Steric Hindrance-Derived Li+ Solvation to Enhance Lithium-Mediated Nitrogen Reduction
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide This study proposes a steric hindrance-derived electrolyte (STE) to generate Li + anion-rich solvation structures to enhance the Li-mediated nitrogen reduction reaction (Li-NRR), a promising electrochemical green ammonia synthesis method. The STE applied methylation of the alpha proton in the tetrahydrofuran (THF) solvent, which dissolved lithium salts, leading to the weak solvation of Li + and generating an anion-rich-solvated structure. The resultant anion-derived solid electrolyte interphase with thin and uniform inorganic properties improved the selectivity, energy efficiency (EE), and stability of the Li-NRR process. Additionally, the anion-rich solvation exhibited antireduction stability and inhibited electrolyte decomposition. Consequently, the STE achieved a 2-fold increase in Faradaic efficiency and NH 3 yield rate (65.8% and 90.8 nmol cm –2 s –1, respectively) compared to the THF-single electrolyte (35.7% and 49.3 nmol cm –2 s –1 ) while increasing the EE by 1.5 times.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Hydrogen Storage and Materials · Inorganic Chemistry and Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Surface Chemistry Laboratory of Electronic Materials (SCHEMA), Department of Chemical Engineering, Research Center for Carbon-zero Green Ammonia Cycling (RCCGAC)
Pohang University of Science and Technology (POSTECH)
Department of Chemical Engineering
Department of Materials Science and Engineering, Research Institute of Advanced Materials
Seoul National University
Funding
National Research Foundation of Korea
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