Department of Physics and Astronomy, University of California, Irvine, CA 92697-4575, USA.
State Key Laboratory of Surface Physics and Key Laboratory for Computational Physical Sciences (MOE) and Department of Physics, Fudan University, Shanghai, 200433, China.
Science. 2019 May 17;364(6441):670-673. doi: 10.1126/science.aaw7505. Epub 2019 May 16.
Magnetic single atoms and molecules are receiving intensifying research focus because of their potential as the smallest possible memory, spintronic, and qubit elements. Scanning probe microscopes used to study these systems have benefited greatly from new techniques that use molecule-functionalized tips to enhance spatial and spectroscopic resolutions and enable new sensing capabilities. We demonstrate a microscopy technique that uses a magnetic molecule, Ni(cyclopentadienyl), adsorbed at the apex of a scanning probe tip, to sense exchange interactions with another molecule adsorbed on a Ag(110) surface in a continuously tunable fashion in all three spatial directions. We further used the probe to image contours of exchange interaction strength, revealing angstrom-scale regions where the quantum states of two magnetic molecules strongly mix. Our results pave the way for new nanoscale imaging capabilities based on magnetic single-molecule sensors.
磁性单原子和单分子由于有望成为最小的存储、自旋电子学和量子比特元件而受到越来越多的研究关注。用于研究这些系统的扫描探针显微镜极大地受益于新技术,这些新技术使用分子功能化尖端来提高空间和光谱分辨率,并实现新的传感功能。我们展示了一种显微镜技术,该技术使用吸附在扫描探针尖端顶点的磁性分子 Ni(环戊二烯基),以连续可调的方式在所有三个空间方向上感应与吸附在 Ag(110)表面上的另一个分子的交换相互作用。我们进一步使用探针来绘制交换相互作用强度的轮廓,揭示出两个磁性分子的量子态强烈混合的埃级区域。我们的结果为基于磁性单分子传感器的新纳米级成像能力铺平了道路。