电容去离子
纳米团簇
材料科学
石墨烯
吸附
化学工程
阳极
纳米技术
插层(化学)
纳米材料
介孔材料
电极
电化学
纳米颗粒
无机化学
化学
有机化学
工程类
物理化学
催化作用
作者
Weiqing Kong,Xu Ge,Desheng Kong,C.C. Liu,Jianpeng Sun,Xiao Fang Zhu,Meng Zhang,Yuanyuan Feng
出处
期刊:Desalination
[Elsevier BV]
日期:2023-12-06
卷期号:573: 117222-117222
被引量:35
标识
DOI:10.1016/j.desal.2023.117222
摘要
BiOCl nanomaterials, because of their unique layered structure and fascinating physicochemical properties, have attracted enormous attention as anode material for capacitive deionization (CDI) towards the relief of global freshwater scarcity. However, the synthesis of ultrasmall BiOCl nanoclusters remains a considerable challenge, while the effect of crystalline surfaces on the Cl− ion intercalation/deintercalation has not yet been explored so far. In this work, highly dispersed BiOCl nanoclusters with the predominant exposure of (110) and (101) planes on graphene sheets (BiOCl@G) are fabricated by nanoconfinement and air-plasma strategy. On one hand, the ultrasmall BiOCl nanoclusters with size of ∼3 nm significantly increased their atomic utilization and electrochemical active sites, whereas the preferred crystalline planes of (110) and (101) favored the Cl− intercalation/deintercalation process within BiOCl. On the other hand, the dominant mesopores, along with a large interlayer distance (∼0.4 nm) between exfoliated graphene sheets, ensured the fast ion transport-adsorption at BiOCl/solution interface. With these novel structural features, the BiOCl@G possesses excellent figure-of-merits in terms of the Cl−-adsorption capacity (109.8 mg g−1), adsorption rate (0.110 mg g−1 s−1), energy consumption, and CDI cycling stability. These results provide new fundamental insights for developing high performance BiOCl-graphene nanocomposites used in CDI desalination and beyond.
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