How absorbed hydrogen affects the catalytic activity of transition metals.

نویسندگان

  • Hristiyan A Aleksandrov
  • Sergey M Kozlov
  • Swetlana Schauermann
  • Georgi N Vayssilov
  • Konstantin M Neyman
چکیده

Heterogeneous catalysis is commonly governed by surface active sites. Yet, areas just below the surface can also influence catalytic activity, for instance, when fragmentation products of catalytic feeds penetrate into catalysts. In particular, H absorbed below the surface is required for certain hydrogenation reactions on metals. Herein, we show that a sufficient concentration of subsurface hydrogen, H(sub) , may either significantly increase or decrease the bond energy and the reactivity of the adsorbed hydrogen, H(ad) , depending on the metal. We predict a representative reaction, ethyl hydrogenation, to speed up on Pd and Pt, but to slow down on Ni and Rh in the presence of H(sub) , especially on metal nanoparticles. The identified effects of subsurface H on surface reactivity are indispensable for an atomistic understanding of hydrogenation processes on transition metals and interactions of hydrogen with metals in general.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A comparative study between transition-metal-substituted Keggin-type tungstosilicates supported on anatase leaf as catalyst for synthesis of symmetrical disulfides

Transition-metal-substituted  (TMS)  polyoxometalates  of  the  general  formula  [SiW9M3O39], (where M = first row transition metal), has been synthesized and supported on anatase by sol–gel method under oil-bath condition. The tetrabutylammonium (TBA) salts of the Keggin-type polyoxotungstates  [SiW9M3O39],  (M = VII, CrII, MnII,  FeII CoII  and NiII),  proved  to  be  green, reusable,  and  ...

متن کامل

Hydrogen evolution from catalytic hydrolysis of NaBH4: Comparative study between the catalytic activity of TiO2 nanotubes with various arrangements

Nowadays, a lot of efforts have been applied to find an appropriate catalyst for generating hydrogen from NaBH4. Hence in the current study, various nanostructures of TiO2 were employed to obtain an insight into how the different support catalysts effect on the hydrolysis rate of NaBH4. For this aim, disordered filaments (DF-NTs) and ordered free-standing TiO2 nanotubes (FS-NTs) were fabricated...

متن کامل

Comparison of Catalytic Effect of Alkali and Alkaline Earth Metals Hydrogen Sulfate: As the Promoter for an Efficient Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones under Solvent-Free Conditions

Alkali and alkaline earth metals hydrogen sulfate catalyzed the one-pot three component condensation reactions of aldehydes, 1,3-dicarbonyl compounds and urea or thiourea under solvent-free conditions leading to 3,4-dihydropyrimidin-2(1H)-ones in high yields at 80 °C. Our results showed that Biginelli reaction not only is pH dependent, but the cation of catalyst plays an importan...

متن کامل

Tailoring the Energy Band Gap of Transition Metal Doped TiO2 Thin Film

Water splitting for hydrogen production under sunlight using TiO2 as photo catalyst provides a better route for solar energy and attracts the attention of many researchers. The photo catalytic activity of TiO2 under sunlight irradiation depends on the band gap energy. The transition metal doped TiO2 shows an edge over TiO2 in optical absorbance and photo catalytic activity. Thin film of Cr dope...

متن کامل

Ag/ZnO Nanocomposites: Preparation, Characterization and Investigation of the Catalytic Activity for Oxidation of Toluene in Liquid Phase

In this research, Ag/ZnO nanocomposites were prepared and characterized by transition electron microscopy (TEM), the energy dispersive X-ray spectrum (EDS) and X-ray diffraction patterns (XRD). These nanocomposites were used as catalysts for the oxidation of toluene to benzaldehyde and benzoic acid with hydrogen peroxide (H2O2) and tert-butylhydroperoxide (TBHP) as oxidizing agent in the liquid...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Angewandte Chemie

دوره 53 49  شماره 

صفحات  -

تاریخ انتشار 2014