An Enhanced Extend Interface via the π–π Interaction to Achieve the Soluble Light‐Assisted Lithium–Oxygen Batteries

Author:

Wang Yue1,Song Li‐Na1,Wang Yi‐Feng1,Wang Xiao‐Xue12,Wu Jia‐Yi12,Sun Yu1,Xu Ji‐Jing12ORCID

Affiliation:

1. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P. R. China

2. International Center of Future Science Jilin University Changchun 130012 P. R. China

Abstract

AbstractThe light‐assisted strategy is considered as an effective way to reduce the overpotential of lithium‐oxygen (Li─O2) batteries, however, the generated solid discharge products are prone to cover active sites of the solid‐state photocatalyst, causing the premature death of the cell. Herein, for the first time, the feasibility of soluble photocatalysts in Li─O2 battery system using Iron (II) Phthalocyanine (FePc) is verified. A micro reaction channel is constructed between the sp2‐carbon cathode and the soluble photocatalyst‐phthalein iron through π–π interaction, which can effectively increase the three‐phase reaction interface, facilitating the rapid separation and the transportation of photogenerated electrons and holes, thus improving the photocatalytic efficiency and the reaction kinetics of Li─O2 battery. Moreover, the FePc soluble photocatalysts induced the dual growth modes of surface growth and solution‐mediated growth pathways for the discharge products lead to an additional discharge capacity in the Li─O2 battery. Accordingly, the battery exhibits a lower overpotential of 0.33 V between discharge and charge plateaus at a current density of 0.01 mA cm−2, displaying the excellent cyclic stability (remaining a round‐trip efficiency of 81.1% after 130 cycles). The novel strategy provides new approaches for the construction of the light‐assisted Li─O2 batteries with reduced overpotential and boosted energy efficiency.

Funder

Higher Education Discipline Innovation Project

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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