Open AccessN, P, and S Codoped Graphene‐Like Carbon Nanosheets for Ultrafast Uranium (VI) Capture with High Capacity
Author(s) -
Chen Zhe,
Chen Wanying,
Jia Dashuang,
Liu Yang,
Zhang Anrui,
Wen Tao,
Liu Jian,
Ai Yuejie,
Song Weiguo,
Wang Xiangke
Publication year - 2018
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.201800235
Subject(s) - heteroatom , graphene , uranium , adsorption , density functional theory , ionic bonding , aqueous solution , x ray photoelectron spectroscopy , carbon fibers , materials science , uranyl , covalent bond , chemical engineering , ion , nanotechnology , chemistry , composite number , ring (chemistry) , organic chemistry , computational chemistry , engineering , metallurgy , composite material
The development of functional materials for the highly efficient capture of radionuclides, such as uranium from nuclear waste solutions, is an important and challenging topic. Here, few‐layered N, P, and S codoped graphene‐like carbon nanosheets (NPS‐GLCs) that are fabricated in the 2D confined spacing of silicate RUB‐15 and applied as sorbents to remove U(VI)ions from aqueous solutions are presented. The NPS‐GLCs exhibit a large capacity, wide pH suitability, an ultrafast removal rate, stability at high ionic strengths, and excellent selectivity for U(VI) as compared to multiple competing metal ions. The 2D ultrathin structure of NPS‐GLCs with large spacing of 1 nm not only assures the rapid mass diffusion, but also exposes a sufficient active site for the adsorption. Strong covalent bonds such as POU and SOU are generated between the heteroatom (N, P, S) with UO 2 2+ according to X‐ray photoelectron spectroscopy analysis and density functional theory theoretical calculations. This work highlights the interaction mechanism of low oxidation state heteroatoms with UO 2 2+ , thereby shedding light on the material design of uranium immobilization in the pollution cleanup of radionuclides.