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The garnet electrolyte presents poor wettability with Li metal, resulting in an extremely large interfacial impedance and drastic growth of Li dendrites. Herein, a novel ultra‐stable conductive composite interface (CCI) consisting of LiySn alloy and Li3N is constructed in situ between Li6.4La3Zr1.4Ta0.6O12 (LLZTO) pellet and Li metal by a conversion reaction of SnNx with Li metal at 300 °C. The LiySn alloy as a continuous and robust bridge between LLZTO and Li metal can effectively reduce the LLZTO/Li interfacial resistance from 4468.0 Ω to 164.8 Ω. Meanwhile, the Li3N as a fast Li‐ion channel can efficiently transfer Li ions and give their uniform distribution at the LLZTO/Li interface. Therefore, the Li/LLZTO@CCI/Li symmetric battery stably cycles for 1200 h without short circuit, and the all‐solid‐state high‐voltage Li/LLZTO@CCI/LiNi0.5Co0.2Mn0.3O2 battery achieves a specific capacity of 161.4 mAh g−1 at 0.25 C with a capacity retention rate of 92.6 % and coulombic efficiency of 100.0 % after 200 cycles at 25 °C. [ABSTRACT FROM AUTHOR]

Due to high ionic conductivity and low cost, Li1.4Al0.4Ti1.6(PO4)3 (LATP) has emerged as a promising solid‐state electrolyte for next‐generation lithium (Li) metal solid‐state batterie with high safety performance and energy density. However, the extremely high impedance and surface instability of LATP with Li metal retard its practical application. Herein, a novel method is proposed to construct an ultrathin ZnO layer that is tightly coated on the LATP pellets, surface (ZnO@LATP) via magnetron sputtering, which in situ reacts with Li to form a low electronic conductivity and multifunctional solid electrolyte interphase (SEI). The formed SEI can not only effectively lower the interfacial resistance, but also overcome the side reactions of LATP with the Li metal anode and suppress the Li dendrite growth. Specifically, the interface resistance decreases from 80 554 to 353 Ω and the overpotential reduces from 1 V to 20 mV. As a result, the Li/ZnO@LATP@ZnO/Li symmetric batteries can stably cycle for more than 2000 h without short circuit at 0.05 mA cm−2 and Li/ZnO@LATP/LiFePO4 batteries show excellent cycle stability for 200 cycles at 0.1 C. This work highlights the significance of multifunctional interphase between LATP and Li metal for improvement of interfacial impedance and instability. [ABSTRACT FROM AUTHOR]

• Arsenic is electrochemically adsorbed by birnessite from mining wastewater. • Electrochemical redox reactions of birnessite contribute to arsenic adsorption. • H 2 O 2 formation and high potential of birnessite anode facilitate As(III) oxidation. • Mn2+ in wastewater can also be effectively removed during arsenic adsorption. • Cell voltage reversal facilitates the continuous use of birnessite electrode. Manganese oxides have been extensively investigated for arsenic (As) adsorption from aqueous solution. However, the effect of electrochemical redox reactions on the adsorption performance and underlying mechanism remain elusive. Herein, birnessite was used for electrochemical adsorption of As from mining wastewater at a constant cell voltage, and the effect of cell voltage and the continuous use (without desorption) performance of birnessite electrode were also evaluated. At 1.2 V for 24 h, the concentrations of total As (As(T)) and As(III) in wastewater decreased from 3808.7 to 73.7 μg L−1 and 682.8 to 21.4 μg L−1, respectively. The As(T) removal ratio increased with increasing cell voltage and reached 98.1% at 1.2 V, which was higher than that at open circuit (84.1%). The Mn2+ concentration also significantly decreased in wastewater during As adsorption. The high potential of birnessite anode and the generation of H 2 O 2 on cathode facilitated As(III) oxidation, and the electrochemical redox reactions of birnessite contributed to the enhancement of As(T) removal. The application of cell voltage reversal could improve the utilization rate of birnessite electrodes by dissolution-recrystallization during continuous use, and the As(T) removal ratio was increased from 73.5% to 85.1% after five cycles of voltage alteration. The present work indicates that birnessite is a promising absorbent for the electrochemical adsorption of As from real wastewaters. [ABSTRACT FROM AUTHOR]