In-situ fabrication of bio-inspired nanocatalysts for enhanced oxygen reduction reaction in alkaline media

被引:8
作者
Aazam, Elham S. [1 ]
Akhtar, Naeem [2 ]
El-Said, Waleed Ahmed [3 ,4 ,5 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Chem Dept, Jeddah 23622, Saudi Arabia
[2] Bahauddin Zakariya Univ BZU, Inst Chem Sci, Multan 60800, Pakistan
[3] Univ Jeddah, Coll Sci, Dept Chem, POB 80327, Jeddah 21589, Saudi Arabia
[4] Assiut Univ, Fac Sci, Dept Chem, Assiut 71516, Egypt
[5] Univ Jeddah, Jeddah, Saudi Arabia
关键词
Oxygen reduction reaction; Bioinspired; Bimetallic; Zeolitic imidazolate framework; N-rich C; ADVANCED ELECTROCATALYSTS; CARBON NANOTUBES; POROUS CARBON; NANOMATERIALS; FRAMEWORKS; PROGRESS; DESIGN;
D O I
10.1016/j.matchemphys.2022.126884
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Designing a fuel cell based on non-precious metal-based electrocatalysts with high reduction potential and stability against methanol/carbon monoxide (MeOH/CO) poisoning is quite challenging. Taking inspiration from naturally occurring enzymes, materials with earth-abundant metal centers embedded in organic framework helps to expedite the kinetics of the oxygen reduction reaction (ORR) by providing more O2 adsorption sites through positively charged N atoms. Thus, herein, we have fabricated novel bioinspired nitrodopamine derived (NDA) N rich C coated bimetallic zeolitic imidazolate framework (NDA@BM-ZIF) through in-situ solvothermal synthesis approach. NDA@BM-ZIF based electrode offers high half wave potential value (E1/2 = 0.915 V) and high tolerance against MeOH poisoning (91.4%) even better than dopamine (DA) derived NC coated BM-ZIF (86.1%) and commercially available Pt/C (87.3%). The remarkable electrocatalytic efficacy of NDA@BM-ZIF could be ascribed to surface compatibility by providing positively charged O2 adsorption sites, increased surface defects and promote heterolytic O-O bond cleavage rather than homolytic cleavage thus resulting in fast electron transportation capability.
引用
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页数:8
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