Hydride-Enhanced CO2 Methanation: Water-Stable BaTiO2.4H0.6 as a New Support

Ya Tang, Yoji Kobayashi, Cédric Tassel, Takafumi Yamamoto, Hiroshi Kageyama

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Catalytic CO2 hydrogenation to CH4 provides a promising approach to producing natural gas, and reducing the emissions of global CO2. However, the efficiency of catalytic CO2 methanation is limited by slow kinetics at low temperatures. This study first demonstrates that an air- and water-stable perovskite oxyhydride BaTiO2.4H0.6 could function as an active support material for Ni-, Ru-based catalysts for CO2 methanation at 300–350 °C, a relatively lower temperature. With the oxyhydride support, the activity for Ni and Ru increases by a factor of 2–7 when compared to the BaTiO3 oxide support. Kinetic analysis shows reduced H2 poisoning probably due to spillover, implying that the activity change is due to the kinetics being influenced by hydride. Furthermore, the oxyhydride-supported Ni catalyst is also durable with its catalytic performance preserved for at least 10 h under a humid environment at elevated temperatures. It is anticipated that these perovskite oxyhydrides will shed new light on the design of high-efficiency metal-based catalysts for water-involved catalytic reactions.
Original languageEnglish (US)
JournalAdvanced Energy Materials
Volume8
Issue number23
DOIs
StatePublished - Aug 16 2018
Externally publishedYes

Bibliographical note

Generated from Scopus record by KAUST IRTS on 2022-09-13

ASJC Scopus subject areas

  • Renewable Energy, Sustainability and the Environment
  • Materials Science(all)

Fingerprint

Dive into the research topics of 'Hydride-Enhanced CO2 Methanation: Water-Stable BaTiO2.4H0.6 as a New Support'. Together they form a unique fingerprint.

Cite this