A high pressure x-ray photoelectron spectroscopy study of CO oxidation over Rh(100).

نویسندگان

  • J Gustafson
  • S Blomberg
  • N M Martin
  • V Fernandes
  • A Borg
  • Z Liu
  • R Chang
  • E Lundgren
چکیده

We have studied the oxidation of CO over Rh(100) using high pressure x-ray photoelectron spectroscopy under CO and O2 pressures ranging from 0.01 to 1 mbar. The results show a very low or no conversion for the CO covered surface found at low temperatures, while the activity rises slightly when the temperature is high enough for some CO to desorb, exposing surface sites for dissociative O2 adsorption. As the temperature is increased further, more CO desorbs and oxygen replaces CO as the dominating species at the surface. At the same time we find a sudden increase in the reactivity, such that all CO that reaches the surface is instantly transformed into CO2. We find that the O coverage in the active state is highly dependent on the total pressure and, although we do not detect any presence of a surface oxide as in previous surface x-ray diffraction studies, the highest O coverage indicates that the surface is close to being oxidized.

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 reactive oxide overlayer on rhodium nanoparticles during CO oxidation and its size dependence studied by in situ ambient-pressure X-ray photoelectron spectroscopy.

Carbon monoxide oxidation is one of the most studied heterogeneous reactions, being scientifically and industrially important, particularly for removal of CO from exhaust streams and preferential oxidation for hydrogen purification in fuel-cell applications. The precious metals Ru, Rh, Pd, Pt, and Au are most commonly used for this reaction because of their high activity and stability. Despite ...

متن کامل

CO Oxidation on Pt-Group Metals from Ultrahigh Vacuum to Near Atmospheric Pressures. 1. Rhodium

The CO oxidation reaction on Rh(111) was studied both at low pressures (e2 × 10-4 Torr) under steadystate conditions and at high pressures (0.01-88 Torr) in a batch reactor at various gaseous reactant compositions. Surface CO and O coverages were determined using polarization modulation infrared reflection absorption spectroscopy (PM-IRAS) and X-ray photoelectron spectroscopy (XPS). CO titratio...

متن کامل

Electronic Interactions in Bimetallic Systems: An X-ray Photoelectron Spectroscopic Study

The electronic interactions in Cu/Rh( loo), Cu/Ru(OOOI), Ni/Ru(0001), Ni/W( 1 lo), and Pd/W( 1 IO) have been examined by means of X-ray photoelectron spectroscopy (XPS). The shifts in core-level binding energies indicate that the adatoms in a monolayer of Ni, Cu, or Pd are electronically perturbed with respect to the surface atoms of Ni(100), Cu( IOO), or Pd(100). The magnitude of the electroni...

متن کامل

New insights into catalytic CO oxidation on Pt-group metals at elevated pressures

Producing a definitive picture of the CO oxidation reaction (CO + O2 ? CO2) on Pt-group metals (Rh, Pd, Pt, and Ru) across the ‘pressure gap’ has proved to be a challenging task. Surface-sensitive techniques amenable to high pressure environments (e.g. PM-IRAS) have sparked a renewed interest in this reaction under realistic pressures. Here, we review recent work in our laboratory examining CO ...

متن کامل

Ethanol Electro-Oxidation on Ternary Platinum−Rhodium−Tin Nanocatalysts: Insights in the Atomic 3D Structure of the Active Catalytic Phase

Novel insights in the synthesis−structure−catalytic activity relationships of nanostructured trimetallic Pt−Rh−Sn electrocatalysts for the electrocatalytic oxidation of ethanol are reported. In particular, we identify a novel single-phase Rh-doped Pt−Sn Niggliite mineral phase as the source of catalytically active sites for ethanol oxidation; we discuss its morphology, composition, chemical sur...

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:
  • ACS nano

دوره 6 12  شماره 

صفحات  -

تاریخ انتشار 2012