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The demand for 'more energy and less carbon' is one of the most important challenges facing humanity. Exploring not only more efficient renewable energy systems, but also advanced energy conversion and storage materials is an essential requisite to achieve the task. Since the emergence of alkali-ion rechargeable batteries, the development of cathode materials has been considered as a key factor that improves the overall performance of batteries. In this respect, understanding the underlying science of the factors affecting the properties and performance of cathode materials and how to ameliorate them have made remarkable progress. There have been several reports about factors ranging from the nano- to the micrometer scale, and now it is time to build an infrastructure to design advanced cathode materials with a selective and comprehensive perspective on those factors. In this Review article, we discuss the key factors contributing to the properties and performance of cathode materials with a comprehensive perspective on various alkali-ion transition metal compounds. It covers a wide scope of factors from atomic to microscopic levels as follows: atomic, electronic, crystal and particle structures. This journal is

The ever-growing demand for high-energy lithium-ion batteries in portable electronics and electric vehicles has triggered intensive research efforts over the past decade. An efficient strategy to boost the energy and power density of lithium-ion batteries is to increase the Ni content in the cathode materials. However, a higher Ni content in the cathode materials gives rise to safety issues. Herein, thermal expansion and oxygen vacancies are proposed as new critical factors that affect the thermal stability of charged Ni-rich cathode materials based on a systematic synchrotron-based X-ray study of Li0.33Ni0.5+ x Co0.2Mn0.3- x O2 (x = 0, 0.1, 0.2) cathode materials during a heating process. Charged cathode materials with higher Ni contents show larger thermal expansion, which accelerates transition metal migration to the Li layers. Oxygen vacancies are formed and accumulate mainly around Ni ions until the layered-to-spinel phase transition begins. The oxygen vacancies also facilitate transition metal migration to the Li layers. Thermal expansion and the presence of oxygen vacancies decrease the energy barrier for cation migration and facilitate the phase transitions in charged cathode materials during the heating process. These results provide valuable guidance for developing new cathode materials with improved safety characteristics.

This review explores the challenges and advancements in the development of high‐energy lithium‐ion batteries (LIBs), particularly focusing on the electrochemical and structural stability of Ni‐rich cathode materials. Despite their potential to increase the energy density of LIBs, these cathode materials encounter issues such as irreversible phase transitions and structural degradation during cycling, which ultimately affect their electrochemical performance. Elemental doping/substitution has emerged as promising strategies to address these challenges. However, the precise mechanisms underlying their performance enhancement remain unclear. The objective is to elucidate the complex reaction mechanisms triggered by doping and substitution in Ni‐rich cathode materials by employing in situ operando analyses to uncover their effects on electrochemical behavior and structural integrity during cycling. This comprehensive investigation aims to clarify the roles of elemental dopants or substituents in the crystal structures of Ni‐rich cathode materials, thereby offering valuable insights for the structural engineering of cathode materials in high‐energy LIBs. By elucidating these intricate mechanisms, this review provides a practical roadmap for future research and significantly contributes to LIB technology by guiding material design and optimization strategies in the development of advanced LIBs. [ABSTRACT FROM AUTHOR]

The exploration of high-energy-density cathode materials is vital to the practical use of K-ion batteries. Layered K-metal oxides have too high a voltage slope due to their large K+–K+ interaction, resulting in low specific capacity and average voltage. In contrast, the 3D arrangement of K+, with polyanions separating them, reduces the strength of the effective K+-K+ repulsion, which in turn increases specific capacity and voltage. Here, stoichiometric KVPO4F for use as a high-energy-density K-ion cathode is developed. The KVPO4F cathode delivers a reversible capacity of ≈105 mAh g−1 with an average voltage of ≈4.3 V (vs K/K+), resulting in a gravimetric energy density of ≈450 Wh kg−1. During electrochemical cycling, the KxVPO4F cathode goes through various intermediate phases at x = 0.75, 0.625, and 0.5 upon K extraction and reinsertion, as determined by ex situ X-ray diffraction characterization and ab initio calculations. This work further explains the role of oxygen substitution in KVPO4+xF1−x: the oxygenation of KVPO4F leads to an anion-disordered structure which prevents the formation of K+/vacancy orderings without electrochemical plateaus and hence to a smoother voltage profile.

Lithium-ion batteries based on intercalation compounds have dominated the advanced portable energy storage market. The positive electrode materials in these batteries belong to a material group of lithium-conducting crystals that contain redox-active transition metal and lithium. Materials without lithium-conducting paths or lithium-free compounds could be rarely used as positive electrodes due to the incapability of reversible lithium intercalation or the necessity of using metallic lithium as negative electrodes. These constraints have significantly limited the choice of materials and retarded the development of new positive electrodes in lithium-ion batteries. Here, we demonstrate that lithium-free transition metal monoxides that do not contain lithium-conducting paths in their crystal structure can be converted into high-capacity positive electrodes in the electrochemical cell by initially decorating the monoxide surface with nanosized lithium fluoride. This unusual electrochemical behaviour is attributed to a surface conversion reaction mechanism in contrast with the classic lithium intercalation reaction. Our findings will offer a potential new path in the design of positive electrode materials in lithium-ion batteries.

