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The manipulation of stress in high-capacity microscale alloying anode materials, which undergo significant volumetric variation during cycling, is crucial prerequisite for improved their cycling capability. In this work, an innovative structural design strategy is proposed for scalable fabrication of a unique 3D highly porous micro structured germanium (Ge) featuring micro-nano hierarchical architecture as viable anode for high-performance lithium-ion batteries (LIBs). The resultant micro-sized Ge, consisting of interconnected nanoligaments and bicontinuous nanopores, is endowed with high activity, decreased Li+ diffusion distance and alleviated volume variation, appealing as an ideal platform for in-depth understanding the relationship between structural design and stress evolution. Such a micro-sized Ge being highly porous delivers a record high initial Coulombic efficiency of 92.5%, large volumetric capacity of 2,421 mAh cm-3 at 1.2 mA cm-2, exceptional rate capability (805.6 mAh g-1 at 10 Ag-11) and cycling stability (over 90% capacity retention after 1000 cycles even at 5 A g-1), largely outperforming the reported Ge-based anodes for LIBs. Furthermore, its underlying Li storage mechanism and stress dispersion behavior are explicitly revealed by combined substantial in situ/ex situ experimental characterizations and theoretical computation. This work provides novel insights into the rational design of high-performance and durable alloying anodes toward high-energy LIBs. [ABSTRACT FROM AUTHOR]

Aqueous zinc ion batteries (AZIBs) demonstrate tremendous competitiveness and application prospects because of their abundant resources, low cost, high safety, and environmental friendliness. Although the advanced electrochemical energy storage systems based on zinc ion batteries have been greatly developed, many severe problems associated with Zn anode impede its practical application, such as the dendrite formation, hydrogen evolution, corrosion and passivation phenomenon. To address these drawbacks, electrolytes, separators, zinc alloys, interfacial modification and structural design of Zn anode have been employed at present by scientists. Among them, the structural design for zinc anode is relatively mature, which is generally believed to enhance the electroactive surface area of zinc anode, reduce local current density, and promote the uniform distribution of zinc ions on the surface of anode. In order to explore new research directions, it is crucial to systematically summarize the structural design of anode materials. Herein, this review focuses on the challenges in Zn anode, modification strategies and the threedimensional (3D) structure design of substrate materials for Zn anode including carbon substrate materials, metal substrate materials and other substrate materials. Finally, future directions and perspectives about the Zn anode are presented for developing high-performance AZIBs. [ABSTRACT FROM AUTHOR]

We present a novel hydrolysis-hydrothermal approach to using lithium residues on the surface of LiNi0.5Co0.2Mn0.3O2 as raw materials to synthesize ultrathin LiAlO2-inlaid LiNi0.5Co0.2Mn0.3O2 cathode materials, for the first time. High-resolution transmission electron microscopy (HRTEM) and fast Fourier transform (FFT) analysis indicate that the spherical particles of LiNi0.5Co0.2Mn0.3O2 are completely coated by crystalline LiAlO2 with an average thickness of 4 nm; cross-section SEM and corresponding EDS results confirm that partial Al[sup 3+] ions are doped into the bulk LiNi0.5Co0.2Mn0.3O2 with gradient distribution. Electrochemical tests show that the modified materials exhibit excellent reversible capacity, enhanced cyclability and rate properties, combining with higher Li ion diffusion coefficient and better differential capacity profiles compared with those of the pristine material. Particularly, the 2 mol% LiAlO2-inlaid sample maintains 202 mA h g-1 with 91% capacity retention after 100 high-voltage cycles (with 4.6 V charge cut-off) at 1 C. The enhanced electrochemical performance can be ascribed to the removal of lithium residues and the unique LiAlO2-inlaid architecture. The removal of lithium residues are believed to decrease side reactions between Li2O and the electrolyte, while the unique LiAlO2-inlaid architecture can buffer the volume change of core and shell during cycles, enhance the composite's lithium ion diffusion ability and inherit the advantages of LiAlO2 coating and doping. [ABSTRACT FROM AUTHOR]