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Yu-Jie Tang

Publications and source records attributed to Yu-Jie Tang.

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Pion radiative decays of excited hidden-charm pentaquark molecules: from $\Sigma_c^{(*)}\bar{D}^{(*)}(2S)$ molecules to the reported $P_c$ states

The discovery of the hidden-charm pentaquarks \(P_c(4312)\), \(P_c(4440)\) and \(P_c(4457)\) by the LHCb Collaboration are very likely to identify as the \(\Sigma_c^{(*)}\bar{D}^{(*)}\) molecules. A natural and crucial extension is the existence of excited molecular partners built from a ground-state charmed baryon and a radially excited anti-charmed meson, namely \(\Sigma_c^{(*)}\bar{D}^{(*)}(2S)\) molecules. In a framework of chiral quark model, we systematic study pion-emission decays of such excited molecules into the known ground-state \(P_c\) molecules. Our results show that the decay widths are sensitive to the spin structures and the coupled-channel interferences, i.e., the \(\Sigma_c\bar{D}(2S)/\Sigma_c\bar{D}^*(2S)/\Sigma_c^*\bar{D}^*(2S)[1/2(1/2^-)]\) state decays to \(P_c(4440)\) with a width of several MeV, while the width to \(P_c(4457)\) is suppressed below \(0.3\) MeV due to destructive interference. The pion-emission decay can be the key to unveiling the excited molecular spectrum of hidden-charm pentaquarks and provides decisive experimental signatures. We expect the future experiments such as the LHCb and PANDA can verify our predictions.

hep-ph

Exploring pion emission properties of (strange) hidden-charm molecular pentaquarks in a chiral quark model

The internal structure of the exotic $P_c$ and $P_{cs}$ pentaquarks remains an open question. To address this, we demonstrate that pion emission serves as a sensitive probe by calculating its properties within a molecular scenario using the chiral quark model and coupled-channel effects. Our results reveal a strong dependence of the decay widths on the internal structure and spatial wave functions. We therefore expect this study to stimulate experimental measurements of these decays, which are crucial for determining the nature of these states and guiding the search for further molecular partners.

hep-ph