High-performance light-driven heterogeneous CO2 catalysis with near-unity selectivity on metal phosphides

Akin to single-site homogeneous catalysis, a long sought-after goal is to achieve reaction site precision in heterogeneous catalysis for chemical control over patterns of activity, selectivity and stability. Herein, we report on metal phosphides as a class of material capable of realizing these attr...

Full description

Saved in:
Bibliographic Details
Published inNature communications Vol. 11; no. 1; p. 5149
Main Authors Xu, Yang-Fan, Duchesne, Paul N., Wang, Lu, Tavasoli, Alexandra, Ali, Feysal M., Xia, Meikun, Liao, Jin-Feng, Kuang, Dai-Bin, Ozin, Geoffrey A.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 13.10.2020
Nature Publishing Group
Nature Portfolio
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Akin to single-site homogeneous catalysis, a long sought-after goal is to achieve reaction site precision in heterogeneous catalysis for chemical control over patterns of activity, selectivity and stability. Herein, we report on metal phosphides as a class of material capable of realizing these attributes and unlock their potential in solar-driven CO 2 hydrogenation. Selected as an archetype, Ni 12 P 5 affords a structure based upon highly dispersed nickel nanoclusters integrated into a phosphorus lattice that harvest light intensely across the entire solar spectral range. Motivated by its panchromatic absorption and unique linearly bonded nickel-carbonyl-dominated reaction route, Ni 12 P 5 is found to be a photothermal catalyst for the reverse water gas shift reaction, offering a CO production rate of 960 ± 12 mmol g cat −1  h −1 , near 100% selectivity and long-term stability. Successful extension of this idea to Co 2 P analogs implies that metal phosphide materials are poised as a universal platform for high-rate and highly selective photothermal CO 2 catalysis. There exists an urgent need to develop new materials to convert CO 2 to useful products. Here, authors demonstrate metal phosphide nanoparticles to enable light-driven CO 2 hydrogenation with high activities and near-unity selectivity.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Natural Sciences and Engineering Research Council of Canada (NSERC)
USDOE Office of Science (SC)
Imperial Oil
University of Toronto Connaught Innovation Fund
Ministry of the Environment and Climate Change
Ontario Centre of Excellence Solutions 2030 Challenge Fund
Alexander von Humboldt Foundation
Ministry of Research Innovation and Science Low Carbon Innovation Fund
Ministry of Economic Development, Employment and Infrastructure
AC02-06CH11357
Best in Science
Ontario Ministry of Research and Innovation
Connaught Global Challenge Fund
National Natural Science Foundation of China (NNSFC)
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-020-18943-2