Synergistic boron-dopants and boron-induced oxygen vacancies in MnO2 nanosheets to promote electrocatalytic nitrogen reduction

The development of highly efficient and durable electrocatalysts for the nitrogen reduction reaction (NRR) is of paramount significance for NH3 electrosynthesis. Herein, we report an effective B-doping strategy for the structural engineering of MnO2 toward the NRR through combined experimental and t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-01, Vol.8 (10), p.5200-5208
Hauptverfasser: Chu, Ke, Liu, Ya-ping, Cheng, Yong-hua, Li, Qing-qing
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The development of highly efficient and durable electrocatalysts for the nitrogen reduction reaction (NRR) is of paramount significance for NH3 electrosynthesis. Herein, we report an effective B-doping strategy for the structural engineering of MnO2 toward the NRR through combined experimental and theoretical studies. Introducing B-dopants into MnO2 nanosheets was found to create abundant O-vacancies which cooperated with B-dopants to promote the conductivity and enhance the intrinsic NRR activity of MnO2. The developed B-doped MnO2 nanosheets grown on carbon cloth (B-MnO2/CC) exhibited a significantly enhanced NRR performance with an NH3 yield of 54.2 mu g h(-1) mg(-1) (-0.4 V) and a faradaic efficiency of 16.8% (-0.2 V), and are among the best Mn-based NRR catalysts reported so far. Density functional theory calculations further revealed the synergistic role of B-dopants and O-vacancies in inducing asymmetric charge distribution, which could activate the neighboring Mn atoms to facilitate the stabilization of the key intermediate *N2H on MnO2, leading to reduced reaction energy barrier and enhanced intrinsic NRR activity.
ISSN:2050-7488
2050-7496
DOI:10.1039/d0ta00220h