摘要：聚合物基固态电解质得益于其易加工性,最有希望应用于下一代固态锂金属电池.目前,聚合物基态电解质的离子电导率提升策略多为加入导锂陶瓷以构建离子传输通道,其提升程度有限.电场在锂离子输运过程中存在重要影响,目前研究中有关电场对锂离子传输的影响机制尚不明确.本文将兼具高离子电导率和高介电常数的铌酸锂嵌入聚偏氟乙烯基体中,设计了一种新型复合固态电解质.铌酸锂颗粒有效调节电解质内部电场结构,增强了离子输运方向电场强度,实现了离子电导率的大幅提升(7.39×10^(-4)S cm^(-1),25℃).该电解质匹配高镍正极和锂金属负极的固态电池可稳定循环1000次以上,容量保持率为72%.该研究为设计下一代固态锂电池用高离子电导复合固态电解质提供了新的策略.

摘要：Efficient,low-cost,and stable electrocatalysts for water splitting are highly ***,three-dimensional(3D)Ni_(2)P nanosheet arrays were fabricated and simultaneously modulated by heterostructure engineering and Mn doping(Mn-doped Ni_(2)O_(3)/Ni_(2)P and Mn-doped Ni_(x)S_(y)/Ni_(2)P)via a facile hydrothermal reaction and subsequent phosphorization and *** to the Mn doping,synergistic effect in the heterostructures,and abundantly exposed active sites from the 3D-nanosheet arrays,Mn-doped Ni_(2)O_(3)/Ni_(2)P and Mn-doped Ni_(x)S_(y)/Ni_(2)P exhibit excellent properties for the hydrogen evolution reaction(HER)and oxygen evolution reaction(OER),*** former achieves an excellent current density of-10 mA cm^(-2) at a low overpotential of 104 mV for HER,while the latter attains 100 mA cm^(-2) for OER at an ultralow overpotential of 290 mV and exhibits superior stability at 50 mA cm^(-2) for 160 ***,the Mndoped Ni_(2)O_(3)/Ni_(2)P//Mn-doped Ni_(x)S_(y)/Ni_(2)P couple show high overall-water-splitting activity with a cell voltage of 1.65 V at 10 mA cm^(-2) and outstanding durability at 50 mA cm^(-2) for 120 h in an alkaline *** work presents an effective strategy to design and synthesize low-cost and highly active non-noble metal electrocatalysts for overall water splitting through the simultaneous application of heterostructure engineering,foreign-metal-atom doping,and a 3Dnanoarray *** strategy brings a paradigm shift toward the mass production of low-cost non-noble metal electrocatalysts for renewable energy devices.

摘要：Ceramic electrolytes are important in ceramic-liquid hybrid electrolytes(CLHEs),which can effectively solve the interfacial issues between the electrolyte and electrodes in solid-state batteries and provide a highly efficient Li-ion transfer for solid–liquid Li metal *** the ionic transport mechanisms in CLHEs and the corresponding role of ceramic electrolytes is crucial for a rational design ***,the Li-ion transfer in the ceramic electrolytes of CLHEs was confirmed by tracking the 6Li and 7Li substitution behavior through solid-state nuclear magnetic resonance *** ceramic and liquid electrolytes simultaneously participate in Li-ion transport to achieve highly efficient Li-ion transfer in CLHEs.A spontaneous Li-ion exchange was also observed between ceramic and liquid electrolytes,which serves as a bridge that connects the ceramic and liquid electrolytes,thereby greatly strengthening the continuity of Li-ion pathways in CLHEs and improving the kinetics of Li-ion *** importance of an abundant solid–liquid interface for CLHEs was further verified by the enhanced electrochemical performance in LiFePO4/Li and LiNi0.8Co0.1Mn0.1O2/Li batteries from the generated *** work provides a clear understanding of the Li-ion transport pathway in CLHEs that serves as a basis to build a universal Li-ion transport model of CLHEs.

摘要：The morphology and electronic structure of a Li4Ti5012 anode are known to determine its electrical and electrochemical properties in lithium rechargeable batteries. Ag-Li4Ti5012 nanofibers have been rationally designed and synthesized by an electrospinning technique to meet the requirements of one-dimensional （1D） morphology and superior electrical conductivity. Herein, we have found that the 1D Ag-Li4Ti5012 nanofibers show enhanced specific capacity, rate capability, and cycling stability compared to bare Li4Ti5012 nanofibers, due to the Ag nanoparticles （〈5 nm）, which are mainly distributed at interfaces between Li4Ti5O12 primary particles. This structural morphology gives rise to 20% higher rate capability than bare Li4Ti5O12 nanofibers by facilitating the charge transfer kinetics. Our findings provide an effective way to improve the electrochemical performance of Li4Ti5O12 anodes for lithium rechargeable batteries.