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Highly Active Oxygen Evolution Reaction of NiMoO4 Sub-1 nm Nanowires Boosts Luminol Electrochemiluminescence
Hao Zang1, Dong Mei Wang1, Wen Jie Dai1
1Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, P. R. China.
Abstract:
In recent years, there has been an increasing research focus on the luminol-H2O electrochemiluminescence (ECL) system due to its ability to address the instability and toxicity of H2O2, which are common issues associated with the conventional luminol-H2O2 ECL system. To enhance the ECL efficiency of the luminol-H2O system, researchers have developed electrocatalytic materials with exceptional oxygen evolution reaction (OER) properties to facilitate water electrolysis into O2 to produce reactive oxygen species (ROS) and act as co-reactant promoters. However, most of these materials are characterized by their nanoscale or microscale dimensions, resulting in relatively large sizes and low specific surface areas, which hinder the application of the luminol-H2O system. To address this challenge, nickel molybdate sub-1 nm nanowires (NiMoO4 S1 NWs) with a large specific surface area is synthesized that can offer many active sites to enhance the performance of the OER to boost the ECL of luminol. This study demonstrates that the large amount of ROS generated by the OER of NiMoO4 S1 NWs play a crucial role in enhancing the ECL intensity of luminol. Finally, a NiMoO4 S1 NWs-based ECL biosensor for the highly sensitive detection of the nucleocapsid proteins of SARS-CoV-2 is successfully constructed.

