Issue 91, 2020

Two dimensional electrocatalyst engineering via heteroatom doping for electrocatalytic nitrogen reduction

Abstract

The electrocatalytic N2 reduction reaction (eNRR) – which can occur under ambient conditions with renewable energy input – became a promising synthetic pathway for ammonia (NH3) and has attracted growing attention in the past few years. Some achievements have been made in the eNRR; however, there remain significant challenges to realize satisfactory NH3 production. Therefore, the rational design of highly efficient and durable eNRR catalysts with N[triple bond, length as m-dash]N bond activating and breaking ability is highly desirable. Two-dimensional (2D) materials have shown great potential in electrocatalysis for energy conversion and storage. Although most 2D materials are inactive toward the eNRR, they can be activated by various modification methods. Heteroatom doping engineering can impact the charge distribution and spin states on catalytic sites, therefore accelerating the dinitrogen adsorption and protonation process. This review summarises the recent research progress of heteroatom-doped 2D materials, including carbon, molybdenum disulfide (MoS2) and metal carbides (MXenes), for the eNRR. In addition, some existing opportunities and future research directions in electrocatalytic nitrogen fixation for ammonia production are discussed.

Graphical abstract: Two dimensional electrocatalyst engineering via heteroatom doping for electrocatalytic nitrogen reduction

Article information

Article type
Feature Article
Submitted
19 Aug 2020
Accepted
06 Oct 2020
First published
07 Oct 2020

Chem. Commun., 2020,56, 14154-14162

Two dimensional electrocatalyst engineering via heteroatom doping for electrocatalytic nitrogen reduction

Y. Yang, R. Wang, L. Yang, Y. Jiao and T. Ling, Chem. Commun., 2020, 56, 14154 DOI: 10.1039/D0CC05635A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements