Chemical Research in Chinese Universities ›› 2026, Vol. 42 ›› Issue (3): 998-1007.doi: 10.1007/s40242-026-6055-7

• Research Articles • Previous Articles     Next Articles

SnO@SnO2 Heterojunction as a Novel and Powerful Electrochemiluminescence (ECL) Co-reactant and Strong Self-enhanced ECL Based on SnO@SnO2-mercaptosuccinic Acid Self-assembled Nanoparticles@Ru(bpy)32+ System

ZHANG Weiwei, YAO Qichen, HUANG Yun, ZHENG Jingcheng, SHAO Jiwei, CHEN Yu, CHEN Yuhong, CHI Yuwu   

  1. MOE Key Laboratory for Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection for Food Safety, College of Chemistry, Fuzhou University, Fuzhou, 350108, P. R. China
  • Received:2026-02-28 Accepted:2026-03-10 Published:2026-06-02
  • Contact: CHI Yuwu,E-mail:y.w.chi@fzu.edu.cn E-mail:y.w.chi@fzu.edu.cn
  • Supported by:
    This work was supported by the National Natural Science Foundation of China (No. 22474021) and the Program for Changjiang Scholars and Innovative Research Team in University, China (No. IRT_15R11).

Abstract: This work revealed for the first time that SnO@SnO2 heterojunction (SnOx, 1<x<2) could act as a novel and powerful electrochemiluminescence (ECL) co-reactant. Heterojunction-containing SnO@SnO2 nanostructures (ca. 20 nm) capped with mercaptosuccinic acid (MSA) were uniformly produced by MSA-etching tin nanoparticles, and could be spontaneously self-assembled into large-sized (ca. 200 nm), well-dispersed, uniform, and spherical nanoparticles (SnO@SnO2-MSA SANs). The synthesized SnO@SnO2-MSA SANs could act as a highly efficient co-reactant for the Ru(bpy)32+ ECL system, outperforming the conventional co-reactant tri-n-propylamine (TPrA). It was revealed that the high co-reactant activity of SnO@SnO2 did not originate from SnO or SnO2 alone, but from the heterojunction of SnO@SnO2 (i.e., SnOx, 1<x<2). The SnOx heterojunction acted as a strong co-reactant, initiating highly energetic electron-transfer with the electrogenerated Ru(bpy)33+ and emitting strong ECL. Utilizing the abundant negative surface charges of SnO@SnO2-MSA SANs, Ru(bpy)32+ complexes were successfully loaded via electrostatic adsorption to construct self-enhanced ECL nanocomposites, i.e., SnO@SnO2-MSA SANs@Ru(bpy)32+. The composites exhibited highly efficient anodic ECL emission peaking at 618 nm without requiring any exogenous species. The nanoscale integration of Ru(bpy)32+ luminophores and SnO@SnO2-MSA SAN co-reactants shortens the electron-transfer pathway and thus improves the interfacial ECL reaction efficiency.

Key words: Tin oxide heterojunction, Electrochemiluminescence, Nano-co-reactant, Self-enhanced, Self-assembled nanoparticle