题名 | Boosting the oxygen evolution reaction using defect-rich ultra-thin ruthenium oxide nanosheets in acidic media |
作者 | |
通讯作者 | Xu,Hu; Zeng,Lin; Gu,Meng; Li,Hui |
共同第一作者 | Zhao,Zhi Liang; Wang,Qi; Huang,Xiang |
发表日期 | 2020-12-01
|
DOI | |
发表期刊 | |
ISSN | 1754-5692
|
EISSN | 1754-5706
|
卷号 | 13期号:12页码:5143-5151 |
摘要 | Developing low cost and highly active catalysts for the oxygen evolution reaction (OER) in an acidic medium is urgently indispensable for proton exchange membrane water electrolyzers (PEMWEs). Herein, we have prepared ultra-thin RuO2 nanosheets (RuO2 NSs) using a simple molten salt method. The as-prepared RuO2 NSs with a thickness of 1-2 nm possess abundant defects. Toward the OER, the RuO2 NSs achieve an extremely low overpotential of 199 mV at a current density of 10 mA cmgeo-2 with a loading of 125 μg cmgeo-2. Furthermore, the RuO2 NSs exhibit specific and mass activities of up to 0.89 mA cmoxide-2 and 0.52 A mgRu-1 at 1.46 V vs. RHE, which are 14.9 and 80.6 times enhanced in specific and mass activity as compared to the commercial RuO2 nanoparticles, respectively. In a homemade PEMWE, with RuO2 NSs as the OER catalyst, the electrolyzer achieves a current density of 0.93 A cm-2 at a cell voltage of 1.65 V without iR drop correction, which is 3 times larger than that of the commercial RuO2 catalyst (0.31 A cm-2). Density functional theory calculations indicate that the Ru vacancy on the RuO2 NS surfaces significantly weakens the binding energy of O∗ with respect to that of OOH∗, which decreases the energy cost in the transformation from O∗ to OOH∗, and thus dramatically enhances the OER performance. The unique defect-rich structure and outstanding performance demonstrate that the RuO2 NSs possess great potential for developing high-performance PEMWEs. This journal is |
相关链接 | [Scopus记录] |
收录类别 | |
语种 | 英语
|
重要成果 | ESI高被引
|
学校署名 | 第一
; 共同第一
; 通讯
|
资助项目 | Shenzhen Peacock Plan[
|
WOS研究方向 | Chemistry
; Energy & Fuels
; Engineering
; Environmental Sciences & Ecology
|
WOS类目 | Chemistry, Multidisciplinary
; Energy & Fuels
; Engineering, Chemical
; Environmental Sciences
|
WOS记录号 | WOS:000599751100041
|
出版者 | |
EI入藏号 | 20210109708671
|
EI主题词 | Binding energy
; Catalysts
; Defects
; Density functional theory
; Electrolytic cells
; Nanosheets
; Oxygen
; Oxygen evolution reaction
|
EI分类号 | Nanotechnology:761
; Physical Chemistry:801.4
; Chemical Products Generally:804
; Probability Theory:922.1
; Solid State Physics:933
; Materials Science:951
|
Scopus记录号 | 2-s2.0-85098327972
|
来源库 | Scopus
|
引用统计 |
被引频次[WOS]:190
|
成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/210914 |
专题 | 工学院_材料科学与工程系 工学院_机械与能源工程系 理学院_物理系 |
作者单位 | 1.Department of Materials Science and Engineering,Southern University of Science and Technology,Shenzhen,518055,China 2.Department of Physics,Southern University of Science and Technology,Shenzhen,518055,China 3.Shenzhen Institutes of Advanced Technology,Chinese Academy of Sciences,Shenzhen,518055, 4.Department of Mechanical and Energy Engineering,Southern University of Science and Technology,Shenzhen,518055,China 5.Shenzhen Key Laboratory of Hydrogen Energy,Southern University of Science and Technology,Shenzhen,518055, 6.Shenzhen Engineering Laboratory for Automotive Fuel Cell Stacks,Southern University of Science and Technology,Shenzhen, Guangdong,518055,China |
第一作者单位 | 材料科学与工程系 |
通讯作者单位 | 物理系; 机械与能源工程系; 材料科学与工程系; 南方科技大学 |
第一作者的第一单位 | 材料科学与工程系 |
推荐引用方式 GB/T 7714 |
Zhao,Zhi Liang,Wang,Qi,Huang,Xiang,et al. Boosting the oxygen evolution reaction using defect-rich ultra-thin ruthenium oxide nanosheets in acidic media[J]. Energy & Environmental Science,2020,13(12):5143-5151.
|
APA |
Zhao,Zhi Liang.,Wang,Qi.,Huang,Xiang.,Feng,Qi.,Gu,Shuang.,...&Li,Hui.(2020).Boosting the oxygen evolution reaction using defect-rich ultra-thin ruthenium oxide nanosheets in acidic media.Energy & Environmental Science,13(12),5143-5151.
|
MLA |
Zhao,Zhi Liang,et al."Boosting the oxygen evolution reaction using defect-rich ultra-thin ruthenium oxide nanosheets in acidic media".Energy & Environmental Science 13.12(2020):5143-5151.
|
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