All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Covalent-Bridged Heterointerfaces via Grafted Triazine Organic Polymers Enable Directed Charge Transfer for Efficient Oxygen Reduction in Zn-Air Batteries

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27640%2F25%3A10258837" target="_blank" >RIV/61989100:27640/25:10258837 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.acs.org/doi/10.1021/acsnano.5c11348" target="_blank" >https://pubs.acs.org/doi/10.1021/acsnano.5c11348</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acsnano.5c11348" target="_blank" >10.1021/acsnano.5c11348</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Covalent-Bridged Heterointerfaces via Grafted Triazine Organic Polymers Enable Directed Charge Transfer for Efficient Oxygen Reduction in Zn-Air Batteries

  • Original language description

    Covalent triazine framework (CTF) derivatives have emerged as promising metal-free electrocatalysts due to their high nitrogen content and intrinsic porosity. However, their performance remains limited by sluggish interfacial charge transport and the inaccessibility of active sites. Herein, we report an interfacial covalent bridging strategy based on grafting polymerization to construct a carbon heterostructure electrocatalyst, featuring vertically aligned nitrogen-doped nanosheets covalently anchored onto graphene (v-N/CNS/Gr) support. The covalently bridged interface promotes interfacial charge transfer across the heterostructure, activating otherwise dormant nitrogen active sites and amplifying the oxygen reduction reaction (ORR) reactivity. In situ spectroscopic analyses and theoretical simulations reveal that the covalent bridged bonding promotes charge transport and oxygen activation, and optimizes the adsorption/desorption of intermediates, collectively contributing to reduced energy barriers along the 4e- ORR pathway. As a result, the v-N/CNS/Gr delivers excellent ORR activity with a half-wave potential of 0.85 V (vs RHE). When employed as the cathode in a Zn-air battery, v-N/CNS/Gr achieves a high-power density and stable operation over 850 h. This work demonstrates a generalizable triazine-polymer-based interfacial bridge strategy for enhancing active site accessibility and charge transport in metal-free electrocatalysts.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    20500 - Materials engineering

Result continuities

  • Project

  • Continuities

    O - Projekt operacniho programu

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    ACS Nano

  • ISSN

    1936-0851

  • e-ISSN

    1936-086X

  • Volume of the periodical

    19

  • Issue of the periodical within the volume

    35

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    31870-31881

  • UT code for WoS article

    001555940200001

  • EID of the result in the Scopus database

    2-s2.0-105015363723