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Controlling NOx Reduction Pathways of Rh Catalysts with Oxygen-Vacancy-Rich ZnO1-x Nanoparticles Derived from a
Liyang Wang1, Zhe Tan2,3, Jie Zheng1
1Institute of Chemical Engineering and Technology, Xi'an Jiaotong University, Innovation Harbour, Xi-xian New District, Xi'an 712000, China.
Abstract:
Surface and lattice vacancies in crystal structures play a critical role in improving properties, but synthesizing vacancy-rich crystals remains a significant challenge. In this research, we proposed a novel method to synthesize ZnO1-x nanoparticles (NPs) with rich oxygen vacancies (VO), by thermally decomposing a H2DAB-Zn2(ox)3 metal-organic framework. The high-concentration VO in ZnO1-x NPs were confirmed by X-ray powder diffraction, X-ray photoelectron spectroscopy, electron paramagnetic resonance, and other measurements. The lattice expansion was observed for ZnO1-x NPs, resulting from electrostatic repulsion between Zn2+ and positive VO. As the support for NOx reduction, the homogeneously dispersed PGM/ZnO1-x (PGM = Ru, Rh, Pd, Ir, and Pt) catalysts were prepared and exhibited remarkable improvement in activities compared with the corresponding PGM/ZnO. The activity enhancement of Rh/ZnO1-x may be attributed to strong CO adsorption and fast NO dissociation induced by the abundant VO, resulting in a short reaction pathway distinct from Rh/ZnO.
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