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This study extends Time-Resolved Terahertz Stark Spectroscopy (TRTSS) to molecules in water, enabling the observation of Stark effects in a highly polar solvent at room temperature. By utilizing intense single-cycle THz pulses, the researchers effectively prevent dipole reorientation, allowing for the measurement of both linear and quadratic Stark effects in Malachite Green and Methyl Orange. The findings, supported by time-dependent density functional theory (TD-DFT) calculations, reveal that solvent interactions significantly influence the Stark parameters of solvated molecules, providing new insights into molecular dynamics in polar environments.
Stark spectroscopy in water reveals how solvent interactions can dramatically alter molecular dipole responses, challenging previous assumptions about molecular behavior in polar environments.
Stark spectroscopy is a powerful method for probing molecular dipole moment changes, charge transfer dynamics, and polarizability under applied electric fields. Time-Resolved Terahertz Stark Spectroscopy (TRTSS), which employs intense single-cycle terahertz (THz) pulses to induce transient Stark shifts, overcomes key limitations of conventional approaches. Unlike static or low-frequency fields, THz pulses oscillate much faster than typical molecular rotation times, effectively preventing dipole reorientation and enabling measurements in solutions at ambient conditions. Here, we extend TRTSS to molecules dissolved in water, the most important polar solvent for chemical and biological systems and report the first demonstration of Stark spectroscopy in water at room temperature. Using Malachite Green and Methyl Orange as model systems, we observe clear THz-induced spectral modulations, demonstrating that TRTSS can successfully reveal THz Stark responses even in highly polar, hydrogen-bonded environments. Measured signals exhibit a combination of linear (dipole-driven) and quadratic (polarizability-driven) Stark effects in both systems, consistent with time-dependent density functional theory (TD-DFT) calculations. Comparison with TD-DFT further suggests that conformational effects can influence the extracted Stark parameters in solvated molecules.
