Breuer S, Uitz M, Wilkening H M R
Christian Doppler Laboratory for Lithium Batteries, and Institute for Chemistry and Technology of Materials , Graz University of Technology , Stremayrgasse 9 , 8010 Graz , Austria.
Alistore-ERI European Research Institute , 33 rue Saint Leu , 80039 Amiens , France.
J Phys Chem Lett. 2018 Apr 19;9(8):2093-2097. doi: 10.1021/acs.jpclett.8b00418. Epub 2018 Apr 12.
Diffusive processes are ubiquitous in nature. In solid state physics, metallurgy and materials science the diffusivity of ions govern the functionality of many devices such as sensors or batteries. Motional processes on surfaces, across interfaces or through membranes can be quite different to that in the bulk. A direct, quantitative description of such local diffusion processes is, however, rare. Here, we took advantage of Li longitudinal nuclear magnetic relaxation to study, on the atomic length scale, the diffusive motion of lithium spins in the interfacial regions of nanocrystalline, orthorhombic LiBH. Magnetization transients and free induction decays revealed a fast subset of Li ions having access to surface pathways that offer activation barriers (0.18 eV) much lower than those in the crystalline bulk regions (0.55 eV). These observations make orthorhombic borohydride a new nanostructured model system to study disorder-induced enhancements in interfacial diffusion processes.
扩散过程在自然界中无处不在。在固态物理学、冶金学和材料科学中,离子的扩散率决定了许多器件(如传感器或电池)的功能。表面、跨界面或通过膜的运动过程可能与本体中的运动过程有很大不同。然而,对这种局部扩散过程的直接、定量描述却很少见。在这里,我们利用锂纵向核磁共振弛豫,在原子长度尺度上研究了锂自旋在纳米晶正交晶系LiBH界面区域的扩散运动。磁化瞬态和自由感应衰减揭示了一部分快速移动的锂离子能够进入表面通道,这些通道提供的激活势垒(0.18电子伏特)比晶体本体区域(0.55电子伏特)的要低得多。这些观察结果使正交硼氢化物成为研究无序诱导的界面扩散过程增强的新型纳米结构模型体系。