Abstract
Designing readily available and highly active electrocatalysts for water splitting is essential for renewable energy technologies. Here we present the construction of FeCo-FeCoP@C hollow nanocubes encapsulated in nitrogen-doped carbon nanocages (FeCo-FeCoP@C@NCCs) through controlled carbonization and subsequent phosphorization of a Prussian blue analogue. With stronger electronic interaction and hollow structure, the as-obtained FeCo-FeCoP@C@NCCs material requires small overpotentials of 91 mV and 280 mV to deliver 10 mA cm−2 in 1 M KOH toward hydrogen and oxygen evolution, respectively. More importantly, applying this material for overall water splitting, it only requires 1.64 V to afford 10 mA cm−2 and exhibits impressively durability over 40 h without obvious performance decay. The present approach inspires potentials for the controllable synthesis of multi-component catalysts for practical applications.
| Original language | English |
|---|---|
| Pages (from-to) | 1-8 |
| Number of pages | 8 |
| Journal | Journal of Energy Chemistry |
| Volume | 53 |
| DOIs | |
| State | Published - Feb 2020 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Electrocatalysts
- Hydrogen evolution reaction
- Metal phosphide
- Overall water splitting
- Oxygen evolution reaction
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