• 文献标题:   Improved nitrogen reduction electroactivity by unique MoS2-SnS2 heterogeneous nanoplates supported on poly(zwitterionic liquids) functionalized polypyrrole/graphene oxide
  • 文献类型:   Article
  • 作  者:   MAO H, YANG HR, LIU JC, ZHANG S, LIU DL, WU Q, SUN WP, SONG XM, MA TY
  • 作者关键词:   mos2, sns2, poly 3 1vinylimidazolium3yl propane1sulfonate functionalized polypyrrole/graphene oxide, nitrogen reduction reaction, irreversible crystal phase transition
  • 出版物名称:   CHINESE JOURNAL OF CATALYSIS
  • ISSN:   0253-9837 EI 1872-2067
  • 通讯作者地址:  
  • 被引频次:   4
  • DOI:   10.1016/S1872-2067(21)63944-X EA MAR 2022
  • 出版年:   2022

▎ 摘  要

Unique MoS2-SnS2 heterogeneous nanoplates have successfully in-situ grown on poly(3-(1-vinylimidazolium-3-yl)propane-1-sulfonate) functionalized polypyrrole/graphene oxide (PVIPS/PPy/GO). PVIPS can attract heptamolybdate ion (Mo7O246-) and Sn4+ as the precursors by the ion-exchange, resulting in the simultaneous growth of 1T'-MoS2 and the berndtite-2T-type hexagonal SnS2 by the interfacial induced effect of PVIPS. The obtained MoS2-SnS2/PVIPS/PPy/GO can serve as electrocatalysts, exhibiting good NRR performance by the synergistic effect. The semi-conducting SnS2 would limit the surface electron accessibility for suppressing HER process of 1T'-MoS2, while metallic 1T'-MoS2 might efficiently improve the NRR electroactivity of SnS2 by the creation of Mo-Sn-Sn trimer catalytic sites. Otherwise, the irreversible crystal phase transition has taken place during the NRR process. Partial 1T'-MoS2 and SnS2 have electrochemically reacted with N-2, and irreversibly converted into Mo2N and SnxNz due to the formation of Mo-N and Sn-N bonding, meanwhile, partial SnS2 has been irreversibly evolved into SnS due to the reduction by the power source in the electrochemical system. It would put forward a new design idea for optimizing the preparation method and electrocatalytic activity of transition metal dichalcogenides. (C) 2022, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.