磺酸
共价键
硝酸
铀酰
共价有机骨架
吸附
化学
材料科学
化学工程
分解
质子
高分子化学
铀
组合化学
无机化学
有机化学
冶金
工程类
物理
量子力学
作者
Ying Xu,Zhiwu Yu,Qingyun Zhang,Feng Luo
标识
DOI:10.1002/advs.202300408
摘要
Abstract Both proton exchange membrane fuel cells and uranium‐based nuclear techniques represent two green and advanced energies. However, both of them still face some intractable scientific and industrial problems. For the former, established proton‐conduction materials always suffer one or another defect such as low proton conductivity, high activation energy, bad durability, or just small‐scale product; while for the later, there still lacks available adsorbent to selectively recover of UO 2 2+ from concentrated nitric acid (>1 M) during the spent fuel reprocessing due to the deactivation of the adsorption site or the decomposition of adsorbent under such rigorous conditions. It is found that the above two issues can be well solved by the construction of sulfonic‐pendent vinylene‐linked covalent organic frameworks (COFs), since these COFs contain abundant sulfonic units for both intrinsic proton conduction and UO 2 2+ capture through strong coordination fixation and vinylene linkage that enhances the stability up to 12 M nitric acid (one of the best materials surviving in 12 M HNO 3 ).
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