skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Computational Design of Active Site Structures with Improved Transition-State Scaling for Ammonia Synthesis

Abstract

Here, the Haber–Bosch process for the reduction of atmospheric nitrogen to ammonia is one of the most optimized heterogeneous catalytic reactions, but there are aspects of the industrial process that remain less than ideal. It has been shown that the activity of metal catalysts is limited by a Brønsted–Evans–Polanyi (BEP) scaling relationship between the reaction and transition-state energies for N 2 dissociation, leading to a negligible production rate at ambient conditions and a modest rate under harsh conditions. In this study, we use density functional theory (DFT) calculations in conjunction with mean-field microkinetic modeling to study the rate of NH 3 synthesis on model active sites that require the singly coordinated dissociative adsorption of N atoms onto transition metal atoms. Our results demonstrate that this ”on-top” binding of nitrogen exhibits significantly improved scaling behavior, which can be rationalized in terms of transition-state geometries and leads to considerably higher predicted activity. While synthesis of these model systems is likely challenging, the stabilization of such an active site could enable thermochemical ammonia synthesis under more benign conditions.

Authors:
ORCiD logo [1];  [1];  [1];  [1]; ORCiD logo [2];  [3]
  1. Stanford Univ., Stanford, CA (United States)
  2. SLAC National Accelerator Lab., Menlo Park, CA (United States); Univ. of Pennsylvania, Philadelphia, PA (United States)
  3. Stanford Univ., Stanford, CA (United States); SLAC National Accelerator Lab., Menlo Park, CA (United States)
Publication Date:
Research Org.:
SLAC National Accelerator Lab., Menlo Park, CA (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
OSTI Identifier:
1459599
Grant/Contract Number:
DGE-1656518; 9455; AC02-76SF00515
Resource Type:
Journal Article: Accepted Manuscript
Journal Name:
ACS Catalysis
Additional Journal Information:
Journal Volume: 8; Journal Issue: 5; Journal ID: ISSN 2155-5435
Publisher:
American Chemical Society (ACS)
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; ammonia synthesis; density functional theory; microkinetic modeling; scaling relations; transition states

Citation Formats

Singh, Aayush R., Montoya, Joseph H., Rohr, Brian A., Tsai, Charlie, Vojvodic, Aleksandra, and Norskov, Jens K. Computational Design of Active Site Structures with Improved Transition-State Scaling for Ammonia Synthesis. United States: N. p., 2018. Web. doi:10.1021/acscatal.8b00106.
Singh, Aayush R., Montoya, Joseph H., Rohr, Brian A., Tsai, Charlie, Vojvodic, Aleksandra, & Norskov, Jens K. Computational Design of Active Site Structures with Improved Transition-State Scaling for Ammonia Synthesis. United States. doi:10.1021/acscatal.8b00106.
Singh, Aayush R., Montoya, Joseph H., Rohr, Brian A., Tsai, Charlie, Vojvodic, Aleksandra, and Norskov, Jens K. Fri . "Computational Design of Active Site Structures with Improved Transition-State Scaling for Ammonia Synthesis". United States. doi:10.1021/acscatal.8b00106.
@article{osti_1459599,
title = {Computational Design of Active Site Structures with Improved Transition-State Scaling for Ammonia Synthesis},
author = {Singh, Aayush R. and Montoya, Joseph H. and Rohr, Brian A. and Tsai, Charlie and Vojvodic, Aleksandra and Norskov, Jens K.},
abstractNote = {Here, the Haber–Bosch process for the reduction of atmospheric nitrogen to ammonia is one of the most optimized heterogeneous catalytic reactions, but there are aspects of the industrial process that remain less than ideal. It has been shown that the activity of metal catalysts is limited by a Brønsted–Evans–Polanyi (BEP) scaling relationship between the reaction and transition-state energies for N2 dissociation, leading to a negligible production rate at ambient conditions and a modest rate under harsh conditions. In this study, we use density functional theory (DFT) calculations in conjunction with mean-field microkinetic modeling to study the rate of NH3 synthesis on model active sites that require the singly coordinated dissociative adsorption of N atoms onto transition metal atoms. Our results demonstrate that this ”on-top” binding of nitrogen exhibits significantly improved scaling behavior, which can be rationalized in terms of transition-state geometries and leads to considerably higher predicted activity. While synthesis of these model systems is likely challenging, the stabilization of such an active site could enable thermochemical ammonia synthesis under more benign conditions.},
doi = {10.1021/acscatal.8b00106},
journal = {ACS Catalysis},
number = 5,
volume = 8,
place = {United States},
year = {Fri Mar 30 00:00:00 EDT 2018},
month = {Fri Mar 30 00:00:00 EDT 2018}
}

Journal Article:
Free Publicly Available Full Text
This content will become publicly available on March 30, 2019
Publisher's Version of Record

Save / Share: