Crucial Role of Surface Hydroxyls on the Activity and Stability in Electrochemical CO2 Reduction

2019 ◽  
Vol 141 (7) ◽  
pp. 2911-2915 ◽  
Author(s):  
Wanyu Deng ◽  
Lei Zhang ◽  
Lulu Li ◽  
Sai Chen ◽  
Congling Hu ◽  
...  
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...


2021 ◽  
Author(s):  
Karla Banjac ◽  
Thanh Hai Phan ◽  
Fernando P. Cometto ◽  
Patrick Alexa ◽  
Yunchang Liang ◽  
...  

The electrochemical reduction of CO2 (CO2RR) into multicarbon compounds is a promising pathway towards renewable chemicals. Structure-product selectivity studies highlight that copper (100) facets favour C2+ product formation. However, the atomic processes leading to the formation of (100)-rich Cu cubes remains elusive. Herein, we use Cu and graphene-protected Cu surfaces to reveal the differences in structure and composition of common Cu-based electrocatalysts, from nano to micrometer scales. We show that stripping/electrodeposition cycles lead to thermodynamically controlled growth of Cu2O micro/nanocubes, while multi-layered Cu nanocuboids form universally during CO2RR upon polarization-driven re-organization of Cu0 atoms. A synergy of electrochemical characterization by scanning tunnelling microscopy (EC-STM), operando EC-Raman and quasi-operando X-Ray Photoemission spectroscopy (XPS) allows us to shed light on the role of oxygen on the dynamic interfacial processes of Cu, and to demonstrate that chloride is not needed for the stabilization of cubic Cu nanostructures.


2019 ◽  
Vol 7 (34) ◽  
pp. 19872-19880 ◽  
Author(s):  
Fuhua Li ◽  
Qing Tang

The functional groups of thiolates strongly affect the catalytic activity and product selectivity of CO2 electroreduction on Au(111).


ACS Catalysis ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 6305-6319 ◽  
Author(s):  
Go Iijima ◽  
Tomohiko Inomata ◽  
Hitoshi Yamaguchi ◽  
Miho Ito ◽  
Hideki Masuda

Author(s):  
Jiayu Li ◽  
Jinxia Li ◽  
Xianglin Liu ◽  
Jiacheng Chen ◽  
Pengfei Tian ◽  
...  

Research ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Zhi-Hua Zhou ◽  
Kai-Hong Chen ◽  
Song Gao ◽  
Zhi-Wen Yang ◽  
Liang-Nian He

In the photoreduction of CO2 to CO, the competitive H2 evolution is always inevitable due to the approximate reduction potentials of H+/H2 and CO2/CO, which results in poor selectivity for CO production. Herein, imidazolium-type ionic liquid- (IL-) modified rhenium bipyridine-based porous organometallic polymers (Re-POMP-IL) were designed as efficient and selective photocatalysts for visible-light CO2 photoreduction to CO based on the affinity of IL with CO2. Photoreduction studies demonstrated that CO2 photoreduction promoted by Re-POMP-IL functioning as the catalyst exhibits excellent CO selectivity up to 95.5% and generate 40.1 mmol CO/g of Re-POMP-IL1.0 (obtained by providing equivalent [(5,5′-divinyl-2,2′-bipyridine)Re(CO)3Cl] and 3-ethyl-1-vinyl-1H-imidazol-3-ium bromide) at 12 h, outperforming that attained with the corresponding Re-POMP analogue without IL, which highlights the crucial role of IL. Notably, CO2 adsorption, light harvesting, and transfer of photogenerated charges as key steps for CO2RR were studied by employing POMPs modified with different amounts of IL as photocatalysts, among which the CO2 affinity as an important factor for POMPs catalyzed CO2 reduction is revealed. Overall, this work provides a practical pathway to improve the CO2 photoreduction efficiency and CO selectivity by employing IL as a regulator.


Author(s):  
Xing Zhi ◽  
Anthony Vasileff ◽  
Yao Zheng ◽  
Yan Jiao ◽  
Shizhang Qiao

The electrochemical CO2 reduction reaction (CRR) is intrinsically complex given the multiple possible reaction pathways and end products. Consequently, selectivity is a persistent challenge for the design and operation of...


Sign in / Sign up

Export Citation Format

Share Document