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Publications (10 of 14) Show all publications
Wani, I. H., Jafri, S. H., Wärnå, J., Hayat, A., Li, H., Shukla, V. A., . . . Leifer, K. (2019). A sub 20 nm metal-conjugated molecule junction acting as a nitrogen dioxide sensor. Nanoscale, 11(14), 6571-6575
Open this publication in new window or tab >>A sub 20 nm metal-conjugated molecule junction acting as a nitrogen dioxide sensor
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2019 (English)In: Nanoscale, ISSN 2040-3364, E-ISSN 2040-3372, Vol. 11, no 14, p. 6571-6575Article in journal (Refereed) Published
Abstract [en]

The interaction of a gas molecule with a sensing material causes the highest change in the electronic structure of the latter, when this material consists of only a few atoms. If the sensing material consists of a short, conductive molecule, the sensing action can be furthermore probed by connecting such molecules to nanoelectrodes. Here, we report that NO2 molecules that adhere to 4,4'-biphenyldithiol (BPDT) bound to Au surfaces lead to a change of the electrical transmission of the BPDT. The related device shows reproducible, stable measurements and is so far the smallest (<20 nm) gas sensor. It demonstrates modulation of charge transport through molecules upon exposure to nitrogen dioxide down to concentrations of 55 ppb. We have evaluated several devices and exposure conditions and obtained a close to linear dependence of the sensor response on the gas concentration.

National Category
Nano Technology
Identifiers
urn:nbn:se:uu:diva-381056 (URN)10.1039/c8nr08417c (DOI)000464454400007 ()30916070 (PubMedID)
Funder
Swedish Research CouncilKnut and Alice Wallenberg FoundationGöran Gustafsson Foundation for Research in Natural Sciences and MedicineCarl Tryggers foundation Swedish Energy AgencySwedish Foundation for Strategic Research
Available from: 2019-04-03 Created: 2019-04-03 Last updated: 2019-05-03Bibliographically approved
Shukla, V. (2019). Computational Studies of 2D Materials: Application to Energy Storage and Electron Transport in Nanoscale Devices. (Doctoral dissertation). Uppsala: Acta Universitatis Upsaliensis
Open this publication in new window or tab >>Computational Studies of 2D Materials: Application to Energy Storage and Electron Transport in Nanoscale Devices
2019 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The field of two-dimensional (2D) layered materials provides a new platform for studying diverse physical phenomena that are scientifically interesting and relevant for technological applications. Novel applications in electronics and energy storage harness the unique electronic, optical, and mechanical properties of 2D materials for design of crucial components. Atomically thin, with large surface to volume ratio, these materials are attractive for broad applications for hydrogen storage, sensing, batteries and photo-catalysis. Theoretical predictions from atomically resolved computational simulations of 2D materials play a pivotal role in designing and advancing these developments.

The central topic of this thesis is 2D materials studied using density functional theory and non-equilibrium Green’s function. The electronic structure and transport properties are discussed for several synthesized and predicted 2D materials, with diverse potential applications in nanoscale electronic devices, gas sensing, and electrodes for rechargeable batteries. Lateral and vertical heterostructures have been studied for applications in nanoscale devices such as graphene/hBN heterostructure nanogap for a potential DNA sequencing device, while in case of twisted bilayer black phosphorus nanojunction, where electronic and transport properties have been explored for diode-like characteristics device. We also have addressed the structural, electronic and transport properties of the recently synthesized polymorphs of 2D borons known as borophenes. We have explored the conventional methods of tuning the material’s properties such as strain in borophene and substitutional doping in black phosphorus with the further investigation of their gas sensing application.

A significant portion of this thesis is also dedicated to the energy storage applications of different 2D materials. Energy storage technologies arise with vital importance in providing effective ways to transport and commercialize the produced energy, aiming at rechargeable batteries with high energy and power density. In this context, first-principles simulations have been applied together with other theoretical tools to evaluate structural properties, ion intercalation kinetics, specific capacity and open circuit voltage of selected 2D materials at the atomic level. The simulation study supports the understanding while improving the properties of the materials to increase their efficiency in battery operation.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2019. p. 101
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1761
Keywords
Density functional theory, Non-equilibrium Green's function, 2D materials, Energy storage, Electron transport
National Category
Condensed Matter Physics Atom and Molecular Physics and Optics
Identifiers
urn:nbn:se:uu:diva-369471 (URN)978-91-513-0547-9 (ISBN)
Public defence
2019-03-01, 80101, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 13:00 (English)
Opponent
Supervisors
Available from: 2019-01-29 Created: 2019-01-05 Last updated: 2019-02-18
Shukla, V., Jena, N. K., Naqvi, S. R., Luo, W. & Ahuja, R. (2019). Modeling High-performing Batteries with Mxenes: The case of S-functionalized two- Dimensional Nitride Mxene Electrode. Nano Energy, 58, 877-885
Open this publication in new window or tab >>Modeling High-performing Batteries with Mxenes: The case of S-functionalized two- Dimensional Nitride Mxene Electrode
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2019 (English)In: Nano Energy, ISSN 2211-2855, E-ISSN 2211-3282, Vol. 58, p. 877-885Article in journal (Refereed) Published
Abstract [en]

