Electrochemical CO2 reduction: water/catalyst interface versus polymer/catalyst interface

Author(s):  
Yixin Ouyang ◽  
Ye-hui Zhang ◽  
Peter Rice ◽  
Li Shi ◽  
Jinlan Wang ◽  
...  

Due to the low solubility and diffusion coefficients of carbon dioxide in aqueous solution, the carbon dioxide electrolytic cells with aqueous electrolytes are difficult to achieve high conversion current density....

2021 ◽  
Author(s):  
Zhen Qi ◽  
Steven A Hawks ◽  
Corie Horwood ◽  
Jürgen Biener ◽  
Monika M. Biener

The reaction rates for electrochemical CO2 reduction in aqueous electrolytes can be limited by the low concentration and diffusion rate of the reactant CO2. To overcome this limitation, we fabricated...


Author(s):  
Dui Ma ◽  
Ting Jin ◽  
Keyu Xie ◽  
Haitao Huang

Converting CO2 into value-added fuels or chemical feedstocks through electrochemical reduction is one of the several promising avenues to reduce atmospheric carbon dioxide levels and alleviate global warming. This approach...


2016 ◽  
Vol 138 (26) ◽  
pp. 8076-8079 ◽  
Author(s):  
Zhe Weng ◽  
Jianbing Jiang ◽  
Yueshen Wu ◽  
Zishan Wu ◽  
Xiaoting Guo ◽  
...  

2018 ◽  
Vol 9 (11) ◽  
pp. 2952-2960 ◽  
Author(s):  
Eva M. Nichols ◽  
Jeffrey S. Derrick ◽  
Sepand K. Nistanaki ◽  
Peter T. Smith ◽  
Christopher J. Chang

The development of catalysts for electrochemical reduction of carbon dioxide offers an attractive approach to transforming this greenhouse gas into value-added carbon products with sustainable energy input.


2019 ◽  
pp. 224-250
Author(s):  
Maximilian Fleischer ◽  
P. Jeanty ◽  
K. Wiesner-Fleischer ◽  
O. Hinrichsen

2001 ◽  
Vol 19 (2) ◽  
pp. 187-198 ◽  
Author(s):  
Yoshiyuki Sato ◽  
Tadao Takikawa ◽  
Shigeki Takishima ◽  
Hirokatsu Masuoka

2019 ◽  
Author(s):  
Michael Tang ◽  
Hongjie Peng ◽  
Philomena Schlexer Lamoureux ◽  
Michal Bajdich ◽  
Frank Abild-Pedersen

Electrochemical reduction of carbon dioxide (CO<sub>2</sub>) over transition metals follows a complex reaction network. Even for products with a single carbon atom (C<sub>1</sub> products), two bifurcated pathways exist: initially between carboxyl (COOH*) and formate (HCOO*) intermediates and the COOH* intermediate is further bifurcated by pathways involving either formyl (CHO*) or COH*. In this study, we combine evidence from the experimental literature with a theoretical analysis of energetics to rationalize that not all steps in the reduction of CO<sub>2</sub> are electrochemical. This insight enables us to create a selectivity map for two-electron products (carbon monoxide (CO) and formate) on elemental metal surfaces using only the CO and OH binding energies as descriptors. In the further reduction of CO<sup>*</sup>, we find that CHO* is formed through a chemical step only whereas COH* follows from an electrochemical step. Notably on Cu(100), the COH pathway becomes dominant at an applied potential lower than −0.5V vs. RHE. For the elemental metals selective towards CO formation, the variation of the CO binding energy is sufficient to further subdivide the map into domains that predominantly form H<sub>2</sub>, CO, and ultimately more reduced products. We find Cu to be the only elemental metal capable of reducing CO<sub>2</sub> to products beyond 2e<sup>− </sup>via the proposed COH pathway and we identify atomic carbon as the key component leading to the production of methane. Our analysis also rationalizes experimentally observed differences in products between thermal and electrochemical reduction of CO<sub>2</sub> on Cu.


2019 ◽  
Author(s):  
Yunchieh Lai ◽  
Ryan J. R. Jones ◽  
Yu Wang ◽  
Lan Zhou ◽  
Matthias Richter ◽  
...  

Electrochemical CO2 reduction to valuable products is a centerpiece of future energy technologies that relies on identificaiton of new catalysts. We present accelerated screening of Cu bimetallic alloys, revealing remarkable sensitivity to alloy concentration that indicates the segregation of alloying elements to critical sites for hydrocarbon formation.


Sign in / Sign up

Export Citation Format

Share Document