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Publications (7 of 7) Show all publications
Belotcerkovtceva, D., Datt, G., Nameirakpam, H., Aitkulova, A., Suntornwipat, N., Majdi, S., . . . Kamalakar, M. V. (2025). Extreme Current Density and Breakdown Mechanism in Graphene on Diamond Substrate. Carbon, 237, Article ID 120108.
Open this publication in new window or tab >>Extreme Current Density and Breakdown Mechanism in Graphene on Diamond Substrate
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2025 (English)In: Carbon, ISSN 0008-6223, E-ISSN 1873-3891, Vol. 237, article id 120108Article in journal (Refereed) Published
Abstract [en]

The high current-carrying capacity of graphene is essential for its use as an interconnect in electronic and spintronic circuits. At the same time, knowing the breakdown limits and mechanism under high fields can enable new device design strategies. In this work, we push the current carrying capacity of the scalable form of chemical vapor deposited (CVD) graphene employing a high-thermal conducting single crystalline diamond substrate. Our experiments on CVD graphene reveal extremely high current densities > 109 A/cm2 in graphene on the diamond with both ohmic (low-resistive) and tunneling tunnel (high-resistive) contacts. Measurements on ferromagnetic (TiOx/Co) and metallic (Ti/Au) contacts demonstrate current densities of ∼1.16×109 A/cm2 and ∼1.7×109 A/cm2, respectively. The tunnel (high-resistive) contacts exhibit a shunting of graphene under high currents via the bottom graphitized diamond, resulting in dielectric breakdown and via alternative conducting paths. Electrical measurements show a distinct threshold for conducting paths of graphitized diamond, in tune accordance with Middleton-Wingreen's theory. Our results of high current densities achieved in CVD graphene, with distinct dependence on ohmic and tunneling, contact resistance, and the observed breakdown mechanism, provide new insights for enabling high-current all carbon circuits.

Place, publisher, year, edition, pages
Elsevier, 2025
Keywords
CVD Graphene, diamond, high current carrying capacity, fractal pattern
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-550657 (URN)10.1016/j.carbon.2025.120108 (DOI)001460969300001 ()2-s2.0-85218100128 (Scopus ID)
Funder
EU, European Research Council, 101002772Olle Engkvists stiftelse, 200–0602Swedish Energy Agency, 48698-1Swedish Energy Agency, 48591-1Swedish Research Council, 2021-05932Swedish Research Council, 22-04186-5Swedish Research Council Formas, 2019-01326Swedish Research Council Formas, 2023-01607Knut and Alice Wallenberg Foundation, 2022.0079
Available from: 2025-02-17 Created: 2025-02-17 Last updated: 2025-11-20Bibliographically approved
Kumar, C., Sharma, R., Pal, S., Datt, G., Sarkar, T., Kamalakar, M. V. & Barman, A. (2024). Additive interfacial Dzyaloshinskii-Moriya interaction in the monolayer-MoS2/Co/Pt asymmetric trilayer system. Physical Review Applied, 22(6), Article ID 064088.
Open this publication in new window or tab >>Additive interfacial Dzyaloshinskii-Moriya interaction in the monolayer-MoS2/Co/Pt asymmetric trilayer system
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2024 (English)In: Physical Review Applied, E-ISSN 2331-7019, Vol. 22, no 6, article id 064088Article in journal (Refereed) Published
Abstract [en]

The observation of a substantial interfacial Dzyaloshinskii-Moriya interaction (IDMI) in twodimensional (2D) transition-metal dichalcogenide (TMD)/ferromagnet (FM) interfaces has opened up the possibility of exploring chiral spin textures and spin dynamics in such systems. This makes the exploration of the additive IDMI in the 2D-TMD/FM/heavy-metal trilayer system an intriguing problem. Here, using the Brillouin light-scattering technique, we have demonstrated the significant contribution of the monolayer-MoS2/Co interface to enhancing the IDMI strength of a widely investigated Co/Pt interface by introducing an additive IDMI when combined to form the MoS2/Co/Pt trilayer stack. Additionally, the FM-layer-thickness-dependent study serves the dual purpose of conducting a comparative analysis of the IDMI strength between Co(t)/Pt(4) and MoS2/Co(t)/Pt(4) systems (where t= 2, 4, and 8 nm), as well as confirming the pure interfacial origin of the DMI in these systems. Our study opens up the promising possibility of using hybrid multilayers to stabilize chiral spin textures, offering potential applications in future spintronic devices.

