Work

Nitrite Reduction at Low Overpotentials on N-Doped Carbon: When Metal Single Atoms Become Poisons

Year: 2025

Type: article

Abstract: High Resolution Image Download MS PowerPoint Slide We report a nitrogen-doped carbon derived from tetracyanoquinodimethane (TCNQ900) that alone catalyzes nitrite reduction (NO 2 – RR) to NH 3 with an onset potential higher than +0.10 V vs RHE and catalytic activity rivaling state-of-the-art transition-metal catalysts. Contrary to the usual view that carbon supports merely modulate metal sites, we show the reverse: atomically dispersed Cu on TCNQ900 poisons active N-rich motifs, preventing the formation of a tandem catalyst in which NO 3 – is first reduced to NO 2 – by Cu and subsequently to NH 3 by TCNQ900. Molecular analogues confirm that Cu coordination blocks N-rich pockets that drive the NO 2 – RR. In contrast, physically mixing Cu nanoparticles with TCNQ900 restores a true tandem effect: Cu NPs reduce NO 3 – to NO 2 –, while unpoisoned TCNQ900 converts NO 2 – to NH 3, achieving 4-fold higher partial currents. These findings overturn the “noninnocent” support concept and highlight the reciprocal influence of metals on carbon catalysts, providing new designing guidelines and pointing to the potential role of carbon supports as active actors in catalysis.

Source: Journal of the American Chemical Society

DOI: 10.1021/jacs.5c15469

Authors: Yizhou Dai, Xinyue Zheng, Markus Antonietti, Mateusz Odziomek

Institution: Max Planck Institute of Colloids and Interfaces

Language: English

Topic: Ammonia Synthesis and Nitrogen Reduction

Subfield: Catalysis

Field: Chemical Engineering

Domain: Physical Sciences

Open Access status: hybrid

Estimated APC paid: $4,500

Funder: Max-Planck-Gesellschaft