Recent upsurge in the two-dimensional (2D) materials have established their larger role on energy storage applications. To this end, Mxene represent a new paradigm extending beyond the realm of oft-explored elemental 2D materials beginning with graphene. Here in, we employed first principles modelling based on density functional theory to investigate the role of S-functionalized Nitride Mxenes as anodes for Li/Na ion batteries. To be specific, V2NS2 and Ti2NS2 have been explored with a focus on computing meaningful descriptors to quantify these 2D materials to be optimally performing electrodes. The Li/Na ion adsorption energies are found to be high (> -2 eV) on both the surfaces and associated with significant charge transfer. Interestingly, this ion intercalation can reach up to multilayers which essentially affords higher specific capacity for the substrate. Particularly, these two 2D materials (V2NS2 and Ti2NS2) have been found to be more suitable for Li-ion batteries with estimated theoretical capacities of 299.52 mAh g(-1) and 308.28 mAh g(-1) respectively. We have also probed the diffusion barriers of ion migration on these two surfaces and these are found to be ultrafast in nature. All these unique features qualify these Mxenes to be potential anode materials for rechargeable batteries and likely to draw imminent attention.

National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-372108 (URN)10.1016/j.nanoen.2019.02.007 (DOI)000461433600100 ()
Funder
Swedish National Infrastructure for Computing (SNIC)Swedish Research Council
Available from: 2019-01-05 Created: 2019-01-05 Last updated: 2019-04-04Bibliographically approved
Prasongkit, J., Shukla, V., Grigoriev, A., Ahuja, R. & Amornkitbamrung, V. (2019). Ultrahigh-sensitive gas sensors based on doped phosphorene: A First-principles investigation. Applied Surface Science, 497, Article ID UNSP 143660.
Open this publication in new window or tab >>Ultrahigh-sensitive gas sensors based on doped phosphorene: A First-principles investigation
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2019 (English)In: Applied Surface Science, ISSN 0169-4332, E-ISSN 1873-5584, Vol. 497, article id UNSP 143660Article in journal (Other academic) Published
Abstract [en]

Recent significant advancements have been made in demonstrating the usage of phosphorene to detect the presence of gases leading to a new breed of gas sensor device. Based on pristine phosphorene, the devices can detect a small concentration of adsorbed molecules with high sensitivity at room temperature. In this work, we propose doping silicon and sulfur impurity atoms into phosphorene to drastically improve its gas sensing performance. We use a combination of density functional theory and non-equilibrium Green's function method to evaluate the sensitivity and selectivity of doped phosphorene nanosensors for four gases (NO, NO2, NH3, and CO). Both devices demonstrate a prominent distinction in conductance when the gas molecules are exposed to the sensor surface. We suggest the doped phosphorene may present advantages over the device based purely on phosphorene due to the ability to discriminate different gases controlled by types of dopants.

National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-372109 (URN)10.1016/j.apsusc.2019.143660 (DOI)000487849800050 ()
Available from: 2019-01-05 Created: 2019-01-05 Last updated: 2019-10-25Bibliographically approved
Shukla, V., Araujo, R. B., Jena, N. K. & Ahuja, R. (2018). Borophene's tryst with stability: exploring 2D hydrogen boride as an electrode for rechargeable batteries. Physical Chemistry, Chemical Physics - PCCP, 20(34), 22008-22016
Open this publication in new window or tab >>Borophene's tryst with stability: exploring 2D hydrogen boride as an electrode for rechargeable batteries
2018 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 20, no 34, p. 22008-22016Article in journal (Refereed) Published
Abstract [en]

