Highly Selective Active Chlorine Generation Electrocatalyzed by Co3O4 Nanoparticles: Mechanistic Investigation through in Situ Electrokinetic and Spectroscopic Analyses

2019 ◽  
Vol 10 (6) ◽  
pp. 1226-1233 ◽  
Author(s):  
Heonjin Ha ◽  
Kyoungsuk Jin ◽  
Sunghak Park ◽  
Kang-Gyu Lee ◽  
Kang Hee Cho ◽  
...  
2009 ◽  
Vol 39 (12) ◽  
pp. 2397-2408 ◽  
Author(s):  
François Zaviska ◽  
Patrick Drogui ◽  
Jean-François Blais ◽  
Guy Mercier

2014 ◽  
Vol 2 (22) ◽  
pp. 8465-8471 ◽  
Author(s):  
Dongbo Yu ◽  
Jianfeng Yao ◽  
Ling Qiu ◽  
Yufei Wang ◽  
Xinyi Zhang ◽  
...  

A new MnO2@Co3O4 hybrid with small-sized Co3O4 nanoparticles grown on α-MnO2 nanotubes exhibited much improved capacitive performances than those of pristine α-MnO2 nanotubes and a physical mixture of α-MnO2 nanotubes and Co3O4 nanoparticles.


2018 ◽  
Vol 20 (38) ◽  
pp. 24858-24868 ◽  
Author(s):  
Fabian Kollhoff ◽  
Johannes Schneider ◽  
Gao Li ◽  
Sami Barkaoui ◽  
Wenjie Shen ◽  
...  

The adsorption of porphyrin derivatives on different, well-defined oxide nanoparticles and their temperature-dependent metalation was investigated using in situ DRIFTS.


Inorganics ◽  
2019 ◽  
Vol 7 (3) ◽  
pp. 27 ◽  
Author(s):  
Ranjit Bag ◽  
Suvam Saha ◽  
Rosmita Borthakur ◽  
Bijan Mondal ◽  
Thierry Roisnel ◽  
...  

In an attempt to expand the library of M2B5 bicapped trigonal-bipyramidal clusters with different transition metals, we explored the chemistry of [Cp*WCl4] with metal carbonyls that enabled us to isolate a series of mixed-metal tungstaboranes with an M2{B4M’} {M = W; M’ = Cr(CO)4, Mo(CO)4, W(CO)4} core. The reaction of in situ generated intermediate, obtained from the low temperature reaction of [Cp*WCl4] with an excess of [LiBH4·thf], followed by thermolysis with [M(CO)5·thf] (M = Cr, Mo and W) led to the isolation of the tungstaboranes [(Cp*W)2B4H8M(CO)4], 1–3 (1: M = Cr; 2: M = Mo; 3: M = W). In an attempt to replace one of the BH—vertices in M2B5 with other group metal carbonyls, we performed the reaction with [Fe2(CO)9] that led to the isolation of [(Cp*W)2B4H8Fe(CO)3], 4, where Fe(CO)3 replaces a {BH} core unit instead of the {BH} capped vertex. Further, the reaction of [Cp*MoCl4] and [Cr(CO)5·thf] yielded the mixed-metal molybdaborane cluster [(Cp*Mo)2B4H8Cr(CO)4], 5, thereby completing the series with the missing chromium analogue. With 56 cluster valence electrons (cve), all the compounds obey the cluster electron counting rules. Compounds 1–5 are analogues to the parent [(Cp*M)2B5H9] (M= Mo and W) that seem to have generated by the replacement of one {BH} vertex from [(Cp*W)2B5H9] or [(Cp*Mo)2B5H9] (in case of 5). All of the compounds have been characterized by various spectroscopic analyses and single crystal X-ray diffraction studies.


2021 ◽  
Vol 854 ◽  
pp. 157234 ◽  
Author(s):  
Xiangxiang Fan ◽  
Yajuan Xu ◽  
Chenyan Ma ◽  
Wuming He

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