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16 Feb 09:12

Back Cover: Catalytically Active Rh Sub-Nanoclusters on TiO2 for CO Oxidation at Cryogenic Temperatures (Angew. Chem. Int. Ed. 8/2016)

by Hongling Guan, Jian Lin, Botao Qiao, Xiaofeng Yang, Lin Li, Shu Miao, Jingyue Liu, Aiqin Wang, Xiaodong Wang, Tao Zhang
Thumbnail image of graphical abstract

Three milestones in the history of CO oxidation are shown in the picture. One century ago, Langmuir investigated CO oxidation using Pt group metals which work at temperatures higher than 373 K. In the 1980s, Haruta et al. discovered that Au nanoparticles with sizes of 2 nm are active for the oxidation of CO at 200 K. In their Communication on page 2820 ff., X. Wang, T. Zhang et al. show that CO is oxidized at 173 K by Rh sub-nanoclusters supported on TiO2.

04 Jan 13:54

The influence of Co3V2O8 morphology on the oxygen evolution reaction activity and stability

Publication date: February 2016
Source:Electrochemistry Communications, Volume 63
Author(s): Suyeon Hyun, Vignesh Ahilan, Hasuck Kim, Sangaraju Shanmugam
The effect of Co3V2O8 morphology on the electrocatalytic oxygen evolution reaction (OER) activity was evaluated using one- and zero-dimensional nanostructures. The microscopic analyses reveal the existence of thin coating of nitrogen-doped amorphous carbon on the surface of Co3V2O8 nanostructures. The 1D-Co3V2O8 electrocatalyst delivers 10mA cm−2 at overpotential of 0.350V versus reversible hydrogen electrode for OER in 0.1M KOH, whereas 0D-Co3V2O8 catalyst showed 0.397V, benefited from the morphological characteristics of 1D. Moreover, the 1D-Co3V2O8 catalyst exhibits much lower OER overpotential than that of commercial noble metal oxide catalysts, RuO2 (0.41V) and Pt/C (0.79V).

Graphical abstract

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07 Jul 08:45

Engineering Complex, Layered Metal Oxides: High-Performance Nickelate Oxide Nanostructures for Oxygen Exchange and Reduction

by Xianfeng Ma, Juliana S. A. Carneiro, Xiang-Kui Gu, Hao Qin, Hongliang Xin, Kai Sun and Eranda Nikolla

TOC Graphic

ACS Catalysis
DOI: 10.1021/acscatal.5b00756