Imaging Anisotropic Proton Intercalation in Photochromic MoO3

Protonation represents a fundamental chemical process with promising applications in the fields of energy, environment, and memory devices. Probing the protonation mechanism, however, presents a formidable challenge owing to the elusiveness of intercalated protons. In this work, we utilize the atomi...

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Veröffentlicht in:Nano letters 2024-08, Vol.24 (31), p.9727-9733
Hauptverfasser: Xu, Zhihang, Lau, Ting Wai, Xiong, Pei, Li, Jiangtong, Li, Molly Meng-Jung, Yin, Jun, Zhu, Ye
Format: Artikel
Sprache:eng
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Zusammenfassung:Protonation represents a fundamental chemical process with promising applications in the fields of energy, environment, and memory devices. Probing the protonation mechanism, however, presents a formidable challenge owing to the elusiveness of intercalated protons. In this work, we utilize the atomic and electronic structure changes associated with protonation to directly image the proton intercalation pathways in α-MoO3 induced by UV illumination. We reveal the anisotropic intercalation behavior which is initiated by photocatalyzed water dissociation preferentially at the (001) edges and then propagates along the c axis, transforming α-MoO3 into H x MoO3 to realize photochromism. This photochromic process can be reversed via heating in air, leading to anisotropic proton deintercalation, also preferentially along the c axis. The observed anisotropic behavior can be attributed to the intrinsically low energy barriers for both proton migration along the c axis and water dissociation/formation at (001) edges.
ISSN:1530-6984
1530-6992
1530-6992
DOI:10.1021/acs.nanolett.4c02601