Asyneuma japonicum is an ornamental flowering plant in East Asia. The genus Asyneuma is difficult to distinguish taxonomically because of its morphological similarities with the genus Campanula. We constructed the first complete plastome of A. japonicum (NCBI accession number: OR805474) using the Illumina platform. This plastome is a circular ring structure with a length of 185,875 base pairs. It is organized into four parts: a pair of inverted repeats (33,084 bp each) as well as large (83,795 bp) and small (35,912 bp) single-copy regions. One hundred nine unique genes were encoded in the assembled plastome. Using structural variations, junction boundaries, rearrangements, divergent hotspots, and phylogenetic analysis, we revealed that A. japonicum was in the closest evolutionary position to Hanabusaya asiatica and it had a large evolutionary divergence from the Campanulaceae family due to gene rearrangements. [ABSTRACT FROM AUTHOR]

Conversion reaction electrodes offer a high specific capacity in rechargeable batteries by utilizing wider valence states of transition metals than conventional intercalation-based electrodes and have thus been intensively studied in recent years as potential electrode materials for high-energy-density rechargeable batteries. However, several issues related to conversion reactions remain poorly understood, including the polarization or hysteresis during charge/discharge processes. Herein, Co3O4 in Na cells is taken as an example to understand the aforementioned properties. The large hysteresis in charge/discharge profiles is revealed to be due to different electrochemical reaction paths associated with respective charge and discharge processes, which is attributed to the mobility gap among inter-diffusing species in a metal oxide compound during de/sodiation. Furthermore, a Co3O4–graphene nanoplatelet hybrid material is demonstrated to be a promising anode for Na rechargeable batteries, delivering a capacity of 756 mAh g−1 with a good reversibility and an energy density of 96 Wh kg−1 (based on the total electrode weight) when combined with a recently reported Na4Fe3(PO4)2(P2O7) cathode.

Developing electrode materials with high-energy densities is important for the development of lithium-ion batteries. Here, we demonstrate a mesoporous molybdenum dioxide material with abnormal lithium-storage sites, which exhibits a discharge capacity of 1,814 mAh g(-1) for the first cycle, more than twice its theoretical value, and maintains its initial capacity after 50 cycles. Contrary to previous reports, we find that a mechanism for the high and reversible lithium-storage capacity of the mesoporous molybdenum dioxide electrode is not based on a conversion reaction. Insight into the electrochemical results, obtained by in situ X-ray absorption, scanning transmission electron microscopy analysis combined with electron energy loss spectroscopy and computational modelling indicates that the nanoscale pore engineering of this transition metal oxide enables an unexpected electrochemical mass storage reaction mechanism, and may provide a strategy for the design of cation storage materials for battery systems.

Lithium iron phosphate (LFP) has attracted tremendous attention as an electrode material for next-generation lithium-rechargeable battery systems due to the use of low-cost iron and its electrochemical stability. While the lithium diffusion in LFP, the essential property in battery operation, is relatively fast due to the one-dimensional tunnel present in the olivine crystal, the tunnel is inherently vulnerable to the presence of FeLi anti-site defects (Fe ions in Li ion sites), if any, that block the lithium diffusion and lead to inferior performance. Herein, we demonstrate that the kinetic issue arising from the FeLi defects in LFP can be completely eliminated in lithium-excess olivine LFP. The presence of an excess amount of lithium in the Fe ion sites (LiFe) energetically destabilizes the FeLi-related defects, resulting in reducing the amount of Fe defects in the tunnel. Moreover, we observe that the spinodal decomposition barrier is notably reduced in lithium-excess olivine LFP. The presence of LiFe and the absence of FeLi in lithium-excess olivine LFP additionally induce faster kinetics, resulting in an enhanced rate capability and a significantly reduced memory effect. The lithium-excess concept in the electrode crystal brings up unexpected properties for the pristine crystal and offers a novel and interesting approach to enhance the diffusivity and open up additional diffusion paths in solid-state ionic conductors.

Developing sustainable Li‐ion batteries requires high‐energy cathodes based on low‐cost, earth‐abundant elements, moving away from low‐reserve nickel and cobalt. Fe‐based oxide cathodes with Fe3+/4+ and O2−/n− redox couples offer potential but face low initial Coulombic efficiency and significant voltage hysteresis. This study investigates Li‐excess Fe‐based disordered rock‐salt (DRX) oxyfluorides (Li2Fe0.5M0.5O2F; M = Fe, Ti, Mn) using combined electrochemical/spectroscopic characterization and first‐principles calculation. Oxygen‐dependent Fe3+/4+ redox, related to Fe 3d–O 2p hybrid state, can be stabilized when combined with Mn3+/4+ redox in DRX structure owing to the unusual decrease in its redox potential. The moderately high charge transfer gap stabilizes Fe4+ against ligand‐to‐metal charge transfer (LMCT) on charge, reduces the amount of oxygen oxidation, thereby increasing Coulombic efficiency. On discharge, it allows metal‐to‐ligand charge transfer (MLCT) without substantial overpotential, reducing hysteresis in oxygen redox. The resulting composition exhibits high capacity (309 mAh g−1) and energy density (998 Wh kg−1), providing insights for next‐generation Ni‐ and Co‐free cathode materials. [ABSTRACT FROM AUTHOR]

Adenophora remotiflora is a wild perennial plant used as oriental medicine and ornamental flowers in East Asia. The haploid genome size of A. remotiflora was estimated at 3.9 Gb with a 2.42% heterozygosity ratio. The chloroplast genome of 174,455 base pairs (bp) shows a circular map structure, and has four conserved regions consisting of a large single-copy region of 108,423 bp, a small single-copy region of 10,444 bp, and a pair of inverted repeats (each 27,794 bp). A total of 108 unique genes were annotated, comprising 74 protein-coding genes, 4 ribosomal RNA genes, and 30 transfer RNA genes. A total of 155 repeat sequences were identified, and comparative genome structures were characterized among the Adenophora species. Phylogenetic diversity showed that A. remotiflora is in a close position within the Adenophora genus, and Adenophora erecta is in the closest evolutionary position. [ABSTRACT FROM AUTHOR]