THE HERMENEUTICAL RECEPTION OF THE CHARACTER OF JORGE DE BURGOS IN UMBERTO ECO\u27S NOVEL "THE NAME OF THE ROSE"

U članku se analiziraju modaliteti Ecova intertekstualnog prisvajanja fikcionalne osobe J.L. Borgesa i pojedinih književnih metafora koje se razvijaju u njegovim pripovijetkama u izgradnji hermeneutičke recepcije lika Jorgea iz Burgosa, glavnog negativca romana Ime ruže Umberta Eca. Dok je prvi aspekt dostatno obrađen u kritičkoj literaturi o Imenu ruže, drugi je ostao zanemaren u nekim bitnim aspektima. Analiza ideoloških i hermeneutičkih aspekata njegovog lika u Ecovu romanu otkriva da u izgradnji ne samo njegova etičkog i teološkog habitusa nego i razvitku glavnog narativnog tijeka romana, čiji je on pokretač, veliku ulogu igraju dvostruko kodirane metafore koje Borges razvija u svojim pripovijetkama Teolozi i Tri tumačenja Jude. U članku se analizira njihova uloga u spomenutim Borgesovim novelama i njihov intertekstualni odjek u Imenu ruže koji se pronalazi na idejnoj i kompozicijsko-pripovjednoj razini. Temeljna Borgesova metafora \u27svi su ljudi jedan čovjek\u27 razrađuje se u romanu raznim figurama ponavljanja, a unutar te primarne metafore značajna je metaforika Jude koju Borges razvija u noveli Tri tumačenja Jude. Analiza hermeneutičke recepcije Jorgeova lika otkriva presudnu ulogu te metafore u njenoj iozgradnji.This article analyses the modalities of Umberto Eco\u27s intertextual adoption of J. L. Borges\u27 \u27fictional person\u27 and the specific literary metaphors Borges developed and used in his short stories when building the hermeneutical reception of the character of Jorge de Burgos, the villain of Eco\u27s novel The Name of the Rose. While the critical literature on The Name of the Rose has devoted considerable attention to the former, the latter has remained neglected in some crucial aspects. The analysis of ideological and hermeneutic aspects of his character in Eco\u27s novel revealed that, in creating his ethical and theological habitus and even in the development of the novel\u27s main narrative, a significant role was played by double coded metaphors developed by Borges in his short stories The Theologians and Three Versions of Judas. This article analyses their role in the aforementioned short stories by Borges and their intertextual resonance in The Name of the Rose visible both, on the level of ideas and the compositional-narrative level. The basic Borges\u27 metaphor, "Whatever one man does, it is as if all men did it", was developed in the novel with the help of various figures of repetition. Within that primary metaphor, an important place is held by the metaphorics of Judas developed by Borges in Three Versions of Judas. Analysis of the hermeneutical reception of Jorge\u27s character has revealed the crucial role of that metaphor in its creation

Spinodal twinning of a deformed crystal

<div><p>We propose the possibility of a spinodal mechanism for deformation twinning in addition to the nucleation and growth mechanism assumed in all existing studies of twinning, using the thermodynamic stability analysis of a homogeneously deformed crystal by examining its energy landscape as a function of strain along the twinning direction obtained from first-principles calculations. Twinning occurs continuously owing to thermodynamic instability with respect to twinning at large shear strains, whereas it can only take place through the nucleation and growth mechanism at small shear strains.</p></div

Colossal Room-Temperature Electrocaloric Effect in Ferroelectric Polymer Nanocomposites Using Nanostructured Barium Strontium Titanates

The electrocaloric effect (ECE) refers to conversion of thermal to electrical energy of polarizable materials and could form the basis for the next-generation refrigeration and power technologies that are highly efficient and environmentally friendly. Ferroelectric materials such as ceramic and polymer films exhibit large ECEs, but each of these monolithic materials has its own limitations for practical cooling applications. In this work, nanosized barium strontium titanates with systematically varied morphologies have been prepared to form polymer nanocomposites with the ferroelectric polymer matrix. The solution-processed polymer nanocomposites exhibit an extraordinary room-temperature ECE <i>via</i> the synergistic combination of the high breakdown strength of a ferroelectric polymer matrix and the large change of polarization with temperature of ceramic nanofillers. It is found that a sizable ECE can be generated under both modest and high electric fields, and further enhanced greatly by tailoring the morphology of the ferroelectric nanofillers such as increasing the aspect ratio of the nanoinclusions. The effect of the geometry of the nanofillers on the dielectric permittivity, polarization, breakdown strength, ECE and crystallinity of the ferroelectric polymer has been systematically investigated. Simulations based on the phase-field model have been carried out to substantiate the experimental results. With the remarkable cooling energy density and refrigerant capacity, the polymer nanocomposites are promising for solid-state cooling applications

Nanoscale Origins of Ferroelastic Domain Wall Mobility in Ferroelectric Multilayers

