4.8 Article

Hydrogen-incorporated vanadium dioxide nanosheets enable efficient uranium confinement and photoreduction

期刊

NANO RESEARCH
卷 15, 期 4, 页码 2943-2951

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-021-3916-8

关键词

VO2 nanosheets; hydroxylated surface; confinement; photoreduction; uranium

资金

  1. National Natural Science Foundaiton of China [21902130, 21976147]
  2. Sichuan Science and Technology Program [2020YFG0160, 2020YFG0191, 2020YFS0345, 2020JDJQ0060, 2020JDRC0089]
  3. State Key Laboratory of Environment-friendly Energy Materials in SWUST [18fksy0218]
  4. SWUST [18zx7149]
  5. Natural Science Foundation of Anhui province [2008085QB81, 2008085QA33]
  6. Education Department of Anhui Province Foundation [KJ2019A0503]

向作者/读者索取更多资源

In this study, hydrogen was successfully incorporated into VO2 nanosheets to enhance the interaction between VO2 and U(VI), resulting in a highly active and stable photocatalyst for U(VI) reduction. The increase in hydrogen content in hydrated VO2 (H-X-VO2) nanosheets led to a reduction in bandgap and increased binding strength of UO22+ on the nanosheets.
Photocatalytic reduction of U(VI) represents a novel and effective manner for the removal of U(VI) pollutant from radioactive wastewater. Herein, we successfully incorporated hydrogen into VO2 nanosheets, which strengthened the interaction between VO2 and U(VI), thereby achieving a highly active and stable photocatalyst for U(VI) reduction. With the increase of H content in hydric VO2 (H-X-VO2) nanosheets, the bandgap shrank from 2.29 to 1.66 eV, whereas the position of conduction bands remained more negative than the reduction potential of U(VI)/U(IV) (0.41 V vs. NHE). When irradiated by simulated sunlight, the U(VI) removal efficiency over H-0.613-VO2 nanosheets reached up to 95.4% within 90 min, which largely outperformed 28.3% of pristine VO2 nanosheets. The mechanistic study demonstrated that the hydroxylated surface gave rise to the balanced O confinement sites in VO2 (011), leading to the stabilized adsorption configuration and increased binding strength of UO22+ on HX--VO2 nanosheets.

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