Electrochemical Nitrate-to-Ammonia Conversion Enabled by Carbon-Decoration of Ni─GaOOH Synthesized via Plasma-Assisted CO 2 Reduction.
Abd H BabikirXin MaoAijun DuJames D RichesKostya Ken OstrikovAnthony Peter O'MullanePublished in: Small (Weinheim an der Bergstrasse, Germany) (2024)
The release of nitrates into the environment leads to contaminated soil and water that poses a health risk to humans and animals. Due to the transition to renewable energy-based technologies, an electrochemical approach is an emerging option that can selectively produce valuable ammonia from nitrate sources. However, traditional metal-based electrocatalysts often suffer from low nitrate adsorption that reduces NH 3 production rates. Here, a Ni-GaOOH-C/Ga electrocatalyst for electrochemical nitrate conversion into NH 3 is synthesized via a low energy atmospheric-pressure plasma process that reduces CO 2 into highly dispersed activated carbon on dispersed Ni─GaOOH particles produced from a liquid metal Ga─Ni alloy precursor. Nitrate conversion rates of up to 26.3 µg h -1 mg -1 cat are achieved with good stability of up to 20 h. Critically, the presence of carbon centers is central to improved performance where both Ni─C and NiO─C interfaces act as NO 3- adsorption and reduction centers during the reaction. Density functional theory (DFT) calculations indicate that the NiO─C and Ni─C reaction sites reduce the Gibbs free energy required for NO 3- reduction to NH 3 compared to NiO and Ni. Importantly, catalysts without carbon centers do not produce NH 3 , emphasizing the unique effects of incorporating carbon nanoparticles into the electrocatalyst.
Keyphrases
- metal organic framework
- drinking water
- density functional theory
- room temperature
- nitric oxide
- health risk
- transition metal
- ionic liquid
- gold nanoparticles
- molecular dynamics
- pet ct
- molecularly imprinted
- heavy metals
- particulate matter
- high resolution
- mass spectrometry
- air pollution
- tandem mass spectrometry
- oxide nanoparticles