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Boosting the oxygen evolution reaction using defect-rich ultra-thin ruthenium oxide nanosheets in acidic media

  • Zhi Liang Zhao (Co-first Author)
  • , Qi Wang (Co-first Author)
  • , Xiang Huang (Co-first Author)
  • , Qi Feng
  • , Shuang Gu
  • , Zhen Zhang
  • , Hu Xu*
  • , Lin Zeng*
  • , Meng Gu*
  • , Hui Li*
  • *Corresponding author for this work

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

Abstract

Developing low cost and highly active catalysts for the oxygen evolution reaction (OER) in an acidic medium is urgently indispensable for proton exchange membrane water electrolyzers (PEMWEs). Herein, we have prepared ultra-thin RuO2 nanosheets (RuO2 NSs) using a simple molten salt method. The as-prepared RuO2 NSs with a thickness of 1-2 nm possess abundant defects. Toward the OER, the RuO2 NSs achieve an extremely low overpotential of 199 mV at a current density of 10 mA cmgeo-2 with a loading of 125 μg cmgeo-2. Furthermore, the RuO2 NSs exhibit specific and mass activities of up to 0.89 mA cmoxide-2 and 0.52 A mgRu-1 at 1.46 V vs. RHE, which are 14.9 and 80.6 times enhanced in specific and mass activity as compared to the commercial RuO2 nanoparticles, respectively. In a homemade PEMWE, with RuO2 NSs as the OER catalyst, the electrolyzer achieves a current density of 0.93 A cm-2 at a cell voltage of 1.65 V without iR drop correction, which is 3 times larger than that of the commercial RuO2 catalyst (0.31 A cm-2). Density functional theory calculations indicate that the Ru vacancy on the RuO2 NS surfaces significantly weakens the binding energy of O∗ with respect to that of OOH∗, which decreases the energy cost in the transformation from O∗ to OOH∗, and thus dramatically enhances the OER performance. The unique defect-rich structure and outstanding performance demonstrate that the RuO2 NSs possess great potential for developing high-performance PEMWEs. © The Royal Society of Chemistry 2020.
Original languageEnglish
Pages (from-to)5143-5151
Number of pages9
JournalEnergy & Environmental Science
Volume13
Issue number12
Online published13 Nov 2020
DOIs
Publication statusPublished - 1 Dec 2020
Externally publishedYes

Funding

This work was financially supported by the Shenzhen Peacock Plan (KQTD2016022620054656 and KQTD20190929173815000), the Shenzhen Clean Energy Research Institute (No.CERI-KY-2019-003), the Shenzhen Key Laboratory project (ZDSYS201603311013489), the Development and Reform Commission of Shenzhen Municipality 2017 (No. 1106), the Guangdong Innovative and Entrepreneurial Research Team Program (2016ZT06N500 and 2019ZT08C044), the National Key Research and Development Program of China (2017YFB0102701), and the National Natural Science Foundation of China (No. 21802065). This work was supported by the Pico Center at SUSTech CRF, which receives support from the Presidential Fund and Development and Reform Commission of Shenzhen Municipality. Z. L. Zhao acknowledges Postdoctoral Science Foundation (2020M672692).

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