Publications Repository - Gdańsk University of Technology

Page settings

polski
Publications Repository
Gdańsk University of Technology

Treść strony

Sub‐Nanometer‐Scale Cu9S5 Enables Efficiently Electrochemical Nitrate Reduction to Ammonia

The sub-nanometer is a key feature size in materials science. Unlike single-atom and nanomaterials, size effects and inter-component cooperative actions in sub-nanomaterials will effective on its performance is more significant. Here, 0.95 nm ordered arrangement Cu9S5 sub-nanowires (Cu9S5 SNWs) are synthesized through the co-assembly effect of inorganic nuclei (Cu9S5) and clusters (phosphotungstic acid-PTA), achieving a significant increase in the specific surface area of the sample and ≈100% atomic exposure rate, which is the key to its high catalytic activity. PTA clusters not only act as a “charge transfer station” to accelerate the inter-component electron transfer process, but also facilitate the dissociation of water and provide more hydrogen protons, thus dramatically facilitating the electrocatalytic process. The experimental results show that the Cu9S5 SNWs exhibited excellent nitrate reduction reaction (NO3−RR) properties. The Faraday efficiency (FE) of NO3−RR is 90.4% at the optimum potential −0.3 VRHE (reversible hydrogen electrode) and the ammonia production is as high as 0.37 mmol h−1 cm−2, which is superior to most reported electrocatalysts. In addition, the Zn-NO3− liquid-flow battery devices assembled using Cu9S5 SNWs as electrode materials show excellent application results. This work provides a reference for the design of highly efficient sub-nanoscale NO3−RR electrocatalysts.

Authors

Additional information

DOI
Digital Object Identifier link open in new tab 10.1002/aenm.202403354
Category
Publikacja w czasopiśmie
Type
artykuły w czasopismach dostępnych w wersji elektronicznej [także online]
Language
angielski
Publication year
2024

Source: MOSTWiedzy.pl - publication "Sub‐Nanometer‐Scale Cu9S5 Enables Efficiently Electrochemical Nitrate Reduction to Ammonia" link open in new tab

Portal MOST Wiedzy link open in new tab