Enhancing d-p orbital hybridization through oxygen vacancies boosting capacity and kinetics of layered double hydroxides for durable aqueous magnesium-ion batteries
Weizhi Kou , Zhitang Fang , Yangyang Sui , Yubo Yang , Cong Liu , Chenyu Yang , Congyan Jiang , Gang Yang , Luming Peng , Xuefeng Guo , Weiping Ding , Wenhua Hou
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引用次数: 0
Abstract
Layered double hydroxides (LDHs) are potential cathode materials for aqueous magnesium-ion batteries (AMIBs). However, the low capacity and sluggish kinetics significantly limit their electrochemical performance in AMIBs. Herein, we find that oxygen vacancies can significantly boost the capacity, electrochemical kinetics, and structure stability of LDHs. The corresponding structure-performance relationship and energy storage mechanism are elaborated through exhaustive in/ex-situ experimental characterizations and density functional theory (DFT) calculations. Specially, in-situ Raman and DFT calculations reveal that oxygen vacancies elevate orbital energy of O 2p and electron density of O atoms, thereby enhancing the orbital hybridization of O 2p with Ni/Co 3d. This facilitates electron transfer between O and adjacent Ni/Co atoms and improves the covalency of Ni–O and Co–O bonds, which activates Ni/Co atoms to release more capacity and stabilizes the Ov-NiCo-LDH structure. Moreover, the distribution of relaxation times (DRT) and molecular dynamics (MD) simulations disclose that the enhanced d-p orbital hybridization optimizes the electronic structure of Ov-NiCo-LDH, which distinctly reduces the diffusion energy barriers of Mg2+ and improves the charge transfer kinetics of Ov-NiCo-LDH. Consequently, the assembled Ov-NiCo-LDH//active carbon (AC) and Ov-NiCo-LDH//perylenediimide (PTCDI) AMIBs can both deliver high specific discharge capacity (182.7 and 59.4 mAh g−1 at 0.5 A g−1, respectively) and long-term cycling stability (85.4% and 89.0% of capacity retentions after 2500 and 2400 cycles at 1.0 A g−1, respectively). In addition, the practical prospects for Ov-NiCo-LDH-based AMIBs have been demonstrated in different application scenarios. This work not only provides an effective strategy for obtaining high-performance cathodes of AMIBs, but also fundamentally elucidates the inherent mechanisms.
期刊介绍:
The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies.
This journal focuses on original research papers covering various topics within energy chemistry worldwide, including:
Optimized utilization of fossil energy
Hydrogen energy
Conversion and storage of electrochemical energy
Capture, storage, and chemical conversion of carbon dioxide
Materials and nanotechnologies for energy conversion and storage
Chemistry in biomass conversion
Chemistry in the utilization of solar energy