Wu Wenjian, Zhao Yufei, Li Shihong, He Baiyin, Liu Hao, Zeng Xingrong, Zhang Jinqiang, Wang Guoxiu
School of Materials Science and Engineering, Dongguan University of Technology, Dongguan 523808, People's Republic of China.
School of Materials Science and Engineering, Dongguan University of Technology, Dongguan 523808, People's Republic of China; Center for Clean Energy Technology, School of Mathematical and Physical Science, Faculty of Science, University of Technology Sydney, NSW 2007, Australia; College of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, People's Republic of China.
J Colloid Interface Sci. 2019 Jul 1;547:291-298. doi: 10.1016/j.jcis.2019.04.004. Epub 2019 Apr 3.
Two-dimensional (2D) molybdenum sulfide (MoS) is considered as a promising catalyst for hydrogen evolution reaction (HER), originated from its abundant hydrogen evolution active sites. However, the HER performance of MoS is currently hindered by the limited exposed density of the active sites and low conductivity. Herein, we report a facile and scalable electrospinning technique to fabricate 2D MoS nanoplates doped with phosphorus within one-dimensional nitrogen doped-carbon nanofibers (NCNFs-MoS|P) as a highly efficient HER catalyst. The space-confined growth with the presence of NCNFs avoided the stacking and aggregation of the MoS nanoplates, resulting in more exposed edge sites. The introduction of phosphorus atoms further activated the surface of MoS and enhanced the electron transfer. The overpotential of NCNFs-MoS|P reached 98 mV at 10 mA cm, exhibiting excellent HER catalytic activity. Besides, almost no decay was observed after the stability test (5000 cycles or 20 h). The density functional calculations (DFT) elucidated that the incorporation of phosphorus atoms significantly improved the electrical conductivity and decreased the H adsorption energy barrier on MoS, leading to a high catalytic performance of NCNFs-MoS|P.
二维(2D)硫化钼(MoS)因其丰富的析氢活性位点而被认为是一种很有前景的析氢反应(HER)催化剂。然而,目前MoS的析氢性能受到活性位点暴露密度有限和电导率低的阻碍。在此,我们报道了一种简便且可扩展的静电纺丝技术,用于在一维氮掺杂碳纳米纤维(NCNFs-MoS|P)中制备掺杂磷的二维MoS纳米片,作为一种高效的析氢催化剂。在NCNFs存在下的空间限制生长避免了MoS纳米片的堆叠和聚集,从而产生了更多暴露的边缘位点。磷原子的引入进一步活化了MoS的表面并增强了电子转移。NCNFs-MoS|P在10 mA cm时的过电位达到98 mV,表现出优异的析氢催化活性。此外,稳定性测试(5000次循环或20小时)后几乎没有观察到衰减。密度泛函计算(DFT)表明,磷原子的掺入显著提高了电导率,并降低了MoS上的H吸附能垒,从而导致NCNFs-MoS|P具有高催化性能。