首页 | 本学科首页   官方微博 | 高级检索  
     


Perovskite ceramic oxide as an efficient electrocatalyst for nitrogen fixation
Authors:Yangsen Xu  Xi Xu  Ning Cao  Xianfen Wang  Xuehua Liu  Marco Fronzi  Lei Bi
Affiliation:1. School of Resource Environment and Safety Engineering, University of South China, Hengyang, 421001, China;2. Institute of Materials for Energy and Environment, College of Materials Science and Engineering, Qingdao University, Ningxia Road No.308, Qingdao, 266071, China;3. IGP College of Engineering and SIT Research Laboratories, Shibaura Institute of Technology, Toyosu, Tokyo, Japan;4. School of Mathematical and Physical Science, University of Technology Sydney, Ultimo, New South Wales, 2007, Australia
Abstract:The electrochemical conversion of N2 to NH3 is an interesting research topic as it provided an alternative and energy-saving method compared with the traditional way of NH3 production. Although different materials have been proposed for N2 reduction, the use of defects in oxides was only reported recently and the relevant working mechanism was not fully revealed. In this study, Sr was used as the dopant for LaFeO3 to create oxygen vacancies, forming the Sr-doped LFO (La0.5Sr0.5FeO3-δ) perovskite oxide. The La0.5Sr0.5FeO3-δ ceramic oxide used as a catalyst achieves an NH3 yield of 11.51 μgh?1 mg?1 and the desirable faradic efficiency (F.E.) of 0.54% at ?0.6 V vs reversible hydrogen electrode (RHE), which surpassed that of LaFeO3 nanoparticles. The 15N isotope labeling method was employed to prove the La0.5Sr0.5FeO3-δ catalyst had the function of converting N2 into NH3 under the electrolysis condition. The first principle calculations were used to investigate the mechanism at the atomistic level, revealing that the free energy barriers changed significantly with the introduction of oxygen vacancies that accelerated the overall nitrogen reduction reaction (NRR) procedure.
Keywords:Perovskite oxides  DFT calculations  Nitrogen reduction  Electrocatalytic  Oxygen vacancy
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号