Evidence for surface effects on the intermolecular interactions in Fe(ii) spin crossover coordination polymers

被引:15
|
作者
Ekanayaka, Thilini K. [1 ]
Kurz, Hannah [2 ]
McElveen, Kayleigh A. [3 ]
Hao, Guanhua [1 ,4 ]
Mishra, Esha [1 ]
N'Diaye, Alpha T. [4 ]
Lai, Rebecca Y. [3 ,5 ]
Weber, Birgit [2 ]
Dowben, Peter A. [1 ]
机构
[1] Univ Nebraska, Dept Phys & Astron, Jorgensen Hall, Lincoln, NE 68588 USA
[2] Univ Bayreuth, Inorgan Chem 4, Univ Str 30,NW 1, D-95447 Bayreuth, Germany
[3] Univ Nebraska, Dept Chem, Hamilton Hall, Lincoln, NE 68588 USA
[4] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
[5] Univ Nebraska, Nebraska Ctr Mat & Nanosci, Voetle Keegan Nano Ctr, Lincoln, NE 68588 USA
基金
美国国家科学基金会;
关键词
X-RAY-STRUCTURE; MAGNETIC-PROPERTIES; THIN-FILMS; THERMAL HYSTERESIS; ELECTRONIC-STRUCTURE; IRON(II); COMPLEX; STATE; FE(PHEN)(2)(NCS)(2); TEMPERATURE;
D O I
10.1039/d1cp04243b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
From X-ray absorption spectroscopy (XAS) and X-ray photoemission spectroscopy (XPS), it is evident that the spin state transition behavior of Fe(ii) spin crossover coordination polymer crystallites at the surface differs from the bulk. A comparison of four different coordination polymers reveals that the observed surface properties may differ from bulk for a variety of reasons. There are Fe(ii) spin crossover coordination polymers with either almost complete switching of the spin state at the surface or no switching at all. Oxidation, differences in surface packing, and changes in coordination could all contribute to making the surface very different from the bulk. Some Fe(ii) spin crossover coordination polymers may be sufficiently photoactive so that X-ray spectroscopies cannot discern the spin state transition.
引用
收藏
页码:883 / 894
页数:12
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