scholarly journals Electrochemical Reduction of CO2: Influence of Pre-treating the Carbon Support

2021 ◽  
Vol 10 (1) ◽  
pp. 1-14
Author(s):  
Nuno M. Pereira ◽  
C. Mateos-Pedrero ◽  
A. Mendes

The production of useful chemicals by electroreducing CO2 it is a promising approach to reduce the levels of this greenhouse gas in the atmosphere. This is not a straightforward process due to the high stability of the CO2 molecule and low selectivity however, these barriers can be overcome by using an appropriate catalyst. This research focus on the effect of pre-treating the carbon supports before incorporating the catalyst on the electroreduction of CO2. We found that the electrochemical behaviour of the carbon supports is modified by the nature of the pre-treatment used. From the structure perspective, the results showed partial destruction of the carbon structure mainly after the oxidative treatments nevertheless, the introduction of defect sites in the carbon structure contributed to catalyst performance. This improvement was proved by the LSV data that showed the reduction of the current associated with the hydrogen reduction reaction.

2017 ◽  
Vol 5 (5) ◽  
pp. 1808-1825 ◽  
Author(s):  
Sheng Sui ◽  
Xiaoying Wang ◽  
Xintong Zhou ◽  
Yuehong Su ◽  
Saffa Riffat ◽  
...  

This paper reviews progress in studies of the mechanism, nanostructure, size effect and carbon supports of Pt electrocatalysts for the ORR.


Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 45
Author(s):  
Julia Hülstede ◽  
Dana Schonvogel ◽  
Henrike Schmies ◽  
Peter Wagner ◽  
Frank Schröter ◽  
...  

Fe-N-C materials are promising non-precious metal catalysts for the oxygen reduction reaction in fuel cells and batteries. However, during the synthesis of these materials less active Fe-containing nanoparticles are formed in many cases which lead to a decrease in electrochemical activity and stability. In this study, we reveal the significant properties of the carbon support required for the successful incorporation of Fe-N-related active sites. The impact of two carbon blacks and two activated biomass-based carbons on the Fe-N-C synthesis is investigated and crucial support properties are identified. Carbon supports having low portions of amorphous carbon, moderate surface areas (>800 m2/g) and mesopores result in the successful incorporation of Fe and N on an atomic level and improved oxygen reduction reaction (ORR) activity. A low surface area and especially amorphous parts of the carbon promote the formation of metallic iron species covered by a graphitic layer. In contrast, highly microporous systems with amorphous carbon provoke the formation of less active iron carbides and carbon nanotubes. Overall, a phosphoric acid activated biomass is revealed as novel and sustainable carbon support for the formation of Fe-Nx sites. Overall, this study provides valuable and significant information for the future development of novel and sustainable carbon supports for Fe-N-C catalysts.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 177 ◽  
Author(s):  
Harold O. Panganoron ◽  
Jethro Daniel A. Pascasio ◽  
Eugene A. Esparcia ◽  
Julie Anne D. del Rosario ◽  
Joey D. Ocon

Sluggish kinetics in oxygen reduction reaction (ORR) requires low-cost and highly durable electrocatalysts ideally produced from facile methods. In this work, we explored the conversion and utilization of waste biomass as potential carbon support for α-MnO2 catalyst in enhancing its ORR performance. Carbon supports were derived from different waste biomass via hydrothermal carbonization (HTC) at different temperature and duration, followed by KOH activation and subsequent heat treatment. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX) and X-Ray diffraction (XRD) were used for morphological, chemical, and structural characterization, which revealed porous and amorphous carbon supports for α-MnO2. Electrochemical studies on ORR activity suggest that carbon-supported α-MnO2 derived from HTC of corncobs at 250 °C for 12 h (CCAC + MnO2 250-12) gives the highest limiting current density and lowest overpotential among the synthesized carbon-supported catalysts. Moreover, CCAC + MnO2 250-12 facilitates ORR through a 4-e‑ pathway, and exhibits higher stability compared to VC + MnO2 (Vulcan XC-72) and 20% Pt/C. The synthesis conditions preserve oxygen functional groups and form porous structures in corncobs, which resulted in a highly stable catalyst. Thus, this work provides a new and cost-effective method of deriving carbon support from biomass that can enhance the activity of α-MnO2 towards ORR.


