Intercalating Bulk Gold Crystal Into Ordered Single Atoms

R Rong Rong W Wenfa Chen (State Key Laboratory of Mechanics and Control of Aerospace Structures and Institute for Frontier Science Key Laboratory for Intelligent Nano Materials and Devices of Ministry of Education Nanjing University of Aeronautics and Astronautics Nanjing China) P Pin Lyu E Erwen Zhang Y Yang Wang J Jiaran Li (State Key Laboratory of Mechanics and Control of Aerospace Structures and Institute for Frontier Science Key Laboratory for Intelligent Nano Materials and Devices of Ministry of Education Nanjing University of Aeronautics and Astronautics Nanjing China) Y Yizhou Zhao (Department of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520-8107, United States) J Jinguo Liu Y Ying Liu F Fanrong Lin (Key Laboratory for Intelligent Nano Materials and Devices of Ministry of Education, and Institute for Frontier Science, Nanjing University of Aeronautics and Astronautics) S Shuiyan Cao Z Zhongxin Chen (School of Science and Engineering) Y Yi Cui W Wei Liu Y Yanpeng Liu

Abstract

ABSTRACT Gold single atoms (GSAs) have attracted considerable attentions due to their potential in electrocatalytic and photocatalytic reactions. However, achieving high gold density in conventional wet‐solution or mechanical approaches remains currently challenging, apart from uncontrolled spatial on‐support distributions, undesired bi‐products and wastes. Here we show that single gold atoms can be synthesized and patterned via a top‐down intercalation method, in which the topmost layer of gold (100) crystal evolves into isolated single atoms (conversion rate up to 25%) chiseled by a phosphorus monolayer. Scanning tunneling microscopy, X‐ray photoemission spectroscopy, and density functional theory calculations reveal that GSAs assemble into well‐ordered (2 × 2) arrays without thermodynamic tendency for coalescence and weakly couple with the underlying non‐planar phosphorus layer toward efficient hydrogen evolution reaction and oxygen evolution reaction catalysis. The on‐surface formation of GSAs can be readily tailored by varying the post‐annealing temperature and durations. This protocol is defect‐free, solvent‐free, eco‐friendly, scalable, and could regenerate a batch‐to‐batch of fresh GSAs arrays via a simple sputtering and intercalation process in case of catalyst deactivation. This work opens a green and sustainable way for the facile preparation of high‐density GSAs for efficient on‐surface electro‐/photo‐catalytic applications.

Article Details

Volume / Issue Vol. 38, Issue 17
Published March 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (15)

R

Rong Rong

W

Wenfa Chen

State Key Laboratory of Mechanics and Control of Aerospace Structures and Institute for Frontier Science Key Laboratory for Intelligent Nano Materials and Devices of Ministry of Education Nanjing University of Aeronautics and Astronautics Nanjing China

P

Pin Lyu

E

Erwen Zhang

Y

Yang Wang

J

Jiaran Li

State Key Laboratory of Mechanics and Control of Aerospace Structures and Institute for Frontier Science Key Laboratory for Intelligent Nano Materials and Devices of Ministry of Education Nanjing University of Aeronautics and Astronautics Nanjing China

Y

Yizhou Zhao

Department of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520-8107, United States

J

Jinguo Liu

Y

Ying Liu

F

Fanrong Lin

Key Laboratory for Intelligent Nano Materials and Devices of Ministry of Education, and Institute for Frontier Science, Nanjing University of Aeronautics and Astronautics

S

Shuiyan Cao

Z

Zhongxin Chen

School of Science and Engineering

Y

Yi Cui

W

Wei Liu

Y

Yanpeng Liu