TY - JOUR
T1 - Water Durable Electride Y5Si3
T2 - Electronic Structure and Catalytic Activity for Ammonia Synthesis
AU - Lu, Yangfan
AU - Li, Jiang
AU - Tada, Tomofumi
AU - Toda, Yoshitake
AU - Ueda, Shigenori
AU - Yokoyama, Toshiharu
AU - Kitano, Masaaki
AU - Hosono, Hideo
N1 - Funding Information:
This work was supported by MEXT Element Strategy Initiative and ACCEL of Japan Science and Technology Agency in Japan. HAXPES measurements were performed with approval of NIMS Synchrotron X-ray Station (proposal nos. 2015A4703 and 2015B4703). S.U. is grateful to HiSOR (Hiroshima University) and JAEA/SPring-8 for the development of HAXPES at BL15XU of SPring-8.
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/4/20
Y1 - 2016/4/20
N2 - We report an air and water stable electride Y5Si3 and its catalytic activity for direct ammonia synthesis. It crystallizes in the Mn5Si3-type structure and confines 0.79/f.u. anionic electrons in the quasi-one-dimensional holes. These anionic electrons strongly hybridize with yttrium 4d electrons, giving rise to improved chemical stability. The ammonia synthesis rate using Ru(7.8 wt %)-loaded Y5Si3 was as high as 1.9 mmol/g/h under 0.1 MPa and at 400 °C with activation energy of ∼50 kJ/mol. Its strong electron-donating ability to Ru metal of Y5Si3 is considered to enhance nitrogen dissociation and reduce the activation energy of ammonia synthesis reaction. Catalytic activity was not suppressed even after Y5Si3, once dipped into water, was used as the catalyst promoter. These findings provide novel insights into the design of simple catalysts for ammonia synthesis.
AB - We report an air and water stable electride Y5Si3 and its catalytic activity for direct ammonia synthesis. It crystallizes in the Mn5Si3-type structure and confines 0.79/f.u. anionic electrons in the quasi-one-dimensional holes. These anionic electrons strongly hybridize with yttrium 4d electrons, giving rise to improved chemical stability. The ammonia synthesis rate using Ru(7.8 wt %)-loaded Y5Si3 was as high as 1.9 mmol/g/h under 0.1 MPa and at 400 °C with activation energy of ∼50 kJ/mol. Its strong electron-donating ability to Ru metal of Y5Si3 is considered to enhance nitrogen dissociation and reduce the activation energy of ammonia synthesis reaction. Catalytic activity was not suppressed even after Y5Si3, once dipped into water, was used as the catalyst promoter. These findings provide novel insights into the design of simple catalysts for ammonia synthesis.
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U2 - 10.1021/jacs.6b00124
DO - 10.1021/jacs.6b00124
M3 - Article
AN - SCOPUS:84964403007
SN - 0002-7863
VL - 138
SP - 3970
EP - 3973
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 12
ER -