Abstract Formation of hydronium and carbonate ions from carbon dioxide in the aqueous phase is a reversible process and can both produce and consume ions. These equilibrium reactions represent molecular electrochemical oscillators in pure water. Reversible switching of ionic dynamics is a chaotic process, which is influenced by the CO2 level, temperature and other factors. As demonstrated in previous works, weak variations of magnetic fields induce different electrochemical reactivity and generate ionic waves caused by mutual synchronization of molecular oscillators. Such waves correlate between transparent electrochemical cells, suggesting macroscopic mechanisms for their interaction. This work explores these observations by monitoring the high-resolution ionic dynamics and temperature of independent fluidic cells with electrochemical impedance spectroscopy. Synchronization effects are shown to occur primarily in the CO2 dissolving scenario on the 3-10 minute scale. Without CO2 access, mutual synchronization is either non-existent or negligible. Maximal correlations with r>0.9 are achieved between 4-6 cells. The number of synchronization events is about five times lower when cells are separated between non-transparent containers. To explain such results, we consider the hypothesis of molecular quantum networks that operate with spin conversion of water isomers, investigation of these mechanisms can lead to new quantum sensing technologies.
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