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Distinguishing the origin of lunar water ice requires in situ isotopic measurements with high sensitivity and robustness under extreme lunar conditions; however, challenges such as uncertain water contents and isotopic fractionation induced by regolith particles restrict isotopic analysis. Herein, we present a miniaturized tunable diode laser absorption spectrometer (TDLAS) developed as the core prototype for the Chang'E-7 Lunar Soil Water Molecule Analyzer (LSWMA). The wavelength range of the instrument is 3659.5-3662.0 cm-1, and the system integrates a Herriott cell for stable multi-isotope (H2 16O, H2 18O, H2 17O, and HD16O) detection and employs regolith samples of known isotopic experiments to quantify adsorption-induced fractionation. Performance evaluations demonstrated a dynamic water detection range of 0.01-2 wt % and isotope precision up to 1.3 parts per thousand for delta D (30.5 s), 0.77 parts per thousand for delta 18O (36 s), and 0.75 parts per thousand for delta 17O (21.5 s) with extended averaging. Repeated injections of three types of standard water revealed a volume-dependent deviation (Delta delta D up to -59.5 parts per thousand) attributed to multilayer adsorption effects, while simulated lunar soil experiments identified additional isotopic fractionation (Delta delta D up to -12.8 parts per thousand) caused by particle binding. These results validate the ability of the spectrometer to resolve subtle isotopic shifts under lunar conditions, providing critical data for distinguishing water origins and advancing future resource utilization strategies.

来源平台：ACS SENSORS