Sequential growth at the sub-10 nm scale of cyanide bridged coordination networks on inorganic surfaces

被引:14
作者
Tricard, Simon [1 ]
Charra, Fabrice [2 ]
Mallah, Talal [1 ]
机构
[1] Univ Paris 11, UMR CNRS 8182, Inst Chim Mol & Mat Orsay, F-91405 Orsay, France
[2] CEA, IRAMIS, SPCSI, Lab Organ Elect & Nanophoton, F-91191 Gif Sur Yvette, France
关键词
FUNCTIONALIZED SI(100) SURFACE; SINGLE-MOLECULE DYNAMICS; PRUSSIAN BLUE ANALOGS; PHOTOINDUCED MAGNETIZATION; SPIN-CROSSOVER; IRON CYANIDE; NANOPARTICLES; FILMS; TEMPERATURE; MAGNETS;
D O I
10.1039/c3dt51636a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The elaboration of coordination networks' nano-objects on surfaces can be realized by sequential growth in solution (SGS). This bottom-up strategy gives the possibility to control the size, the isolation and the organization of the objects with a precision going up to the molecular scale. Detailed descriptions of the growth of the nickel(II)-iron(II) Prussian blue analog and of the copper-molybdenum cyanide-bridged coordination network are reported to give insight about the mechanisms of the growth. Then a comparative XPS analysis has been performed to explain the different reactivity of the precursors of the growth of the nickel(II)-iron(II) and nickel(II)-chromium(III) Prussian blue analogs. This perspective article proves that SGS can be optimized for each coordination system to build molecular superstructures on surfaces, with interesting physical properties towards chemical devices.
引用
收藏
页码:15835 / 15845
页数:11
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