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Verified CAS / Academic Author2 Decoded Studies

Prof. ZHENG Shourong

State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China

Co-Affiliations:State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University

Research Publications & English Decoded Briefs

Showing 2 publications
Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2025012901

Strong Impact of Support Morphology on Catalytic Decomposition of N2O over Rh/CeO2 Catalysts

N2O is a potent greenhouse gas, and its catalytic decomposition is of significant environmental importance. In this study, three CeO2 supports with different morphologies—nanorods (NR), nanocubes (NC), and nanooctahedra (NO)—were prepared via a hydrothermal method. Rh catalysts supported on these CeO2 materials were synthesized using a deposition-precipitation method, and their catalytic performance for N2O decomposition was evaluated. Results demonstrate that Rh/CeO2-NR exhibits superior catalytic activity compared to Rh/CeO2-NC and Rh/CeO2-NO under identical reaction conditions, including in the presence of O2 and H2O. Characterization reveals that Rh/CeO2-NR possesses abundant oxygen vacancies and a relatively high number of intrinsic defect sites, which facilitate the transfer of O intermediates. Additionally, Rh/CeO2-NR exhibits an appropriate Rh0/Rhn+ ratio, promoting the redox cycle between Rh species and reactants, thereby enhancing catalytic activity. The study underscores the critical role of CeO2 support morphology in optimizing Rh-based catalysts for N2O decomposition, offering a strategy to improve catalytic efficiency and stability for industrial applications.

Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2024042404

CaO-Doped Rh/Al2O3 as a Highly Effective Catalyst for Catalytic N2O Decomposition

The direct catalytic decomposition of the greenhouse gas N2O into nitrogen and oxygen holds significant environmental importance. In this study, CaO-modified Rh-based catalysts were prepared via a stepwise impregnation method. The catalyst structures were characterized, and their catalytic performances for N2O decomposition were investigated. The characterization results demonstrate that CaO doping significantly enhances catalytic activity and water resistance. Specifically, the 0.5Rh/Al2O3 catalyst exhibited a N2O conversion below 5% at 300 °C, whereas the 0.5Rh-4Ca/Al2O3 catalyst achieved 50% conversion under identical conditions, indicating markedly improved low-temperature activity. Compared to the undoped catalyst (0.5Rh/Al2O3), CaO doping (0.5Rh-xCa/Al2O3) strengthens metal-support interactions, improves Rh dispersion on the support surface, and modulates the electron density around Rh, thereby substantially boosting N2O decomposition capability. The catalyst also demonstrated excellent stability, maintaining essentially constant conversion over 40 h of reaction. These findings underscore the potential of alkaline earth metal oxide doping as an effective strategy for designing high-performance noble metal catalysts for N2O abatement.