{"title":"Unlocking high stability and selectivity in reverse water–gas shift over a synergistic MoCO catalyst","authors":"Xiaolong Li, Manni Sun, Zhiyan Yang, Xiru Wang, Yongning Ma, Junli Zhu, Zhuoya Zhao, Yuhao Yang","doi":"10.1002/aic.70111","DOIUrl":null,"url":null,"abstract":"The reverse water‐gas shift (RWGS) reaction is vital for CO<jats:sub>2</jats:sub> utilization and carbon cycling, yet catalyst stability and CO selectivity remain major challenges due to its endothermic nature and competing methanation. Here, a synergistic α‐Mo<jats:sub>2</jats:sub>C:MoO<jats:sub>2</jats:sub> (MoCO) catalyst with carbide–oxide interactions was in situ constructed via a one‐step temperature‐programmed calcination, achieving high dispersion and synergy. MoCO‐3.5 (Mo/C = 1:3.5) reached near‐equilibrium CO<jats:sub>2</jats:sub> conversions (50.56% at 500°C, 74.71% at 800°C) and >99.6% CO selectivity under H<jats:sub>2</jats:sub>/CO<jats:sub>2</jats:sub> = 3:1 at industrial space velocity (8400 mL·g<jats:sub>cat</jats:sub><jats:sup>−1</jats:sup>·h<jats:sup>−1</jats:sup>), maintaining stability for 120 h without coking. Mechanistic studies revealed a hydrogen‐assisted formate pathway, and weak CO adsorption enabled rapid desorption, effectively suppressing methanation. This synergy‐driven structural regulation strategy offers a promising strategy for designing highly stable and CO‐selective non‐noble metal RWGS catalysts.","PeriodicalId":120,"journal":{"name":"AIChE Journal","volume":"21 1","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AIChE Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/aic.70111","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The reverse water‐gas shift (RWGS) reaction is vital for CO2 utilization and carbon cycling, yet catalyst stability and CO selectivity remain major challenges due to its endothermic nature and competing methanation. Here, a synergistic α‐Mo2C:MoO2 (MoCO) catalyst with carbide–oxide interactions was in situ constructed via a one‐step temperature‐programmed calcination, achieving high dispersion and synergy. MoCO‐3.5 (Mo/C = 1:3.5) reached near‐equilibrium CO2 conversions (50.56% at 500°C, 74.71% at 800°C) and >99.6% CO selectivity under H2/CO2 = 3:1 at industrial space velocity (8400 mL·gcat−1·h−1), maintaining stability for 120 h without coking. Mechanistic studies revealed a hydrogen‐assisted formate pathway, and weak CO adsorption enabled rapid desorption, effectively suppressing methanation. This synergy‐driven structural regulation strategy offers a promising strategy for designing highly stable and CO‐selective non‐noble metal RWGS catalysts.
期刊介绍:
The AIChE Journal is the premier research monthly in chemical engineering and related fields. This peer-reviewed and broad-based journal reports on the most important and latest technological advances in core areas of chemical engineering as well as in other relevant engineering disciplines. To keep abreast with the progressive outlook of the profession, the Journal has been expanding the scope of its editorial contents to include such fast developing areas as biotechnology, electrochemical engineering, and environmental engineering.
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