The nanoscale origins of ferroelastic domain wall motion in ferroelectric multilayer thin films that lead to giant electromechanical responses are investigated. We present direct evidence for complex underpinning factors that result in ferroelastic domain wall mobility using a combination of atomic-level aberration corrected scanning transmission electron microscopy and phase-field simulations in model epitaxial (001) tetragonal (T) PbZr_<i>x</i>Ti_1–<i>x</i>O₃ (PZT)/rhombohedral (R) PbZr_<i>x</i>Ti_1–<i>x</i>O₃ (PZT) bilayer heterostructures. The local electric dipole distribution is imaged on an atomic scale for a ferroelastic domain wall that nucleates in the R-layer and cuts through the composition breaking the T/R interface. Our studies reveal a highly complex polarization rotation domain structure that is nearly on the knife-edge at the vicinity of this wall. Induced phases, namely tetragonal-like and rhombohedral-like monoclinic were observed close to the interface, and exotic domain arrangements, such as a half-4-fold closure structure, are observed. Phase field simulations show this is due to the minimization of the excessive elastic and electrostatic energies driven by the enormous strain gradient present at the location of the ferroelastic domain walls. Thus, in response to an applied stimulus, such as an electric field, any polarization reorientation must minimize the elastic and electrostatic discontinuities due to this strain gradient, which would induce a dramatic rearrangement of the domain structure. This insight into the origins of ferroelastic domain wall motion will allow researchers to better “craft” such multilayered ferroelectric systems with precisely tailored domain wall functionality and enhanced sensitivity, which can be exploited for the next generation of integrated piezoelectric technologies

Fast Magnetic Domain-Wall Motion in a Ring-Shaped Nanowire Driven by a Voltage

Magnetic domain-wall motion driven by a voltage dissipates much less heat than by a current, but none of the existing reports have achieved speeds exceeding 100 m/s. Here phase-field and finite-element simulations were combined to study the dynamics of strain-mediated voltage-driven magnetic domain-wall motion in curved nanowires. Using a ring-shaped, rough-edged magnetic nanowire on top of a piezoelectric disk, we demonstrate a fast voltage-driven magnetic domain-wall motion with average velocity up to 550 m/s, which is comparable to current-driven wall velocity. An analytical theory is derived to describe the strain dependence of average magnetic domain-wall velocity. Moreover, one 180° domain-wall cycle around the ring dissipates an ultrasmall amount of heat, as small as 0.2 fJ, approximately 3 orders of magnitude smaller than those in current-driven cases. These findings suggest a new route toward developing high-speed, low-power-dissipation domain-wall spintronics

Nanovoid Formation and Annihilation in Gallium Nanodroplets under Lithiation–Delithiation Cycling

The irreversible chemomechanical degradation is a critical issue in the development of high-capacity electrode materials for the next-generation lithium (Li)-ion batteries. Here we report the self-healing behavior of gallium nanodroplets (GaNDs) under electrochemical cycling at room temperature, observed with <i>in situ</i> transmission electron microscopy (TEM). During lithiation, the GaNDs underwent a liquid-to-solid phase transition, forming a crystalline phase (Li_<i>x</i>Ga) with ∼160% volume expansion. Owing to the uneven Li flow during lithiation, the fully lithiated GaNDs exhibited highly distorted morphologies. Upon delithiation, the reverse phase transition occurred, accompanied with the nucleation and growth of a nanosized void. After the GaNDs were fully delithiated, the nanovoid gradually annihilated. Our analysis, along with phase field modeling and experimental measurements of the void growth and annihilation, provides mechanistic insights into the void formation and annihilation mechanism. The GaNDs may function as an effective healing agent in durable composite electrodes for high-performance Li-ion batteries, wherein active components, such as Si, are susceptible to fracture

Insight into the Mechanism of Thermal Stability of α‑Diimine Nickel Complex in Catalyzing Ethylene Polymerization

The union of experimental and computational methods can accelerate the development of polymerization catalysts for industrial applications. Herein, we report complementary experimental and computational studies of the thermal stability of α-diimine nickel complexes by using thermally stable <b>Cat. 1</b> and a typical Brookhart catalyst (<b>B-Cat</b>) as models. Experimentally, we found that many more nickel atoms could be activated for <b>Cat. 1</b> at elevated temperature during the ethylene polymerization process compared to those for <b>B-Cat</b>. Computationally, first-principle calculations showed that the decomposition energies of <b>Cat. 1</b> were found to be higher than those of <b>B-Cat</b>, contributing to the activation observed for <b>Cat. 1</b>. We found that the presence of ethydene evidently affected the conformation of C1–N1–Ni–N2–C2 five-membered ring (where the nickel center is located) of <b>Cat. 1</b>, turning the envelope conformation (<b>B-Cat</b>) into a half-chair conformation (<b>Cat. 1</b>). According to calculations, the decomposition energy of the latter was 17.4 kJ/mol higher than that of the former. These results provide information to elucidate the mechanism of thermal stability of α-diimine nickel catalyst and significantly advance the development of thermally stable α-diimine nickel catalysts used in industry

Nanovoid Formation and Annihilation in Gallium Nanodroplets under Lithiation–Delithiation Cycling

The irreversible chemomechanical degradation is a critical issue in the development of high-capacity electrode materials for the next-generation lithium (Li)-ion batteries. Here we report the self-healing behavior of gallium nanodroplets (GaNDs) under electrochemical cycling at room temperature, observed with <i>in situ</i> transmission electron microscopy (TEM). During lithiation, the GaNDs underwent a liquid-to-solid phase transition, forming a crystalline phase (Li_<i>x</i>Ga) with ∼160% volume expansion. Owing to the uneven Li flow during lithiation, the fully lithiated GaNDs exhibited highly distorted morphologies. Upon delithiation, the reverse phase transition occurred, accompanied with the nucleation and growth of a nanosized void. After the GaNDs were fully delithiated, the nanovoid gradually annihilated. Our analysis, along with phase field modeling and experimental measurements of the void growth and annihilation, provides mechanistic insights into the void formation and annihilation mechanism. The GaNDs may function as an effective healing agent in durable composite electrodes for high-performance Li-ion batteries, wherein active components, such as Si, are susceptible to fracture