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Creators/Authors contains: "Alvarez, M_A G"

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  1. Abstract This work presents MARS (Modular apparatus for nuclear reactions spectroscopy) and its characterization prior to its first application to measure$$^6$$ 6 Li+$$^{12}$$ 12 C nuclear reactions. Measurements were performed at the 3 MV tandem accelerator of the CNA (National Accelerator Center), in Seville, Spain. The$$^{6}$$ 6 Li projectiles were accelerated at energies around the$$^6$$ 6 Li+$$^{12}$$ 12 C Coulomb barrier ($$V^{\text {cm}}_{B}\sim 3.0$$ V B cm 3.0 MeV - center of mass and$$V^{\text {lab}}_{B}\sim 4.5$$ V B lab 4.5 MeV - laboratory frame). Using a$$^{6}\hbox {Li}^{2+}$$ 6 Li 2 + beam, we measured at 13 laboratory energies from 4.00 to 7.75 MeV. Thus, we present the excitation function of$$^{12}$$ 12 C($$^6$$ 6 Li,$$^4$$ 4 He)$$^{14}\hbox {N}^{g.s.}$$ 14 N g . s . reaction, at 2 backward angles ($$110.0^\circ $$ 110 . 0 and$$140.0^\circ $$ 140 . 0 ). The projectile dissociation, leading to this reaction, increases with the bombarding energies around the Coulomb barrier. This dissociation is favored at an optimum energy$$E_{b}^{\text {op}}$$ E b op $$\ge $$ $$V_{B}$$ V B +$$|Q_{bu}|$$ | Q bu | , where$$V_{B}$$ V B is the Coulomb barrier of the system, and$$|Q_{bu}|$$ | Q bu | is the module ofQ-value for the$$^6$$ 6 Li dissociation into$$^4$$ 4 He+$$^2$$ 2 H. This result corroborates a systematic analysis of weakly bound projectiles reacting on several targets [1]. 
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    Free, publicly-accessible full text available May 1, 2026
  2. Abstract This work investigates the elastic scattering of10B on119Sn at several energies around the Coulomb barrier. The experimental angular distributions are analyzed within the optical model framework using two different nuclear interactions: the São Paulo potential (SPP) and its updated version, SPP2. The analysis shows that SPP2 provides a better overall description of the data, with the main differences between the two interactions stemming from the matter density adopted for the10B projectile. The optical potentials obtained in this study are expected to serve as a reliable starting point for describing cross sections of other reaction channels for this system within the coupled-channel formalism. 
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    Free, publicly-accessible full text available July 25, 2026