Pt Atom-Substituted MoC Single-Atom Catalyst for Enhancing H2 Production

被引:2
作者
Tang, Nanfang [1 ]
Liu, Dongyuan [2 ]
Chen, Shuai [1 ]
Wang, Zhenyu [1 ,3 ]
Ma, Yuxia [1 ]
Li, Qi [1 ,4 ]
Li, Yunshuai [1 ,3 ]
Xu, Guoliang [1 ]
Wu, Chuntian [1 ]
Kang, Liqun [5 ]
Luo, Wenhao [6 ]
Qiao, Botao [1 ]
Zhu, Houyu [2 ]
Cong, Yu [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, CAS Key Lab Sci & Technol Appl Catalysis, Dalian 116023, Peoples R China
[2] China Univ Petr East China, Sch Mat Sci & Engn, Qingdao 266580, Shandong, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Dalian Maritime Univ, Dalian 116026, Peoples R China
[5] Max Planck Inst Chem Energy Convers, Dept Inorgan Spect, D-45470 Mulheim, Germany
[6] Inner Mongolia Univ, Sch Chem & Chem Engn, Hohhot 010021, Peoples R China
来源
ACS CATALYSIS | 2024年 / 14卷 / 19期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
single-atom catalyst; water gas shift reaction; H-2; production; H2O activation; catalyst design; GAS SHIFT REACTION; IN-SITU; ALPHA-MOC; WATER; INTERFACE; HYDROGEN; SURFACE; IR; NANOPARTICLES; ACTIVATION;
D O I
10.1021/acscatal.4c01821
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Single-atom catalysts with a maximum atom utilization efficiency have shown great potential for application in energy conversion and storage fields. Herein, a highly stable single-atom Pt catalyst (Pt-1/alpha-MoC) on alpha-MoC nanoribbons with Pt loading up to 2% is fabricated using an atom substitution strategy for the water-gas shift (WGS) reaction, which exhibits a very high H-2 production rate of 1094 mu mol(CO)/g(cat)s at 200 degrees C, indicating one of the highest activity levels compared with the reported state-of-the-art WGS catalysts. Complementary advanced characterizations, including aberration-corrected scanning transmission electron microscopy (STEM), synchrotron X-ray absorption spectroscopy (XAS), and density functional theory (DFT) calculations, demonstrate that single Pt atoms are uniformly dispersed on the outermost surface of alpha-MoC and strongly confined within the crystalline lattice of molybdenum carbides. In situ spectroscopic studies and DFT calculations reveal that the Pt-MoC interface serves as a primary active site of the water gas shift (WGS) reaction, boosting H2O molecule activation, to form the key OH* intermediates. Our findings offer an efficient method for the rational design of high-activity single-atom catalysts and lay a good foundation for their industrial application.
引用
收藏
页码:14297 / 14307
页数:11
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