Synergistic reductive catalytic effects of an organic and inorganic hybrid covalent organic framework for hydrogen fuel production

被引:1
|
作者
Rani, Sonia [1 ]
Nadeem, Muhammad [2 ]
Alrahili, Mazen R. [3 ]
Shalash, Marwan [4 ]
Bhatti, Moazzam H. [2 ]
Munawar, Khurram Shahzad [5 ,6 ]
Tariq, Muhammad [1 ]
Asif, Hafiz Muhammad [1 ]
El-Bahy, Zeinhom M. [7 ]
机构
[1] Bahauddin Zakariya Univ Multan, Inst Chem Sci, Inorgan Res Lab, Multan 60800, Pakistan
[2] Allama Iqbal Open Univ, Dept Chem, Islamabad, Pakistan
[3] Taibah Univ, Sch Sci, Phys Dept, Janadah Bin Umayyah Rd, Medina 42353, Saudi Arabia
[4] Northern Border Univ, Coll Sci & Arts Turaif, Dept Chem, Ar Ar, Saudi Arabia
[5] Univ Sargodha, Inst Chem, Sargodha 40100, Punjab, Pakistan
[6] Univ Mianwali, Dept Chem, Mianwali 42200, Punjab, Pakistan
[7] Al Azhar Univ, Fac Sci, Dept Chem, Cairo, Egypt
关键词
FLUORESCENCE QUANTUM YIELD; OXYGEN EVOLUTION; BIFUNCTIONAL ELECTROCATALYST; PORPHYRIN; COBALT; POLYOXOMETALATE; SPECTROSCOPY; GRAPHENE; DEGRADATION; TEMPERATURE;
D O I
10.1039/d4dt00788c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Electrocatalytic hydrogen generation in alkaline medium has become widely used in a variety of sectors. However, the possibility for additional performance improvement is hampered by slow kinetics. Because of this restriction, careful control over processes such as water dissociation, hydroxyl desorption and hydrogen recombination is required. Covalent organic frameworks (COFs) based on porphyrin and polyoxometalates (POMs) show encouraging electrocatalytic performance, offering a viable route for effective and sustainable hydrogen generation. Their specific architectures lead to increased electrocatalytic activity, which makes them excellent choices for developing water electrolysis as a clean energy conversion method in the alkaline medium. In this regard, TTris@ZnPor and Lindqvist POM were coordinated to create a new eco-friendly and highly active covalent organic framework (TP@VL-COF). In order to describe TP@VL-COF, extensive structural and morphological investigations were carried out through FTIR, 1H NMR, elemental analysis, SEM, fluorescence, UV-visible, PXRD, CV, N2-adsorption isotherm, TGA and DSC analyses. In an alkaline medium, the electrocatalytic capability of 20%C/Pt, TTris@ZnPor, Lindqvist POM and TP@VL-COF was explored and compared for the hydrogen evolution reaction (HER). The TP@VL-COF showed the best catalytic efficiency for HER in an alkaline electrolyte, requiring just a 75 mV overpotential to drive 10 mA cm-2 and outperforming 20%C/Pt, TTris@ZnPor, Lindqvist POM and other reported catalysts. The Tafel slope value also indicates faster kinetics for TP@VL-COF (114 mV dec-1) than for 20%C/Pt (182 mV dec-1) TTris@ZnPor (116 mV dec-1) and Lindqvist POM (125 mV dec-1). The electrocatalysis of 20%C/Pt, precursors and TP@VL-COF for HER in an alkaline electrolyte was assessed. The TP@VL-COF showed just 75 mV overpotential, which is due to the covalent linkage of Lindqvist POM creating synergistic effects.
引用
收藏
页码:10875 / 10889
页数:15
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