Graphene's emergence can be viewed as a positive upheaval in 2D materials research. Along the same line, the realization of a related elemental 2D material, borophene, is another breakthrough. To circumvent the stability issues of borophene, which is reported to have been synthesized on metallic substrates under extreme conditions, hydrogenation of borophene (otherwise called as borophane or hydrogen boride or boron hydride) has been a plausible solution, but only proposed computationally. A recent report (H. Nishino, T. Fujita, N. T. Cuong, S. Tominaka, M. Miyauchi, S. Iimura, A. Hirata, N. Umezawa, S. Okada, E. Nishibori, A. Fujino, T. Fujimori, S. Ito, J. Nakamura, H. Hosono and T. Kondo, J. Am. Chem. Soc., 2017, 139(39), 13761-13769) brings to fore its experimental realization. Our current study delves into the possibilities of employing this intriguing 2D hydrogen boride as anodes in Li/Na ion batteries. Using first-principles density functional theory methods, we computed relevant properties such as the ion (Li/Na) adsorption behavior, the possible pathways of ionic diffusion with the estimation of barriers as well as the theoretical specific capacities and average voltages to uniquely demonstrate that this material is of particular significance for battery applications. It is noted that the use of hydrogen boride leads to a high specific capacity of 861.78 mA h g(-1) for Li ions, which is remarkably higher than the value reported in relation to its computationally predicted structure. Furthermore, Na ion intercalation leads to negative voltage profiles, implying the unsuitability of 2D hydrogen boride for this particular ion. Our findings are timely and pertinent towards adding insightful details relevant to the progress of applications of 2D materials for energy storage.

Place, publisher, year, edition, pages
ROYAL SOC CHEMISTRY, 2018
National Category
Materials Chemistry
Identifiers
urn:nbn:se:uu:diva-369513 (URN)10.1039/c8cp03686a (DOI)000449394100021 ()30109880 (PubMedID)
Funder
Swedish Research CouncilCarl Tryggers foundation StandUp
Available from: 2018-12-17 Created: 2018-12-17 Last updated: 2019-01-05Bibliographically approved
Shukla, V., Grigoriev, A., Jena, N. K. & Ahuja, R. (2018). Strain controlled electronic and transport anisotropies in two-dimensional borophene sheets. Physical Chemistry, Chemical Physics - PCCP, 20(35), 22952-22960
Open this publication in new window or tab >>Strain controlled electronic and transport anisotropies in two-dimensional borophene sheets
2018 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 20, no 35, p. 22952-22960Article in journal (Refereed) Published
Abstract [en]

Two recent reports on realization of an elemental 2D analogue of graphene:borophene (Science, 2015, 350, 1513-1516; Nat. Chem., 2016, 8, 563-568) focus on the inherent anisotropy and directional dependence of the electronic properties of borophene polymorphs. Achieving stable 2D borophene structures may lead to some degree of strain in the system because of the substrate-lattice mismatch. We use first principles density functional theory (DFT) calculations to study the structural, electronic and transport properties of (12) and -borophene polymorphs. We verified the directional dependency and found the tunable anisotropic behavior of the transport properties in these two polymorphs. We find that strain as low as 6% brings remarkable changes in the properties of these two structures. We further investigate current-voltage (I-V) characteristics in the low bias regime after applying a strain to see how the anisotropy of the current is affected. Such observations like the sizeable tuning of transport and I-V characteristics at the expense of minimal strain suggest the suitability of 2D borophene for futuristic device applications.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2018
National Category
Materials Chemistry
Identifiers
urn:nbn:se:uu:diva-363428 (URN)10.1039/c8cp03815e (DOI)000445220500055 ()30156222 (PubMedID)
Funder
Swedish Research CouncilSwedish National Infrastructure for Computing (SNIC), SNIC2017-11-28 SNIC2017-5-8 SNIC2017-1-237
Available from: 2018-10-18 Created: 2018-10-18 Last updated: 2019-01-05Bibliographically approved
Jena, N. K., Araujo, R. B., Shukla, V. & Ahuja, R. (2017). Borophane as a Benchmate of Graphene: A Potential 2D Material for Anode of Li and Na-Ion Batteries. ACS Applied Materials and Interfaces, 9(19), 16148-16158
Open this publication in new window or tab >>Borophane as a Benchmate of Graphene: A Potential 2D Material for Anode of Li and Na-Ion Batteries
2017 (English)In: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 9, no 19, p. 16148-16158Article in journal (Refereed) Published
Abstract [en]

