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Immobilizing Molecular Metal Dithiolene–Diamine Complexes on 2D Metal–Organic Frameworks for Electrocatalytic H 2 Production
Author(s) -
Dong Renhao,
Zheng Zhikun,
Tranca Diana C.,
Zhang Jian,
Chandrasekhar Naisa,
Liu Shaohua,
Zhuang Xiaodong,
Seifert Gotthard,
Feng Xinliang
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201605337
Subject(s) - catalysis , metal , diamine , carbon fibers , metal organic framework , protonation , graphene , chemistry , inorganic chemistry , materials science , polymer chemistry , nanotechnology , organic chemistry , composite number , ion , adsorption , composite material
Carbon electrocatalysts consisting of metal complexes such as MN x or MS x are promising alternatives to high‐cost Pt catalysts for the hydrogen evolution reaction (HER). However, the exact HER active sites remain elusive. Here, molecular metal dithiolene‐diamine (MS 2 N 2 , M=Co and Ni), metal bis(dithiolene) (MS 4 ), and metal bis(diamine) (MN 4 ) complexes were selectively incorporated into carbon‐rich 2D metal–organic frameworks (2D MOFs) as model carbon electrocatalysts. The 2D MOF single layers, powders, and composites with graphene were thus prepared and showed definite active sites for H 2 generation. The electrocatalytic HER activity of the 2D MOF‐based catalysts with different metal complexes follow the order of MS 2 N 2 >MN 4 >MS 4 . Moreover, the protonation preferentially occurred on the metal atoms, and the concomitant heterolytic elimination of H 2 was favored on the M–N units in the MS 2 N 2 active centers. The results provide an in‐depth understanding of the catalytic active sites, thus making way for the future development of metal complexes in carbon‐rich electrode materials for energy generation.