Abstract

The electrochemical performance of lithium-oxygen (Li-O2) batteries can be markedly improved through designing the architecture of cathode electrodes with sufficient spaces to facilitate the diffusion of oxygen and accommodate the discharge products, and optimizing the cathode catalyst to promote the oxygen reduction reaction and oxygen evolution reaction (OER). Herein, we report the synthesis of ruthenium (Ru) nanocrystal-decorated vertically aligned graphene nanosheets (VGNS) grown on nickel (Ni) foam. As an effective binder-free cathode catalyst for Li-O2 batteries, the Ru-decorated VGNS@Ni foam can significantly reduce the charge overpotential via the effects on the OER and achieve high specific capacity, leading to an enhanced electrochemical performance. The Ru-decorated VGNS@Ni foam electrode has demonstrated low charge overpotential of ~0.45 V and high reversible capacity of 23 864 mAh g−1 at the current density of 200 mA g−1, which can be maintained for 50 cycles under full charge and discharge testing condition in the voltage range of 2.0–4.2 V. Furthermore, Ru nanocrystal decorated VGNS@Ni foam can be cycled for more than 200 cycles with a low overpotential of 0.23 V under the capacity curtained to be 1000 mAh g−1 at a current density of 200 mA g−1. Ru-decorated VGNS@Ni foam electrodes have also achieved excellent high rate and long cyclability performance. This superior electrochemical performance should be ascribed to the unique three-dimensional porous nanoarchitecture of the VGNS@Ni foam electrodes, which provide sufficient pores for the diffusion of oxygen and storage of the discharge product (Li2O2), and the effective catalytic effect of Ru nanocrystals on the OER, respectively. Ex situ field emission scanning electron microscopy, X-ray diffraction, Raman and Fourier transform infrared measurements revealed that Ru-decorated VGNS@Ni foam can effectively decompose the discharge product Li2O2, facilitate the OER and lead to a high round-trip efficiency. Therefore, Ru-decorated VGNS@Ni foam is a promising cathode catalyst for rechargeable Li-O2 batteries with low charge overpotential, long cycle life and high specific capacity. A three-dimensional graphene-based material has an architecture that enhances lightweight lithium-oxygen batteries in multiple ways. A team led by Guoxiu Wang from the University of Technology Sydney in Australia searchs for a cathode that would alleviate some problems associated with lithium-oxygen batteries, such as their poor cycling stability and the high voltages needed to recharge them. The researchers designed a more porous type of cathode that contained vertical graphene nanosheets to prevent oxygen pathways becoming clogged by discharge products. Attaching the open-network, highly conductive carbon nanomaterials to nickel foam yielded a material containing many channels and voids for lithium by-products. Adding catalytic ruthenium nanoparticles to the graphene network resulted in a cathode that dropped recharging overpotentials significantly — from 1.5 to 0.23–V — while remaining stable for over 200 cycles. We report the synthesis of ruthenium nanocrystal-decorated vertically aligned graphene nanosheets grown on nickel foam. As an effective binder-free cathode for Li-O2 batteries, it can significantly reduce the charge overpotential via their effects on the oxygen evolution reaction and achieve high specific capacity, leading to an enhanced electrochemical performance.

Highlights

  • From the magnified field emission scanning electron microscopy (FESEM) image (Figures 1d–f), it can be observed that the as-prepared vertical graphene nanosheets (VGNS) exhibit strong binding to the Ni foam with a vertical orientation and form a honeycomb structure enclosed by the neighboring VGNS walls

  • In summary, we report the synthesis of VGNS@Ni foam and Rudecorated VGNS@Ni foam as an efficient cathode catalyst for Li-O2 batteries

  • The electrochemical testing shows that the Ru-decorated VGNS@Ni foam is an effective cathode catalyst for Li-O2 batteries, which can significantly reduce the charge overpotential and achieves a high specific capacity, leading to an enhanced electrochemical performance

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Summary

Introduction

Rechargeable Li-O2 batteries have been considered to be one of the most promising systems as future power sources for electric vehicles owing to their high theoretical energy density of 3505 Wh kg − 1.1–4. The development of practical Li-O2 batteries faces several serious challenges, including high overpotential between charge and discharge, poor cycling stability, low Coulombic efficiency and low rate capability.[5,6,7,8] The reaction mechanism in a Li-O2 cell involves an oxygen reduction reaction (ORR) in the discharge process and an oxygen evolution reaction (OER) in the charge process, during which molecular O2 reacts reversibly with Li+ ions (Li++O2+2e − ↔ Li2O2, with an equilibrium voltage of 2.96 V vs Li).[9,10] This mechanism is very different from the traditional intercalation reactions of Li-ion batteries. The theoretical overpotential for a Li2O2 film is only 0.2 V, the practical overpotential normally reaches as high as. It has been identified that catalysts and appropriate non-aqueous electrolytes can effectively overcome these problems.[6,7,12] Various catalysts, such as metal oxides, metal nitrides and noble metals have been investigated as suitable cathode catalysts in Engineering, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Korea

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