基于低维MoS2\TiO2核壳结构的析氢控制合成

Duc Nguyen Anh, Xuan Dieu Nguyen Thi
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摘要

在本报告中,我们提出了低维壳核(2D\1D)纳米结构的合成,其中TiO2纳米棒(tnr)作为核心,被连续单层MoS2 (1L-MoS2)作为外壳覆盖。获得的1L-MoS2\ tnr直接生长在导电石墨箔上,无需任何转移过程,从而最大限度地减少了从电极到最外层工作表面的电荷转移电阻。首先,采用AF溅射法设计TiO2种子层,然后采用水热法生长tnr。然后,通过金属-有机化学气相沉积技术在tnr表面涂覆连续单层MoS2,得到1L-MoS2\ tnr纳米材料。结构、振动和形态特征表明样品具有较高的结晶度。有趣的是,1L-MoS2\ tnr表现出高效的电化学HER活性,最小的起始过电位为-140 mV vs RHE,相应的Tafel斜率为80 mV / 10年,远低于原始的1L-MoS2和tnr。
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Controlled synthesis of low-dimensional MoS2\TiO2 based core-shell structure for hydrogen evolution reaction
In this report, we present the synthesis of low dimensional shell-core (2D\1D) nanostructures, in which the TiO2 nanorods (TNRs) as the core are covered by a continuous monolayer MoS2 (1L-MoS2) as the shell. The obtain 1L-MoS2\TNRs was directly grown on the conduct graphite foil without any transfer process, thus minimizing the charge transfer resistance from the electrode to the outer most working surface. For the first steps, the TiO2 seed layer was designed by the AF sputtering method, then the TNRs were grown by hydrothermal approach. Thereafter, the TNRs were conformally coated by a continuous monolayer MoS2 via a metal-organic chemical vapor deposition technique, resulting in 1L-MoS2\TNRs nanomaterial. The structural, vibrational, and morphological characteristics demonstrated that the samples are high crystallinity. Interestingly, the 1L-MoS2\TNRs showed highly efficient in electrochemical HER activity with the smallest onset overpotential of -140 mV vs RHE and a corresponding Tafel slope of 80 mV per decade, which were much lower compared to the pristine 1L-MoS2 and TNRs.
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