Enhancement of catalytic activity of Pd-PVP colloid for direct H2O2 synthesis from H2 and O2 in water with addition of 0.5 atom% Pt or Ir

2018 ◽  
Vol 8 (4) ◽  
pp. 1002-1015 ◽  
Author(s):  
Takashi Deguchi ◽  
Hitoshi Yamano ◽  
Sho Takenouchi ◽  
Masakazu Iwamoto

Atomically dispersed Pt or Ir atoms enhance H2O2 and H2O formation on Pd nano-particles leaving the H2O2 hydrogenation rate unchanged, while Ru, Rh, or Au atoms show little effect.

2008 ◽  
Vol 139 ◽  
pp. 41-46 ◽  
Author(s):  
K. Okazaki-Maeda ◽  
Y. Morikawa ◽  
Shingo Tanaka ◽  
Masanori Kohyama

Pt nano-particles are supported on carbon materials at the electrode catalysts of protonexchange menbrane fuel cells. Pt nano-particles are desirable to be strongly adsorbed on carbon materials for high dispersion, although strong Pt-C interactions may affect the catalytic activity of small clusters. Thus we have examined H-atom absorption on Pt clusters supported or unsupported on graphene sheets, using first-principles calculations. For Pt-atom/graphene systems, a H atom is more weakly adsorbed than for a free Pt atom, and the H-Pt interaction becomes weaker if the interaction between a Pt atom and graphene becomes stronger. For the Ptn-cluster/graphene systems (n=2-4), the H-Pt interactions are also substantially changed from those for free Pt clusters. In the Pt clusters on graphene, the Pt-Pt distances are substantially changed associated with the electronicstructure changes by the Pt-C interactions. These structural and electronic changes in the Pt clusters as well as the presence of graphene itself seem to cause the changes in the absorption energies and preferential sites of H-atom absorption.


2009 ◽  
Vol 2 (1) ◽  
pp. 35-41 ◽  
Author(s):  
Fatemeh F. Bamoharram ◽  
Majid M. Heravi ◽  
Mina Roushani ◽  
Maryam R. Toosi ◽  
Ladan Jodeyre

2013 ◽  
Vol 57 (1-4) ◽  
pp. 273-281 ◽  
Author(s):  
Egill Skúlason ◽  
Avan A. Faraj ◽  
Lilja Kristinsdóttir ◽  
Javed Hussain ◽  
Anna L. Garden ◽  
...  

2015 ◽  
Vol 15 (11) ◽  
pp. 8494-8501 ◽  
Author(s):  
Young Eun Jeong ◽  
Pullur Anil Kumar ◽  
Hee Lack Choi ◽  
Kwan-Young Lee ◽  
Heon Phil Ha

2014 ◽  
Vol 10 (2) ◽  
pp. 312-317 ◽  
Author(s):  
Ali Reza Rajabi ◽  
Saeid Jabbarzare ◽  
Mohammad Reza Mohammad Shafiee ◽  
Majid Ghashang

2016 ◽  
Vol 2 (1) ◽  
pp. 75 ◽  
Author(s):  
Sh.S. Itkulova ◽  
G.D. Zakumbaeva

<p>Bimetallic cobalt-containing catalysts supported on alumina have been studied in the Fischer-Tropsch synthesis. It has been shown that a promotion of Co/Al<sub>2</sub>O<sub>3</sub> by iridium leads to dispergation of both metals. It was supposed that the metal dispergation occurred due to M-M interaction with formation of the bimetallic nano-particles of cluster type. These particles have the high catalytic activity, selectivity and stability in the Fischer-Tropsch synthesis. It was observed that by regulation of the process conditions it is possible to obtain the definite hydrocarbon fractions. Thus, the increase both CO+H<sub>2</sub> ratio and space velocity is accompanied by high olefin yield.</p>


2015 ◽  
Vol 3 (20) ◽  
pp. 11048-11056 ◽  
Author(s):  
Yifei Sun ◽  
Jianhui Li ◽  
Yimin Zeng ◽  
Babak Shalchi Amirkhiz ◽  
Mengni Wang ◽  
...  

Introduction of A-site deficiency on Ni-doped LaSrCrO3 anodes helps form highly mobile oxygen vacancies and remarkably enhances Ni nanoparticle reducibility, and significantly increases electronic conductivity and catalytic activity.


2020 ◽  
Vol 16 ◽  
Author(s):  
Shatendra Sharma ◽  
Monika Vats ◽  
Jyotsna Sharma ◽  
Arvind Chhabra ◽  
R. K. Rakesh Kumar ◽  
...  

Background: Tin oxide nano-particles also show good photo-catalytic efficiency because of its wide band gap and high recombination rates of photo-generated electron-hole pairs. Being non-toxic and chemically stable, the tin oxide nano-particles are used as dynamic photo-catalyst for the degradation. Tin oxide nano-crystals suitable for charge storage devices are synthesized using co-precipitation technique. Objectives: Synthesis of Tin oxide nano-crystals by using co-precipitation method for photo-catalytic activity under sunlight that can be used for photo-degradation. The method of synthesis and characterization are discussed. Materials and Methods: The nano-crystals are prepared by co-precipitation method using stannic chloride and sodium carbonate. sodium carbonate is added under constant stirring drop by drop for 90 minutes. The solution is settled for 4 hours. The precipitates are first washed using de-ionized water and then with ethyl alcohol. The dried powder of nanocrystals is then calcinated at 500oC for one hour in a muffle furnace. The structural, morphological, optical and electrical characterization of these synthesized crystals is done using (XRD), (FESEM), (TEM), (UV-Visible), (FT-Raman), Zeta potential and dielectric constant measurements. Results and Discussion: The sizes of synthesized nano-crystals vary from 25 nm to 100 nm and are found to be optically transparent. The dielectric constant of nano-crystals is measured in the frequency range of 100Hz-1MHz and it can be seen that it declines from ~2000 at frequency 100Hz to ~30 at 1MHz.However, this decline in dielectric constant with frequency can be explained well on the basis of strong space charge polarization and rotational direction polarization processes in nanostructures. In the high frequency regions, these processes cannot follow the electrical field frequency variations that results in the rapid decrease of dielectric constant. Photo-catalytic activity: The photo-catalytic activity of the particles under sun light is also investigated which shows that the crystals show degradation of the methylene blue dye under sunlight irradiation. Theoretical investigations with DFT: The band gap of the particles is also calculated from the UV-VIS spectra which is found to be ~3.6 eV and this experimentally observed value of band gap matches with that calculated theoretically from Density Functional Theory (DFT) using Local Density Approximation (LDA). Conclusion: The method of synthesis reported in the present paper is scalable and can be used for commercial synthesis of SnO2 nano-crystals for electrodes and energy storage devices.


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