Borophene, single atomic-layer sheet of boron (Science 2015, 350, 1513), is a rather new entrant into the burgeoning class of 2D materials. Borophene exhibits anisotropic metallic properties whereas its hydrogenated counterpart borophane is reported to be a gapless Dirac material lying on the same bench with the celebrated graphene. Interestingly, this transition of borophane also rendered stability to it considering the fact that borophene was synthesized under ultrahigh vacuum conditions on a metallic (Ag) substrate. On the basis of first-principles density functional theory computations, we have investigated the possibilities of borophane as a potential Li/Na-ion battery anode material. We obtained a binding energy of -2.58 (-1.08 eV) eV for Li (Na)-adatom on borophane and Bader charge analysis revealed that Li(Na) atom exists in Li+(Na+) state. Further, on binding with Li/Na, borophane exhibited metallic properties as evidenced by the electronic band structure. We found that diffusion pathways for Li/Na on the borophane surface are anisotropic with x direction being the favorable one with a barrier of 0.27 and 0.09 eV, respectively. While assessing the Li-ion anode performance, we estimated that the maximum Li content is Li0.445B2H2, which gives rises to a material with a maximum theoretical specific capacity of 504 mAh/g together with an average voltage of 0.43 V versus Li/Li+. Likewise, for Na-ion the maximum theoretical capacity and average voltage were estimated to be 504 mAh/g and 0.03 V versus Na/Na+, respectively. These findings unambiguously suggest that borophane can be a potential addition to the map of Li and Na-ion anode materials and can rival some of the recently reported 2D materials including graphene.

Place, publisher, year, edition, pages
AMER CHEMICAL SOC, 2017
Keywords
borophene, borophane, Dirac material, Li-ion battery, Na-ion battery, Li/Na-diffusion
National Category
Materials Chemistry
Identifiers
urn:nbn:se:uu:diva-327151 (URN)10.1021/acsami.7b01421 (DOI)000401782500026 ()28443653 (PubMedID)
Funder
Swedish Research CouncilStandUpCarl Tryggers foundation
Available from: 2017-08-25 Created: 2017-08-25 Last updated: 2019-01-05Bibliographically approved
Gond, R., Meena, S. S., Yusuf, S. M., Shukla, V., Jena, N. K., Ahuja, R., . . . Barpanda, P. (2017). Enabling the Electrochemical Activity in Sodium Iron Metaphosphate [NaFe(PO3)(3)] Sodium Battery Insertion Material: Structural and Electrochemical Insights. Inorganic Chemistry, 56(10), 5918-5929
Open this publication in new window or tab >>Enabling the Electrochemical Activity in Sodium Iron Metaphosphate [NaFe(PO3)(3)] Sodium Battery Insertion Material: Structural and Electrochemical Insights
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2017 (English)In: Inorganic Chemistry, ISSN 0020-1669, E-ISSN 1520-510X, Vol. 56, no 10, p. 5918-5929Article in journal (Refereed) Published
Abstract [en]

Sodium-ion batteries are widely pursued as an economic alternative to lithium-ion battery technology, where Fe- and Mn-based compounds are particularly attractive owing to their elemental abundance. Pursuing phosphate-based polyanionic chemistry, recently solid-state prepared NaFe(PO3)(3) metaphosphate was unveiled as a novel potential sodium insertion material, although it was found to be electrochemically inactive. In the current work, employing energy-savvy solution combustion synthesis, NaFe2+(PO3)(3) was produced from low-cost Fe3+ precursors. Owing to the formation of nanoscale carbon-coated product, electrochemical activity was enabled in NaFe(PO3)(3) for the first time. In congruence with the first principles density functional theory (DFT) calculations, an Fe3+/Fe2+ redox activity centered at 2.8 V (vs Na/Na+) was observed. Further, the solid-solution metaphosphate family Na(Fe1-xMnx)(PO3)(3) (x = 0-1) was prepared for the first time. Their structure and distribution of transition metals (TM = Fe/Mn) was analyzed with synchrotron diffraction, X-ray photoelectron spectroscopy, and Mossbauer spectroscopy. Synergizing experimental and computational tools, NaFe(PO3)(3) metaphosphate is presented as an electrochemically active sodium insertion host material.

