塔菲尔方程
钴
催化作用
电催化剂
肺表面活性物质
无机化学
晶体结构
分子
化学工程
化学
电化学
材料科学
结晶学
物理化学
电极
有机化学
工程类
生物化学
作者
Ya‐Pan Wu,Wei Zhou,Jun Zhao,Wen‐Wen Dong,Ya‐Qian Lan,Dong‐Sheng Li,Chenghua Sun,Xianhui Bu
标识
DOI:10.1002/anie.201707238
摘要
Abstract 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 H 2 O 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.
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