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Title: Stable iridium dinuclear heterogeneous catalysts supported on metal-oxide substrate for solar water oxidation

Abstract

Atomically dispersed catalysts refer to substrate-supported heterogeneous catalysts featuring one or a few active metal atoms that are separated from one another. They represent an important class of materials ranging from single-atom catalysts (SACs) and nanoparticles (NPs). While SACs and NPs have been extensively reported, catalysts featuring a few atoms with well-defined structures are poorly studied. The difficulty in synthesizing such structures has been a critical challenge. We report a facile photochemical method that produces catalytic centers consisting of two Ir metal cations, bridged by O and stably bound to a support. Direct evidence unambiguously supporting the dinuclear nature of the catalysts anchored on α-Fe2O3 is obtained by aberration-corrected scanning transmission electron microscopy (AC-STEM). Experimental and computational results further reveal that the threefold hollow binding sites on the OH-terminated surface of α-Fe2O3 anchor the catalysts to provide outstanding stability against detachment or aggregation. The resulting catalysts exhibit high activities toward H2O photooxidation.

Authors:
 [1];  [2];  [3];  [4];  [5];  [6];  [1];  [1];  [1];  [7];  [2];  [5];  [1];  [6];  [8]; ORCiD logo [9];  [10];  [6];  [5];  [2] more »;  [2]; ORCiD logo [1] « less
  1. Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, MA 02467,
  2. Department of Chemistry, Yale Energy Sciences Institute, Yale University, New Haven, CT 06520,
  3. Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany,, National Center for Electron Microscopy in Beijing, School of Materials Science and Engineering, Tsinghua University, 100084 Beijing, China,
  4. National Laboratory of Solid State Microstructures, College of Engineering and Applied Sciences, Nanjing University, 210093 Nanjing, China,, Collaborative Innovation Center of Advanced Microstructures, Nanjing University, 210093 Nanjing, China,, Department of Chemical Engineering and Materials Science, University of California, Irvine, CA 92697,
  5. Department of Chemical and Biological Engineering, Tufts University, Medford, MA 02155,
  6. Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720,
  7. Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany,
  8. National Center for Electron Microscopy in Beijing, School of Materials Science and Engineering, Tsinghua University, 100084 Beijing, China,
  9. National Laboratory of Solid State Microstructures, College of Engineering and Applied Sciences, Nanjing University, 210093 Nanjing, China,, Collaborative Innovation Center of Advanced Microstructures, Nanjing University, 210093 Nanjing, China,
  10. Department of Chemical Engineering and Materials Science, University of California, Irvine, CA 92697,, Department of Physics and Astronomy, University of California, Irvine, CA 92697
Publication Date:
Research Org.:
Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Energy Frontier Research Centers (EFRC) (United States). Argonne-Northwestern Solar Energy Research Center (ANSER)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF); National Key Research and Development Program (China); National Basic Research Program of China; National Natural Science Foundation of China (NSFC); Natural Science Foundation of Jiangsu Province (China); Fundamental Research Funds for the Central Universities (China)
OSTI Identifier:
1423731
Alternate Identifier(s):
OSTI ID: 1506300
Grant/Contract Number:  
SC0001059; SC0024430; AC02-05CH11231; SC0014430; FG02-05ER15730; DMR 1055762; 2016YFB0700402; 2015CB654901; 11474147; BK20151383; 021314380077
Resource Type:
Published Article
Journal Name:
Proceedings of the National Academy of Sciences of the United States of America
Additional Journal Information:
Journal Name: Proceedings of the National Academy of Sciences of the United States of America Journal Volume: 115 Journal Issue: 12; Journal ID: ISSN 0027-8424
Publisher:
Proceedings of the National Academy of Sciences
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; catalyst; water splitting; solar energy; STEM; spectroscopy

