TY - JOUR
T1 - Ru/La0.5Pr0.5O1.75 Catalyst for Low-Temperature Ammonia Synthesis
AU - Ogura, Yuta
AU - Tsujimaru, Kotoko
AU - Sato, Katsutoshi
AU - Miyahara, Shin Ichiro
AU - Toriyama, Takaaki
AU - Yamamoto, Tomokazu
AU - Matsumura, Syo
AU - Nagaoka, Katsutoshi
N1 - Funding Information:
This research was supported by a grant from the CREST, JST program (no. JPMJCR1341). STEM observations were performed as part of a program conducted by the Advanced Characterization Nanotechnology Platform Japan, sponsored by the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan. K. Sato thanks the Program for Elements Strategy Initiative for Catalysts & Batteries (ESICB) commissioned by MEXT. The authors thank Mr. Y. Wada (Oita University) for his assistance with characterization techniques.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/12/3
Y1 - 2018/12/3
N2 - To exploit the use of hydrogen as a source of sustainable energy, development of an efficient process for synthesizing an energy carrier such as ammonia under mild conditions will be necessary. Here, we show that Ru/La0.5Pr0.5O1.75 prereduced at an extraordinary high temperature of 650 °C catalyzes high NH3-synthesis rates under mild conditions. At 400 °C under 1.0 MPa, the synthesis rate was comparable with that of most active oxide-supported Ru catalysts. Kinetic analysis revealed that hydrogen poisoning, which is a typical drawback for oxide-supported Ru catalysts such as Cs+/Ru/MgO, was effectively suppressed over Ru/La0.5Pr0.5O1.75. The high activity induced by high-temperature reduction was attributable to the good thermal stability of the support and a phase change of the La0.5Pr0.5O1.75 support during prereduction. Fourier transform-infrared spectroscopy measurements after N2 adsorption on the catalyst revealed that electrons were efficiently donated from trigonal La0.5Pr0.5O1.5 to the antibonding π orbital of the N≡N bond of N2 via Ru atoms. Cleavage of the N≡N bond, the rate-determining step for ammonia synthesis, was thus accelerated. Our results expand the range of possibilities for developing more effective ammonia synthesis catalysts under mild conditions. Such catalysts will be needed to enable development of hydrogen-based sustainable energy resources.
AB - To exploit the use of hydrogen as a source of sustainable energy, development of an efficient process for synthesizing an energy carrier such as ammonia under mild conditions will be necessary. Here, we show that Ru/La0.5Pr0.5O1.75 prereduced at an extraordinary high temperature of 650 °C catalyzes high NH3-synthesis rates under mild conditions. At 400 °C under 1.0 MPa, the synthesis rate was comparable with that of most active oxide-supported Ru catalysts. Kinetic analysis revealed that hydrogen poisoning, which is a typical drawback for oxide-supported Ru catalysts such as Cs+/Ru/MgO, was effectively suppressed over Ru/La0.5Pr0.5O1.75. The high activity induced by high-temperature reduction was attributable to the good thermal stability of the support and a phase change of the La0.5Pr0.5O1.75 support during prereduction. Fourier transform-infrared spectroscopy measurements after N2 adsorption on the catalyst revealed that electrons were efficiently donated from trigonal La0.5Pr0.5O1.5 to the antibonding π orbital of the N≡N bond of N2 via Ru atoms. Cleavage of the N≡N bond, the rate-determining step for ammonia synthesis, was thus accelerated. Our results expand the range of possibilities for developing more effective ammonia synthesis catalysts under mild conditions. Such catalysts will be needed to enable development of hydrogen-based sustainable energy resources.
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U2 - 10.1021/acssuschemeng.8b04683
DO - 10.1021/acssuschemeng.8b04683
M3 - Article
AN - SCOPUS:85056516272
SN - 2168-0485
VL - 6
SP - 17258
EP - 17266
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 12
ER -