4.8 Article

Compensating Electronic Effect Enables Fast Site-to-Site Electron Transfer over Ultrathin RuMn Nanosheet Branches toward Highly Electroactive and Stable Water Splitting

Journal

ADVANCED MATERIALS
Volume 33, Issue 51, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202105308

Keywords

2D nanosheets; doping; oxygen evolution reaction; ruthenium; water splitting

Funding

  1. Ministry of Science and Technology [2017YFA0208200, 2016YFA0204100]
  2. National Natural Science Foundation of China [22025108, 21771156]
  3. Natural Science Foundation of Jiangsu Higher Education Institutions [17KJB150032]
  4. project of scientific and technologic infrastructure of Suzhou [SZS201708]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  6. Xiamen University

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Heteroatom doping and two-dimensional nanostructure design have been demonstrated as effective strategies for improving the electroactivity and stability of electrocatalysts. Mn-doped ultrathin Ru nanosheet branches (RuMn NSBs) exhibit bifunctionalities of hydrogen evolution reaction and oxygen evolution reaction with high electroactivity and durability. The shortened Ru-O bonds and flexible modulation on the valence states of Ru sites by the introduction of Mn are key factors that lead to improved electrochemical performances.
To improve the electroactivity and stability of electrocatalysts, various modulation strategies have been applied in nanocatalysts. Among different methods, heteroatom doping has been considered as an effective method, which modifies the local bonding environments and the electronic structures. Meanwhile, the design of novel two-dimensional (2D) nanostructures also offers new opportunities for achieving efficient electrocatalysts. In this work, Mn-doped ultrathin Ru nanosheet branches (RuMn NSBs), a newly reported 2D nanostructure, is synthesized. With the ultrathin and naturally abundant edges, the RuMn NSBs have exhibited bifunctionalities of hydrogen evolution reaction and oxygen evolution reaction with high electroactivity and durability in different electrolytes. Experimental characterizations have revealed that Ru-O bonds are shortened due to Mn doping, which is the key factor that leads to improved electrochemical performances. Density functional theory (DFT) calculations have confirmed that the introduction of Mn enables flexible modulations on the valence states of Ru sites. The inversed redox state evolutions of Ru and Mn sites not only improve the electroactivity for the water splitting but also the long-term stability due to the pinning effect of Ru sites. This work has provided important inspirations for the design of future advanced Ru-based electrocatalysts with high performances and durability.

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