Tsuchimoto Akihisa, Shi Xiang-Mei, Kawai Kosuke, Mortemard de Boisse Benoit, Kikkawa Jun, Asakura Daisuke, Okubo Masashi, Yamada Atsuo
Department of Chemical System Engineering, School of Engineering, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo, 113-8656, Japan.
National Institute for Materials Science (NIMS), Tsukuba, Ibaraki, 305-0044, Japan.
Nat Commun. 2021 Jan 27;12(1):631. doi: 10.1038/s41467-020-20643-w.
Reversibility of an electrode reaction is important for energy-efficient rechargeable batteries with a long battery life. Additional oxygen-redox reactions have become an intensive area of research to achieve a larger specific capacity of the positive electrode materials. However, most oxygen-redox electrodes exhibit a large voltage hysteresis >0.5 V upon charge/discharge, and hence possess unacceptably poor energy efficiency. The hysteresis is thought to originate from the formation of peroxide-like O dimers during the oxygen-redox reaction. Therefore, avoiding O-O dimer formation is an essential challenge to overcome. Here, we focus on NaMnO, which we recently identified to exhibit a large reversible oxygen-redox capacity with an extremely small polarization of 0.04 V. Using spectroscopic and magnetic measurements, the existence of stable O was identified in NaMnO. Computations reveal that O is thermodynamically favorable over the peroxide-like O dimer as a result of hole stabilization through a (σ + π) multiorbital Mn-O bond.
电极反应的可逆性对于具有长电池寿命的高能效可充电电池至关重要。额外的氧氧化还原反应已成为实现正极材料更大比容量的一个密集研究领域。然而,大多数氧氧化还原电极在充电/放电时表现出大于0.5 V的大电压滞后,因此具有不可接受的低能量效率。这种滞后被认为源于氧氧化还原反应过程中过氧化物样O二聚体的形成。因此,避免O-O二聚体的形成是一个必须克服的关键挑战。在这里,我们关注NaMnO,我们最近发现它具有大的可逆氧氧化还原容量,极化极小,仅为0.04 V。通过光谱和磁性测量,在NaMnO中确定了稳定O的存在。计算表明,由于通过(σ + π)多轨道Mn-O键实现空穴稳定,O在热力学上比过氧化物样O二聚体更有利。