期刊
ACS ENERGY LETTERS
卷 5, 期 3, 页码 736-741出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.9b02812
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资金
- Australian Research Council [CE140100012, DP170102267, DP200101878]
- Australian Renewable Energy Agency (ARENA) [2018/RND009]
- Russian Ministry of Science and Higher Education [AAAA-A16-116121510087-5]
As research on sustainable ammonia synthesis via electrochemical and photochemical N-2 reduction progresses to include a wider variety of aqueous and aprotic electrolytes, H-1 NMR spectroscopy is increasingly adopted as a means for ammonium quantification. However, this method is highly sensitive to experimental parameters, as demonstrated herein using a highly versatile and robust NMR pulse program. We demonstrate the sensitivity of the measurement to the final pH of the analyzed solution and identify a [H+] concentration range enabling robust quantification. We compare direct quantification versus calibration approaches to show that the former is highly sensitive to spin relaxation effects and identify the latter as the most reliable approach. This method, when optimized, enables direct, rapid quantification of both (NH4+)-N-14 and (NH4+)-N-15 within 12-22 min. The limit of detection of 5-10 mu M, depending on the solvent, which meets the needs of current electrochemical and photochemical N-2 reduction research.
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