Reaction‐Induced Dynamic Evolution of In 2 O 3 During the Reverse Water‐Gas Shift (RWGS) Reaction

ABSTRACT The In 2 O 3 based catalysts are promising for the reverse water‐gas shift (RWGS) reaction owing to their high selectivity. However, the dynamic structural and chemical evolution of In 2 O 3 under reactive atmosphere remains poorly understood. Herein, we elucidate the nanoscale dynamic evolution of In 2 O 3 during the RWGS reaction using in situ transmission electron microscopy (TEM), in situ X‐ray diffraction (XRD), quasi in situ X‐ray photoelectron spectroscopy (XPS), and in situ Raman spectroscopy. Our results reveal that In 2 O 3 undergoes substantial surface reconstruction at the early reaction stage in an H 2 /CO 2 atmosphere, forming mobile worm‐like In 2 O 3‐x nanorods even at temperatures as low as 150°C. These nanorods migrate and grow, increasing in width from 2.6 nm at 150°C to 8.5 nm at 400°C. Following this early‐stage transformation, the particle size of In 2 O 3 remains almost unchanged. The system subsequently enters a steady stage, governed by a dynamic balance between oxygen‐vacancy formation by H 2 reduction and vacancy ‘'re‐filling'’ by CO 2 . This work thus verifies the reaction‐induced dynamic evolution of In 2 O 3 for the RWGS reaction, where hydrogen acts as a key promoter and reaction temperature serves as a critical accelerator.

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Small
Published
2026-11-02
DOI
https://doi.org/10.1002/smll.76473
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
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article

Reaction‐Induced Dynamic Evolution of In 2 O 3 During the Reverse Water‐Gas Shift (RWGS) Reaction

Menghui Liu, Changjun Liu, Shilong Xiong, Langli Luo et al.
3 links
Small
Catalysts for Methane Reforming
article

Reaction‐Induced Dynamic Evolution of In 2 O 3 During the Reverse Water‐Gas Shift (RWGS) Reaction

Menghui Liu, Changjun Liu, Shilong Xiong, Langli Luo, Xiaotong Qiu, Linlin Wu, Lin Gu, Jingting Hu, Rui Zou, Jili Xu
article en

Abstract

ABSTRACT The In 2 O 3 based catalysts are promising for the reverse water‐gas shift (RWGS) reaction owing to their high selectivity. However, the dynamic structural and chemical evolution of In 2 O 3 under reactive atmosphere remains poorly understood. Herein, we elucidate the nanoscale dynamic evolution of In 2 O 3 during the RWGS reaction using in situ transmission electron microscopy (TEM), in situ X‐ray diffraction (XRD), quasi in situ X‐ray photoelectron spectroscopy (XPS), and in situ Raman spectroscopy. Our results reveal that In 2 O 3 undergoes substantial surface reconstruction at the early reaction stage in an H 2 /CO 2 atmosphere, forming mobile worm‐like In 2 O 3‐x nanorods even at temperatures as low as 150°C. These nanorods migrate and grow, increasing in width from 2.6 nm at 150°C to 8.5 nm at 400°C. Following this early‐stage transformation, the particle size of In 2 O 3 remains almost unchanged. The system subsequently enters a steady stage, governed by a dynamic balance between oxygen‐vacancy formation by H 2 reduction and vacancy ‘'re‐filling'’ by CO 2 . This work thus verifies the reaction‐induced dynamic evolution of In 2 O 3 for the RWGS reaction, where hydrogen acts as a key promoter and reaction temperature serves as a critical accelerator.

Small
Tianjin University (CN), Dalian Institute of Chemical Physics (CN), Collaborative Innovation Center of Chemical Science and Engineering Tianjin (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN), State Key Laboratory of Catalysis (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 38%
Catalysts for Methane Reforming
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