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    Coherent absorption dynamics: The dual role of off-diagonal couplings in weakly bound nuclei

    Hao Liu, Jin Lei*, and Zhongzhou Ren

    • *Contact author: jinl@tongji.edu.cn

    Phys. Rev. C 113, 054601 – Published 4 May, 2026

    DOI: https://doi.org/10.1103/bgwc-x5wj

    Abstract

    Disentangling reaction mechanisms in weakly bound nuclei remains a long-standing challenge, complicated by the common practice of treating absorption as an incoherent sum of channel contributions. Within the Continuum-Discretized Coupled-Channels (CDCC) framework, we apply the generalized optical theorem [S. R. Cotanch, Nucl. Phys. A 842, 48 (2010)] and show that the total absorption cross section, σA∝−〈Ψ|W|Ψ〉, decomposes as σA=σD+σB+σint, where σint is a coherent interference term between channel components. For the systems and complex fragment-target optical potentials considered, σint is negative and comparable in magnitude to the direct absorption terms. The off-diagonal imaginary couplings play a dual role: they redistribute flux among channels and generate σint, which is required for flux-balance consistency. In calculations for d+Nb93 and Li6+Co59/Pb208, retaining the full nondiagonal coupling matrix nearly doubles the breakup-channel absorption for the heavy target, while reducing the total absorption through σint. We demonstrate that neglecting the off-diagonal imaginary couplings Wij (i≠j) is not merely an approximation but leads to a systematically biased physical picture: the total absorption is overestimated while the breakup absorption component is severely underestimated. Experimental analyses that employ incoherent-sum models to extract direct and breakup cross sections from data will inherit this bias. The full coupling matrix is therefore essential for mechanism-resolved cross-section extraction, and we advocate that experimentalists adopt full-coupling CDCC calculations as the standard for consistent interpretation of absorption data in weakly bound systems.

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