4.8 Article

Ultrafine Pt Nanoclusters Confined in a Calixarene-Based {Ni24} Coordination Cage for High-Efficient Hydrogen Evolution Reaction

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 138, Issue 50, Pages 16236-16239

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b11218

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Funding

  1. National Natural Science Foundation of China [21571172, 21521092, 21633008, 21575134, 51222404]
  2. National Key Research and Development Plan [2016YFA0203200]

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To obtain stable and ultrafine Pt nano clusters, a trigonal prismatic coordination cage with the sulfur atoms on the edges was solvothermally synthesized to confine them. In the structure of {Ni-24(TC4A-SO2)(6)(TD C)(12) (H2O)(6)} (H(4)TC4A-SO2 = p-tert-butylsulfonylcalix[4]arene; H2TDC = 2,5-thiophenedicarboxylic acid), three Ni-4-(TC4A-SO2) SBUs are bridged by three TDC ligands into a triangle and two such triangles are pillared by three pairs of TDC ligands to form a trigonal prism. The cage cavity has 12 sulfur atoms on the surface. Because of the porous structure and strong covalent interaction between metal and sulfur, ultrafine Pt nanoclusters composed of less than similar to 18 Pt atoms can be facilely confined in the present trigonal prismatic cage (Pt@CIAC-121). The as-synthesized Pt NCs exhibit higher electrocatalytic activity than commercial Pt/C toward hydrogen evolution reaction.

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