CNRS, Sorbonne Université, IRD, MNHN , Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie , UMR7590 , 75252 Paris cedex 05 , France.
Institut de Chimie Moléculaire et des Matériaux d'Orsay , Université Paris-Sud, CNRS, Université Paris-Saclay , 91405 Orsay cedex , France.
Inorg Chem. 2018 Jul 2;57(13):7610-7619. doi: 10.1021/acs.inorgchem.8b00508. Epub 2018 Jun 13.
CoFe Prussian blue analogues (PBAs) are well-known for their magnetic bistability tuned by external stimuli. The photoswitching properties are due to the electron transfer from Co-NC-Fe to Co-NC-Fe linkage, accompanied by the spin change of the Co ions (HS stands for high spin and LS for low spin). In this work, we investigated 100 nm particles of the RbCo[Fe(CN)]·11HO PBA (named RbCoFe). The photoexcited state of the PBA was reached by red laser excitation (λ = 635 nm) and observed by X-ray absorption spectroscopy and X-ray magnetic circular dichroism (XMCD) that are element-specific probes. The XMCD measurements at the Co and Fe L edges, probing the magnetic 3d orbitals, have provided a direct evidence of the antiferromagnetic interaction between the Co and the Fe ions belonging to the core of the particles, thus confirming the previously published, though indirect XMCD measurements at K edges. Because of the surface sensitivity of XMCD at the L edges, the magnetic properties of the particle surface were also revealed. Surface Co-Fe pairs exhibit a weak ferromagnetic interaction. Thus, the magnetic structure of the photomagnetic RbCoFe 100 nm particles can be described as a ferrimagnetic core surrounded by a ferromagnetic shell. This finding brings new insights into the understanding of the complex magnetic properties of photoexcited RbCoFe and shows that the surface can have different magnetic behavior than the core. This should impact the nature of magnetic coupling in nanoparticles of CoFe PBA, where surface effect will dominate.
钴铁普鲁士蓝类似物 (PBAs) 以其对外界刺激可调的磁双稳性而闻名。光致变色性质归因于 Co-NC-Fe 到 Co-NC-Fe 键的电子转移,伴随着 Co 离子的自旋变化(HS 代表高自旋,LS 代表低自旋)。在这项工作中,我们研究了 RbCo[Fe(CN)]·11HO PBA(命名为 RbCoFe)的 100nm 颗粒。PBA 的光激发态通过红光激光激发(λ=635nm)实现,并通过 X 射线吸收光谱和 X 射线磁圆二色性(XMCD)进行观察,后者是元素特异性探针。在 Co 和 Fe L 边缘的 XMCD 测量中,探测了磁性 3d 轨道,为 Co 和 Fe 离子之间的反铁磁相互作用提供了直接证据,这些离子属于颗粒的核心,从而证实了之前发表的、尽管是间接的 K 边缘的 XMCD 测量。由于 L 边缘的 XMCD 具有表面灵敏度,因此还揭示了颗粒表面的磁性。表面 Co-Fe 对表现出弱铁磁相互作用。因此,光磁 RbCoFe 100nm 颗粒的磁结构可以描述为铁磁核心被铁磁壳包围。这一发现为理解光激发 RbCoFe 的复杂磁性提供了新的见解,并表明表面可能具有与核心不同的磁性行为。这应该会影响 CoFe PBA 纳米颗粒中磁耦合的性质,其中表面效应将占主导地位。