2019 ◽  
Author(s):  
Sahithi Ananthaneni ◽  
Rees Rankin

<div>Electrochemical reduction of CO2 to useful chemical and fuels in an energy efficient way is currently an expensive and inefficient process. Recently, low-cost transition metal-carbides (TMCs) are proven to exhibit similar electronic structure similarities to Platinum-Group-Metal (PGM) catalysts and hence can be good substitutes for some important reduction reactions. In this work, we test graphenesupported WC (Tungsten Carbide) nanocluster as an electrocatalyst for the CO2 reduction reaction. Specifically, we perform DFT studies to understand various possible reaction mechanisms and determine the lowest thermodynamic energy landscape of CO2 reduction to various products such as CO, HCOOH, CH3OH, and CH4. This in-depth study of reaction energetics could lead to improvements and develop more efficient electrocatalysts for CO2 reduction.<br></div>


Author(s):  
Yingchun Zhang ◽  
Changsheng Cao ◽  
Xintao Wu ◽  
Qi-Long Zhu

Bismuth (Bi)-based nanomaterials are considered as the promising electrocatalysts for electrocatalytic CO2 reduction reaction (CO2RR), but it is challenging to achieve high current density and selectivity in a wide potential...


2021 ◽  
Author(s):  
Hong Zhu ◽  
Qingjun Chen ◽  
Jinghua Yu ◽  
Qian Zhou ◽  
Fanghui Wang ◽  
...  

The corrosion of carbon support is one of key factors causing deactivation of Pt-based oxygen reduction reaction (ORR) catalysts for proton exchange membrane fuel cells. In this work, a highly...


2021 ◽  
Author(s):  
Guokang Han ◽  
Yongrong Sun ◽  
Yuxin Liu ◽  
Lingfeng Li ◽  
Xudong Li ◽  
...  

The nature of carbon support has huge effects on the catalytic properties of supported catalysts. When utilized for electrochemical purposes as support for precious metal in acid media, the oxygen...


2021 ◽  
Author(s):  
Jinsun Lee ◽  
Xinghui Liu ◽  
Ashwani Kumar ◽  
Yosep Hwang ◽  
Eunji Lee ◽  
...  

This work highlights the importance of a rational design for more energetically suitable nitrogen reduction reaction routes and mechanisms by regulating the electronic band structures with phase-selective defect sites.


Catalysts ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. 328 ◽  
Author(s):  
Alagar Paulraj ◽  
Yohannes Kiros ◽  
Mats Göthelid ◽  
Malin Johansson

This article reports the two-step synthesis of NiFeOx nanomaterials and their characterization and bifunctional electrocatalytic activity measurements in alkaline electrolyte for metal-air batteries. The samples were mostly in layered double hydroxide at the initial temperature, but upon heat treatment, they were converted to NiFe2O4 phases. The electrochemical behaviour of the different samples was studied by linear sweep voltammetry and cyclic voltammetry on the glassy carbon electrode. The OER catalyst activity was observed for low mass loadings (0.125 mg cm−2), whereas high catalyst loading exhibited the best performance on the ORR side. The sample heat-treated at 250 °C delivered the highest bi-functional oxygen evolution and reduction reaction activity (OER/ORR) thanks to its thin-holey nanosheet-like structure with higher nickel oxidation state at 250 °C. This work further helps to develop low-cost electrocatalyst development for metal-air batteries.


Author(s):  
Aldona Kostuch ◽  
Sebastian Jarczewski ◽  
Marcin K. Surówka ◽  
Piotr Kuśtrowski ◽  
Zbigniew Sojka ◽  
...  

Mn–Co spinel/carbon electrocatalyst performance exhibits a volcano-type shape which results from a trade-off between electrical conductivity and the amount of oxygen groups.


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