TY - JOUR
T1 - Phase-Selective Epitaxial Growth of Heterophase Nanostructures on Unconventional 2H-Pd Nanoparticles
AU - Ge, Yiyao
AU - Huang, Zhiqi
AU - Chen, Bo
AU - Liu, Guigao
AU - Zhou, Ming
AU - Zhang, Xiao
AU - Cheng, Hongfei
AU - Liu, Guanghua
AU - Du, Yonghua
AU - Sun, Cheng Jun
AU - Tan, Chaoliang
AU - Huang, Jingtao
AU - Yin, Pengfei
AU - Fan, Zhanxi
AU - Chen, Ye
AU - Yang, Nailiang
AU - Zhang, Hua
N1 - Funding Information:
Z.F. and H.Z. acknowledge the financial support from ITC via the Hong Kong Branch of National Precious Metals Material Engineering Research Center (NPMM) and Start-Up Grants (Project Nos. 9610480, 7200651, and 9380100) and grants (Project Nos. 9610478, 7005512, and 1886921) from the City University of Hong Kong. The authors thank the Facility for Analysis, Characterization, Testing, and Simulation, Nanyang Technological University, Singapore, for their electron microscopy (and/or X-ray) facilities. This research used resources of the Advanced Photon Source, an Office of Science User Facility operated for the U.S. Department of Energy (DOE) Office of Science by Argonne National Laboratory, supported by the U.S. DOE under Contract No. DE-AC02-06CH11357, and the Canadian Light Source and its funding partners.
Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/11/4
Y1 - 2020/11/4
N2 - Heterostructured, including heterophase, noble-metal nanomaterials have attracted much interest due to their promising applications in diverse fields. However, great challenges still remain in the rational synthesis of well-defined noble-metal heterophase nanostructures. Herein, we report the preparation of Pd nanoparticles with an unconventional hexagonal close-packed (2H type) phase, referred to as 2H-Pd nanoparticles, via a controlled phase transformation of amorphous Pd nanoparticles. Impressively, by using the 2H-Pd nanoparticles as seeds, Au nanomaterials with different crystal phases epitaxially grow on the specific exposed facets of the 2H-Pd, i.e., face-centered cubic (fcc) Au (fcc-Au) on the (002)h facets of 2H-Pd while 2H-Au on the other exposed facets, to achieve well-defined fcc-2H-fcc heterophase Pd@Au core-shell nanorods. Moreover, through such unique facet-directed crystal-phase-selective epitaxial growth, a series of unconventional fcc-2H-fcc heterophase core-shell nanostructures, including Pd@Ag, Pd@Pt, Pd@PtNi, and Pd@PtCo, have also been prepared. Impressively, the fcc-2H-fcc heterophase Pd@Au nanorods show excellent performance toward the electrochemical carbon dioxide reduction reaction (CO2RR) for production of carbon monoxide with Faradaic efficiencies of over 90% in an exceptionally wide applied potential window from -0.9 to -0.4 V (versus the reversible hydrogen electrode), which is among the best reported CO2RR catalysts in H-type electrochemical cells.
AB - Heterostructured, including heterophase, noble-metal nanomaterials have attracted much interest due to their promising applications in diverse fields. However, great challenges still remain in the rational synthesis of well-defined noble-metal heterophase nanostructures. Herein, we report the preparation of Pd nanoparticles with an unconventional hexagonal close-packed (2H type) phase, referred to as 2H-Pd nanoparticles, via a controlled phase transformation of amorphous Pd nanoparticles. Impressively, by using the 2H-Pd nanoparticles as seeds, Au nanomaterials with different crystal phases epitaxially grow on the specific exposed facets of the 2H-Pd, i.e., face-centered cubic (fcc) Au (fcc-Au) on the (002)h facets of 2H-Pd while 2H-Au on the other exposed facets, to achieve well-defined fcc-2H-fcc heterophase Pd@Au core-shell nanorods. Moreover, through such unique facet-directed crystal-phase-selective epitaxial growth, a series of unconventional fcc-2H-fcc heterophase core-shell nanostructures, including Pd@Ag, Pd@Pt, Pd@PtNi, and Pd@PtCo, have also been prepared. Impressively, the fcc-2H-fcc heterophase Pd@Au nanorods show excellent performance toward the electrochemical carbon dioxide reduction reaction (CO2RR) for production of carbon monoxide with Faradaic efficiencies of over 90% in an exceptionally wide applied potential window from -0.9 to -0.4 V (versus the reversible hydrogen electrode), which is among the best reported CO2RR catalysts in H-type electrochemical cells.
UR - http://www.scopus.com/inward/record.url?scp=85095667898&partnerID=8YFLogxK
U2 - 10.1021/jacs.0c09461
DO - 10.1021/jacs.0c09461
M3 - Journal article
C2 - 33086784
AN - SCOPUS:85095667898
SN - 0002-7863
VL - 142
SP - 18971
EP - 18980
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 44
ER -