Effect of Cation Species on Pressure-driven Electrokinetic Energy Conversion in Charged Conical Nanochannels

Electrokinetic energy conversion (EEC) offers a promising avenue for transforming elusive natural energy into electric power, showing a wide application spectrum. Unlike prevalent studies that chiefly utilize symmetrical electrolyte solution (e.g., KCl) and uniformly structured negatively charged nanochannels for EEC, this paper delves into a thorough examination of EEC characteristics—streaming current, streaming potential, and output power—in both positively and negatively charged conical nanochannels with symmetrical and asymmetric (CaCl2 and LaCl3) electrolytes solutions. Operating under the assumption that the electrolyte solutions (KCl, CaCl2, and LaCl3) possess equivalent ionic strength and, thereby, a common Debye length, our findings reveal a significant dependency of EEC characteristics and their regulation parameters on the electrolyte type, nanochannel charge polarity, and ionic strength. As the ionic strength increases, both the streaming current and output power initially rise to a peak before subsequently declining, with the ionic strength at the peak being influenced by the cation valence: lower valence leads to lower ionic strength. In asymmetric electrolyte scenarios, optimal EEC characteristic is observed in positively charged conical nanochannels under a reverse pressure difference, attributed to the ion-selective and ionic concentration distribution in the charged conical nanochannels. Moreover, the complex behaviors of the regulation parameters of EEC characteristics are unveiled. Notably, a tri-valent electrolyte's regulation parameters exceed those of a bi-valent electrolyte, indicating that ionic valence asymmetry enhances the regulation effects on EEC in conical nanochannels.