Place, publisher, year, edition, pages
American Physical Society, 2024
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-547576 (URN)10.1103/PhysRevApplied.22.064088 (DOI)001390386400001 ()
Funder
EU, European Research Council, 101002772Swedish Research Council, 2021-05932Swedish Research Council Formas, 2019-01326Swedish Research Council Formas, 2023-01607Knut and Alice Wallenberg Foundation, 2022.0079Swedish Research Council, 2021-03675
Available from: 2025-01-24 Created: 2025-01-24 Last updated: 2025-01-24Bibliographically approved
Belotcerkovtceva, D., Nameirakpam, H., Datt, G., Noumbe, U. & Kamalakar, M. V. (2024). High current treated-passivated graphene (CTPG) towards stable nanoelectronic and spintronic circuits. Nanoscale Horizons, 9(3), 456-464
Open this publication in new window or tab >>High current treated-passivated graphene (CTPG) towards stable nanoelectronic and spintronic circuits
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2024 (English)In: Nanoscale Horizons, ISSN 2055-6764, E-ISSN 2055-6756, Vol. 9, no 3, p. 456-464Article in journal (Refereed) Published
Abstract [en]

Achieving enhanced and stable electrical quality of scalable graphene is crucial for practical graphene device applications. Accordingly, encapsulation has emerged as an approach for improving electrical transport in graphene. In this study, we demonstrate high-current treatment of graphene passivated by AlOx nanofilms as a new means to enhance the electrical quality of graphene for its scalable utilization. Our experiments and electrical measurements on large-scale chemical vapor-deposited (CVD) graphene devices reveal that high-current treatment causes persistent and irreversible de-trapping density in both bare graphene and graphene covered by AlOx. Strikingly, despite possible interfacial defects in graphene covered with AlOx, the high-current treatment enhances its carrier mobility by up to 200% in contrast to bare graphene samples, where mobility decreases. Spatially resolved Raman spectroscopy mapping confirms that surface passivation by AlOx, followed by the current treatment, reduces the number of sp3 defects in graphene. These results suggest that for current treated-passivated graphene (CTPG), the high-current treatment considerably reduces charged impurity and trapped charge densities, thereby reducing Coulomb scattering while mitigating any electromigration of carbon atoms. Our study unveils CTPG as an innovative system for practical utilization in graphene nanoelectronic and spintronic integrated circuits.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2024
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-526688 (URN)10.1039/d3nh00338h (DOI)001140998600001 ()2-s2.0-85182721062 (Scopus ID)
Funder
Swedish Research Council, 2021-05932Swedish Energy Agency, 48698–1Swedish Research Council Formas, 2019–01326Olle Engkvists stiftelse, 200–0602EU, European Research Council, Project SPINNER
Available from: 2024-04-15 Created: 2024-04-15 Last updated: 2025-02-18Bibliographically approved
Schulz, N., Chanda, A., Datt, G., Ong, C. S., Sorgenfrei, F., Ambardar, S., . . . Srikanth, H. (2023). Surface Termination-Enhanced Magnetism at Nickel Ferrite/2D Nanomaterial Interfaces: Implications for Spintronics. ACS Applied Nano Materials, 6(12), 10402-10412
Open this publication in new window or tab >>Surface Termination-Enhanced Magnetism at Nickel Ferrite/2D Nanomaterial Interfaces: Implications for Spintronics
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2023 (English)In: ACS Applied Nano Materials, E-ISSN 2574-0970, Vol. 6, no 12, p. 10402-10412Article in journal (Refereed) Published
Abstract [en]

