Electrocatalysts for oxygen-reduction and oxygen-evolution reactions (ORR and OER) are crucial for metal-air batteries, where more costly Pt- and Ir/Ru-based materials are the benchmark catalysts for ORR and OER, respectively. Herein, for the first time Ni is combined with MnO species, and a 3D porous graphene aerogel-supported Ni/MnO (Ni-MnO/rGO aerogel) bifunctional catalyst is prepared via a facile and scalable hydrogel route. The synthetic strategy depends on the formation of a graphene oxide (GO) crosslinked poly(vinyl alcohol) hydrogel that allows for the efficient capture of highly active Ni/MnO particles after pyrolysis. Remarkably, the resulting Ni-MnO/rGO aerogels exhibit superior bifunctional catalytic performance for both ORR and OER in an alkaline electrolyte, which can compete with the previously reported bifunctional electrocatalysts. The MnO mainly contributes to the high activity for the ORR, while metallic Ni is responsible for the excellent OER activity. Moreover, such bifunctional catalyst can endow the homemade Zn-air battery with better power density, specific capacity, and cycling stability than mixed Pt/C + RuO catalysts, demonstrating its potential feasibility in practical application of rechargeable metal-air batteries.

Li La Zr O -based Li-rich garnets react with water and carbon dioxide in air to form a Li-ion insulating Li CO layer on the surface of the garnet particles, which results in a large interfacial resistance for Li-ion transfer. Here, we introduce LiF to garnet Li La Zr Ta O (LLZT) to increase the stability of the garnet electrolyte against moist air; the garnet LLZT-2 wt % LiF (LLZT-2LiF) has less Li CO on the surface and shows a small interfacial resistance with Li metal, a solid polymer electrolyte, and organic-liquid electrolytes. An all-solid-state Li/polymer/LLZT-2LiF/LiFePO battery has a high Coulombic efficiency and long cycle life; a Li-S cell with the LLZT-2LiF electrolyte as a separator, which blocks the polysulfide transport towards the Li-metal, also has high Coulombic efficiency and kept 93 % of its capacity after 100 cycles.

Nitrogen coordinated metal single atoms in carbon have aroused extensive interest recently and have been growing as the active research frontier in a wide range of key renewable energy reactions and devices. However, single-atom catalysts with isolated metallic active components cannot satisfy the demand of electrocatalysis with the requirement in selectivity. Herein, we develop a step-by-step self-assembly strategy to allocate nickel (Ni) and iron (Fe) single atoms respectively on the inner and outer walls of graphene hollow nanospheres (GHSs), for the first time realizing the separate-sided different single-atom functionalization of hollow graphene. The Ni or Fe single atom is demonstrated to be coordinated with four N atoms via the formation of a Ni-N 4 or Fe-N 4 planar experimental observations. As a proof-of-concept demonstration for realistic application, the Ni-N 4 /GHSs/Fe-N 4 endows the rechargeable Zn-air battery with excellent energy efficiency and cycling stability as an air-cathode, outperforming the performance of benchmark Pt/C+RuO 2 air-cathode. The current work paves a new avenue for precise control of single-atom sites on carbon surface for the high-performance and selective electrocatalysts.

NASICON (Na super ionic conductor) structures of NaMV(PO) (M = Mn, Fe, Ni) were prepared, characterized by aberration-corrected STEM and synchrotron radiation, and demonstrated to be durable cathode materials for rechargeable sodium-ion batteries. In NaMnV(PO), two redox couples of Mn/Mn and V/V are accessed with two voltage plateaus located at 3.6 and 3.3 V and a capacity of 101 mAh g at 1 C. Furthermore, the NaMnV(PO) cathode delivers a high initial efficiency of 97%, long durability over 1000 cycles, and good rate performance to 10 C. The robust framework structure and stable electrochemical performance makes it a reliable cathode materials for sodium-ion batteries.