Lin Zhao, Diru Liu, Yiying Wang, Mengyuan Zhang, Qiang Wang, Guangyan Xu and Hong He
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引用次数: 0
Abstract
Ethanol steam reforming (ESR) is a promising technique for sustainable hydrogen production, achieving high hydrogen yields. Herein, we prepare a series of Rh–Ce/Al2O3 catalysts with enhanced catalytic performance by modulating the interaction between active Rh and the CeO2 promoter. Various characterization techniques, including HAADF-STEM and XAFS, demonstrated that new Rh–O–Ce sites were formed by the effective trapping of single-atom Rh species by CeO2 nanoparticles on the Rh–Ce5/Al2O3 catalyst. In situ DRIFTS-MS combined with isotopic kinetic analysis further revealed that Rh–O–Ce sites significantly enhanced water activation, which promoted the production of acetate, a reactive intermediate in ESR. Acetate was dehydrogenated to CO, which subsequently reacted with H2O to form formate in the water–gas shift (WGS) reaction, a critical step in ESR. Similarly, the enhanced water activation also promoted the formation of formate, which ultimately decomposed to H2 and CO2. Consequently, the Rh–Ce5/Al2O3 catalyst exhibited an excellent hydrogen production rate of 22.4 mmol g−1 min−1 at 450 °C and remarkable stability in the ESR reaction. The findings revealed the role of Rh–O–Ce sites in enhancing the performance of Rh-based catalysts in ESR, beneficial for the design of efficient ESR catalysts.
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