A High‐Rate and Long‐Life Aqueous Rechargeable Mg‐Ion Battery Based on an Organic Anode Integrating Diimide and Triazine

Author:

Cang Ruibai1,Zhang Mingyi1,Zhou Xuejiao1,Zhu Kai2,Zhang Xitian1,Cao Dianxue2ORCID

Affiliation:

1. Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of Education School of Physics and Electronic Engineering Harbin Normal University 150025 Harbin P. R. China

2. Key Laboratory of Superlight Materials and Surface Technology of Ministry of Education College of Materials Science and Chemical Engineering Harbin Engineering University 150001 Harbin P. R. China

Abstract

AbstractAqueous Mg‐ion batteries (MIBs) lack reliable anode materials. This study concerns the design and synthesis of a new anode material – a π‐conjugate of 3D‐poly(3,4,9,10‐perylenetracarboxylic diimide‐1,3,5‐triazine‐2,4,6‐triamine) [3D‐P(PDI‐T)] – for aqueous MIBs. The increased aromatic structure inhibits solubility in aqueous electrolytes, enhancing its structural stability. The 3D‐P(PDI‐T) anode exhibits several notable characteristics, including an extremely high rate capacity of 358 mAh g−1 at 0.05 A g−1, A 3D‐P(PDI‐T)‖Mg2MnO4 full cell exhibits a reversible capacity of 148 mAh g−1 and a long cycle life of 5000 cycles at 0.5 A g−1. The charge storage mechanism reveals a synergistic interaction of Mg2+ and H+ cations with C−N/C=O groups. The assembled 3D‐P(PDI‐T)‖Mg2MnO4 full cell exhibits a capacity retention of around 95 % after 5000 cycles at 0.5 A g−1. This 3D‐P(PDI‐T) anode sustained its framework structure during the charge–discharge cycling of Mg‐ion batteries. The reported results provide a strong basis for a cutting‐edge molecular engineering technique to afford improved organic materials that facilitate efficient charge‐storage behavior of aqueous Mg‐ion batteries.

Funder

National Natural Science Foundation of China

Harbin Engineering University

Publisher

Wiley

Subject

General Energy,General Materials Science,General Chemical Engineering,Environmental Chemistry

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