TY - JOUR
T1 - Ternary intermetallic LaCoSi as a catalyst for N2 activation
AU - Gong, Yutong
AU - Wu, Jiazhen
AU - Kitano, Masaaki
AU - Wang, Junjie
AU - Ye, Tian Nan
AU - Li, Jiang
AU - Kobayashi, Yasukazu
AU - Kishida, Kazuhisa
AU - Abe, Hitoshi
AU - Niwa, Yasuhiro
AU - Yang, Hongsheng
AU - Tada, Tomofumi
AU - Hosono, Hideo
N1 - Publisher Copyright:
© 2018 The Author(s) 2018, under exclusive licence to Macmillan Publishers Ltd, part of Springer Nature.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Activating high-energy multiple bonds using earth-abundant metals is one of the most significant challenges in catalysis. Here, we show that LaCoSi - a ternary intermetallic compound - is an efficient and stable catalyst for N2 activation to produce NH3. The ammonia synthesis is significantly promoted by shifting the reaction bottleneck from the sluggish N2 dissociation to NH x formation, which few catalysts have achieved. Theoretical calculations reveal that the negatively charged cobalt mediates electron transfer from lanthanum to the adsorbed N2, which further reduces the activation barrier of N2 dissociation. Most importantly, the specific LaCoSi geometric configuration stabilizes the N2 adsorption with a strong exothermic effect, which dramatically decreases the apparent energy barrier of N2 activation. Consequently, LaCoSi shows a superior activity (1,250 μmol g-1 h-1), with a 60-fold increase over the activity of supported cobalt catalysts under mild reaction conditions (400 °C, 0.1 MPa).
AB - Activating high-energy multiple bonds using earth-abundant metals is one of the most significant challenges in catalysis. Here, we show that LaCoSi - a ternary intermetallic compound - is an efficient and stable catalyst for N2 activation to produce NH3. The ammonia synthesis is significantly promoted by shifting the reaction bottleneck from the sluggish N2 dissociation to NH x formation, which few catalysts have achieved. Theoretical calculations reveal that the negatively charged cobalt mediates electron transfer from lanthanum to the adsorbed N2, which further reduces the activation barrier of N2 dissociation. Most importantly, the specific LaCoSi geometric configuration stabilizes the N2 adsorption with a strong exothermic effect, which dramatically decreases the apparent energy barrier of N2 activation. Consequently, LaCoSi shows a superior activity (1,250 μmol g-1 h-1), with a 60-fold increase over the activity of supported cobalt catalysts under mild reaction conditions (400 °C, 0.1 MPa).
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U2 - 10.1038/s41929-017-0022-0
DO - 10.1038/s41929-017-0022-0
M3 - Article
AN - SCOPUS:85047541232
SN - 2520-1158
VL - 1
SP - 178
EP - 185
JO - Nature Catalysis
JF - Nature Catalysis
IS - 3
ER -