4.8 Article

Heterostructuring Mesoporous 2D Iridium Nanosheets with Amorphous Nickel Boron Oxide Layers to Improve Electrolytic Water Splitting

Journal

SMALL METHODS
Volume 5, Issue 10, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smtd.202100679

Keywords

2D materials; amorphous-crystalline interfaces; electrochemical water splitting; heterostructures; mesoporous materials

Funding

  1. China Scholarship Council (CSC)
  2. JST-ERATO Yamauchi Materials Space-Tectonics Project [JPMJER2003]
  3. National Natural Science Foundation of China [22106106]
  4. Natural Science Foundation of Shanghai [21ZR1446600]

Ask authors/readers for more resources

A 2D heterostructure consisting of amorphous nickel boron oxide and crystalline mesoporous iridium has been designed for water splitting, showing superior electrochemical performance in both oxygen evolution reaction and hydrogen evolution reaction. The well-defined heterostructure and strong interfacial coupling contribute to abundant catalytically active heterointerfaces and boosted exposure of active sites. Tuning the electronic state of the iridium sites by hybridizing with nickel boron oxide layers further enhances the overall performance of the heterostructures.
2D heterostructures exhibit a considerable potential in electrolytic water splitting due to their high specific surface areas, tunable electronic properties, and diverse hybrid compositions. However, the fabrication of well-defined 2D mesoporous amorphous-crystalline heterostructures with highly active heterointerfaces remains challenging. Herein, an efficient 2D heterostructure consisting of amorphous nickel boron oxide (Ni-B-i) and crystalline mesoporous iridium (meso-Ir) is designed for water splitting, referred to as Ni-B-i/meso-Ir. Benefiting from well-defined 2D heterostructures and strong interfacial coupling, the resulting mesoporous dual-phase Ni-B-i/meso-Ir possesses abundant catalytically active heterointerfaces and boosts the exposure of active sites, compared to their crystalline and amorphous mono-counterparts. The electronic state of the iridium sites is tuned favorably by hybridizing with Ni-B-i layers. Consequently, the Ni-B-i/meso-Ir heterostructures show superior and stable electrochemical performance toward both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in an alkaline electrolyte.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available