过饱和度
电解质
化学
强电解质
碘酸盐
离解(化学)
结晶
模板
化学工程
降水
纳米材料
金属
纳米颗粒
无机化学
纳米技术
碘化物
材料科学
物理化学
有机化学
气象学
工程类
物理
电极
作者
Wei‐Hong Lai,Yunxiao Wang,Yong Wang,Minghong Wu,Jiazhao Wang,Huan Liu,Shulei Chou,Jun Chen,Shi Xue Dou
出处
期刊:Nature Chemistry
[Springer Nature]
日期:2019-07-24
卷期号:11 (8): 695-701
被引量:98
标识
DOI:10.1038/s41557-019-0298-6
摘要
The precise control of the morphology of inorganic materials during their synthesis is important yet challenging. Here we report that the morphology of a wide range of inorganic materials, grown by rapid precipitation from a metal cation solution, can be tuned during their crystallization from one- to three-dimensional (1D to 3D) structures without the need for capping agents or templates. This control is achieved by adjusting the balance between the electrolytic dissociation (α) of the reactants and the supersaturation (S) of the solutions. Low-α, weak electrolytes promoted the growth of anisotropic (1D and 2D) samples, with 1D materials favoured in particular at low S. In contrast, isotropic 3D polyhedral structures could only be prepared in the presence of strong electrolyte reactants (α ≈ 1) with low S. Using this strategy, a wide range of materials were prepared, including metal oxides, hydroxides, carbonates, molybdates, oxalates, phosphates, fluorides and iodate with a variety of morphologies.
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