X-ray Science Division, Advanced Photon Source, Center for Nanoscale Materials, Argonne National Laboratory , Argonne, Illinois 60439, United States.
Center for Functional Nanomaterials, Brookhaven National Laboratory , Upton, New York 11973, United States.
ACS Nano. 2017 Feb 28;11(2):1443-1454. doi: 10.1021/acsnano.6b06708. Epub 2017 Feb 7.
Emergent lithium-ion (Li) batteries commonly rely on nanostructuring of the active electrode materials to decrease the Li ion diffusion path length and to accommodate the strains associated with the insertion and de-insertion of Li, but in many cases these nanostructures evolve during electrochemical charging-discharging. This change in the nanostructure can adversely impact performance, and challenges remain regarding how to control these changes from the perspective of morphological design. In order to address these questions, operando grazing-incidence small-angle X-ray scattering and X-ray diffraction (GISAXS/GIXD) were used to assess the structural evolution of a family of model ordered mesoporous NiCoO anode films during battery operation. The pore dimensions were systematically varied and appear to impact the stability of the ordered nanostructure during the cycling. For the anodes with small mesopores (≈9 nm), the ordered nanostructure collapses during the first two charge-discharge cycles, as determined from GISAXS. This collapse is accompanied by irreversible Li-ion insertion within the oxide framework, determined from GIXD and irreversible capacity loss. Conversely, anodes with larger ordered mesopores (17-28 nm) mostly maintained their nanostructure through the first two cycles with reversible Li-ion insertion. During the second cycle, there was a small additional deformation of the mesostructure. This preservation of the ordered structure lead to significant improvement in capacity retention during these first two cycles; however, a gradual loss in the ordered nanostructure from continuing deformation of the ordered structure during additional charge-discharge cycles leads to capacity decay in battery performance. These multiscale operando measurements provide insight into how changes at the atomic scale (lithium insertion and de-insertion) are translated to the nanostructure during battery operation. Moreover, small changes in the nanostructure can build up to significant morphological transformations that adversely impact battery performance through multiple charge-discharge cycles.
新兴的锂离子(Li)电池通常依赖于活性电极材料的纳米结构化来减小 Li 离子扩散路径长度,并适应与 Li 的插入和脱插相关的应变,但在许多情况下,这些纳米结构在电化学充电-放电过程中会发生演变。这种纳米结构的变化会对性能产生不利影响,并且在从形态设计的角度控制这些变化方面仍然存在挑战。为了解决这些问题,使用掠入射小角 X 射线散射和 X 射线衍射(GISAXS/GIXD)来评估一系列模型有序介孔 NiCoO 阳极薄膜在电池运行过程中的结构演变。系统地改变了孔径尺寸,并且似乎会影响循环过程中有序纳米结构的稳定性。对于具有小介孔(≈9nm)的阳极,有序纳米结构在头两个充放电循环中坍塌,这是通过 GISAXS 确定的。这种坍塌伴随着氧化物骨架内不可逆的 Li 离子插入,这是通过 GIXD 和不可逆容量损失确定的。相反,具有较大有序介孔(17-28nm)的阳极在头两个循环中主要通过可逆 Li 离子插入来维持其纳米结构。在第二个循环中,介孔结构有一个小的附加变形。这种有序结构的保留导致在前两个循环中显著提高了容量保持率;然而,在额外的充放电循环中,有序结构的持续变形导致有序纳米结构的逐渐损失,从而导致电池性能的容量衰减。这些多尺度原位测量提供了深入了解原子尺度上的变化(Li 的插入和脱插)如何在电池运行过程中转化为纳米结构。此外,纳米结构的微小变化会逐渐累积到显著的形态转变,从而通过多个充放电循环对电池性能产生不利影响。