Bifunctional Transition Metal Hydroxysulfides: Room-Temperature Sulfurization and Their Applications in Zn–Air Batteries

Hao Fan Wang, Cheng Tang, Bin Wang, Bo Quan Li, Qiang Zhang*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

395 Citations (Scopus)

Abstract

Bifunctional electrocatalysis for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) constitutes the bottleneck of various sustainable energy devices and systems like rechargeable metal–air batteries. Emerging catalyst materials are strongly requested toward superior electrocatalytic activities and practical applications. In this study, transition metal hydroxysulfides are presented as bifunctional OER/ORR electrocatalysts for Zn–air batteries. By simply immersing Co-based hydroxide precursor into solution with high-concentration S2−, transition metal hydroxides convert to hydroxysulfides with excellent morphology preservation at room temperature. The as-obtained Co-based metal hydroxysulfides are with high intrinsic reactivity and electrical conductivity. The electron structure of the active sites is adjusted by anion modulation. The potential for 10 mA cm−2 OER current density is 1.588 V versus reversible hydrogen electrode (RHE), and the ORR half-wave potential is 0.721 V versus RHE, with a potential gap of 0.867 V for bifunctional oxygen electrocatalysis. The Co3FeS1.5(OH)6 hydroxysulfides are employed in the air electrode for a rechargeable Zn–air battery with a small overpotential of 0.86 V at 20.0 mA cm−2, a high specific capacity of 898 mAh g−1, and a long cycling life, which is much better than Pt and Ir-based electrocatalyst in Zn–air batteries.

Original languageEnglish
Article number1702327
JournalAdvanced Materials
Volume29
Issue number35
DOIs
Publication statusPublished - 20 Sept 2017
Externally publishedYes

Keywords

  • CoFe hydroxysulfides
  • Zn–air batteries
  • bifunctional air cathodes
  • layered double hydroxides
  • oxygen evolution reaction
  • oxygen reduction reaction

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