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Highly efficient H 2 production from H 2 S via a robust graphene-encapsulated metal catalyst
The electrocatalytic decomposition of the abundant and toxic H 2 S from industrial by-products is a promising energy conversion technology for H 2 production and simultaneously removing this environmental pollutant. However, the development of such a technology has been hindered by the lack of low-c...
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Published in: | Energy & environmental science 2020-01, Vol.13 (1), p.119-126 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The electrocatalytic decomposition of the abundant and toxic H
2
S from industrial by-products is a promising energy conversion technology for H
2
production and simultaneously removing this environmental pollutant. However, the development of such a technology has been hindered by the lack of low-cost, efficient and robust electrocatalysts. Herein, we reported a remarkable graphene-encapsulated metal catalyst,
i.e.
, nitrogen-doped graphene encapsulating a non-precious CoNi nanoalloy as the anode for highly efficient electrocatalytic H
2
production from H
2
S. This optimized catalyst could drive the anode reaction at an onset potential of 0.25 V, which was 1.24 V lower than that required for the water oxidation reaction, and delivered almost twice current density than that of Pt/C. Meanwhile, it exhibited approximately 98% H
2
faradaic efficiency and maintained long-term durability for more than 500 h without any decay. The density functional theory calculations revealed that the CoNi and nitrogen dopants synergistically facilitated the formation of polysulfides on graphene's surfaces. Furthermore, a demo showed 1200 h stability for removing H
2
S impurities from industrial syngas to produce hydrogen by this graphene-encapsulated metal catalyst, demonstrating its great potential for hydrogen production toward sustainable energy applications. |
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ISSN: | 1754-5692 1754-5706 |
DOI: | 10.1039/C9EE03231B |