Understanding the structure and properties of the elusive non-stoichiometric lead dioxide

Tiffany L. Kinnibrugh, Tim Fister, Xiaoping Wang, D. Bazak, Ajay Karakoti, Vijayakumar Murugesan
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Abstract

Underutilization of the active material on the positive plate has been a persistent restriction on the performance of lead - acid batteries. Initial utilization of chemically - prepared and PbO2 phases formed in a battery during charge suggests that the stoichiometries change with cycling1 and proximity to oxygen evolution. Moreover, the lifetime of the battery is often limited by the ratio of α and β -Pb O2 and the adhesion between PbO2 and the underlying Pb current collector. This interface, referred to as the “corrosion layer” is thought to contain lead oxides with intermediate composition between PbO and PbO2. Similar phases have previously been identified by mass loss or color change during thermal decomposition of PbO2 to PbO, suggesting at least two phases2, 3. Here, we identify the structure of these phases using multiple in situ analysis techniques. Isolation of PbOx phase/s using TGA enabled determination of a PbOx structure and further analysis with NMR and XPS to provide Pb oxidation states and Pb environments. Finally, we compare these results to data collected from industrial battery plates.
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了解难以捉摸的非化学计量二氧化铅的结构和性质
正极板活性材料利用率不足一直是限制铅酸电池性能的一个因素。对化学制备的电池和充电过程中形成的 PbO2 相的初步利用表明,电池的化学计量学会随着循环1 和氧气进化的接近而改变。此外,电池的寿命通常受限于 α 和 β -Pb O2 的比率以及 PbO2 与底层 Pb 集流体之间的附着力。这个界面被称为 "腐蚀层",据认为其中含有介于 PbO 和 PbO2 之间的铅氧化物。以前曾通过 PbO2 热分解为 PbO 过程中的质量损失或颜色变化确定过类似的相,这表明至少有两种相2、3。在此,我们利用多种原位分析技术确定了这些相的结构。利用 TGA 分离出 PbOx 相/相,从而确定了 PbOx 结构,并利用 NMR 和 XPS 进行进一步分析,以提供铅氧化态和铅环境。最后,我们将这些结果与从工业电池板收集的数据进行了比较。
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