Metal-free rGO/GO hybrid microelectrode array for sensitive and in-situ hydrogen peroxide sensing

2019 ◽  
Vol 326 ◽  
pp. 134967
Author(s):  
Jing Zhang ◽  
Ming Zhao ◽  
Jun Yang ◽  
Gang Wu ◽  
Huaping Wu ◽  
...  
2019 ◽  
Vol 252 ◽  
pp. 128-137 ◽  
Author(s):  
André Torres-Pinto ◽  
Maria J. Sampaio ◽  
Cláudia G. Silva ◽  
Joaquim L. Faria ◽  
Adrián M.T. Silva

Author(s):  
Sara Yacob ◽  
Michael J. Caulfield ◽  
Timothy A. Barckholtz

Partial oxidation catalysts capable of efficiently operating at low temperatures may limit the over-oxidation of alkane substrates and thereby improve selectivity. This work focuses on examining alkane oxidation using completely metal-free organocatalysts, dioxiranes. The dioxiranes employed here are synthesized by oxidation of a ketone using a terminal oxidant, such as hydrogen peroxide. Our work generates the dioxirane in situ , so that the process can be catalytic with respect to the ketone. To date, we have demonstrated selective partial oxidation of adamantane using ketone catalysts resulting in yields upwards of 60% towards 1-adamantanol with greater than 99% selectivity. Furthermore, we have demonstrated that changing the electrophilic character of the ketone R groups to contain more electron-donating ligands facilitates the dioxirane ring formation and improves overall oxidation yields. Isotopic labelling studies using H 2 18 O 2 show the preferential incorporation of an 18 O label into the parent ketone, providing evidence for a dioxirane intermediate formed in situ . The isotopic labelling studies, along with solvent effect studies, suggest the formation of peracetic acid as a reactive intermediate. This article is part of a discussion meeting issue ‘Providing sustainable catalytic solutions for a rapidly changing world’.


Carbon ◽  
2015 ◽  
Vol 95 ◽  
pp. 949-963 ◽  
Author(s):  
Valentina Perazzolo ◽  
Christian Durante ◽  
Roberto Pilot ◽  
Andrea Paduano ◽  
Jian Zheng ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Qingyao Wu ◽  
Jingjing Cao ◽  
Xiao Wang ◽  
Yan Liu ◽  
Yajie Zhao ◽  
...  

A Correction to this paper has been published: https://doi.org/10.1038/s41467-021-21490-z


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yongmeng Wu ◽  
Cuibo Liu ◽  
Changhong Wang ◽  
Yifu Yu ◽  
Yanmei Shi ◽  
...  

AbstractElectrocatalytic alkyne semi-hydrogenation to alkenes with water as the hydrogen source using a low-cost noble-metal-free catalyst is highly desirable but challenging because of their over-hydrogenation to undesired alkanes. Here, we propose that an ideal catalyst should have the appropriate binding energy with active atomic hydrogen (H*) from water electrolysis and a weaker adsorption with an alkene, thus promoting alkyne semi-hydrogenation and avoiding over-hydrogenation. So, surface sulfur-doped and -adsorbed low-coordinated copper nanowire sponges are designedly synthesized via in situ electroreduction of copper sulfide and enable electrocatalytic alkyne semi-hydrogenation with over 99% selectivity using water as the hydrogen source, outperforming a copper counterpart without surface sulfur. Sulfur anion-hydrated cation (S2−-K+(H2O)n) networks between the surface adsorbed S2− and K+ in the KOH electrolyte boost the production of active H* from water electrolysis. And the trace doping of sulfur weakens the alkene adsorption, avoiding over-hydrogenation. Our catalyst also shows wide substrate scopes, up to 99% alkenes selectivity, good reducible groups compatibility, and easily synthesized deuterated alkenes, highlighting the promising potential of this method.


2021 ◽  
Vol 9 (12) ◽  
pp. 7556-7565
Author(s):  
Guojian Chen ◽  
Yadong Zhang ◽  
Ke Liu ◽  
Xiaoqing Liu ◽  
Lei Wu ◽  
...  

Constructing phenanthroline-based cationic radical porous hybrid polymers as versatile metal-free heterogeneous catalysts for both oxidation of sulfides and CO2 conversion.


2021 ◽  
Author(s):  
Shankar S. Narwade ◽  
Shivsharan M. Mali ◽  
Bhaskar R. Sathe

A study on the in situ decoration of ethylenediamine (EDA) on acid functionalized multi-walled carbon nanotubes (O-MWCNTs) for overall water splitting reactions at all pH as an efficient and inexpensive metal-free multifunctional electrocatalyst.


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