Premium
Hydride‐Enhanced CO 2 Methanation: Water‐Stable BaTiO 2.4 H 0.6 as a New Support
Author(s) -
Tang Ya,
Kobayashi Yoji,
Tassel Cédric,
Yamamoto Takafumi,
Kageyama Hiroshi
Publication year - 2018
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201800800
Subject(s) - methanation , catalysis , materials science , hydride , substitute natural gas , chemical engineering , perovskite (structure) , inorganic chemistry , kinetics , metal , oxide , chemistry , metallurgy , syngas , organic chemistry , engineering , physics , quantum mechanics
Catalytic CO 2 hydrogenation to CH 4 provides a promising approach to producing natural gas, and reducing the emissions of global CO 2 . However, the efficiency of catalytic CO 2 methanation is limited by slow kinetics at low temperatures. This study first demonstrates that an air‐ and water‐stable perovskite oxyhydride BaTiO 2.4 H 0.6 could function as an active support material for Ni‐, Ru‐based catalysts for CO 2 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 BaTiO 3 oxide support. Kinetic analysis shows reduced H 2 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.