Photocatalytic Extraction of Uranium from Seawater Using Covalent Organic Framework Nanowires

In the push to achieve net-zero emissions by 2050, nuclear power will play an essential role alongside renewable wind and solar power, and correspondingly global interest and investment in this well-established technology is accelerating. The uranium present in seawater could support nuclear power generation for centuries, but traditional adsorptive separation strategies have proven ineffective for the selective extraction of uranium from this vast resource. Here, we report the synthesis of nanowires of a triazine-linked two-dimensional covalent organic framework via a solvent modulation approach, which can be used to access nanowire external diameters ranging from 50 to 200 nm. The 100 nm nanowires are exceptionally promising for the capture of uranium(VI) via photocatalytic reduction. Under simulated sunlight and without the use of sacrificial agents, the nanowires achieve a uranium uptake of 10.9 g/g from a 100 ppm uranyl(VI) solution, which is the highest reported to date among materials studied for photo and electrocatalytic uranium capture. Significantly, these nanowires exhibit a uranium adsorption capacity of 34.5 mg/g after exposure to seawater under irradiation for 42 days, a record among all materials reported to date for uranium capture.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-08-09
DOI
https://doi.org/10.1021/jacs.4c07699
Citations
86
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
13.63

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article

Photocatalytic Extraction of Uranium from Seawater Using Covalent Organic Framework Nanowires

Katie R. Meihaus, Ye Yuan, Guangshan Zhu, Jeffrey R. Long et al.
86 citations
Journal of the American Chemical Society
Radioactive element chemistry and processing
13.63
article

Photocatalytic Extraction of Uranium from Seawater Using Covalent Organic Framework Nanowires

Katie R. Meihaus, Ye Yuan, Guangshan Zhu, Jeffrey R. Long, Yajie Yang, Xujiao Ma, Yuebing Zheng, Jixiang Li, Biao Jiang, Yan‐Qin Zhao, Fengchao Cui
article en
86 citations

Abstract

In the push to achieve net-zero emissions by 2050, nuclear power will play an essential role alongside renewable wind and solar power, and correspondingly global interest and investment in this well-established technology is accelerating. The uranium present in seawater could support nuclear power generation for centuries, but traditional adsorptive separation strategies have proven ineffective for the selective extraction of uranium from this vast resource. Here, we report the synthesis of nanowires of a triazine-linked two-dimensional covalent organic framework via a solvent modulation approach, which can be used to access nanowire external diameters ranging from 50 to 200 nm. The 100 nm nanowires are exceptionally promising for the capture of uranium(VI) via photocatalytic reduction. Under simulated sunlight and without the use of sacrificial agents, the nanowires achieve a uranium uptake of 10.9 g/g from a 100 ppm uranyl(VI) solution, which is the highest reported to date among materials studied for photo and electrocatalytic uranium capture. Significantly, these nanowires exhibit a uranium adsorption capacity of 34.5 mg/g after exposure to seawater under irradiation for 42 days, a record among all materials reported to date for uranium capture.

Journal of the American Chemical SocietyVol. 146(33)
Lawrence Berkeley National Laboratory (US), Northeast Normal University (CN), Chinese Academy of Sciences (CN), Shanghai Advanced Research Institute (CN), University of Chinese Academy of Sciences (CN), University of California, Berkeley (US)
National Natural Science Foundation of China, Department of Science and Technology of Jilin Province, Higher Education Discipline Innovation Project, China National Nuclear Corporation, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Life below water
Openalex Percentile: Top 0%
Radioactive element chemistry and processing
13.63
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