纳米笼
纳米晶
铜
纳米材料
硫化铜
晶体结构
纳米技术
硫化镉
离子
离子交换
氧化物
材料科学
化学
无机化学
结晶学
冶金
催化作用
有机化学
生物化学
作者
Hsin-Lun Wu,Ryota Sato,Atsushi Yamaguchi,Masato Kimura,Mitsutaka Haruta,Hiroki Kurata,Toshiharu Teranishi
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2016-03-18
卷期号:351 (6279): 1306-1310
被引量:129
标识
DOI:10.1126/science.aad5520
摘要
The crystal structure of ionic nanocrystals (NCs) is usually controlled through reaction temperature, according to their phase diagram. We show that when ionic NCs with different shapes, but identical crystal structures, were subjected to anion exchange reactions under ambient conditions, pseudomorphic products with different crystal systems were obtained. The shape-dependent anionic framework (surface anion sublattice and stacking pattern) of Cu2O NCs determined the crystal system of anion-exchanged products of CuxS nanocages. This method enabled us to convert a body-centered cubic lattice into either a face-centered cubic or a hexagonally close-packed lattice to form crystallographically unusual, multiply twinned structures. Subsequent cation exchange reactions produced CdS nanocages while preserving the multiply-twinned structures. A high-temperature stable phase such as wurtzite ZnS was also obtained with this method at ambient conditions.
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