跳到主要导航 跳到搜索 跳到主要内容

Facile synthesis of Fe-modified manganese oxide with high content of oxygen vacancies for efficient airborne ozone destruction

  • Jingbo Jia
  • , Wenjuan Yang
  • , Pengyi Zhang*
  • , Junying Zhang
  • *此作品的通讯作者
  • Tsinghua University
  • Yulin University

科研成果: 期刊稿件文章同行评审

摘要

Oxygen vacancy engineering is an efficient strategy to improve the catalytic performance of nanomaterials. In this work, a highly active Fe-modified manganese oxide (Fe-MnOx) was synthesized and used for airborne ozone decomposition. The addition of Fe3+ during MnO2 synthesis led to higher specific surface area, greatly increased content of oxygen vacancies, evidenced by XPS, H2-TPR analysis and lower oxygen vacancy formation energy (decreased by ∼1.2 eV) based on the density functional theory calculations. The ozone conversion over Fe-MnOx kept 97% after 24 h reaction, while it over MnO2 slowed down to 85% under dry condition. Remarkably, under humid condition (RH = 60%), the ozone conversion over Fe-MnOx kept 73% after 6 h reaction, while ozone conversion over pure MnO2 decreased to 50% within 1 h under the conditions of 100 ppm inlet ozone concentration and weight space velocity of 660 L g−1 h−1. The intermediate peroxide species (O22−) formed on the surface oxygen vacancies of Fe-MnOx and MnO2 during ozone decomposition reaction were observed using in situ Raman spectroscopy. The concentration and depletion rate of O22− on the surface of Fe-MnOx was higher than that on MnO2, illustrating that O22− acted as the key species to boost the catalytic process. The content and dispersity of oxygen vacancies were identified to be mainly responsible for the performance difference. This provides a promising idea for designing novel nanomaterial catalyst for gaseous ozone decomposition.

源语言英语
页(从-至)79-86
页数8
期刊Applied Catalysis A: General
546
DOI
出版状态已出版 - 25 9月 2017

指纹

探究 'Facile synthesis of Fe-modified manganese oxide with high content of oxygen vacancies for efficient airborne ozone destruction' 的科研主题。它们共同构成独一无二的指纹。

引用此