Pt nanoparticles on titania nanotubes prepared by vapor-phase impregnation–decomposition method

2010 ◽  
Vol 495 (2) ◽  
pp. 458-461 ◽  
Author(s):  
C. Encarnación Gómez ◽  
J.R. Vargas García ◽  
J.A. Toledo Antonio ◽  
M.A. Cortes Jacome ◽  
C. Ángeles Chávez
2020 ◽  
Vol 600 ◽  
pp. 117631
Author(s):  
C. Encarnación-Gómez ◽  
M.A. Cortés-Jácome ◽  
A.K. Medina-Mendoza ◽  
C. Angeles- Chávez ◽  
M.G. Hernández-Cruz ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 949
Author(s):  
Lucas Warmuth ◽  
Gülperi Nails ◽  
Maria Casapu ◽  
Sheng Wang ◽  
Silke Behrens ◽  
...  

Titania nanotubes (TNTs) impregnated with Pd and Pt nanoparticles are evaluated as heterogeneous catalysts in different conditions in two reactions: catalytic CO oxidation (gas phase, up to 500 °C) and H2O2 direct synthesis (liquid phase, 30 °C). The TNTs are obtained via oxidation of titanium metal and the intermediate layer-type sodium titanate Na2Ti3O7. Thereafter, the titanate layers are exfoliated and show self-rolling to TNTs, which, finally, are impregnated with Pd or Pt nanoparticles at room temperature by using Pd(ac)2 and Pt(ac)2. The resulting crystalline Pd/TNTs and Pt/TNTs are realized with different lengths (long TNTs: 2.0–2.5 µm, short TNTs: 0.23–0.27 µm) and a specific surface area up to 390 m2/g. The deposited Pd and Pt particles are 2–5 nm in diameter. The TNT-derived catalysts show good thermal (up to 500 °C) and chemical stability (in liquid-phase and gas-phase reactions). The catalytic evaluation results in a low CO oxidation light-out temperature of 150 °C for Pt/TNTs (1 wt-%) and promising H2O2 generation with a productivity of 3240 molH2O2 kgPd−1 h−1 (Pd/TNTs, 5 wt-%, 30 °C). Despite their smaller surface area, long TNTs outperform short TNTs with regard to both CO oxidation and H2O2 formation.


2005 ◽  
Vol 876 ◽  
Author(s):  
Huifang Xu ◽  
Ganesh Vanamu ◽  
Ziming Nie ◽  
Jonathan Phillips ◽  
Yifeng Wang

AbstractPresent work shows that simple, standard methods of metal addition, without the need for ion implantation or other complex and expensive processes, can dramatically improve the performance of titania based structures compared to P25 for (i.e. hydrocarbon oxidation) photocatalytic reactions. In this work, Au and Pt were incorporated into titania nanotubes, and their photocatalytic activities were investigated in detail. The samples were analyzed using a JEOL FEG-2010F field emission gun scanning transmission electron microscopy (STEM) with attached Oxford Instruments' X-ray energy-dispersive spectroscopy (EDS) system and Gatan imaging filtering (GIF) system. Both high-resolution TEM (HRTEM) images and high angle annular dark-field (HAAD) images were recorded for the specimens. The performance of the samples was tested for the oxidation of acetaldehyde using a continuous flow reactor. The pure nanotube is more photoreactive than commercial P25 titania. Both Au and Pt treated nanotube samples increased the photo reactivity. The most significant result of this work is that the activity of Pt (< 1 nm) containing nanotube is more than 10 times the rate of P25, and more than 6 times the rate of the pure nanotube. However, sizes of the Au and Pt nanoparticles on the nanotube surfaces likely affected the photo-reactivity. Large size of the Au and Pt particles decreased the photo-reactivity. Specifically, the addition of platinum without formation of obvious nanoparticles on the nanotube surfaces increased the maximum activity significantly, and increased the total yield.


2019 ◽  
Vol 25 (8) ◽  
pp. 763-770 ◽  
Author(s):  
Chen Jin ◽  
Marie Holz ◽  
Wei Xia ◽  
Bastian Mei ◽  
Shankhamala Kundu ◽  
...  

Author(s):  
Nithin Poonkottil ◽  
Ranjith K. Ramachandran ◽  
Eduardo Solano ◽  
Nadadur Veeraraghavan Srinath ◽  
Ji-Yu Feng ◽  
...  
Keyword(s):  

1987 ◽  
Vol 29 (1) ◽  
pp. 107-115 ◽  
Author(s):  
Satoshi Sato ◽  
Shin Hasebe ◽  
Hiroaki Sakurai ◽  
Kazuo Urabe ◽  
Yusuke Izumi

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