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Updated: Jun 4, 2025
A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
Asymmetric Rh-O-Co bridge sites enable superior bifunctional catalysis for hydrazine-assisted hydrogen production
Jinrui Hu1, Xuan Wang1, Yi Zhou1
1Jiangsu Key Laboratory of New Power Batteries, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University Nanjing 210023 China tangyawen@njnu.edu.cn gengtaofu@njnu.edu.cn.
Abstract:
Hydrazine-assisted water splitting is a promising strategy for energy-efficient hydrogen production, yet challenges remain in developing effective catalysts that can concurrently catalyze both the hydrogen evolution reaction (HER) and hydrazine oxidation reaction (HzOR) in acidic media. Herein, we report an effective bifunctional catalyst consisting of Rh clusters anchored on Co3O4 branched nanosheets (Rh-Co3O4 BNSs) synthesized via an innovative arginine-induced strategy. The Rh-Co3O4 BNSs exhibit unique Rh-O-Co interfacial sites that facilitate charge redistribution between Rh clusters and the Co3O4 substrate, thereby optimizing their valence electronic structures. When the current density reaches 10 mA cm-2, the Rh-Co3O4 BNSs require working potentials of only 32 mV for the HER and 0.26 V for the HzOR, far surpassing commercial Pt/C. Furthermore, the Rh-Co3O4 BNSs can work efficiently for hydrazine-assisted water electrolysis with a low voltage of 0.34 V at 10 mA cm-2 and excellent stability. Theoretical calculations reveal that the optimized valence electronic structure within interfacial Rh-O-Co sites not only reduces the adsorption energy barrier of Co3O4 for H* in the HER; but also optimizes the hydrazine adsorption in the HzOR and lowers the free energy change in the potential-determining step, where the facilitated dehydrogenation is observed in in situ Raman spectra. This work provides a viable approach for designing efficient bifunctional catalysts for future hydrazine-assisted hydrogen production.
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