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Updated: Oct 10, 2025

High-Temperature and High-Pressure In situ Magic Angle Spinning Nuclear Magnetic Resonance Spectroscopy
Published on: October 9, 2020
Unraveling the Surface Hydroxyl Network on In2O3 Nanoparticles with High-Field Ultrafast Magic Angle Spinning Nuclear
Qiao Han1,2, Pan Gao1, Lixin Liang1,2
1State Key Laboratory of Catalysis, National Laboratory for Clean Energy, 2011-Collaborative Innovation Center of Chemistry for Energy Materials, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, China.
Abstract:
Hydroxyl groups are among the major active surface sites over metal oxides. However, their spectroscopic characterizations have been challenging due to limited resolutions, especially on hydroxyl-rich surfaces where strong hydroxyl networks are present. Here, using nanostructured In2O3 as an example, we show significantly enhanced discrimination of the surface hydroxyl groups, owing to the high-resolution 1H NMR spectra performed at a high magnetic field (18.8 T) and a fast magic angle spinning (MAS) of up to 60 kHz. A total of nine kinds of hydroxyl groups were distinguished and their assignments (μ1, μ2, and μ3) were further identified with the assistance of 17O NMR. The spatial distribution of these hydroxyl groups was further explored via two-dimensional (2D) 1H-1H homonuclear correlation experiments with which the complex surface hydroxyl network was unraveled at the atomic level. Moreover, the quantitative analysis of these hydroxyl groups with such high resolution enables further investigations into the physicochemical property and catalytic performance characterizations (in CO2 reduction) of these hydroxyl groups. This work provides insightful understanding on the surface structure/property of the In2O3 nanoparticles and, importantly, may prompt general applications of high-field ultrafast MAS NMR techniques in the study of hydroxyl-rich surfaces on other metal oxide materials.
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