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Zhitao Shen

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2 published item(s)

preprint2026arXiv

Explaining the "Why": A Unified Framework for the Additive Attribution of Changes in Arbitrary Measures

Explaining why aggregated measures change is a critical challenge in data analytics that existing systems struggle to address. While current attribution methods exist, they lack a unified solution that is simultaneously general for arbitrary measures, holistic across both data dimensions and measure composition, and rigorous in its interpretability. To bridge this gap, we introduce a principled framework that reframes attribution through the powerful lens of cooperative game theory. Our key contribution is a classification of measures based on their mathematical structure, which enables a spectrum of algorithms-from general approximations to exact, closed-form solutions-that offer a principled trade-off between generality and performance. We demonstrate our framework's superiority through a multi-faceted evaluation: simulations first confirm its numerical accuracy and then its generality for non-additive measures; a case study on Simpson's Paradox showcases its unique interpretability; and a final experiment proves its practical utility by significantly outperforming existing root cause analysis systems.

preprint2021arXiv

Magnetic moment preservation and emergent Kondo resonance of Co-phthalocyanine on semimetallic Sb(111)

Magnetic molecules on surfaces have been widely investigated to reveal delicate interfacial couplings and for potential technological applications. In these endeavors, one prevailing challenge is how to preserve or recover the molecular spins, especially on highly metallic substrates that can readily quench the magnetic moments of the ad-molecules. Here we use scanning tunneling microscopy/spectroscopy to exploit the semimetallic nature of antimony and observe, surprisingly yet pleasantly, that the spin of Co-phthalocyanine is well preserved on Sb(111), as unambiguously evidenced by the emergent strong Kondo resonance across the molecule. Our first-principles calculations further confirm that the optimal density of states near the Fermi level of the semimetal is a decisive factor, weakening the overall interfacial coupling, while still ensuring sufficiently effective electron-spin scattering in the many-body system. Beyond isolated ad-molecules, we discover that each of the magnetic moments in a molecular dimer or a densely packed island is distinctly preserved as well, rendering such molecular magnets immense potentials for ultra-high density memory devices.