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Research Article | Open Access | Just Accepted

NIR photothermal enhancement to achieve high-efficiency nitrogen reduction to ammonia by polyoxometalates@Fe-polydopamine

Xiaofei Chen1Lixin Wu2( )Feng Bai1( )

1 Key Laboratory for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-Efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, Henan University, Kaifeng 475004, China

2 State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, China

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Abstract

The development of atmospheric pressure N2 reduction to NH3 is attracting much attention in green chemistry, yet it is still a challenge to obtain satisfactory activity under mild conditions. Herein, an efficient NIR photothermal catalysis reduction of N2 constitutes an occurrence is reported. With or without V-substitute polyoxometalates (POMs) loaded on the surface of Fe-chelated polydopamine (Fe-PDA) photothermal support through the electrostatic interactions, NIR photothermal catalysts POMs@Fe-PDA are fabricated. The induction of “FeV” cofactor facilitates electron transfer between V(V)/V(IV)&Fe(III)/Fe(II) and N2, thereby activating N2 molecule. The synergy between the catalytic activity of V-POMs and the local NIR photothermal effect of Fe-PDA dramatically enhances N2 reduction. Noticeably, PMo10V2@Fe-PDA exhibits a significantly enhanced NH3 production rate of 181.1 μmol/L with a turnover frequency of 1006.1 mmol M−1 h−1 under 808 nm NIR laser radiation, being the highest values reported at atmospheric pressure. We expect that this work could provide an alternative approach for photothermal catalysis N2 reduction under mild conditions.

Nano Research
Cite this article:
Chen X, Wu L, Bai F. NIR photothermal enhancement to achieve high-efficiency nitrogen reduction to ammonia by polyoxometalates@Fe-polydopamine. Nano Research, 2024, https://doi.org/10.26599/NR.2025.94907006

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Received: 31 July 2024
Revised: 23 August 2024
Accepted: 25 August 2024
Available online: 26 August 2024

© The author(s) 2025

This article is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the original author(s) and the source, provide a link to the license, and indicate if changes were made.

See https://creativecommons.org/licenses/by/4.0/

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