scholarly journals Concerted Cation–Electron Transfer Mechanism for CO2 Electroreduction

Author(s):  
Seung-Jae Shin ◽  
Hansol Choi ◽  
Stefan Ringe ◽  
Da Hye Won ◽  
Chang Hyuck Choi ◽  
...  

Converting carbon dioxide (CO2) into valuable products is one of the most important processes for a sustainable society. Especially, the electrochemical CO2 reduction reaction (CO2RR) offers an effective means, but its reaction mechanism is not yet fully understood. Here, we demonstrate that concerted cation–electron transfer (CCET) is a key catalytic step in the CO2RR to carbon monoxide. The first-principles-based multiscale simulation identifies a single cation that coordinates a CO2− intermediate adsorbed on Ag electrode. The CCET is experimentally verified by a collapse of the CO2RR polarization curves upon correcting for the thermodynamic activity of the cation. As further confirmation, a kinetic study shows that the CO2RR obeys first-order kinetics on the local cation concentration at the electric double layer (estimated by measuring the electrode surface charge). Finally, this work unveils the fundamental origin of different CO2RR activity depending on the species of alkali metal cation, and further highlights the importance of ion-pairing tendency of the cations for electrochemical interface design to achieve high-performance CO2 electrolysis.

2021 ◽  
Author(s):  
Seung-Jae Shin ◽  
Hansol Choi ◽  
Stefan Ringe ◽  
Da Hye Won ◽  
Chang Hyuck Choi ◽  
...  

Converting carbon dioxide (CO2) into valuable products is one of the most important processes for a sustainable society. Especially, the electrochemical CO2 reduction reaction (CO2RR) offers an effective means, but its reaction mechanism is not yet fully understood. Here, we demonstrate that cation-coupled electron transfer (CCET) is a rate-determining step in the CO2RR to carbon monoxide. The first-principles-based multiscale simulation identifies a single cation that coordinates a CO2− intermediate adsorbed on Ag electrode. The CCET is experimentally verified by a collapse of the CO2RR polarization curves upon correcting Nernstianly for a bulk cation concentration. As further confirmation, a kinetic study shows that the CO2RR obeys first-order kinetics on a local cation concentration. Finally, this work unveils that the cation effect on CO2RR originates from the local colligative property, and further highlights the importance of ion-pairing tendency for electrochemical interface design to achieve high-performance CO2 electrolysis.


2021 ◽  
Author(s):  
Seung-Jae Shin ◽  
Hansol Choi ◽  
Stefan Ringe ◽  
Da Hye Won ◽  
Chang Hyuck Choi ◽  
...  

Abstract Converting carbon dioxide (CO2) into valuable products is one of the most important processes for a sustainable society. Especially, the electrochemical CO2 reduction reaction (CO2RR) offers an effective means, but its reaction mechanism is not yet fully understood. Here, we demonstrate that cation-coupled electron transfer (CCET) is a rate-determining step in the CO2RR to carbon monoxide. The first-principles-based multiscale simulation identifies a single cation that coordinates a CO2− intermediate adsorbed on Ag electrode. The CCET is experimentally verified by a collapse of the CO2RR polarization curves upon correcting Nernstianly for a bulk cation concentration. As further confirmation, a kinetic study shows that the CO2RR obeys first-order kinetics on a local cation concentration. Finally, this work unveils that the cation effect on CO2RR originates from the local colligative property, and further highlights the importance of ion-pairing tendency for electrochemical interface design to achieve high-performance CO2 electrolysis.


Author(s):  
Xu Hu ◽  
Sai Yao ◽  
Letian Chen ◽  
Xu Zhang ◽  
Menggai Jiao ◽  
...  

Electrochemical CO2 reduction reaction (CO2RR) is a very important approach to realize sustainable development. Single-atom catalysts show advantages in both homogeneous and heterogeneous catalysis, and considerable progress has been made...


2018 ◽  
Vol 3 (10) ◽  
pp. 2527-2532 ◽  
Author(s):  
Xu Lu ◽  
Yueshen Wu ◽  
Xiaolei Yuan ◽  
Ling Huang ◽  
Zishan Wu ◽  
...  

2020 ◽  
Author(s):  
Xinyue Wang ◽  
Xiahan Sang ◽  
Chung-Li Dong ◽  
Siyu Yao ◽  
Ling Shuai ◽  
...  

Abstract Electrocatalysts play a key role in accelerating the sluggish electrochemical CO2 reduction (ECR) involving multi-electron and proton transfer. Herein, we develop a proton capture strategy via accelerating the water dissociation reaction catalyzed by transition metal nanoparticles (NPs) adjacent to atomically dispersed Ni-Nx active sites (Ni@NiNCM) to accelerate the proton transfer to the latter for boosting the intermediate protonation step, and hence the whole ECR process. For the first time, the accelerated protonation process is amply demonstrated experimentally. Aberration-corrected scanning transmission electron microscopy and synchrotron radiation X-ray absorption spectroscopy, together with DFT calculations, revealed that the Ni NPs accelerated the adsorbed H (Had) generation and transfer to the adjacent Ni-Nx sites for boosting the intermediate protonation and the overall ECR processes. This proton capture strategy is highly general, which can be extended to the design and preparation of various high-performance catalysts for diverse electrochemical reactions even beyond ECR.


2016 ◽  
Vol 22 (40) ◽  
pp. 14158-14161 ◽  
Author(s):  
Jaecheol Choi ◽  
Tania M. Benedetti ◽  
Rouhollah Jalili ◽  
Ashley Walker ◽  
Gordon G. Wallace ◽  
...  

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