Iron-molybdenum sulfides heterostructured nanosheet arrays for highly efficient hydrogen evolution reaction

被引:0
|
作者
Jin, Doudou [1 ,2 ]
Liu, Xingjia [1 ,2 ]
Cao, Jian [1 ,2 ]
Wei, Maobin [1 ,2 ]
Liu, Xiaoyan [1 ,2 ]
Chen, Yanli [1 ,2 ]
Li, Xin [1 ,2 ]
Wu, Qiong [1 ,2 ]
Dong, Zhaoxu [1 ,2 ]
Liu, Huilian [1 ,2 ]
机构
[1] Jilin Normal Univ, Coll Phys, Changchun 130103, Peoples R China
[2] Jilin Normal Univ, Natl Demonstrat Ctr Expt Phys Educ, Siping 136000, Peoples R China
关键词
1T MoS2; Nanosheets array; Overall water splitting; Seawater; IN-SITU GROWTH; MOS2; PERFORMANCE; FOAM;
D O I
10.1016/j.ijhydene.2025.02.243
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
1T MoS2 is identified as a hopeful rising star to substitute noble-metal catalysts for the electrocatalytic application. But the insufficient active sites and poor stability impede its large-scale applications. In this study, the novel Fe7S8/1T MoS2 heterostructured nanosheet arrays were prepared on iron foam through a facile hydrothermal approach as the highly efficient electrocatalysts for the first time. Fe7S8/1T MoS2 AA0.03 nanosheet arrays exhibited the extra low overpotential of 9 mV and 162 mV at 10 mA/cm2 and 100 mA/cm2 for HER, and the low overpotential of 183 mV at 10 mA/cm2 for OER. The assembled Fe7S8/1T MoS2 AA0.03//Fe7S8/1T MoS2 AA0.03 cell only need 1.41 V (2.15 V) to drive 10 mA/cm2 for overall alkaline water (natural seawater) splitting with remarkable cycle stability for 48 h. This novel strategy provides a pathway for the rational design of dualfunction electrocatalysts.
引用
收藏
页码:617 / 627
页数:11
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