4.5 Article

Bimetallic AuPd@CeO2 Nanoparticles Supported on Potassium Titanate Nanobelts: A Highly Efficient Catalyst for the Reduction of NO with CO

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CATALYSIS LETTERS
卷 151, 期 9, 页码 2483-2491

出版社

SPRINGER
DOI: 10.1007/s10562-020-03502-7

关键词

NO reduction with CO; Bimetallic AuPd; CeO2; Potassium titanate nanobelts; In situ diffuse reflectance fourier transform IR spectroscopy; Modulation excitation spectroscopy

资金

  1. Natural Science Foundation of China (NSFC) [21377017]
  2. Dalian University of Technology [DUT13RC(03)04, DUT13RC(3)26]
  3. National Thousand Talents Program of China
  4. Fundamental Research Funds for the Central Universities of China

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The nanocomposite consisting of bimetallic AuPd nanoparticles modified with CeO2 and deposited on potassium titanate nanobelts exhibited outstanding catalytic performance in the selective catalytic reduction of NO with CO. The favorable synergies between the components led to full NO conversion and high selectivity to N-2. The alloying of Au with Pd enhanced the ability to adsorb CO and NO on the surface, contributing to the high conversion and selectivity.
A nanocomposite consisting of bimetallic AuPd nanoparticles, which were modified with CeO2 (AuPd@CeO2), and deposited on potassium titanate nanobelts (KTN) as support, is shown to exhibit outstanding catalytic performance in the selective catalytic reduction of NO with CO. Transmission electron microscopy and energy dispersive X-Ray elemental mapping indicated that the AuPd nanoparticles surrounded by CeO2 were well-mixed forming an alloy. The potassium titanate support consisted of 1-3 mu m long and 8-14 nm wide nanobelts. The AuPd@CeO2/KTN catalyst showed full NO conversion at 100 % selectivity to N-2 at a gas-hourly space velocity (GHSV) of 15,000 h(-1) and 200 degrees C. The outstanding performance of the AuPd@CeO2/KNT catalyst is attributed to favorable synergies between its components. Corresponding monometallic Au catalysts supported on KTN (Au@CeO2/KNT), as well as bimetallic AuPd supported on TiO2 (AuPd@CeO2/TiO2), showed inferior catalytic performance, indicating the absence of a beneficial synergy between the different components. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) combined with modulation excitation spectroscopy (MES) proved that alloying of Au with Pd enhances the ability to adsorb CO and NO on the surface in an on-top configuration and that the deposition of the bimetallic AuPd nanoparticles on KTN facilitates the crucial formation of isocyanate (-NCO) species, resulting in high conversion and selectivity. [GRAPHICS] .

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