4.7 Article

Superhydrophilic Heteroporous MoS2/Ni3S2 for Highly Efficient Electrocatalytic Overall Water Splitting

期刊

ACS APPLIED ENERGY MATERIALS
卷 1, 期 8, 页码 3929-3936

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.8b00665

关键词

electrocatalysis; superhydrophilic; heteroporous; high activity; overall water splitting

资金

  1. NSFC [21477136 ajd 21471155]
  2. Beijing Natural Science Foundation [2182077]
  3. Henan Educational Committee Foundation [13B150024]
  4. Natural Science Foundation of Henan Province [182300410196]
  5. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB17030300]

向作者/读者索取更多资源

Water molecular adsorption, intermediate species transformation, and product desorption are three main steps for the water splitting that are subject to the corresponding factors of surface wettability, exposed active sites, and mass transfer, respectively. Suitable catalyst with the tailored architecture should be highly regarded to optimize the consistency and systematicness of these three procedures. Herein, highly hydrophilic heteroporous MoS2/Ni3S2 on nickel foam (p-MoS2/Ni3S2/NF) is fabricated through a two-steps strategy including electrodeposition and solvothermalreaction. Intensive water affinity relevant with the porous structure and composition is identified by the contact angle test. Electrochemical surface area results demonstrate the upsurge of active sites for the porous structure in comparison with other samples. The fast mass diffusion feature of the p-MoS2/Ni3S2/NF catalyst is further proved by the multistep chronoamperometric for HER and OER process. Attributed to the above nature superiorities, the electrochemical activity of this p-MoS2/Ni3S2/NF has been greatly enhanced. The overpotentials at a geometric current density of 10 mA cm(-2) for OER and HER significantly reduce to 185 mV and 99 mV in alkaline media, respectively. The as-prepared catalyst p-MoS2/Ni3S2/NF only needs the cell voltages of 1.50, 1.62, and 1.71 V at current densities of 10, 20, and 50 mA cm(-2) to drive water splitting and performs with the good stability for at least 48 h in total. This fascinating material is designed by multiscale principles that stemmed from a better insight on the structure-activity relationship, and it can also afford constructive inspirations for the forward development of various catalytic reactions.

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