journal article·2026-06Open access

KI‐Doped α‐Mo 2 C Stably Catalyze Near‐Equilibrium CO 2 to CO Beyond 1000 Hours

Haipeng Wang, Chunshan Li, Zhiguo Lv, Tao Zhuang, Jinguang Hu, Fujin Sun, Chao Zhang

Carbon Energy· Volume 8· Issue 6

Abstract

ABSTRACT α‐Mo 2 C has demonstrated excellent potential in the catalytic conversion of CO 2 to CO. However, it tends to be reduced to thermodynamically stable β‐Mo 2 C under H 2 atmosphere, leading to deactivation during reverse water–gas shift (RWGS) reaction. In addition, α‐Mo 2 C cannot achieve an equilibrium CO yield below 500°C. This work first found that KI‐doped α‐Mo 2 C can achieve near‐equilibrium CO yields beyond 1000 h at 400°C, 4 bar in the RWGS reaction while maintaining the original α‐Mo 2 C crystal structure. Further research indicates that the doped KI effectively stabilized the oxygen content in α‐Mo 2 C, which is critical for stable catalytic activity. This modification not only reduces the formation‐desorption energy barriers for CO and H 2 O, but also markedly suppresses methane side reaction. Moreover, the incorporation of the KI reduces the oxidation state of Mo, thereby enhancing the surface alkalinity. This enhancement leads to an increased CO 2 conversion rate, thereby achieving near‐equilibrium CO yields at 400°C, 4 bar.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Catalysis and Oxidation Reactions · Catalysts for Methane Reforming · Catalysis and Hydrodesulfurization Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory Base for Eco‐chemical Engineering, College of Chemical Engineering Qingdao University of Science and Technology Qingdao China

School of Chemical Engineering University of Chinese Academy of Sciences Beijing China

Key Laboratory of Rubber‐Plastics, Ministry of Education/Shandong Provincial Key Laboratory of Rubber‐plastics Qingdao University of Science & Technology Qingdao Shandong China

Department of Chemical and Petroleum Engineering University of Calgary, 2500 University Drive Calgary AB Canada

Funding

National Natural Science Foundation of China · Natural Science Foundation of Shandong Province

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