Electrocatalyst for hydrogen evolution and H2O2 recognition on composite carbon paste electrodes with three new Ag(I) MOFs

• Published in: Journal of molecular structure Vol. 1311; p. 138448
• Main Authors: Zhang, Jiaqi, Gao, Wei, Lv, Yue, Fei, Cailing, Wu, Zhengwei, Wu, Huilu
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 05.09.2024
• Subjects: Ag-MOFs; Composite carbon paste electrodes; Electrocatalysis; H2O2 recognition; Hydrogen evolution reaction; Ag-MOFs; Electrocatalysis; Hydrogen evolution reaction; H2O2 recognition; Composite carbon paste electrodes
• ISSN: 0022-2860; 1872-8014
• DOI: 10.1016/j.molstruc.2024.138448

•Three new Ag(Ⅰ) MOFs were synthesized and characterized.•Electrodes composited by Ag(Ⅰ) MOFs show effective HER activity.•The highest HER activity of Ag-MOF-2@CPE may be attributed to coordinated water.•Three Ag-MOF-1∼3@CPE have good H2O2-sensing and exhibit good anti-interference. Three new Ag(I) metal-organic frameworks (Ag-MOFs) containing bisbenzimidazole-derived ligand, namely, {[Ag2(L)(TP)](H2O)}n (1), {[Ag2(L)(HBTC))(H2O)](CH3CH2OH)(H2O)}n (2) and {[Ag4(L)2(IP)2](CH3CN)3(H2O)16}n (3) (L = bis(1-(pyridin-4-ylmethyl)-benzimidazol-2-yl methyl) ether, TP = Terephthalate, BTC = Benzenetricarboxylate, IP = Isophthalate), have been synthesized by volatilization method and systematic adjustment of solvent and aromatic polyacid co-ligand. Single crystal structural analysis showed that although three Ag-MOFs have a three-dimensional (3D) network backbone structure, their topological structures are different. Electrocatalytic hydrogen evolution reaction (HER) of carbon paste composite electrodes (Ag-MOF-1∼3@CPE) prepared by mixing graphite powder with Ag-MOFs were investigated in 0.5 M H2SO4 electrolyte. The HER measurements show that the overpotential η10293K of Ag-MOF-1∼3@CPE are -634, -533 and -615 mV compared with sCPCE (blank electrode, -966 mV), and the Tafel slope of sCPCE and Ag-MOF-1∼3@CPE were 276, 251, 123 and 220 mV dec−1, respectively. The results prove that Ag-MOF-1∼3@CPE could effectively catalyze and accelerate the HER behavior, with electrocatalytic activity order being Ag-MOF-2@CPE > Ag-MOF-3@CPE > Ag-MOF-1@CPE > sCPE. The highest HER activity of Ag-MOF-2@CPE can be attributed to the fact that Ag-MOF-2 contains coordination water molecule, while the higher activity of Ag-MOF-3@CPE than Ag-MOF-1@CPE is due to steric hindrance. Furthermore, the recognition performance of Ag-MOF-1∼3@CPE for H2O2 was further studied by chronoamperometry in 0.2 M phosphate buffer solution (PBS, pH = 6). The three sensors can detect H2O2 in a linear range from 0.5 μM to 4 mM with sensitivities of 103, 34.5 and 138 μA·mM−1·cm−2, and also revealed long-term stability and good selectivity. Our study provides a new approach for designing efficient, non-precious metal electrochemical catalysts. Three new Ag(Ⅰ) MOFs have been synthesized by systematically tuning the solvent and aromatic polyacid co-ligand. Crystallographic analysis revealed that the three Ag(I)-MOFs exhibit different topological channel structures. The Ag-MOF-1∼3@CPE have more positive overpotentials (η10293K), smaller Tafel slopes and lower activation energies in the HER process compared to the blank sCPE, demonstrating that the Ag-MOF-1∼3@CPE have effective electrocatalytic hydrogen evolution activity. The highest electrocatalytic HER activity of Ag-MOF-2@CPE may be attributed to the presence of coordinated water. Moreover, the Ag-MOF-1∼3@CPE have good detection ability for H2O2, and exhibit good stability and anti-interference properties. [Display omitted]