In this study, one-dimensional porous silicon nanowire (1D–PSiNW) arrays were fabricated by one-step metal-assisted chemical etching (MACE) to etch phosphorus-doped silicon wafers. The as-prepared mesoporous 1D–PSiNW arrays here had especially high specific surface areas of 323.47 m2·g−1 and were applied as anodes to achieve fast charge–discharge performance for lithium ion batteries (LIBs). The 1D–PSiNWs anodes with feature size of ~7 nm exhibited reversible specific capacity of 2061.1 mAh·g−1 after 1000 cycles at a high current density of 1.5 A·g−1. Moreover, under the ultrafast charge–discharge current rate of 16.0 A·g−1, the 1D–PSiNWs anodes still maintained 586.7 mAh·g−1 capacity even after 5000 cycles. This nanoporous 1D–PSiNW with high surface area is a potential anode candidate for the ultrafast charge–discharge in LIBs with high specific capacity and superior cycling performance.

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Novelty Cu2O multi-branched nanowires and nanoparticles with size ranging from [Formula: see text]15[Formula: see text]nm to [Formula: see text]60[Formula: see text]nm have been synthesized by one-step hydrothermal process. These Cu2O nanostructures when used as anode materials for lithium-ion batteries exhibit the excellent electrochemical cycling stability and reduced polarization during the repeated charge/discharge process. The specific capacity of the Cu2O nanoparticles, multi-branched nanowires and microscale are maintained at 201.2[Formula: see text]mAh/g, 259.6[Formula: see text]mAh/g and 127.4[Formula: see text]mAh/g, respectively, under the current density of 0.1[Formula: see text]A/g after 50 cycles. The enhanced electrochemical performance of the Cu2O nanostructures compared with microscale counterpart can be attributed to the larger contact area between active Cu2O nanostructures/electrolyte interface, shorter diffusion length of Li[Formula: see text] within nanostructures and the improved stress release upon lithiation/delithiation.

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