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Boosting and stabilizing oxygen evolution reaction through Ru single atoms anchored amorphous NiMoOx electrocatalyst
透過錨定於非晶態 NiMoOx 上的 Ru 單原子提升並穩定析氧反應


Jiayi Li, Yiming Zhu, Changyuan Li, Qian Zhang, Ju Rong, Shasha Guo, Nicolas Alonso-Vante, Long Yang, Min-Hsin Yeh, Wei-Hsiang Huang, Xiaohua Yu, Hongfei Cheng & Jiwei Ma
https://doi.org/10.1038/s41467-025-63870-9
SEED Member: Min-Hsin Yeh, Wei-Hsiang Huang

 

Structural characterizations of amorphous RuNiMo oxides (a-RNMO)

 

Major Contributions
 

1.Amorphous NiMoOx anchored with Ru single atoms (a-RNMO) was synthesized via a one-step room-temperature co-precipitation method, achieving low overpotential (1.78 V at 1 A cm⁻²) and high stability (>100 h) in anion exchange membrane water electrolyzers. 

2.Operando spectroscopy and DFT calculations reveal dynamic reconstruction into amorphous/crystalline NiOOH, with Ru single atoms modulating the electronic structure to enhance intermediate adsorption and OER activity through a complementary amorphous–electronic mechanism. 

3.a-RNMO outperforms commercial RuO₂ in mass and specific activities, demonstrating that anchoring metal single atoms on amorphous supports can balance high performance with economic efficiency for practical alkaline OER applications.




主要貢獻
 

1.一步室溫合成與高效性能:透過一步室溫共沉澱法(one-step room-temperature co-precipitation),合成了錨定釕(Ru)單原子的非晶態 NiMoOx (a-RNMO)。該材料在陰離子交換膜水電解槽(AEMWE)中展現優異性能:低過電位:在 1 A\cm-2 的大電流密度下,電壓僅需 1.78 V。高穩定性:穩定運行超過 100 小時。

2.動態重構與電子調控機制:原位光譜(Operando spectroscopy)與 DFT 計算揭示,催化劑在反應中會動態重構(dynamic reconstruction) 為非晶態/結晶態混合的 NiOOH 物種。Ru 單原子透過調節電子結構,以一種互補的「非晶態—電子機制」增強了中間體的吸附能力與析氧反應(OER)活性。

3.超越商用標準與經濟效益:a-RNMO 在質量活性(mass activity)與比活性(specific activity)上均優於商用 RuO2。這證明了在非晶態載體上錨定金屬單原子,能有效平衡高性能與經濟效益,適用於實際的鹼性 OER 應用。