Citation Formats

Zhao, Yanyan, Yang, Ke R., Wang, Zechao, Yan, Xingxu, Cao, Sufeng, Ye, Yifan, Dong, Qi, Zhang, Xizi, Thorne, James E., Jin, Lei, Materna, Kelly L., Trimpalis, Antonios, Bai, Hongye, Fakra, Sirine C., Zhong, Xiaoyan, Wang, Peng, Pan, Xiaoqing, Guo, Jinghua, Flytzani-Stephanopoulos, Maria, Brudvig, Gary W., Batista, Victor S., and Wang, Dunwei. Stable iridium dinuclear heterogeneous catalysts supported on metal-oxide substrate for solar water oxidation. United States: N. p., 2018. Web. doi:10.1073/pnas.1722137115.
Zhao, Yanyan, Yang, Ke R., Wang, Zechao, Yan, Xingxu, Cao, Sufeng, Ye, Yifan, Dong, Qi, Zhang, Xizi, Thorne, James E., Jin, Lei, Materna, Kelly L., Trimpalis, Antonios, Bai, Hongye, Fakra, Sirine C., Zhong, Xiaoyan, Wang, Peng, Pan, Xiaoqing, Guo, Jinghua, Flytzani-Stephanopoulos, Maria, Brudvig, Gary W., Batista, Victor S., & Wang, Dunwei. Stable iridium dinuclear heterogeneous catalysts supported on metal-oxide substrate for solar water oxidation. United States. https://doi.org/10.1073/pnas.1722137115
Zhao, Yanyan, Yang, Ke R., Wang, Zechao, Yan, Xingxu, Cao, Sufeng, Ye, Yifan, Dong, Qi, Zhang, Xizi, Thorne, James E., Jin, Lei, Materna, Kelly L., Trimpalis, Antonios, Bai, Hongye, Fakra, Sirine C., Zhong, Xiaoyan, Wang, Peng, Pan, Xiaoqing, Guo, Jinghua, Flytzani-Stephanopoulos, Maria, Brudvig, Gary W., Batista, Victor S., and Wang, Dunwei. Mon . "Stable iridium dinuclear heterogeneous catalysts supported on metal-oxide substrate for solar water oxidation". United States. https://doi.org/10.1073/pnas.1722137115.
@article{osti_1423731,
title = {Stable iridium dinuclear heterogeneous catalysts supported on metal-oxide substrate for solar water oxidation},
author = {Zhao, Yanyan and Yang, Ke R. and Wang, Zechao and Yan, Xingxu and Cao, Sufeng and Ye, Yifan and Dong, Qi and Zhang, Xizi and Thorne, James E. and Jin, Lei and Materna, Kelly L. and Trimpalis, Antonios and Bai, Hongye and Fakra, Sirine C. and Zhong, Xiaoyan and Wang, Peng and Pan, Xiaoqing and Guo, Jinghua and Flytzani-Stephanopoulos, Maria and Brudvig, Gary W. and Batista, Victor S. and Wang, Dunwei},
abstractNote = {Atomically dispersed catalysts refer to substrate-supported heterogeneous catalysts featuring one or a few active metal atoms that are separated from one another. They represent an important class of materials ranging from single-atom catalysts (SACs) and nanoparticles (NPs). While SACs and NPs have been extensively reported, catalysts featuring a few atoms with well-defined structures are poorly studied. The difficulty in synthesizing such structures has been a critical challenge. We report a facile photochemical method that produces catalytic centers consisting of two Ir metal cations, bridged by O and stably bound to a support. Direct evidence unambiguously supporting the dinuclear nature of the catalysts anchored on α-Fe2O3 is obtained by aberration-corrected scanning transmission electron microscopy (AC-STEM). Experimental and computational results further reveal that the threefold hollow binding sites on the OH-terminated surface of α-Fe2O3 anchor the catalysts to provide outstanding stability against detachment or aggregation. The resulting catalysts exhibit high activities toward H2O photooxidation.},
doi = {10.1073/pnas.1722137115},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
number = 12,
volume = 115,
place = {United States},
year = {Mon Mar 05 00:00:00 EST 2018},
month = {Mon Mar 05 00:00:00 EST 2018}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record
https://doi.org/10.1073/pnas.1722137115

Citation Metrics:
Cited by: 154 works
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Figures / Tables:

Fig. 1 Fig. 1: Synthesis procedure of Ir DHC. It starts with the immobilization of molecular Ir catalysts, followed by photochemical removal of organic ligands. The binding details of H2O and OH groups are proposed.

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Figures/Tables have been extracted from DOE-funded journal article accepted manuscripts.