Understanding the Growth of Electrodeposited PtNi Nanoparticle Films Using Correlated In Situ Liquid Cell Transmission Electron Microscopy and Synchrotron Radiation

被引:2
作者
Parlinska-Wojtan, Magdalena [1 ]
Tarnawski, Tomasz Roman [1 ]
Depciuch, Joanna [1 ,2 ]
De Marco, Maria Letizia [3 ,4 ]
Sobczak, Kamil [5 ]
Matlak, Krzysztof [6 ]
Pawlyta, Miroslawa [7 ]
Schaeublin, Robin E. [8 ]
Chee, See Wee [3 ]
机构
[1] Polish Acad Sci, Inst Nucl Phys, PL-31342 Krakow, Poland
[2] Med Univ Lublin, Dept Biochem & Mol Biol, PL-20093 Lublin, Poland
[3] Max Planck Gesell, Dept Interface Sci, Fritz Haber Inst, D-14195 Berlin, Germany
[4] Univ Strasbourg, Inst Phys & Chim Mat Strasbourg, UMR 7504 CNRS, 23 Rue Loess,BP 43, F-67034 Strasbourg 2, France
[5] Fac Chem, Biol & Chem Res Ctr, PL-02089 Warsaw, Poland
[6] Jagiellonian Univ, Solaris Natl Synchrotron Radiat Ctr, PL-30392 Krakow, Poland
[7] Silesian Tech Univ, Mat Res Lab, PL-44100 Gliwice, Poland
[8] Swiss Fed Inst Technol, ScopeM Sci Ctr Opt & Electron Microscopy, CH-8093 Zurich, Switzerland
基金
美国国家科学基金会;
关键词
PtNi nanoparticles; LC-TEM; electrodeposition; STXM; in situ; OXYGEN REDUCTION; PLATINUM; METAL; NMR; COMPLEXES; CATALYSTS;
D O I
10.1021/acs.nanolett.4c02228
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrodeposition is a versatile method for synthesizing nanostructured films, but controlling the morphology of films containing two or more elements requires a detailed understanding of the deposition process. We used liquid cell transmission electron microscopy to follow the electrodeposition of PtNi nanoparticle films on a carbon electrode during cyclic voltammetry. These in situ observations show that the film thickness increases with each cycle, and by the fourth cycle, branched and porous structures could be deposited. Synchrotron studies using in situ transmission X-ray microscopy further revealed that Ni was deposited in the oxide phase. Ex situ studies of bulk electrodeposited PtNi nanoparticle films indicated the number of cycles and the scanning rate were the most influential parameters, resulting in a different thickness, a different homogeneity, a different nanoparticle size, and a different surface structure, while the precursor concentration did not have a significant influence. By varying the potential range, we were able to obtain films with different elemental compositions.
引用
收藏
页码:12361 / 12367
页数:7
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