Lithium metal anodes hold great promise to enable high-energy battery systems. However, lithium dendrites at the interface between anode and separator pose risks of short circuits and fire, impeding the safe application. In contrast to conventional approaches of suppressing dendrites, here we show a deposition-regulating strategy by electrically passivating the top of a porous nickel scaffold and chemically activating the bottom of the scaffold to form conductivity/lithiophilicity gradients, whereby lithium is guided to deposit preferentially at the bottom of the anode, safely away from the separator. The resulting lithium anodes significantly reduce the probability of dendrite-induced short circuits. Crucially, excellent properties are also demonstrated at extremely high capacity (up to 40 mAh cm −2 ), high current density, and/or low temperatures (down to −15 °C), which readily induce dendrite shorts in particular. This facile and viable deposition-regulating strategy provides an approach to preferentially deposit lithium in safer positions, enabling a promising anode for next-generation lithium batteries.

Hydrogen production is the key step for the future hydrogen economy. As a promising H production route, electrolysis of water suffers from high overpotentials and high energy consumption. This study proposes an N-doped CoP as the novel and effective electrocatalyst for hydrogen evolution reaction (HER) and constructs a coupled system for simultaneous hydrogen and sulfur production. Nitrogen doping lowers the d-band of CoP and weakens the H adsorption on the surface of CoP because of the strong electronegativity of nitrogen as compared to phosphorus. The H adsorption that is close to thermos-neutral states enables the effective electrolysis of the HER. Only -42 mV is required to drive a current density of -10 mA cm for the HER. The oxygen evolution reaction in the anode is replaced by the oxidation reaction of Fe , which is regenerated by a coupled H S absorption reaction. The coupled system can significantly reduce the energy consumption of the HER and recover useful sulfur sources.

A design methodology for developing lead-free bulk ceramics with large recoverable energy storage density was proposed in this study.

The findings in this study could broaden the applications of KNN materials in a new field.

We propose to realize ultra-wideband polarization conversion metasurfaces in microwave regime through multiple plasmon resonances. An ultra-wideband polarization conversion metasurface is designed using a double-head arrow structure and is further demonstrated both numerically and experimentally. Four plasmon resonances are generated by electric and magnetic resonances, which lead to bandwidth expansion of cross-polarization reflection. The simulated results show that the maximum conversion efficiency is nearly 100% at the four plasmon resonance frequencies and a 1:4 3 dB bandwidth can be achieved for both normally incident x- and y-polarized waves. Experimental results agree well with simulation ones.