SearcharxivSearch

arXiv subjects

G. Mohan Muralikrishna

Publications and source records attributed to G. Mohan Muralikrishna.

2 recordsLinked to original sources

Impact of interstitial carbon on local lattice distortions in CoCrFeMnNi high-entropy alloys

Here, we explore component-dependent local lattice distortions in polycrystalline, equiatomic, face-centered cubic CrMnFeCoNi high-entropy alloys and their modifications induced by dilute interstitial carbon. Multi-edge extended X-ray absorption fine structure spectroscopy combined with reverse Monte Carlo analysis reveals that the Cr component experiences the most substantial local distortions, independent of the temperature of prolonged annealing treatments (993 K or 1373 K) and the nominal carbon content (0 to 0.8 at.%). The static disorder around Cr atoms was found to increase markedly and monotonically upon carbon alloying, whereas Mn, Fe, Co, and Ni demonstrate weaker and non-monotonic tendencies. The carbon-induced lattice distortions extend over several coordination shells, indicating the pronounced effect of the carbon presence on the local environment around Cr absorbers. First-principles density functional theory and finite-temperature molecular dynamics simulations confirm the greater impact of carbon on the local lattice distortions around Cr than around the other $3d$ constituent elements, based on the previous finding that carbon preferentially occupies Cr-rich interstitial sites. These results provide decisive hints towards the atomistic origin of the non-monotonic diffusion behavior previously reported for carbon-doped CrMnFeCoNi alloys, and are noticeable for understanding the carbon-induced phase transitions in compositionally complex systems.

cond-mat.mtrl-sci

Interface-Driven Thermo-Electric Switching Performance of VO$^+$ Diffused Soda-Lime Glass

Strongly confined NaVO$^+$ segregation and its thermo-responsive functionality at the interface between simple sputter-deposited amorphous vanadium oxide thin films and soda-lime glass was substantiated in the present study by in-situ temperature-controlled Time of Flight Secondary Ion Mass Spectrometry (ToF-SIMS). The obtained ToF-SIMS depth profiles provided unambiguous evidence for a reversible transformation that caused systematic switching of the NaVO$^+$/ Na$^+$ and Na$^+$/ VO$^+$ intensities upon cycling the temperature between 25 $^\circ$C and 340 $^\circ$C. Subsequently, NaVO complexes were found to be reversibly formed (at 300 $^\circ$C) in vanadium oxide diffused glass, leading to thermo-responsive electrical behaviour of the thin film glass system. This new segregation -- and diffusion-dependent multifunctionality of NaVO$^+$ -- points towards applications as an advanced material for thermo-optical switches, in smart windows or in thermal sensors.

physics.app-ph