Electrochemical Synthesis of 2D Polymeric Fullerene for Broadband Photodetection

Y Yuxuan Zhang (College of Chemistry) Y Yifan Xie H Hao Mei (University of Mississippi, Jackson, MS, USA.) H Hui Yu (Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry) M Minjuan Li (Frontiers Science Center For Transformative Molecules State Key Laboratory of Synergistic Chem‐Bio Synthesis,School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai China) Z Zexiang He (Frontiers Science Center for Transformative Molecules State Key Laboratory of Synergistic Chem‐Bio Synthesis School of Chemistry and Chemical Engineering and Zhangjiang Institute for Advanced Study Shanghai Jiao Tong University Shanghai P. R. China) W Wentao Fan P Panpan Zhang A Antonio Gaetano Ricciardulli (University of Strasbourg, CNRS, ISIS UMR 7006, 8 allée Gaspard Monge, F-67000 Strasbourg, France) P Paolo Samorì (CNRS, ISIS UMR 7006, University of Strasbourg, 8 Allée Gaspard Monge, Strasbourg F-67000, France) M Mengmeng Li S Sheng Yang (Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research, Ministry of Education, Institute of Interdisciplinary Studies, College of Chemistry and Chemical Engineering)

Abstract

Abstract 2D polymeric fullerene scaffolds, composed of covalently bonded superatomic C 60 nanoclusters, are emerging semiconductors possessing unique hierarchical electronic structures. Hitherto their synthesis has relied on complex and time‐consuming reactions, thereby hindering scalable production and limiting the technological relevance. Here, the study demonstrates a facile electrochemical exfoliation strategy based on the intercalation and expansion of a layered fullerene superlattice, to produce large size (≈52.5 µm 2 ) and monolayer thick 2D polymeric C 60 with high exfoliation yield (≈83%). In situ reduction of solvated protons (H + ) weakens the interlayer interactions thereby promoting the rapid and uniform intercalation of tetra‐n‐butylammonium (TBA + ), ensuring gram‐scale throughput and high structural integrity of exfoliated 2D polymeric C 60 . As a proof of concept, the solution‐processed 2D polymeric C 60 nanosheets have been integrated into thin‐film photodetectors, exhibiting a broad spectral photoresponse ranging from 405 to 1200 nm, with a peak photocurrent at 850 nm and a stable response time. This efficient and scalable exfoliation method holds great promise for the advancement of multifunctional composites and optoelectronic devices based on 2D polymeric C 60 .

Article Details

Volume / Issue Vol. 37, Issue 14
Published April 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (12)

Y

Yuxuan Zhang

College of Chemistry

Y

Yifan Xie

H

Hao Mei

University of Mississippi, Jackson, MS, USA.

H

Hui Yu

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry

M

Minjuan Li

Frontiers Science Center For Transformative Molecules State Key Laboratory of Synergistic Chem‐Bio Synthesis,School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai China

Z

Zexiang He

Frontiers Science Center for Transformative Molecules State Key Laboratory of Synergistic Chem‐Bio Synthesis School of Chemistry and Chemical Engineering and Zhangjiang Institute for Advanced Study Shanghai Jiao Tong University Shanghai P. R. China

W

Wentao Fan

P

Panpan Zhang

A

Antonio Gaetano Ricciardulli

University of Strasbourg, CNRS, ISIS UMR 7006, 8 allée Gaspard Monge, F-67000 Strasbourg, France

P

Paolo Samorì

CNRS, ISIS UMR 7006, University of Strasbourg, 8 Allée Gaspard Monge, Strasbourg F-67000, France

M

Mengmeng Li

S

Sheng Yang

Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research, Ministry of Education, Institute of Interdisciplinary Studies, College of Chemistry and Chemical Engineering