital Interaction in Spinel LiNiMnO Cathode for High-Voltage and High-Rate Li-Ion Batteries.

High voltage cobalt-free spinel LiNiMnO (LNMO) is well organized as a high-power cathode material for lithium (Li)-ion batteries, however, the weak interaction between the 3d orbital of the transition metal (TM) ions and the 2p orbital of oxygen (O) leads to the instability of crystal structural, hindering the long-term stable cycling of LNMO cathode especially at high temperatures. Here, a design strategy of orbital interaction is initiated to strengthen TM 3d-O 2p framework in P-doped LNMO (P-LNMO) by choosing phytic acid as P dopant, which can realize more uniform doping compared to regular phosphate. The results show that the enhancement of TM 3d-O 2p orbital interaction in P-LNMO can suppress the Jahn-Teller effect and subsequent dissolution of Mn, as well as lowers the energy barrier for Li ion insertion/extraction kinetics.

Upgrading the Separators Integrated with Desolvation and Selective Deposition toward the Stable Lithium Metal Batteries.

A practical and effective approach to improve the cycle stability of high-energy density lithium metal batteries (LMBs) is to selectively regulate the growth of the lithium anode. The design of desolvation and lithiophilic structure have proved to be significant means to regulate the lithium deposition process. Here, a fluorinated polymer lithiophilic separator (LS) loaded with a metal-organic framework (MOF801) is designed, which facilitates the rapid transfer of Li within the separator owing to the MOF801-anchored PF from the electrolyte, Li deposition is confined in the plane resulting from the polymer fiber layer rich in lithiophilic groups (C─F).

Insights into the solvation chemistry in liquid electrolytes for lithium-based rechargeable batteries.

Lithium-based rechargeable batteries have dominated the energy storage field and attracted considerable research interest due to their excellent electrochemical performance. As indispensable and ubiquitous components, electrolytes play a pivotal role in not only transporting lithium ions, but also expanding the electrochemical stable potential window, suppressing the side reactions, and manipulating the redox mechanism, all of which are closely associated with the behavior of solvation chemistry in electrolytes. Thus, comprehensively understanding the solvation chemistry in electrolytes is of significant importance.

MOF-derived porous carbon inlaid with MnO nanoparticles as stable aqueous Zn-ion battery cathodes.

Cathodes derived from metal-organic framework materials offer unique advantages in terms of improved structural reversibility and electron conduction efficiency. Nevertheless, the capacity contribution of cathodes based on the carbon framework system has not been clearly discussed or is controversial in aqueous batteries. In this essay, we have uncovered the capacity contribution arising from the adsorption of anions/cations onto the carbon surface by examining the bonds of the carbon and the details of unsteady voltage in the CV/GITT during the discharge.

Rational Construction of FeN@C Yolk-Shell Nanoboxes as Multifunctional Hosts for Ultralong Lithium-Sulfur Batteries.

Rationally constructing inexpensive sulfur hosts that have high electronic conductivity, large void space for sulfur, strong chemisorption, and rapid redox kinetics to polysulfides is critically important for their practical use in lithium-sulfur (Li-S) batteries. Herein, we have designed a multifunctional sulfur host based on yolk-shelled FeN@C nanoboxes (FeN@C NBs) through a strategy of etching combined with nitridation for high-rate and ultralong Li-S batteries. The highly conductive carbon shell physically confines the active material and provides efficient pathways for fast electron/ion transport.

Effectively enhanced structural stability and electrochemical properties of LiNiMnO cathode materials poly-(3,4-ethylenedioxythiophene)- coated for high voltage Li-ion batteries.

Spinel LiNiMnO shows promise as a potential candidate for Li-ion batteries due to its high energy density and high rate performance. However, LiNiMnO (LNMO) spinel oxides usually deliver poor cycle life because of the increasing impedance and gradually dissolving Mn resulting in the destruction of crystal structure. Here, a conductive polymer poly-(3,4-ethylenedioxythiophene) (PEDOT) surface modified strategy is introduced to settle the above challenges.

A 3D conductive network of porous carbon nanoparticles interconnected with carbon nanotubes as the sulfur host for long cycle life lithium-sulfur batteries.

Constructing an interlinked three-dimensional conductive carbon structure as a sulfur host is considered to be an effective strategy for suppressing the capacity decay over long-term cycling and improving the rate performance of lithium-sulfur (Li-S) batteries, because it can not only facilitate rapid electronic and ionic transportation in the cathode, but also be conducive to confine lithium polysulfide (LiPS) dissolution and shuttling. In this report, we designed a novel 3D conductive network structure (CNTs/Co-NC), which is composed of Co-NC (cobalt embedded in an N-doped porous carbon composite) derived from ZIF-67 polyhedra and inserted carbon nanotubes (CNTs), and applied it as a sulfur host for Li-S batteries. The CNT/Co-NC network structure is firstly prepared via the in situ nucleation of small ZIF-67 crystals on the surface of CNTs and eventually grown into CNT/ZIF-67 hybrid materials; after subsequent carbonization and infiltration of sulfur procedures, the S@CNT/Co-NC cathode is obtained.

Enhanced Li storage performance of LiNi(0.5)Mn(1.5)O(4)-coated 0.4Li(2)MnO(3)·0.6LiNi(1/3)Co(1/3)Mn(1/3)O(2) cathode materials for li-ion batteries.

In this study, Li-rich cathode, 0.4Li2MnO3·0.6LiNi1/3Co1/3Mn1/3O2 was synthesized by a resorcinol formaldehyde assisted sol-gel method for the first time.