| Literature DB >> 33473229 |
Xiao Zhang1,2, Mengtao Zhang1, Yuchen Deng1, Mingquan Xu3, Luca Artiglia4, Wen Wen5,6, Rui Gao7,8,9, Bingbing Chen2, Siyu Yao10, Xiaochen Zhang1, Mi Peng1, Jie Yan1, Aowen Li3, Zheng Jiang5,6, Xingyu Gao5,6, Sufeng Cao11, Ce Yang12,13, A Jeremy Kropf12, Jinan Shi3, Jinglin Xie1, Mingshu Bi2, Jeroen A van Bokhoven4,14, Yong-Wang Li7,8, Xiaodong Wen7,8, Maria Flytzani-Stephanopoulos11, Chuan Shi15, Wu Zhou16,17, Ding Ma18.
Abstract
The water-gas shift (WGS) reaction is an industrially important source of pure hydrogen (H2) at the expense of carbon monoxide and water1,2. This reaction is of interest for fuel-cell applications, but requires WGS catalysts that are durable and highly active at low temperatures3. Here we demonstrate that the structure (Pt1-Ptn)/α-MoC, where isolated platinum atoms (Pt1) and subnanometre platinum clusters (Ptn) are stabilized on α-molybdenum carbide (α-MoC), catalyses the WGS reaction even at 313 kelvin, with a hydrogen-production pathway involving direct carbon monoxide dissociation identified. We find that it is critical to crowd the α-MoC surface with Pt1 and Ptn species, which prevents oxidation of the support that would cause catalyst deactivation, as seen with gold/α-MoC (ref. 4), and gives our system high stability and a high metal-normalized turnover number of 4,300,000 moles of hydrogen per mole of platinum. We anticipate that the strategy demonstrated here will be pivotal for the design of highly active and stable catalysts for effective activation of important molecules such as water and carbon monoxide for energy production.Entities:
Year: 2021 PMID: 33473229 DOI: 10.1038/s41586-020-03130-6
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962