Surfactant‐Assisted Phase‐Selective Synthesis of New Cobalt MOFs and Their Efficient Electrocatalytic Hydrogen Evolution Reaction

Reported herein are two new polymorphic Co‐MOFs (CTGU‐5 and ‐6) that can be selectively crystallized into the pure 2D or 3D net using an anionic or neutral surfactant, respectively. Each polymorph contains a H2O molecule, but differs dramatically in its bonding to the framework, which in turn affect...

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Veröffentlicht in:Angewandte Chemie International Edition 2017-10, Vol.56 (42), p.13001-13005
Hauptverfasser: Wu, Ya‐Pan, Zhou, Wei, Zhao, Jun, Dong, Wen‐Wen, Lan, Ya‐Qian, Li, Dong‐Sheng, Sun, Chenghua, Bu, Xianhui
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Sprache:eng
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Zusammenfassung:Reported herein are two new polymorphic Co‐MOFs (CTGU‐5 and ‐6) that can be selectively crystallized into the pure 2D or 3D net using an anionic or neutral surfactant, respectively. Each polymorph contains a H2O molecule, but differs dramatically in its bonding to the framework, which in turn affects the crystal structure and electrocatalytic performance for hydrogen evolution reaction (HER). Both experimental and computational studies find that 2D CTGU‐5 which has coordinates water and more open access to the cobalt site has higher electrocatalytic activity than CTGU‐6 with the lattice water. The integration with co‐catalysts, such as acetylene black (AB) leads to a composite material, AB&CTGU‐5 (1:4) with very efficient HER catalytic properties among reported MOFs. It exhibits superior HER properties including a very positive onset potential of 18 mV, low Tafel slope of 45 mV dec−1, higher exchange current density of 8.6×10−4 A cm−2, and long‐term stability. HER choice of surfactants: Two new Co‐MOFs phase‐selected by anionic and neutral surfactants exhibit differential affinity for entrapped water molecules, leading to a difference in the spatial accessibility of active metal sites. A composite material made from such Co‐MOFs shows impressive performance in electrocatalytic hydrogen evolution reaction (HER) as well as long‐term stability.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201707238