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Nitrogen-Rich Covalent Organic Polymer for Metal-Free Tandem Catalysis and Postmetalation-Actuated High-Performance Water Oxidation.
Seal, Nilanjan; Karmakar, Arun; Mondal, Partha Pratim; Kundu, Subrata; Neogi, Subhadip.
Afiliación
  • Seal N; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
  • Karmakar A; Inorganic Materials & Catalysis Division, CSIR-Central Salt & Marine Chemicals Research Institute, Bhavnagar, Gujarat 364002, India.
  • Mondal PP; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
  • Kundu S; Electrochemical Process Engineering (EPE) Division, CSIR-Central Electrochemical Research Institute (CECRI), Karaikudi, Tamil Nadu 630003, India.
  • Neogi S; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
ACS Appl Mater Interfaces ; 16(32): 41721-41733, 2024 Aug 14.
Article en En | MEDLINE | ID: mdl-39087733
ABSTRACT
Development of high-performing catalytic materials for selective and mild chemical transformations through adhering to the principles of sustainability remains a central focus in modern chemistry. Herein, we report the template-free assembly of a thermochemically robust covalent organic polymer (COP 1) from 2,2'-bipyridine-5,5'-dicarbonyl dichloride and 2,4,6-tris(4-aminophenyl)triazine as [2 + 3] structural motifs. The two-dimensional (2D) layered architecture contains carboxamide functionality, delocalized π-cloud, and free pyridyl-N site-decked pores. Such trifunctionalization benefits this polymeric network exhibiting tandem alcohol oxidation-Knoevenagel condensation. In contrast to common metal-based catalysts, 1 represents a one of a kind metal-free alcohol oxidation reaction via extended π-cloud delocalization-mediated free radical pathway, as comprehensively supported from diverse control experiments. In addition to reasonable recyclability and broad substrate scope, the mild reaction condition underscores its applicability in benign synthesis of valuable product benzylidene malononitrile. Integration of 2,2'-bipyridyl units in this 2D COP favors anchoring non-noble metal ions to devise 1-M (M Ni2+/ Co2+) that demonstrate outstanding electrochemical oxygen evolution reaction in alkaline media with high chronoamperometric stability. Electrochemical parameters of both 1-Co and 1-Ni outperform some benchmark, commercial, as well as a majority of contemporary OER catalysts. Specifically, the overpotential and Tafel slope (280 mV, 58 mV/dec) for 1-Ni is better than 1-Co (360 mV, 78 mV/dec) because of increased charge accumulation as well as a higher number of active sites compared to the former. In addition, the turnover frequency of 1-Ni is found to be 6 times higher than that of 1-Co and ranks among top-tier water oxidation catalysts. The results provide valuable insights in the field of metal-free tandem catalysis as well as promising electrochemical water splitting at the interface of task-specific functionality fuelling in polymeric organic networks.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos