A review of carbon-based and non-carbon-based catalyst supports for the selective catalytic reduction of nitric oxide

• Shahreen Binti Izwan Anthonysamy,
• Syahidah Binti Afandi,
• Mehrnoush Khavarian and
• Abdul Rahman Bin Mohamed

Beilstein J. Nanotechnol. 2018, 9, 740–761, doi:10.3762/bjnano.9.68

Fabrication of CeO₂–MO_x (M = Cu, Co, Ni) composite yolk–shell nanospheres with enhanced catalytic properties for CO oxidation

• Ling Liu,
• Jingjing Shi,
• Hongxia Cao,
• Ruiyu Wang and
• Ziwu Liu

Beilstein J. Nanotechnol. 2017, 8, 2425–2437, doi:10.3762/bjnano.8.241

• (CeO2) has attracted a great deal of research attention due to its high oxygen storage capacity (OSC) and good redox properties [1][2][3]. Because of these unique characteristics, CeO2 has been widely used as environmental catalysts for the removal of harmful pollutants from exhaust gases, such as

Template-directed synthesis and characterization of microstructured ceramic Ce/ZrO₂@SiO₂ composite tubes

• Jörg J. Schneider and
• Meike Naumann

Beilstein J. Nanotechnol. 2014, 5, 1152–1159, doi:10.3762/bjnano.5.126

• ., for solid oxide fuel cells), SOFCs [3][5] and electrochromic smart window applications [11]. Adding silica as a support enhances the oxygen storage capacity (OSC) of such ceria–zirconia composite materials [2][4]. Besides synthetic methods such as the thermal decomposition of precursors [12], co

Catalytic activity of nanostructured Au: Scale effects versus bimetallic/bifunctional effects in low-temperature CO oxidation on nanoporous Au

• Lu-Cun Wang,
• Yi Zhong,
• Haijun Jin,
• Daniel Widmann,
• Jörg Weissmüller and
• R. Jürgen Behm

Beilstein J. Nanotechnol. 2013, 4, 111–128, doi:10.3762/bjnano.4.13

• are discussed. Keywords: AuAg alloy; AuCu alloy; CO oxidation; dynamic studies; kinetics; nanoporous Au (NPG) catalyst; oxygen storage capacity (OSC); temporal analysis of products (TAP); Introduction Porous metallic materials with well-controlled morphologies and surface properties have attracted

• CO pulses (oxygen storage capacity, OSC), was also determined by TAP reactor measurements. Here, the NPG samples were first exposed to O2 in a continuous flow of 10% O2/N2 with a gas flow of 20 NmL·min−1 at atmospheric pressure (30 min at 30 °C); afterwards the amount of stable adsorbed oxygen