Issue 18, 2023

Single silicon-doped CNT as a metal-free electrode for robust nitric oxide reduction utilizing a Lewis base site: an ingenious electronic “Reflux-Feedback” mechanism

Abstract

The electrocatalytic reduction of nitric oxide (NO) has become the most charming approach for the sustainable synthesis of ammonia (NH3), however, the development of a valid catalyst endowed with low cost, high efficiency, and long-term endurance still faces an enormous challenge. In view of the famous concept of “donate and accept”, various transition metal-based electrodes have been predicted and brought into production for electrocatalysis, but metal-free materials or novel activation mechanisms are rarely reported. Here, metal-free electrocatalysts, namely individual silicon (Si) atom-embedded single-walled carbon nanotubes (CNTs), for the NO reduction reaction (NORR) were put forward by performing first-principles calculations. The results disclose that the discarded NO can be converted into value-added NH3 on Si-CNT(10, 0) with a limiting potential of −0.25 V. Importantly, the doped Si atom acts as a Lewis base site that drives some of the p-orbital electrons to return to the surrounding carbon atoms and then feed adequate electron back to intermediates, rendering it more flat for the electroreduction progress. In summary, the designed carbon-based electrode holds great promise for experimental trial and offers a certain degree of theoretical guidance.

Graphical abstract: Single silicon-doped CNT as a metal-free electrode for robust nitric oxide reduction utilizing a Lewis base site: an ingenious electronic “Reflux-Feedback” mechanism

Supplementary files

Article information

Article type
Paper
Submitted
11 Feb 2023
Accepted
14 Apr 2023
First published
17 Apr 2023

Phys. Chem. Chem. Phys., 2023,25, 13072-13079

Single silicon-doped CNT as a metal-free electrode for robust nitric oxide reduction utilizing a Lewis base site: an ingenious electronic “Reflux-Feedback” mechanism

L. Yang, J. Fan and W. Zhu, Phys. Chem. Chem. Phys., 2023, 25, 13072 DOI: 10.1039/D3CP00677H

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