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In situ strain evolution during a disconnection event in a battery nanoparticle

机译:电池纳米粒子断开连接过程中的原位应变演化

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Lithium ion batteries are the dominant form of energy storage in mobile devices, increasingly employed in transportation, and likely candidates for renewable energy storage and integration into the electrical grid. To fulfil their powerful potential, electrodes with increased capacity, faster charge rates, and longer cycle life must be developed. Understanding the mechanics and chemistry of individual nanoparticles under in situ conditions is a crucial step to improving performance and mitigating damage. Here we reveal three-dimensional strain evolution within a single nanoparticle of a promising high voltage cathode material, LiNi0.5Mn1.5O4, under in situ conditions. The particle becomes disconnected during the second charging cycle. This is attributed to the formation of a cathode electrolyte interphase layer with slow ionic conduction. The three-dimensional strain pattern within the particle is independent of cell voltage after disconnection, indicating that the particle is unable to redistribute lithium within its volume or to its neighbours. Understanding the disconnection process at the single particle level and the equilibrium or non-equilibrium state of nanoparticles is essential to improving performance of current and future electrochemical energy storage systems.
机译:锂离子电池是移动设备中能量存储的主要形式,越来越多地用于交通运输中,并且可能是可再生能源存储和集成到电网的候选者。为了发挥其强大的潜力,必须开发出具有更高容量,更快充电速率和更长循环寿命的电极。了解原位条件下单个纳米颗粒的力学和化学性质是改善性能和减轻损伤的关键步骤。在这里,我们揭示了有希望的高压阴极材料LiNi0.5Mn1.5O4在原位条件下在单个纳米粒子中的三维应变演化。在第二个充电周期中,颗粒断开连接。这归因于形成具有缓慢离子传导的阴极电解质中间相层。断开连接后,颗粒内的三维应变模式与电池电压无关,这表明颗粒无法将锂重新分配到其体积内或附近。了解单粒子水平的断开过程以及纳米粒子的平衡或非平衡状态对于提高当前和未来的电化学储能系统的性能至关重要。

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