Rotating ring-disk voltammetry: Diagnosis of catalytic activity of metallic copper catalysts toward CO2 electroreduction

2017 ◽  
Vol 53 (10) ◽  
pp. 1194-1203 ◽  
Author(s):  
A. Wadas ◽  
I. A. Rutkowska ◽  
M. Bartel ◽  
S. Zoladek ◽  
K. Rajeshwar ◽  
...  
2017 ◽  
Vol 129 (23) ◽  
pp. 6568-6572 ◽  
Author(s):  
Xin-Ming Hu ◽  
Magnus H. Rønne ◽  
Steen U. Pedersen ◽  
Troels Skrydstrup ◽  
Kim Daasbjerg

2019 ◽  
Vol 59 (8) ◽  
pp. 92-97
Author(s):  
Ludmila A. Brusnitsina ◽  
◽  
Elena I. Stepanovskih ◽  
Tatiana A. Alekseeva ◽  
◽  
...  

Methods of chemical activation of the dielectric surface, in which metal-catalyst particles are formed on it as a result of chemical transformations, are more universal, since they allow to vary the compositions of solutions of chemical deposition of metal and to precipitate metals on substrates of different chemical nature with different morphology and surface structure. Noble metal compounds and colloidal solutions characterized by limited storage stability due to the coagulation process are mainly used for surface activation. Palladium-free activation is used for metallization of the surface of unfolded dielectrics and metallization of through holes of printed circuit boards. As a dielectric material used inorganic materials (ceramics, polycore, various types of ceramics) and organic fiberglass with epoxiconazole adhesive layer. The aim of this work is to improve the technology of activation of non-conductive surfaces by true solutions based on copper(I) by optimizing the composition of the activator. It is shown that the drying temperature affects the composition of the activator layer. Activates the layer obtained by drying at 323-373 K, is composed of CuCl2∙2H2O and Cu2O. The optimum mode of drying an activating solution based on copper(I) (T = 353-373 K, τ = 15-20 minutes). The compounds formed during the drying of the activating solution based on copper monochloride do not have catalytic activity sufficient to initiate chemical and electrochemical metallization reactions. Therefore, it is necessary to carry out an additional operation-acceleration in solutions of reducing agents. Solutions of hydrazine chloride (N2H4∙HCl), sodium hypophosphite (NaH2PO4∙H2O), hydroxylammonium chloride (NH2OH∙HCl), the concentration of which varied in the range (0.1-0.5) mol∙l‒1, as well as a solution of alkaline formaldehyde were taken as these solutions. The technology of activator acceleration in a solution of the following composition: hydroxylammonium chloride (NH2OH∙HCl)  0.5 mol∙l-1; pH = 8-10; T = 298 K, which allows to significantly increase the surface concentration of catalytically active centers on the dielectric surface. In order to determine the durability and performance of the activating solution, the stability of the copper (I)  based solution was studied. The durability and performance of the activating solution is ensured by the presence of copper monochloride in it. This is possible if the solution will constantly undergo a reaction of reduction of divalent copper to a monovalent state. For this purpose, sodium hypophosphite in an amount of 0.5 mol∙l‒1 and metallic copper with a concentration of 30 g∙l‒1 were introduced into the activating solution as a reducing agent. The optimal composition of the activating solution containing (mol∙l‒1): copper chloride(I) ‒ 3.10; hydrochloric acid ‒ 3.10; surfactant OP-10  0.01; metallic copper 0.47 was established. Methods of regeneration of copper(I) concentration in activation solutions have been developed, which can significantly extend their service life.


2018 ◽  
Vol 6 (40) ◽  
pp. 19438-19444 ◽  
Author(s):  
Xu-Jun He ◽  
Jin-Xian Feng ◽  
Qian Ren ◽  
Gao-Ren Li

Ni nanoparticle-decorated-MnO2 nanodendrites supported on carbon fibers (Ni NPs/MnO2 NDs-CFs) are reported as efficient electrocatalysts for CO2 reduction to formate, and they exhibit low CO2/HCOO− reduction overpotential, superior catalytic activity, high formate selectivity and high faradaic efficiency of over 85%.


ACS Catalysis ◽  
2018 ◽  
Vol 8 (4) ◽  
pp. 3035-3040 ◽  
Author(s):  
Etosha R. Cave ◽  
Chuan Shi ◽  
Kendra P. Kuhl ◽  
Toru Hatsukade ◽  
David N. Abram ◽  
...  

2020 ◽  
Vol 602 ◽  
pp. 117710 ◽  
Author(s):  
Giovanni Pampararo ◽  
Gabriella Garbarino ◽  
Paola Riani ◽  
Maria Villa García ◽  
Vicente Sánchez Escribano ◽  
...  

2016 ◽  
Vol 70 (1) ◽  
Author(s):  
Tomislav Pintauer

Fundamentals of copper catalyzed atom transfer radical addition (ATRA) and mechanistically similar polymerization (ATRP) were discussed. Special emphasis was placed on structural characterization and electrochemical properties of copper complexes. Recent advances in the development of highly active copper complexes for both processes were also reviewed. It was found that electron-donating groups (methoxy and methyl in the 4 and 3,5 positions, respectively) of the pyridine rings in tris(2-pyridylmethyl)amine (TPMA) ligand, significantly increase the catalytic activity in copper mediated ATRA/ATRP.


2021 ◽  
Author(s):  
Qian Sun ◽  
Wenhao Ren ◽  
Yong Zhao ◽  
Chuan Zhao

Single-atom catalysts (SACs) have attracted much interest for electrochemical CO2 reduction because of their high metal utilization and excellent catalytic activity. However, the practical applications of SACs were restricted by...


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Philipp Grosse ◽  
Aram Yoon ◽  
Clara Rettenmaier ◽  
Antonia Herzog ◽  
See Wee Chee ◽  
...  

AbstractTo rationally design effective and stable catalysts for energy conversion applications, we need to understand how they transform under reaction conditions and reveal their underlying structure-property relationships. This is especially important for catalysts used in the electroreduction of carbon dioxide where product selectivity is sensitive to catalyst structure. Here, we present real-time electrochemical liquid cell transmission electron microscopy studies showing the restructuring of copper(I) oxide cubes during reaction. Fragmentation of the solid cubes, re-deposition of new nanoparticles, catalyst detachment and catalyst aggregation are observed as a function of the applied potential and time. Using cubes with different initial sizes and loading, we further correlate this dynamic morphology with the catalytic selectivity through time-resolved scanning electron microscopy measurements and product analysis. These comparative studies reveal the impact of nanoparticle re-deposition and detachment on the catalyst reactivity, and how the increased surface metal loading created by re-deposited nanoparticles can lead to enhanced C2+ selectivity and stability.


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