| Literature DB >> 26783062 |
Shan Gao1, Xingchen Jiao1, Zhongti Sun1, Wenhua Zhang1, Yongfu Sun2, Chengming Wang1, Qitao Hu1, Xiaolong Zu1, Fan Yang1, Shuyang Yang1, Liang Liang1, Ju Wu1, Yi Xie3.
Abstract
Electroreduction of CO2 into hydrocarbons could contribute to alleviating energy crisis and global warming. However, conventional electrocatalysts usually suffer from low energetic efficiency and poor durability. Herein, atomic layers for transition-metal oxides are proposed to address these problems through offering an ultralarge fraction of active sites, high electronic conductivity, and superior structural stability. As a prototype, 1.72 and 3.51 nm thick Co3O4 layers were synthesized through a fast-heating strategy. The atomic thickness endowed Co3O4 with abundant active sites, ensuring a large CO2 adsorption amount. The increased and more dispersed charge density near Fermi level allowed for enhanced electronic conductivity. The 1.72 nm thick Co3O4 layers showed over 1.5 and 20 times higher electrocatalytic activity than 3.51 nm thick Co3O4 layers and bulk counterpart, respectively. Also, 1.72 nm thick Co3O4 layers showed formate Faradaic efficiency of over 60% in 20 h.Entities:
Keywords: CO2 electroreduction; atomic layers; cobalt oxide; formate
Year: 2015 PMID: 26783062 DOI: 10.1002/anie.201509800
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336