Li Ting-Ting, Mei Yan, Li Hongwei, Qian Jinjie, Wu Miao, Zheng Yue-Qing
Chemistry Institute for Synthesis and Green Application, School of Materials Science and Chemical Engineering, Ningbo University, Ningbo 315211, China.
College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325000, China.
Inorg Chem. 2020 Oct 5;59(19):14184-14192. doi: 10.1021/acs.inorgchem.0c01977. Epub 2020 Sep 16.
The electrochemical reduction of CO using intermittent renewable electricity is an attractive strategy for producing value-added fuels and chemicals, but until now, it has been greatly hindered by the shortage of high-performance electrocatalysts. In this study, we have demonstrated a type of molecular-catalyst-based hybrid material by the polymerization of cobalt phthalocyanine (CoPc) on a three-dimensional (3D) g-CN nanosheet-carbon nanotube support for the aqueous electrochemical reduction of CO. The electrocatalytic results show that the obtained composite can selectively transform CO to CO with considerable Faradaic efficiency (FE) of 95 ± 1.8%, a turnover frequency of 4.9 ± 0.2 s, and excellent long-term stability over 24 h at -0.8 V vs the reversible hydrogen electrode (RHE). In comparison to the analogous hybrid electrocatalysts prepared by the drop-drying or dip-coating method, the polymeric form of the molecular catalyst immobilized on 3D carbonaceous materials with an interconnected network enlarges the electrochemically active surface area and enhances the structural and operational robustness.
利用间歇性可再生电力对CO进行电化学还原是生产增值燃料和化学品的一种有吸引力的策略,但到目前为止,高性能电催化剂的短缺严重阻碍了该过程。在本研究中,我们通过在三维(3D)g-CN纳米片-碳纳米管载体上聚合钴酞菁(CoPc),展示了一种用于CO水性电化学还原的基于分子催化剂的杂化材料。电催化结果表明,所获得的复合材料能够以95±1.8%的可观法拉第效率(FE)将CO选择性地转化为CO,周转频率为4.9±0.2 s-1,并且在相对于可逆氢电极(RHE)为-0.8 V的条件下24小时内具有出色的长期稳定性。与通过滴干或浸涂法制备的类似杂化电催化剂相比,固定在具有互连网络的3D碳质材料上的分子催化剂的聚合物形式扩大了电化学活性表面积,并增强了结构和操作的稳健性。