Ultra-low-voltage observation of battery materials by scanning electron microscopy.

Yoichiro Hashimoto, Yutaka Nagaoka, Toru Aiso, Shuhei Yabu, Masahiro Sasajima
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Abstract

The mechanism of voltage contrast formation under ultra-low landing energy condition is discussed, by which a binder contained in lithium-ion battery anode material has been visualized with high contrast. Since the anode material is a complex experimental system with multiple contrast formation factors, a standard sample simulating it was fabricated for simplification. The binder was observed darker than the substrate at landing energies of 30 eV to 50 eV. The binder exhibited a distinct appearance reflecting its shape (in the 3D-particle mode) at 20 eV. The mirroring phenomenon occurred at 10 eV, in which the primary electrons bounced off the sample before irradiating on the surface. The surface potential at the electron beam irradiation moment was presumed to affect the contrast formation, but direct measurement of it was difficult. Thus, the sample was transferred to an AFM without exposure to the atmosphere to measure the "residual" potential of the binder in KPFM mode after the SEM observations. Under darker binder observed conditions of 30 eV to 50 eV, KPFM measured residual potential was positive relative to the substrate. Under conditions of the 3D-particle mode at 20 eV and the mirroring phenomenon at 10 eV, the residual potentials were negative. Therefore, a correlation between the behavior of the voltage contrast and the residual potential was obtained. Finer landing-energy step measurement revealed hysteresis responses of voltage contrast and the residual potential to the landing energy. The Cause of the hysteresis was discussed. The mechanism of voltage contrast formation under ultra-low landing energy condition is discussed, by which a binder contained in lithium-ion battery material has been visualized with high contrast. We confirmed that the contrast change is caused by the surface potential change depending on the landing energy of the primary electron.

电池材料的超低电压扫描电镜观察。
探讨了超低落地能条件下形成电压对比的机理,实现了锂离子电池负极材料中粘结剂的高对比度可视化。由于阳极材料是一个复杂的实验系统,具有多个对比形成因素,为了简化,制作了一个模拟它的标准样品。在30 ~ 50 eV的能量范围内,粘结剂比衬底颜色更深。在20ev下,粘结剂表现出明显的反映其形状的外观(在3d粒子模式下)。在10 eV时发生了镜像现象,其中初级电子在照射到样品表面之前从样品上反弹。假设电子束辐照时刻的表面电位影响着造影剂的形成,但直接测量它是困难的。因此,样品被转移到AFM中,而不暴露于大气中,以测量扫描电镜观察后KPFM模式下粘合剂的“残余”电位。在30 eV至50 eV的较暗粘结剂条件下,KPFM测量的残余电位相对于衬底为正。在20 eV的3d粒子模式和10 eV的镜像现象条件下,剩余电位为负。因此,得到了电压对比性能与剩余电位之间的相关性。精细的着陆能量阶跃测量揭示了电压对比和剩余电位对着陆能量的滞后响应。讨论了磁滞产生的原因。探讨了超低落地能条件下电压对比形成的机理,实现了锂离子电池材料中粘结剂的高对比度可视化。我们证实了对比的变化是由表面电位的变化引起的,这取决于一次电子的着陆能量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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