In Situ Observation of Thermal Proton Transport through Graphene Layers

被引:12
作者
Zhu, Daming [1 ,2 ]
Liu, Xing [1 ,2 ]
Gao, Yi [1 ]
Li, Yadong [1 ,2 ]
Wang, Rui [1 ]
Xu, Zijian [1 ]
Ji, Gengwu [1 ,2 ]
Jiang, Sheng [1 ]
Zhao, Bin [1 ]
Yin, Guangzhi [1 ]
Li, Li [1 ]
Yang, Tieying [1 ]
Wang, Yong [1 ]
Yi, Lin [3 ]
Li, Xiaolong [1 ]
Tai, Renzhong [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Huazhong Univ Sci & Technol, Sch Phys, Wuhan 430074, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
in situ technique; graphene; thermal proton; synchrotron X-ray; transport; CHEMICAL-VAPOR-DEPOSITION; SINGLE-LAYER; REVERSIBLE HYDROGENATION; MONOLAYER GRAPHENE; POROUS GRAPHENE; LARGE-AREA; GROWTH; THICKNESS; CRYSTALS; FILMS;
D O I
10.1021/acsnano.7b03359
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Protons can penetrate through single-layer graphene, but thicker graphene layers (more than 2 layers), which possess more compact electron density, are thought to be unfavorable for penetration by protons at room temperature and elevated temperatures. In this work, we developed an in situ subsecond time-resolved grazing incidence X-ray diffraction technique, which fully realizes the real-time observation of the thermal proton interaction with the graphene layers at high temperature. By following the evolution of interlayer structure during the protonation process, we demonstrated that thermal protons can transport through multilayer graphene (more than 8 layers) on nickel foil at 900 degrees C. In comparison,, under the same conditions, the multilayer graphenes are impermeable to argon, nitrogen, helium, and their derived ions. Complementary in situ transport measurements simultaneously verify the penetration phenomenon at high temperature. Moreover, the direct transport of protons through graphene is regarded as the dominant contribution to the penetration phenomenon. The thermal activation, weak interlayer interaction between layers, and the affinity of the nickel catalyst may all contribute to the proton transport. We believe that this method could become one of the established approaches for the characterization of the ions intercalated with 2D materials in situ and in real-time.
引用
收藏
页码:8970 / 8977
页数:8
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