Engineering of interfacial magnetic properties provides an extra edge in designing heterostructures with desired properties for spintronics and spincaloritronics, without drastically changing the structure of the neighboring nonmagnetic material. Here, we report on the surface termination-enhanced magnetic properties of the ferrimagnetic insulator (FMI) nickel ferrite (NFO) with the inclusion of graphene (Gr) and monolayer hexagonal boron nitride (hBN). Depth-dependent X-ray photoelectron spectroscopy (XPS) measurements reveal the presence of a layer of adsorbed oxygen at the NFO/Gr and NFO/hBN interfaces. Magnetometry and transverse susceptibility measurements indicate that the inclusion of monolayer Gr increases the saturation magnetization (Ms) by 40% and decreases the effective magnetic anisotropy by 50% across 5 K ≤ T ≤ 300 K. A similar but less pronounced effect is observed for the inclusion of hBN. Density functional theory calculations further indicate that the increase in MS due to the inclusion of Gr or hBN arises on oxygen-terminated NFO, as observed in XPS measurements. These results present ways for engineering strong interfacial magnetic effects in FMI/2D nanomaterial systems, controlling magnetism by surface termination, and developing advanced spinterfaces for applications in spincaloritronics and spin insulatronics.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2023
Keywords
magnetism, interfaces, 2D materials, spintronics, ferrimagnets, graphene, hexagonalboron nitride
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-522444 (URN)10.1021/acsanm.3c01352 (DOI)001010225000001 ()
Funder
EU, European Research Council, 854843Knut and Alice Wallenberg FoundationSwedish Energy AgencySwedish Research Council, 2021-03675EU, European Research Council, 101002772-SPINNERStandUpeSSENCE - An eScience CollaborationSwedish National Infrastructure for Computing (SNIC)
Available from: 2024-02-08 Created: 2024-02-08 Last updated: 2024-02-08Bibliographically approved
Muscas, G., Prabahar, K., Congiu, F., Datt, G. & Sarkar, T. (2022). Nanostructure-driven complex magnetic behavior of Sm2CoMnO6 double perovskite. Journal of Alloys and Compounds, 906, Article ID 164385.
Open this publication in new window or tab >>Nanostructure-driven complex magnetic behavior of Sm2CoMnO6 double perovskite
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2022 (English)In: Journal of Alloys and Compounds, ISSN 0925-8388, E-ISSN 1873-4669, Vol. 906, article id 164385Article in journal (Refereed) Published
Abstract [en]

Magnetic double perovskite oxides have steadily emerged as an important class of functional materials. A clear understanding of the complex interactions that govern the magnetic behavior, and thereby, the functionality in these mixed valence compounds, however, remains elusive. In this study, we show that the complex nanostructure that forms in these compounds is at the root of their magnetic behavior. Using complementary experimental and micromagnetic simulation results, we have uncovered the complex nanostructure of polycrystalline Sm2CoMnO6, a typical double perovskite oxide, and established how the nanostructure drives its magnetic behavior. Our results show that Sm2CoMnO6 exhibits a Griffiths phase with the formation of ferromagnetic clusters above the ordering temperature. The isothermal magnetization curves show no sign of saturation, even at the highest measured field (9 T), and irreversibility in the entire magnetic field range. Despite a very clear indication of the presence of antiferromagnetic antisite defects, surprisingly, no antisite defect-induced exchange bias occurs. This is explained from the micro magnetic simulations that confirm the presence of ferromagnetic nanoclusters and nanosized, random, and uncorrelated antisite defects, resulting in no exchange bias. This work provides a clear understanding of the role of antisite defects, in particular, on how their structure can lead to the presence/absence of exchange bias. The fundamental insight offered in this work fills an important knowledge gap in the field and will be of immense value in realizing the true potential of double perovskite oxides for future technological applications. (C)& nbsp;2022 The Author(s). Published by Elsevier B.V.

Place, publisher, year, edition, pages
ElsevierElsevier BV, 2022
Keywords
Magnetic materials, Strongly correlated systems, Structure-property correlations, Nanostructured functional materials, Magnetic measurements
National Category
Other Materials Engineering Metallurgy and Metallic Materials
Identifiers
urn:nbn:se:uu:diva-473768 (URN)10.1016/j.jallcom.2022.164385 (DOI)000779670300004 ()
Funder
Swedish Research Council, 200-0559Swedish Research Council, 2017-05030Swedish Research Council, 2021-03675
Available from: 2022-05-04 Created: 2022-05-04 Last updated: 2024-01-15Bibliographically approved
Schulz, N., Chanda, A., Datt, G., Kamalakar, M. V., Sarkar, T., Phan, M. H. & Srikanth, H. (2022). Proximity enhanced magnetism at NiFe2O4/Graphene interface. Paper presented at 15th Joint MMM-INTERMAG Conference, JAN 10-14, 2022, New Orleans, LA. AIP Advances, 12(3), Article ID 035132.
Open this publication in new window or tab >>Proximity enhanced magnetism at NiFe2O4/Graphene interface
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2022 (English)In: AIP Advances, E-ISSN 2158-3226, Vol. 12, no 3, article id 035132Article in journal (Refereed) Published
Abstract [en]