Place, publisher, year, edition, pages
AMER CHEMICAL SOC, 2017
National Category
Inorganic Chemistry
Identifiers
urn:nbn:se:uu:diva-327152 (URN)10.1021/acs.inorgchem.7b00561 (DOI)000401593800049 ()28462996 (PubMedID)
Funder
Carl Tryggers foundation Swedish Research CouncilSwedish Energy Agency
Available from: 2017-08-25 Created: 2017-08-25 Last updated: 2017-08-25Bibliographically approved
Shukla, V., Jena, N. K., Grigoriev, A. & Ahuja, R. (2017). Prospects of Graphene-hBN Heterostructure Nanogap for DNA Sequencing. ACS Applied Materials and Interfaces, 9(46), 39945-39952
Open this publication in new window or tab >>Prospects of Graphene-hBN Heterostructure Nanogap for DNA Sequencing
2017 (English)In: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 9, no 46, p. 39945-39952Article in journal (Refereed) Published
Abstract [en]

Recent advances in solid-state nano-device-based DNA sequencing are at the helm of the development of a new paradigm, commonly referred to as personalized medicines. Paying heed to a timely need for standardizing robust nanodevices for cheap, fast, and scalable DNA detection, in this article, the nanogap formed by the lateral heterostructure of graphene and hexagonal boron nitride (hBN) is explored as a potential architecture. These heterostructures have been realized experimentally, and our study boasts the idea that the passivation of the edge of the graphene electrode with hBN will solve many of practical problems, such as high reactivity of the graphene edge and difficulty in controlled engineering of the graphene edge structure, while retaining the nanogap setup as a useful nanodevice for sensing applications. Employing first-principle density-functional-theory-based nonequilibrium Greens function methods, we identify that the DNA building blocks, nucleobases, uniquely couple with the states of the nanogap, and the resulting induced states can be attributed as leaving a fingerprint of the DNA sequence in the computed current-voltage (I-V) characteristic. Two bias windows are put forward: lower (1-1.2 V) and higher (2.7-3 V), where unique identification of all four bases is possible from the current traces, although higher sensitivity is obtained at the higher voltage window. Our study can be a practical guide for experimentalists toward development of a nanodevice DNA sensor based on graphene-hBN heterostructures.

Keywords
DNA sequencing, graphene-hBN heterostructure, nonequilibrium Green's function, density functional theory, I-V characteristics
National Category
Physical Sciences
Identifiers
urn:nbn:se:uu:diva-343317 (URN)10.1021/acsami.7b06827 (DOI)000416614600012 ()
Funder
Swedish Research CouncilStandUpCarl Tryggers foundation
Available from: 2018-03-13 Created: 2018-03-13 Last updated: 2019-01-05Bibliographically approved
Ji, C., Goncharov, A. F., Shukla, V., Jena, N. K., Popov, D., Li, B., . . . Mao, H.-K. (2017). Stability of Ar(H2)2 to 358 GPa. Proceedings of the National Academy of Sciences of the United States of America, 114(14), 3596-3600
Open this publication in new window or tab >>Stability of Ar(H2)2 to 358 GPa
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2017 (English)In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 114, no 14, p. 3596-3600Article in journal (Refereed) Published
Abstract [en]

"Chemical precompression" through introducing impurity atoms into hydrogen has been proposed as a method to facilitate metallization of hydrogen under external pressure. Here we selected Ar(H-2)(2), a hydrogen-rich compound with molecular hydrogen, to explore the effect of "doping" on the intermolecular interaction of H-2 molecules and metallization at ultrahigh pressure. Ar(H-2)(2) was studied experimentally by synchrotron X-ray diffraction to 265 GPa, by Raman and optical absorption spectroscopy to 358 GPa, and theoretically using the density-functional theory. Our measurements of the optical bandgap and the vibron frequency show that Ar(H-2)(2) retains 2-eV bandgap and H-2 molecular units up to 358 GPa. This is attributed to reduced intermolecular interactions between H-2 molecules in Ar(H-2)(2) compared with that in solid H-2. A splitting of the molecular vibron mode above 216 GPa suggests an orientational ordering transition, which is not accompanied by a change in lattice symmetry. The experimental and theoretical equations of state of Ar(H-2)(2) provide direct insight into the structure and bonding of this hydrogen-rich system, suggesting a negative chemical pressure on H-2 molecules brought about by doping of Ar.

Keywords
ultrahigh pressure, hydrogen-rich compound, intermolecular interaction, metallization
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-320633 (URN)10.1073/pnas.1700049114 (DOI)000398159000037 ()28289218 (PubMedID)
Funder
Swedish National Infrastructure for Computing (SNIC), SNIC-2015-10-19Swedish Research Council
Available from: 2017-08-08 Created: 2017-08-08 Last updated: 2017-08-08Bibliographically approved
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