Abstract
Hydrous hydrazine (H2NNH2·H2O) has generally been considered a promising hydrogen storage carrier because of inherent advantages such as its high hydrogen content and easy recharging as a liquid. Unfortunately, the decomposition of hydrous hydrazine to H2 is terribly sluggish and/or not entirely favored - a competing decomposition to ammonia may be preferred. This has been the case using noble-metal catalysts and using non-precious-metal-based catalysts, even at elevated temperatures. To overcome this challenge, non-precious-metal-based Cu@Fe5Ni5 core@shell nanocatalysts are prepared using an in situ seeding-growth approach. Unexpectedly, the catalyst exerts 100% H 2 selectivity and excellent activity and stability toward the complete decomposition of hydrous hydrazine, which is due to the synergistic effect of the core@shell structure. These promising results will certainly promote the effective application of hydrous hydrazine as a potential hydrogen storage material.
| Original language | English |
|---|---|
| Pages (from-to) | 7073-7077 |
| Number of pages | 5 |
| Journal | Advanced Functional Materials |
| Volume | 24 |
| Issue number | 45 |
| DOIs | |
| State | Published - 3 Dec 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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