@article{Liu2026, 
author = {Xingyan Liu and Kaili Wu and Yue Li and Youzhou He and Yuyu Fang and Min Fu and Ben Lei and Yuhan Li},
title = {Steering oxidation pathways via Au-mediated transition from type-II to Z-scheme for high-efficiency NO deep oxidation with near-zero NO2 emission},
year = {2026},
journal = {Nano Research},
volume = {19},
number = {8},
pages = {94908660},
keywords = {MOF-based heterojunction, NO removal, Z-scheme, reactive oxygen species modulation, NO2 inhibition},
url = {https://www.sciopen.com/article/10.26599/NR.2026.94908660},
doi = {10.26599/NR.2026.94908660},
abstract = {Fundamentally, the type-II and Z-scheme heterojunctions exhibit identical band alignments but diverge in the charge carriers transfer mechanisms. Here, we demonstrate that the Au-mediated heterojunction transition from type-II to Z-scheme dictates the subsequent photocatalytic NO reaction pathway to obtain excellent activity and selectivity. As proven by density functional theory (DFT) calculations, Kelvin probe force microscopy (KPFM), and in-situ X-ray photoelectron spectroscopy (XPS), the type-II to Z-scheme heterojunction transition is regulated by incorporating Au nanoparticles as electron bridges within in-situ fabricated NH2-MIL-125/TiO2 through controllable hydrolysis. This transition maintains robust redox potentials to generate more reactive active species through effectively separated charge carriers under the high-efficient built-in electric field. As a result, the Z-scheme (NH2-MIL-125/Au/TiO2) exhibits an impressive NO removal efficiency of 82.0%, surpassing the original NH2-MIL-125 by 3.7 times and the type-II (NH2-MIL-125/TiO2) by 1.2 times, while shows a selectivity of almost 100% toward NO2−/NO3−. The in-situ Fourier transform infrared (FT-IR) and DFT reveal that, in comparison with the type-II favored NO+ intermediates, the Z-scheme favors NO− intermediates with enhanced O2/H2O activation, enabling ideal Gibbs free energy for NO-to-NO3− conversion. This study achieves a metal-nanoparticle-mediated strategy for precisely engineering metal-organic framework (MOF)-based heterojunction architectures, which regulates the NO reaction pathways for efficient environmental purification.}
}