摘要
Electrochemically converting nitrate (NO3−) to value-added ammonia (NH3) is a complex process involving an eight-electron transfer and numerous intermediates, presenting a significant challenge for optimization. A multi-elemental synergy strategy to regulate the local electronic structure at the atomic level is proposed, creating a broad adsorption energy landscape in high-entropy alloy (HEA) catalysts. This approach enables optimal adsorption and desorption of various intermediates, effectively overcoming energy-scaling limitations for efficient NH3 electrosynthesis. The HEA catalyst achieved a high Faradaic efficiency of 94.5 ± 4.3% and a yield rate of 10.2 ± 0.5 mg h−1 mgcat−1. It also demonstrated remarkable stability over 250 h in an integrated three-chamber device, coupling electrocatalysis with an ammonia recovery unit for continuous NH3 collection. This work elucidates the catalytic mechanisms of multi-functional HEA systems and offers new perspectives for optimizing multi-step reactions by circumventing adsorption-energy scaling limitations.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 2415739 |
| 期刊 | Advanced Materials |
| 卷 | 37 |
| 期 | 9 |
| DOI | |
| 出版状态 | 已出版 - 5 3月 2025 |
| 已对外发布 | 是 |
指纹
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