Photoemission yield spectroscopy (PYS) is widely used for evaluating the electronic states of materials. As automated materials discovery advances, unsupervised extraction of physical information from ambient-air PYS data becomes important. Conventional fixed-exponent analyses and logarithmic transformations suffer from heteroscedasticity, which destabilizes estimation in low-signal regions. To address this, we propose a data-driven analysis framework based on the 1/n-Scan method, which operates directly in the original signal space, removing the geometric bias inherent in log-transform approaches. We further integrate a self-diagnostic quality-evaluation system that quantifies estimation uncertainty with Akaike weights, together with independent residual metrics–the normalized mean absolute error (NMAE), the RMSE-to-MAE ratio (RMR), the Durbin-Watson (DW) statistic, and a macroscopic metric ()–that distinguish hardware-related data degradation from a physical-model mismatch. Applying the framework to differently doped Si and a polycrystalline Au reference in air, we demonstrate autonomous detection, without assumptions on the emission mechanism, of the breakdown of the single-component approximation in heavily doped p-type Si, arising from the overlap of two emission components with different thresholds, as a statistical anomaly–a decrease in DW below its critical value with an auxiliary increase in , despite sound NMAE and RMR–independently confirmed by a two-component fit (AIC 57, DW recovering from 0.8 to 2.0). For heavily doped n-type Si, the gradual surface evolution was classified as a change within the single-component description. This framework provides a robust, self-diagnosing analysis engine for closed-loop autonomous materials exploration.

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