Here, we explore the change in effective magnetic anisotropy of the ferrimagnetic (FM) insulator nickel ferrite (NFO) thin film due to the inclusion of monolayer graphene (MLG) grown on top of the NFO layer. This was done by performing radio frequency (RF) transverse susceptibility (TS) measurements on bare NFO and NFO/MLG bilayer samples for both in-plane (IP) and out-of-plane (OOP) configurations utilizing a tunnel diode oscillator technique. Our magnetometry measurements indicated an enhancement in the overall saturation magnetization of the NFO/MLG bilayer with respect to the bare NFO film. The TS measurements reveal that the inclusion of MLG reduces the effective magnetic anisotropy for both IP and OOP configurations drastically, by up to a factor of 2 over the temperature range 40 K <= T <= 280 K. Since NFO is a magnetic substrate, it is possible that NFO could induce magnetic ordering in MLG at the NFO/MLG interface via the magnetic proximity effect. Furthermore, since NFO is insulating and MLG is a semimetal, there likely exists a large conductivity difference at the interface, making charge transfer plausible. These two effects could modify the interfacial magnetism leading to a change in the effective magnetic anisotropy. These results highlight the importance of understanding the interfacial magnetism of FM/MLG heterostructures.

Place, publisher, year, edition, pages
American Institute of Physics (AIP)AIP Publishing, 2022
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-474329 (URN)10.1063/9.0000271 (DOI)000784325300017 ()
Conference
15th Joint MMM-INTERMAG Conference, JAN 10-14, 2022, New Orleans, LA
Funder
EU, European Research Council, 101002772Swedish Research Council, 2017-05030Swedish Research Council, 2021-03675Swedish Research Council, 2016-03278Swedish Research Council Formas, 2019-01326Carl Tryggers foundation , CTS 18:340
Available from: 2022-05-18 Created: 2022-05-18 Last updated: 2024-01-15Bibliographically approved
Datt, G., Kotnana, G., Maddu, R., Vallin, Ö., Joshi, D. C., Peddis, D., . . . Sarkar, T. (2021). Combined Bottom-Up and Top-Down Approach for Highly Ordered One-Dimensional Composite Nanostructures for Spin Insulatronics. ACS Applied Materials and Interfaces, 13(31), 37490-37499
Open this publication in new window or tab >>Combined Bottom-Up and Top-Down Approach for Highly Ordered One-Dimensional Composite Nanostructures for Spin Insulatronics
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2021 (English)In: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 13, no 31, p. 37490-37499Article in journal (Refereed) Published
Abstract [en]

Engineering magnetic proximity effects-based devices requires developing efficient magnetic insulators. In particular, insulators, where magnetic phases show dramatic changes in texture on the nanometric level, could allow us to tune the proximity-induced exchange splitting at such distances. In this paper, we report the fabrication and characterization of highly ordered two-dimensional arrays of LaFeO3 (LFO)-CoFe2O4 (CFO) biphasic magnetic nanowires, grown on silicon substrates using a unique combination of bottom-up and top-down synthesis approaches. The regularity of the patterns was confirmed using atomic force microscopy and scanning electron microscopy techniques, whereas magnetic force microscopy images established the magnetic homogeneity of the patterned nanowires and absence of any magnetic debris between the wires. Transmission electron microscopy shows a close spatial correlation between the LFO and CFO phases, indicating strong grain-to-grain interfacial coupling, intrinsically different from the usual core-shell structures. Magnetic hysteresis loops reveal the ferrimagnetic nature of the composites up to room temperature and the presence of a strong magnetic coupling between the two phases, and electrical transport measurements demonstrate the strong insulating behavior of the LFO-CFO composite, which is found to be governed by Mottvariable range hopping conduction mechanisms. A shift in the Raman modes in the composite sample compared to those of pure CFO suggests the existence of strain-mediated elastic coupling between the two phases in the composite sample. Our work offers ordered composite nanowires with strong interfacial coupling between the two phases that can be directly integrated for developing multiphase spin insulatronic devices and emergent magnetic interfaces.

Place, publisher, year, edition, pages
American Chemical Society (ACS)American Chemical Society (ACS), 2021
Keywords
one-dimensional nanostructures, bimagnetic nanocomposites, spin insulatronics, oxide electronics, strain coupling
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-453481 (URN)10.1021/acsami.1c09582 (DOI)000685245800081 ()34325507 (PubMedID)
Funder
Swedish Research Council, 188-0179Swedish Research Council, 184-546Wenner-Gren Foundations, UPD2018-0003Wenner-Gren Foundations, UPD2019-0166Swedish Research Council, 2017-05030Swedish Research Council, 2016-03278
Available from: 2021-09-22 Created: 2021-09-22 Last updated: 2024-01-15Bibliographically approved
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0001-8463-9431

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