Deep‐Learning‐Enhanced Bioimaging Via Energy Traps Regulated Lanthanide Nanoparticles

R Renrui Sun (Department of Chemistry College of Sciences Shanghai University Shanghai China) M Mengyang Lu Z Zhihua Wang (School of Materials Science and Engineering, Tianjin Key Laboratory of Metal and Molecular Materials Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tongyan Road 38, Tianjin 300350, P. R. China) W Wen Gao J Jiabo Chen (Department of Chemistry, College of Sciences) X Xin Liu H Hongxin Zhang (Department of Chemistry, Laboratory of Advanced Materials, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, China) A Artur Bednarkiewicz (Institute of Low Temperature and Structure Research Polish Academy of Sciences Wrocław Poland) F Fan Zhang L Lining Sun (Department of Chemistry, College of Sciences)

Abstract

ABSTRACT High‐resolution biological imaging in deep tissues holds substantial importance for advancing precision medicine. Currently, the lanthanide‐doped nanoparticles enable in vivo near‐infrared imaging but face a critical trade‐off: Er 3 + ‐based emission at around 1530 nm enables high optical resolution yet suffers from limited tissue penetration due to water absorption, whereas nanoprobes emitting at approximately 980/1060 nm offer deeper penetration with high brightness but compromised resolution due to higher tissue scattering at shorter wavelength. This fundamental contradiction between imaging depth and resolution remains a key challenge. Herein, we introduce the concept of energy traps to actively regulate energy distribution within lanthanide nanoparticles via excitation‐wavelength switching and directional energy transfer modulation. This strategy enables controlled access to either sensitizers (Yb 3+ , Nd 3+ ) self‐emission or efficient sensitization of activators (Er 3+ ), thereby allowing selective enhancement of emission channels. By integrating the deep‐tissue penetration capability of short‐wavelength sensitizers (980 and 1060 nm) with the high‐resolution emission of long‐wavelength activators (1530 nm) through a deep‐learning‐based network, we successfully achieved a 93% enhancement in imaging performance for short‐wavelength probes, offering a robust and adaptable platform for high‐contrast deep‐tissue bioimaging and future point‐of‐care diagnostics.

Article Details

Volume / Issue Vol. 1, Issue 1
Published June 26, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

R

Renrui Sun

Department of Chemistry College of Sciences Shanghai University Shanghai China

M

Mengyang Lu

Z

Zhihua Wang

School of Materials Science and Engineering, Tianjin Key Laboratory of Metal and Molecular Materials Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tongyan Road 38, Tianjin 300350, P. R. China

W

Wen Gao

J

Jiabo Chen

Department of Chemistry, College of Sciences

X

Xin Liu

H

Hongxin Zhang

Department of Chemistry, Laboratory of Advanced Materials, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, China

A

Artur Bednarkiewicz

Institute of Low Temperature and Structure Research Polish Academy of Sciences Wrocław Poland

F

Fan Zhang

L

Lining Sun

Department of Chemistry, College of Sciences