格式化
法拉第效率
电导率
原子层沉积
过渡金属
材料科学
电阻率和电导率
吸附
化学工程
催化作用
电极
纳米技术
分析化学(期刊)
电化学
图层(电子)
化学
物理化学
电气工程
工程类
生物化学
色谱法
作者
Shan Gao,Xingchen Jiao,Zhongti Sun,Wenhua Zhang,Yongfu Sun,Chengming Wang,Qitao Hu,Xiaolong Zu,Fan Yang,Shuyang Yang,Liang Liang,Ju Wu,Yi Xie
标识
DOI:10.1002/anie.201509800
摘要
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.
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