Back to Search Start Over

Electrochemical Synthesis of Ammonia Directly fromWet N2 Using La0.6Sr0.4Fe0.8Cu0.2O3-δ-Ce0.8Gd0.18Ca0.02O2-δ Composite Catalyst.

Authors :
Ibrahim A. Amar
Rong Lan
Shanwen Tao
Source :
Journal of The Electrochemical Society; 2014, Vol. 161 Issue 6, pH350-H354, 5p
Publication Year :
2014

Abstract

La<subscript>0.6</subscript>Sr<subscript>0.4</subscript>Fe<subscript>0.8</subscript>Cu<subscript>0.2</subscript>O<subscript>3-δ</subscript> was prepared via combined EDTA-citrate complexing sol-gel process, characterized by X-ray diffraction and SEM. Ammonia synthesis was successfully synthesized directly from wet nitrogen based on an electrolytic cell using La<subscript>0.6</subscript>Sr<subscript>0.4</subscript>Fe<subscript>0.8</subscript>Cu<subscript>0.2</subscript>O<subscript>3-δ</subscript>-Ce<subscript>0.8</subscript>Gd<subscript>0.18</subscript>Ca<subscript>0.02</subscript>O2-δ composite cathode, Ce<subscript>0.8</subscript>Gd<subscript>0.18</subscript>Ca<subscript>0.02</subscript>O<subscript>2-δ-</subscript>(Li/Na/K)<subscript>2</subscript>CO<subscript>3</subscript> composite electrolyte and Sm<subscript>0.5</subscript>Sr<subscript>0.5</subscript>CoO<subscript>3-δ</subscript>-Ce<subscript>0.8</subscript>Gd<subscript>0.18</subscript>Ca<subscript>0.02</subscript>O<subscript>2-δ</subscript> composite anode. The O<superscript>2-</superscript> conduction of the composite electrolyte was used for ammonia synthesis. The maximum ammonia formation rate of 5 x 10<superscript>-11</superscript> mol s<superscript>-1</superscript> cm<superscript>-2</superscript> was observed at 400°C when a voltage of 1.4 V was applied which is two orders of magnitude higher than that of previous report when ammonia was synthesized from N<subscript>2</subscript> and H<subscript>2</subscript>O at 650°C. Besides ammonia, hydrogen is also co-generated at the cathode. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00134651
Volume :
161
Issue :
6
Database :
Supplemental Index
Journal :
Journal of The Electrochemical Society
Publication Type :
Academic Journal
Accession number :
108684738
Full Text :
https://doi.org/10.1149/2.021406jes