Reinhard Marco, Kunnus Kristjan, Ledbetter Kathryn, Biasin Elisa, Zederkof Diana Bregenholt, Alonso-Mori Roberto, van Driel Tim Brandt, Nelson Silke, Kozina Michael, Borkiewicz Olaf J, Lorenc Maciej, Cammarata Marco, Collet Eric, Sokaras Dimosthenis, Cordones Amy A, Gaffney Kelly J
SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States.
Department of Physics, Stanford University, Stanford, California 94305, United States.
ACS Nano. 2024 Jun 18;18(24):15468-15476. doi: 10.1021/acsnano.3c10042. Epub 2024 Jun 4.
Spin transition (ST) materials are attractive for developing photoswitchable devices, but their slow material transformations limit device applications. Size reduction could enable faster switching, but the photoinduced dynamics at the nanoscale remains poorly understood. Here, we report a femtosecond optical pump multimodal X-ray probe study of polymeric nanorods. Simultaneously tracking the ST order parameter with X-ray emission spectroscopy and structure with X-ray diffraction, we observe photodoping of the low-spin-lattice within ∼150 fs. Above a ∼16% photodoping threshold, the transition to the high-spin phase occurs following an incubation period assigned to vibrational energy redistribution within the nanorods activating the molecular spin switching. Above ∼60% photodoping, the incubation period disappears, and the transition completes within ∼50 ps, preceded by the elastic nanorod expansion in response to the photodoping. These results support the feasibility of ST material-based GHz optical switching applications.
自旋转变(ST)材料对于开发光开关器件具有吸引力,但其缓慢的材料转变限制了器件应用。减小尺寸可以实现更快的切换,但纳米尺度下的光致动力学仍知之甚少。在此,我们报告了对聚合物纳米棒的飞秒光泵浦多模态X射线探针研究。通过X射线发射光谱同时跟踪ST序参量,并利用X射线衍射跟踪结构,我们观察到在约150飞秒内低自旋晶格的光掺杂。在约16%的光掺杂阈值以上,在一段分配给纳米棒内振动能量重新分布以激活分子自旋切换的潜伏期后,向高自旋相的转变发生。在约60%的光掺杂以上,潜伏期消失,转变在约50皮秒内完成,之前是纳米棒因光掺杂而发生的弹性膨胀。这些结果支持了基于ST材料的GHz光开关应用的可行性。