Theoretical search for novel Au or Ag bimetallic alloys capable of transforming CO2 into hydrocarbons

2019 ◽  
Vol 7 (36) ◽  
pp. 20567-20573
Author(s):  
Nian Wu ◽  
Li Xiao ◽  
Lin Zhuang

Designing efficient catalysts with a high selectivity toward hydrocarbons at a relatively low overpotential is of great significance for the application of the CO2 electrochemical reduction reaction (CO2RR).

2017 ◽  
Vol 10 (5) ◽  
pp. 1180-1185 ◽  
Author(s):  
Wenchao Sheng ◽  
Shyam Kattel ◽  
Siyu Yao ◽  
Binhang Yan ◽  
Zhixiu Liang ◽  
...  

In situtransformation of Pd into β-PdH is the origin of the high selectivity for CO in the electrochemical CO2reduction reaction using Pd as the electrocatalyst.


2018 ◽  
Vol 6 (12) ◽  
pp. 5025-5031 ◽  
Author(s):  
Kuilin Lv ◽  
Yanchen Fan ◽  
Ying Zhu ◽  
Yi Yuan ◽  
Jinrong Wang ◽  
...  

3D macroporous hierarchical Ag-G-NCF can efficiently convert CO2 to ethanol with a low overpotential, high faradaic efficiency and high selectivity.


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>


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yang Xia ◽  
Xunhua Zhao ◽  
Chuan Xia ◽  
Zhen-Yu Wu ◽  
Peng Zhu ◽  
...  

AbstractOxygen reduction reaction towards hydrogen peroxide (H2O2) provides a green alternative route for H2O2 production, but it lacks efficient catalysts to achieve high selectivity and activity simultaneously under industrial-relevant production rates. Here we report a boron-doped carbon (B-C) catalyst which can overcome this activity-selectivity dilemma. Compared to the state-of-the-art oxidized carbon catalyst, B-C catalyst presents enhanced activity (saving more than 210 mV overpotential) under industrial-relevant currents (up to 300 mA cm−2) while maintaining high H2O2 selectivity (85–90%). Density-functional theory calculations reveal that the boron dopant site is responsible for high H2O2 activity and selectivity due to low thermodynamic and kinetic barriers. Employed in our porous solid electrolyte reactor, the B-C catalyst demonstrates a direct and continuous generation of pure H2O2 solutions with high selectivity (up to 95%) and high H2O2 partial currents (up to ~400 mA cm−2), illustrating the catalyst’s great potential for practical applications in the future.


2021 ◽  
pp. 133035
Author(s):  
Xiaoxia Zhou ◽  
Erhong Song ◽  
Zhaoyu Kuang ◽  
Zhe Gao ◽  
Han Zhao ◽  
...  

2020 ◽  
Vol 65 (10) ◽  
pp. 796-802 ◽  
Author(s):  
Dong-Rui Yang ◽  
Ling Liu ◽  
Qian Zhang ◽  
Yi Shi ◽  
Yue Zhou ◽  
...  

2019 ◽  
Author(s):  
Peter T. Smith ◽  
Younghoon Kim ◽  
Bahiru Punja Benke ◽  
Kimoon Kim ◽  
Christopher Chang

<div> <div> <div> <p>We report a supramolecular design strategy for promoting the selective reduction of O2 for direct electrosynthesis of H2O2. Specifically, we utilized cobalt tetraphenylporphyrin (Co-TPP), a non-selective oxygen reduction reaction (ORR) catalyst, as a building block to assemble the permanently porous supramolecular cage Co-PB-1(6) bearing six Co-TPP subunits connected through twenty-four imine bonds. Reduction of these imine linkers to amines yields the more flexible porous cage Co-rPB-1(6). Both Co-PB-1(6) and Co-rPB-1(6) cages produce 90-100% H2O2 from electrochemical ORR catalysis in neutral pH water, and we attribute this high selectivity to site isolation of the discrete molecular units, as the analogous Co-TPP monomer generates only a 50% mixture of H2O2 and H2O from electrochemical ORR under the same conditions. The ability to control reaction selectivity in supramolecular structures beyond traditional host-guest interactions offers new opportunities for designing such architectures for a broader range of catalytic applications. </p> </div> </div> </div>


2018 ◽  
Vol 20 (16) ◽  
pp. 3705-3710 ◽  
Author(s):  
Dexin Yang ◽  
Qinggong Zhu ◽  
Xiaofu Sun ◽  
Chunjun Chen ◽  
Lu Lu ◽  
...  

Nanoporous Cu/Ni oxide composites can improve CO2reduction activity for producing formic acid in an aqueous electrolyte with a low overpotential.


2018 ◽  
Vol 140 (4) ◽  
pp. 1496-1501 ◽  
Author(s):  
Yao Yao ◽  
Shangqian Zhu ◽  
Haijiang Wang ◽  
Hui Li ◽  
Minhua Shao

2019 ◽  
Vol 55 (66) ◽  
pp. 9805-9808 ◽  
Author(s):  
Ruru Chen ◽  
Minna Cao ◽  
Weiguang Yang ◽  
Huimin Wang ◽  
Suyuan Zhang ◽  
...  

Well-dispersed palladium nanoparticles based on a supramolecular assembly exhibit high selectivity, activity and stability for the conversion of CO2 to CO.


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