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A physical catalyst for the electrolysis of nitrogen to ammonia
Author(s) -
Yang Song,
D. W. Johnson,
Rui Peng,
Dale K. Hensley,
Peter V. Bonnesen,
Liangbo Liang,
Jingsong Huang,
Fengchang Yang,
Fei Zhang,
Rui Qiao,
Arthur P. Baddorf,
Timothy J. Tschaplinski,
Nancy L. Engle,
Marta C. Hatzell,
Zili Wu,
David A. Cullen,
Harry M. Meyer,
Bobby G. Sumpter,
Adam J. Rondi
Publication year - 2018
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.1700336
Subject(s) - catalysis , electrolysis , ammonia , ammonia production , nitrogen , carbon fibers , materials science , environmental chemistry , inorganic chemistry , chemical engineering , environmental science , nanotechnology , chemistry , organic chemistry , electrode , composite material , composite number , engineering , electrolyte
Ammonia synthesis consumes 3 to 5% of the world's natural gas, making it a significant contributor to greenhouse gas emissions. Strategies for synthesizing ammonia that are not dependent on the energy-intensive and methane-based Haber-Bosch process are critically important for reducing global energy consumption and minimizing climate change. Motivated by a need to investigate novel nitrogen fixation mechanisms, we herein describe a highly textured physical catalyst, composed of N-doped carbon nanospikes, that electrochemically reduces dissolved N gas to ammonia in an aqueous electrolyte under ambient conditions. The Faradaic efficiency (FE) achieves 11.56 ± 0.85% at -1.19 V versus the reversible hydrogen electrode, and the maximum production rate is 97.18 ± 7.13 μg hour cm. The catalyst contains no noble or rare metals but rather has a surface composed of sharp spikes, which concentrates the electric field at the tips, thereby promoting the electroreduction of dissolved N molecules near the electrode. The choice of electrolyte is also critically important because the reaction rate is dependent on the counterion type, suggesting a role in enhancing the electric field at the sharp spikes and increasing N concentration within the Stern layer. The energy efficiency of the reaction is estimated to be 5.25% at the current FE of 11.56%.

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