Sulfur-doped graphene anchoring of ultrafine Au₂₅ nanoclusters for electrocatalysis

Abstract

The biggest challenge of exploring the catalytic properties of under-coordinated nanoclusters is the issue of stability. We demonstrate herein that chemical dopants on sulfur-doped graphene (S-G) can be utilized to stabilize ultrafine (sub-2 nm) Au₂₅ (PET)₁₈ clusters to enable stable nitrogen reduction reaction (NRR) without significant structural degradation. The Au₂₅@S-G exhibits an ammonia yield rate of 27.5μg_(NH₃)⋅mgAu⁻¹⋅h⁻¹ at −0.5 V with faradic efficiency of 2.3%. More importantly, the anchored clusters preserve ∼ 80% NRR activity after four days of continuous operation, a significant improvement over the 15% remaining ammonia production rate for clusters loaded on undoped graphene tested under the same conditions. Isotope labeling experiments confirmed the ammonia was a direct reaction product of N₂ feeding gas instead of other chemical contaminations. Ex-situ X-ray photoelectron spectroscopy and X-ray absorption near-edge spectroscopy of post-reaction catalysts reveal that the sulfur dopant plays a critical role in stabilizing the chemical state and coordination environment of Au atoms in clusters. Further ReaxFF molecular dynamics (RMD) simulation confirmed the strong interaction between Au nanoclusters (NCs) and S-G. This substrate-anchoring process could serve as an effective strategy to study ultrafine nanoclusters' electrocatalytic behavior while minimizing the destruction of the under-coordinated surface motif under harsh electrochemical reaction conditions.

Group Members

William A. Goddard III

Charles and Mary Ferkel Professor