1] Department of Chemistry, The University of Texas at Austin, 1 University Station, Austin, Texas 78712, USA [2].
1] Texas Materials Institute, The University of Texas at Austin, 1 University Station, Austin, Texas 78712, USA [2].
Nat Mater. 2014 Jul;13(7):726-32. doi: 10.1038/nmat4000. Epub 2014 Jun 1.
Perovskite oxides have attracted significant attention as energy conversion materials for metal-air battery and solid-oxide fuel-cell electrodes owing to their unique physical and electronic properties. Amongst these unique properties is the structural stability of the cation array in perovskites that can accommodate mobile oxygen ions under electrical polarization. Despite oxygen ion mobility and vacancies having been shown to play an important role in catalysis, their role in charge storage has yet to be explored. Herein we investigate the mechanism of oxygen-vacancy-mediated redox pseudocapacitance for a nanostructured lanthanum-based perovskite, LaMnO3. This is the first example of anion-based intercalation pseudocapacitance as well as the first time oxygen intercalation has been exploited for fast energy storage. Whereas previous pseudocapacitor and rechargeable battery charge storage studies have focused on cation intercalation, the anion-based mechanism presented here offers a new paradigm for electrochemical energy storage.
钙钛矿氧化物因其独特的物理和电子特性,作为金属-空气电池和固体氧化物燃料电池电极的能量转换材料,引起了人们的极大关注。在这些独特的性质中,钙钛矿中阳离子阵列的结构稳定性是突出的,在电极化下可以容纳可移动的氧离子。尽管已经表明氧离子迁移率和空位在催化中起着重要作用,但它们在电荷存储中的作用尚未得到探索。在此,我们研究了纳米结构的镧基钙钛矿 LaMnO3 中氧空位介导的氧化还原赝电容的机理。这是首例阴离子插层赝电容,也是首次利用氧嵌入实现快速储能。虽然之前的赝电容器和可充电电池的电荷存储研究主要集中在阳离子嵌入,但这里提出的基于阴离子的机制为电化学储能提供了一个新的范例。