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铁(II)自旋交叉配合物的超薄薄膜:可见光和真空紫外光致电子结构和自旋态转变。

Iron(II) spin-crossover complexes in ultrathin films: electronic structure and spin-state switching by visible and vacuum-UV light.

机构信息

Institut für Experimentelle und Angewandte Physik, Christian-Albrechts-Universität zu Kiel, 24098 Kiel (Germany) www.ieap.uni-kiel.de/surface/ag-kipp.

出版信息

Angew Chem Int Ed Engl. 2014 Mar 10;53(11):3019-23. doi: 10.1002/anie.201307968. Epub 2014 Feb 12.

DOI:10.1002/anie.201307968
PMID:24519743
Abstract

The electronic structure of the iron(II) spin crossover complex [Fe(H2bpz)2(phen)] deposited as an ultrathin film on Au(111) is determined by means of UV-photoelectron spectroscopy (UPS) in the high-spin and in the low-spin state. This also allows monitoring the thermal as well as photoinduced spin transition in this system. Moreover, the complex is excited to the metastable high-spin state by irradiation with vacuum-UV light. Relaxation rates after photoexcitation are determined as a function of temperature. They exhibit a transition from thermally activated to tunneling behavior and are two orders of magnitude higher than in the bulk material.

摘要

通过在 Au(111) 上沉积的超薄薄膜中铁(II)自旋交叉配合物[Fe(H2bpz)2(phen)]的紫外光电子能谱(UPS),确定了其电子结构,该配合物在高自旋态和低自旋态下均能进行测定。这也允许对该系统中的热诱导和光诱导自旋转变进行监测。此外,该配合物通过真空紫外光照射被激发到亚稳态的高自旋态。光激发后的弛豫速率随温度的变化而确定。它们表现出从热激活到隧道行为的转变,并且比体材料中的弛豫速率高两个数量级。

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