Si-Doped Fe Catalyst for Ammonia Synthesis at Dramatically Decreased Pressures and Temperatures

被引:41
作者
An, Qi [1 ]
Mcdonald, Molly [1 ]
Fortunelli, Alessandro [2 ,3 ]
Goddard, William A., III [2 ]
机构
[1] Univ Nevada, Dept Chem & Mat Engn, Reno, NV 89577 USA
[2] CALTECH, Mat & Proc Simulat Ctr MSC, Pasadena, CA 91125 USA
[3] CNR, ICCOM, ThC2 Lab, I-56124 Pisa, Italy
关键词
TOTAL-ENERGY CALCULATIONS; PROMOTED FE(111); TRANSITION-METAL; NITROGEN; SURFACES; IRON; DINITROGEN; RUTHENIUM; OXIDE;
D O I
10.1021/jacs.9b13996
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Haber-Bosch (HB) process combining nitrogen (N-2) and hydrogen (H-2) into ammonia (NH3) gas plays an essential role in the synthesis of fertilizers for food production and many other commodities. However, HB requires enormous energy resources (2% of world energy production), and the high pressures and temperatures make NH3 production facilities very expensive. Recent advances in improving HB catalysts have been incremental and slow. To accelerate the development of improved HB catalysts, we developed a hierarchical high-throughput catalyst screening (HHTCS) approach based on the recently developed complete reaction mechanism to identify non-transition-metal (NTM) elements from a total set of 18 candidates that can significantly improve the efficiency of the most active Fe surface, Fe-bcc(111), through surface and subsurface doping. Surprisingly, we found a very promising subsurface dopant, Si, that had not been identified or suggested previously, showing the importance of the subsurface Fe atoms in N-2 reduction reactions. Then we derived the full reaction path of the HB process for the Si doped Fe-bcc(111) from QM simulations, which we combined with kinetic Monte Carlo (kMC) simulations to predict a similar to 13-fold increase in turnover frequency (TOF) under typical extreme HB conditions (200 atm reactant pressure and 500 degrees C) and a similar to 43-fold increase in TOF under ideal HB conditions (20 atm reactant pressure and 400 degrees C) for the Si-doped Fe catalyst, in comparison to pure Fe catalyst. Importantly, the Si-doped Fe catalyst can achieve the same TOF of pure Fe at 200 atm/500 degrees C under much milder conditions, e.g. at a much decreased reactant pressure of 20 atm at 500 degrees C, or alternatively at temperature and reactant pressure decreased to 400 degrees C and 60 atm, respectively. Production plants using the new catalysts that operate under such milder conditions could be much less expensive, allowing production at local sites needing fertilizer.
引用
收藏
页码:8223 / 8232
页数:10
相关论文
共 41 条
[1]   ACTIVATION OF NITROGEN BY ALKALI-METAL PROMOTED TRANSITION-METAL .1. AMMONIA SYNTHESIS OVER RUTHENIUM PROMOTED BY ALKALI-METAL [J].
AIKA, K ;
OZAKI, A ;
HORI, H .
JOURNAL OF CATALYSIS, 1972, 27 (03) :424-&
[2]   QM-Mechanism-Based Hierarchical High-Throughput in Silico Screening Catalyst Design for Ammonia Synthesis [J].
An, Qi ;
Shen, Yidi ;
Fortunelli, Alessandro ;
Goddard, William A., III .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (50) :17702-17710
[3]  
Appl M., 2006, Ullmann's Encyclopedia of Industrial Chemistry
[4]   GREEN-FUNCTION APPROACH TO LINEAR RESPONSE IN SOLIDS [J].
BARONI, S ;
GIANNOZZI, P ;
TESTA, A .
PHYSICAL REVIEW LETTERS, 1987, 58 (18) :1861-1864
[5]  
Bielawa H, 2001, ANGEW CHEM INT EDIT, V40, P1061, DOI 10.1002/1521-3773(20010316)40:6<1061::AID-ANIE10610>3.3.CO
[6]  
2-2
[7]   Beyond fossil fuel-driven nitrogen transformations [J].
Chen, Jingguang G. ;
Crooks, Richard M. ;
Seefeldt, Lance C. ;
Bren, Kara L. ;
Bullock, R. Morris ;
Darensbourg, Marcetta Y. ;
Holland, Patrick L. ;
Hoffman, Brian ;
Janik, Michael J. ;
Jones, Anne K. ;
Kanatzidis, Mercouri G. ;
King, Paul ;
Lancaster, Kyle M. ;
Lymar, Sergei V. ;
Pfromm, Peter ;
Schneider, William F. ;
Schrock, Richard R. .
SCIENCE, 2018, 360 (6391)
[8]  
Dove M. T., 1993, Introduction to Lattice Dynamics
[9]  
ERTL G, 1982, SURF SCI, V114, P527, DOI [10.1016/0039-6028(82)90703-8, 10.1016/0039-6028(82)90702-6]
[10]   Reactions at surfaces: From atoms to complexity (Nobel lecture) [J].
Ertl, Gerhard .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (19) :3524-3535