Affiliation:
1. Department of Chemistry National Dong Hwa University No. 1, Sec. 2, Da Hsueh Rd. Shoufeng Hualien 97401 Taiwan R. O. C.
2. Department of Chemistry Yonsei University Seoul 03722 Republic of Korea
3. Univ Rennes CNRS ISCR-UMR 6226 35000 Rennes France
Abstract
AbstractThe first hydride‐containing 2‐electron palladium/copper alloys, [PdHCu11{S2P(OiPr)2}6(C≡CPh)4] (PdHCu11) and [PdHCu12{S2P(OiPr)2}5{S2PO(OiPr)} (C≡CPh)4] (PdHCu12), are synthesized from the reaction of [PdH2Cu14{S2P(OiPr)2}6(C≡CPh)6] (PdH2Cu14) with trifluoroacetic acid (TFA). X‐ray diffraction reveals that the PdHCu11 and PdHCu12 kernels consist of a central PdH unit encapsulated within a vertex‐missing Cu11 cuboctahedron and complete Cu12 cuboctahedron, respectively. DFT calculations indicate that both PdHCu11 and PdHCu12 can be considered as axially‐distorted 2‐electron superatoms. PdHCu11 shows excellent HER activity, unprecedented within metal nanoclusters, with an onset potential of −0.05 V (at 10 mA cm−2), a Tafel slope of 40 mV dec−1, and consistent HER activity during 1000 cycles in 0.5 M H2SO4. Our study suggests that the accessible central Pd site is the key to HER activity and may provide guidelines for correlating catalyst structures and HER activity.
Funder
Ministry of Science and Technology
Cited by
1 articles.
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