TY - JOUR
T1 - Novel issues of morphology, size, and structure of Pt nanoparticles in chemical engineering
T2 - Surface attachment, aggregation or agglomeration, assembly, and structural changes
AU - Long, Nguyen Viet
AU - Thi, Cao Minh
AU - Nogami, Masayuki
AU - Ohtaki, Michitaka
PY - 2012/6
Y1 - 2012/6
N2 - In this paper, the polyhedral Pt nanoparticles were prepared by a modified polyol method using AgNO3 as a nanostructure-shaping agent. TEM and HRTEM images of Pt nanoparticles show the particle size in the 10 nm range for the well-controlled case. In contrast, Pt nanoparticles have the particle size in the 50 nm range for the uncontrolled case. To understand the important issues of morphology, size, surface and structure, the as-prepared Pt nanoparticles were investigated through UV-vis spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and high-resolution (HR)TEM measurements. In the two cases, the as-prepared Pt nanoparticles with and without the control procedures exhibit surface attachment, aggregation or agglomeration and assembly. The mechanisms can lead to the formation of the ultra-porous mesostructure of the as-prepared Pt nanoparticles by using various sophisticated control methods. Therefore, the experimental findings and observations showed the formations of the porous Pt nanostructures as the new Pt textures from self-aggregation or self-agglomeration and self-assembly of extreme importance in designing great superlattices under experimentally chemical and physical methods. This also proved the important role of PVP polymer in the protection of the as-prepared nanoparticles. In particular, a new phenomenon was found in the randomly natural collapse and self-breaking in the Pt nanostructures originating from the naked Pt nanoparticles without protective polymer agents. As a result, a porous meso-nanostructure was formed by the structural changes of Pt nanoparticles without stabilization of the PVP polymer. Finally, the discoveries of surface structure changes of polyhedral Pt shapes and morphologies in future are very important in further catalysis investigation.
AB - In this paper, the polyhedral Pt nanoparticles were prepared by a modified polyol method using AgNO3 as a nanostructure-shaping agent. TEM and HRTEM images of Pt nanoparticles show the particle size in the 10 nm range for the well-controlled case. In contrast, Pt nanoparticles have the particle size in the 50 nm range for the uncontrolled case. To understand the important issues of morphology, size, surface and structure, the as-prepared Pt nanoparticles were investigated through UV-vis spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and high-resolution (HR)TEM measurements. In the two cases, the as-prepared Pt nanoparticles with and without the control procedures exhibit surface attachment, aggregation or agglomeration and assembly. The mechanisms can lead to the formation of the ultra-porous mesostructure of the as-prepared Pt nanoparticles by using various sophisticated control methods. Therefore, the experimental findings and observations showed the formations of the porous Pt nanostructures as the new Pt textures from self-aggregation or self-agglomeration and self-assembly of extreme importance in designing great superlattices under experimentally chemical and physical methods. This also proved the important role of PVP polymer in the protection of the as-prepared nanoparticles. In particular, a new phenomenon was found in the randomly natural collapse and self-breaking in the Pt nanostructures originating from the naked Pt nanoparticles without protective polymer agents. As a result, a porous meso-nanostructure was formed by the structural changes of Pt nanoparticles without stabilization of the PVP polymer. Finally, the discoveries of surface structure changes of polyhedral Pt shapes and morphologies in future are very important in further catalysis investigation.
UR - http://www.scopus.com/inward/record.url?scp=84865659149&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84865659149&partnerID=8YFLogxK
U2 - 10.1039/c2nj40027h
DO - 10.1039/c2nj40027h
M3 - Article
AN - SCOPUS:84865659149
SN - 1144-0546
VL - 36
SP - 1320
EP - 1334
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 6
ER -