磷钨酸
化学
透射电子显微镜
扫描电子显微镜
电化学
纳米结构
无机化学
化学工程
晶体结构
结晶学
电极
催化作用
有机化学
物理化学
物理
量子力学
工程类
作者
Björn Greijer,Wannes De Turck,Geoffrey Daniel,Jayeeta Saha,Mats Johnsson,Gulaim A. Seisenbaeva,Vadim G. Kessler
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-02-07
卷期号:63 (7): 3428-3435
被引量:1
标识
DOI:10.1021/acs.inorgchem.3c04122
摘要
Subjecting phosphotungstic acid solutions to low pH in combination with introduction of polyvalent cations led to the formation of nanostructured microspheres of approximately 2 μm in size, as shown by scanning electron microscopy, which were almost insoluble and resistant to degradation at neutral and high pH. These microspheres were composed of secondary nanospheres with diameters around 20 nm as revealed by transmission electron microscopy and atomic force microscopy. Investigations of the crystal structure of a potential intermediate of this process, namely, acidic lanthanum phosphotungstate, [La(H2O)9](H3O)3[PW12O40]2(H2O)19, showed a tight network of hydrogen bonding, permitting closer packing of phosphotungstic acid anions, thereby confirming the mechanism of the observed self-assembly process. The new material demonstrated promising electrochemical properties in oxygen evolution reactions with the high stability of the obtained electrode material.
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