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Title: Catalysis Enabled by Plasma Activation of Strong Chemical Bonds: A Review

Journal Article · · ACS Energy Letters
ORCiD logo [1];  [1]; ORCiD logo [2]; ORCiD logo [1]; ORCiD logo [1]
  1. Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States
  2. Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States, Department of Aerospace and Mechanical Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States

Nonthermal plasma-driven catalysis is an emerging subfield of heterogeneous catalysis that is particularly promising for the chemical transformation of hard-to-activate molecules (e.g., N2, CO2, CH4). In this Review, we illustrate this promise of plasma-enhanced catalysis, focusing on the ammonia synthesis and methane dry reforming reactions, two reactions that have received wide attention and that illustrate the potential for plasma excitations to mitigate kinetic and thermodynamic obstacles to chemical conversions. We highlight how plasma activation of reactants can provide access to overall reaction rates, conversions, product yields, and/or product distributions unattainable by thermal catalysis at similar temperatures and pressures. Particular emphasis is given to efforts aimed at discerning the underlying mechanisms at play in these systems. We discuss opportunities for and challenges to the advancement of the field.

Research Organization:
University of Notre Dame, IN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0016543
OSTI ID:
1509775
Alternate ID(s):
OSTI ID: 1512270
Journal Information:
ACS Energy Letters, Journal Name: ACS Energy Letters Vol. 4 Journal Issue: 5; ISSN 2380-8195
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 181 works
Citation information provided by
Web of Science

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