Nitrogen-triggered plasmonic bifunctionality in ruthenium/titanium oxynitride Schottky catalyst for energized hydrazine-seawater hydrogen production

Plasmon-coupled hydrazine-seawater electrolysis emerges as an advanced hydrogen generation approach characterized by enhanced product efficiency and renewable utilization. Though the integration of plasmonic effects with bifunctional catalysts promises to revolutionize system design, the design of such catalysts with plasmonic bifunctionality remains a huge challenge. Our work breaks new ground by employing nitrogen as a "molecular switch" to trigger plasmonic bifunctionality in ruthenium/titanium oxynitride (Ru/TiNO 0.6 ), achieving intrinsically and plasmon-energized hydrogen evolution reaction (overpotential: 13.5 mV) and hydrazine oxidation reaction (overpotential: 222.3 mV). The plasmonic two-electrode system demonstrates remarkable performance enhancement, boosting current density by 34.6% (127.5→171.6 mA cm -2 at 0.2V) with maintaining near 100% selective conversion to H 2 /N 2 . Through advanced characterization and theoretical analysis, we decode nitrogen's triple role: it narrows band gap of substrate and enhances both photoelectronic and photothermal effects; it enhances Mott-Schottky effects to generate metastable amorphous Ru species, and induces interface charge polarization with creating built-in electric fields that synergistically lower activation barriers. These concerted effects yield optimal hydrogen adsorption energetics (ΔG *H ) while facilitating *N 2 H 3 intermediate formation and shift of rate determining step, establishing a new paradigm for plasmon-driven bifunctional electrocatalysis. Breaks new ground using N as a "molecular switch" to achieve plasmonic bifunctionality in Ru/TiNO 0.6 with ultra-low overpotentials for hydrogen evolution reaction (HER, 13.5 mV) and hydrazine oxidation reaction (HzOR, 222.3 mV). The system boosts current density by 34.6% (171.6 mA cm -2 ) at 0.2 V while maintaining ∼100% H 2 /N 2 selectivity, establishing a new electrocatalysis paradigm. • Plasmon-coupled hydrazine-seawater electrolysis enhances renewable H 2 generation efficiency. • Plasmonic effects lead to an ultra-low HER overpotential at 13.5 mV. • Plasmon induces a HzOR overpotential of 222.3 mV with ∼100% H 2 /N 2 selectivity. • Nitrogen's triple role enables plasmonic bifunctionality in Ru/TiNO 0.6 catalyst.

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Publication Details

Journal
Advanced Powder Materials
Published
2025-11-21
DOI
https://doi.org/10.1016/j.apmate.2025.100384
Citations
1
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.36
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article

Nitrogen-triggered plasmonic bifunctionality in ruthenium/titanium oxynitride Schottky catalyst for energized hydrazine-seawater hydrogen production

Yaobing Wang, Hui Xue, Jingyun Mao, Haoran Jiang et al.
1 citations
Advanced Powder Materials
Electrocatalysts for Energy Conversion
0.36
article

Nitrogen-triggered plasmonic bifunctionality in ruthenium/titanium oxynitride Schottky catalyst for energized hydrazine-seawater hydrogen production

Yaobing Wang, Hui Xue, Jingyun Mao, Haoran Jiang, Shuangjuan Shen, Yiyin Huang, Rui Yang, Congyuan Zeng, Yuanyuan Sun, Jiajun Luo
article en
1 citations

Abstract

Plasmon-coupled hydrazine-seawater electrolysis emerges as an advanced hydrogen generation approach characterized by enhanced product efficiency and renewable utilization. Though the integration of plasmonic effects with bifunctional catalysts promises to revolutionize system design, the design of such catalysts with plasmonic bifunctionality remains a huge challenge. Our work breaks new ground by employing nitrogen as a "molecular switch" to trigger plasmonic bifunctionality in ruthenium/titanium oxynitride (Ru/TiNO 0.6 ), achieving intrinsically and plasmon-energized hydrogen evolution reaction (overpotential: 13.5 mV) and hydrazine oxidation reaction (overpotential: 222.3 mV). The plasmonic two-electrode system demonstrates remarkable performance enhancement, boosting current density by 34.6% (127.5→171.6 mA cm -2 at 0.2V) with maintaining near 100% selective conversion to H 2 /N 2 . Through advanced characterization and theoretical analysis, we decode nitrogen's triple role: it narrows band gap of substrate and enhances both photoelectronic and photothermal effects; it enhances Mott-Schottky effects to generate metastable amorphous Ru species, and induces interface charge polarization with creating built-in electric fields that synergistically lower activation barriers. These concerted effects yield optimal hydrogen adsorption energetics (ΔG *H ) while facilitating *N 2 H 3 intermediate formation and shift of rate determining step, establishing a new paradigm for plasmon-driven bifunctional electrocatalysis. Breaks new ground using N as a "molecular switch" to achieve plasmonic bifunctionality in Ru/TiNO 0.6 with ultra-low overpotentials for hydrogen evolution reaction (HER, 13.5 mV) and hydrazine oxidation reaction (HzOR, 222.3 mV). The system boosts current density by 34.6% (171.6 mA cm -2 ) at 0.2 V while maintaining ∼100% H 2 /N 2 selectivity, establishing a new electrocatalysis paradigm. • Plasmon-coupled hydrazine-seawater electrolysis enhances renewable H 2 generation efficiency. • Plasmonic effects lead to an ultra-low HER overpotential at 13.5 mV. • Plasmon induces a HzOR overpotential of 222.3 mV with ∼100% H 2 /N 2 selectivity. • Nitrogen's triple role enables plasmonic bifunctionality in Ru/TiNO 0.6 catalyst.

Advanced Powder MaterialsVol. 5(3)
Fujian Normal University (CN), Anhui Agricultural University (CN), Tianjin University (CN), Fujian Institute of Research on the Structure of Matter (CN), Yangzhou University (CN)
Openalex Percentile: Top 36%
Electrocatalysts for Energy Conversion
0.36
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