Geng Bo, Yan Feng, Zhang Xiao, He Yuqian, Zhu Chunling, Chou Shu-Lei, Zhang Xiaoli, Chen Yujin
Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Harbin Engineering University, Harbin, 150001, China.
College of Physics and Optoelectronic Engineering, Harbin Engineering University, Harbin, 150001, China.
Adv Mater. 2021 Dec;33(49):e2106781. doi: 10.1002/adma.202106781. Epub 2021 Oct 8.
Metal-organic frameworks (MOFs) with intrinsically porous structures and well-dispersed metal sites are promising candidates for electrocatalysis; however, the catalytic efficiencies of most MOFs are significantly limited by their impertinent adsorption/desorption energy of intermediates formed during electrocatalysis and very low electrical conductivity. Herein, Co is introduced into conductive Cu-catecholate (Cu-CAT) nanorod arrays directly grown on a flexible carbon cloth for hydrogen evolution reaction (HER). Electrochemical results show that the Co-incorporated Cu-CAT nanorod arrays only need 52 and 143 mV overpotentials to drive a current density of 10 mA cm in alkaline and neutral media for HER, respectively, much lower than most of the reported non-noble metal-based electrocatalysts and comparable to the benchmark Pt/C electrocatalyst. Density functional theory calculations show that the introduction of Co can optimize the adsorption energy of hydrogen (ΔG ) of Cu sites, almost close to that of Pt (111). Furthermore, the adsorption energy of water ( ) of Co sites in the CuCo-CAT is significantly lower than that of Cu sites upon coupling Cu with Co, effectively accelerating the Volmer step in the HER process. The findings, synergistic effect of bimetals, open a new avenue for the rational design of highly efficient MOF-based electrocatalysts.
具有固有多孔结构和分散良好的金属位点的金属有机框架(MOF)是电催化领域很有前景的候选材料;然而,大多数MOF的催化效率受到电催化过程中形成的中间体不适当的吸附/解吸能量以及极低电导率的显著限制。在此,将钴引入直接生长在柔性碳布上的导电铜-儿茶酚(Cu-CAT)纳米棒阵列中用于析氢反应(HER)。电化学结果表明,掺入钴的Cu-CAT纳米棒阵列在碱性和中性介质中驱动HER达到10 mA cm电流密度时分别仅需要52和143 mV的过电位,远低于大多数已报道的非贵金属基电催化剂,且与基准Pt/C电催化剂相当。密度泛函理论计算表明,钴的引入可以优化铜位点的氢吸附能(ΔG),几乎接近Pt(111)的氢吸附能。此外,在Cu与Co耦合后,CuCo-CAT中钴位点的水吸附能( )显著低于铜位点,有效加速了HER过程中的Volmer步骤。这些关于双金属协同效应的发现为合理设计高效的基于MOF的电催化剂开辟了一条新途径。