Tiered Electron Anions in Multiple Voids of LaScSi and Their Applications to Ammonia Synthesis
Related Experiment Video
Updated: Feb 25, 2026

Ammonia Synthesis at Low Pressure
Published on: August 23, 2017
Jiazhen Wu1,2, Yutong Gong1,2, Takeshi Inoshita1,3
1Materials Research Center for Element Strategy, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, 226-8503, Japan.
Abstract:
Electrides-compounds in which electrons localized in interstitial spaces periodically serve as anions-have attracted broad attention for their exotic properties, such as extraordinary electron-donating ability. In our efforts to expand this small family of phases, LaScSi emerges as a promising candidate. Its electron count is 2e- f.u.-1 in excess of that expected from the Zintl concept, while its structure offers interstitial spaces that can accommodate these extra electrons. Herein, this potential is explored through density functional theory (DFT) calculations and property measurements on LaScSi. DFT calculations (validated by heat capacity and electrical transport measurements) reveal electron density peaks at two symmetry-distinct interstitial sites. Importantly, this electride-like character is combined with chemical stability in air and water, an advantage for catalysis. Ru-loaded LaScSi shows outstanding catalytic activity for ammonia synthesis, with a turnover frequency (0.1 s-1 at 0.1 MPa, 400 °C) an order of magnitude higher than those of oxide-based Ru catalysts, e.g., Ru/MgO. As with other electrides, LaScSi's ability to reversibly store hydrogen prevents the hydrogen poisoning of Ru surfaces. The better performance of LaScSi, however, hints at the importance of the high concentration (>1.6 × 1022 cm-3 ) and tiered nature of its anionic electrons, which offers guidance toward new catalysts.
More Related Videos
12:05Preparation of Hydrophobic Metal-Organic Frameworks via Plasma Enhanced Chemical Vapor Deposition of Perfluoroalkanes for the Removal of Ammonia
Published on: October 10, 2013
06:35Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Related Concept Videos
Structure of Amines
Preparation of Amines: Alkylation of Ammonia and Amines
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Acid Halides to Amides: Aminolysis
In the first step of the aminolysis mechanism, the amine attacks the carbonyl carbon of the acyl chloride to form a tetrahedral intermediate. In the second step, the carbonyl group is re-formed with the elimination of a chloride...
Lewis Acids and Bases
VSEPR Theory and the Effect of Lone Pairs