Cheng Suqin, Xue Zhijie, Li Can, Liu Yufeng, Xiang Longjun, Ke Youqi, Yan Kaking, Wang Shiyong, Yu Ping
School of Physical Science and Technology, ShanghaiTech University, 201210, Shanghai, China.
Key Laboratory of Artificial Structures and Quantum Control (Ministry of Education), Shenyang National Laboratory for Materials Science, School of Physics and Astronomy, Shanghai Jiao Tong University, 200240, Shanghai, China.
Nat Commun. 2022 Mar 31;13(1):1705. doi: 10.1038/s41467-022-29371-9.
Triangulene and its homologues are of considerable interest for molecular spintronics due to their high-spin ground states as well as the potential for constructing high spin frameworks. Realizing triangulene-based high-spin system on surface is challenging but of particular importance for understanding π-electron magnetism. Here, we report two approaches to generate triangulene trimers on Au(111) by using surface-assisted dehydration and alkyne trimerization, respectively. We find that the developed dehydration reaction shows much higher chemoselectivity thus resulting in significant promotion of product yield compared to that using alkyne trimerization approach, through cutting the side reaction path. Combined with spin-polarized density functional theory calculations, scanning tunneling spectroscopy measurements identify the septuple (S = 3) high-spin ground state and quantify the collective ferromagnetic interaction among three triangulene units. Our results demonstrate the approaches to fabricate high-quality triangulene-based high spin systems and understand their magnetic interactions, which are essential for realizing carbon-based spintronic devices.
由于其高自旋基态以及构建高自旋框架的潜力,三角烯及其同系物在分子自旋电子学领域备受关注。在表面实现基于三角烯的高自旋体系具有挑战性,但对于理解π电子磁性尤为重要。在此,我们报告了分别通过表面辅助脱水和炔烃三聚反应在Au(111)上生成三角烯三聚体的两种方法。我们发现,与使用炔烃三聚反应方法相比,所开发的脱水反应具有更高的化学选择性,通过切断副反应路径,从而显著提高了产物产率。结合自旋极化密度泛函理论计算,扫描隧道谱测量确定了七重态(S = 3)的高自旋基态,并量化了三个三角烯单元之间的集体铁磁相互作用。我们的结果展示了制备高质量基于三角烯的高自旋体系并理解其磁相互作用的方法,这对于实现碳基自旋电子器件至关重要。