L'état supraconducteur étant un condensat de paires de Cooper constitué d'électrons de moments et de spins opposés, il peut être fortement influencé par des effets de spin. Au cours de cette thèse, nous étudions l'effet d'un fort champ d'échange et d'un effet spin-orbite de type Rashba sur les propriétés supraconductrices. Dans une première partie, on étudie les effets associés à l'interaction entre supraconductivité et fort champ d'échange, se caractérisant par une transition de phase vers un état supraconducteur inhomogène découvert par Fulde, Ferrell, Larkin et Ovchinnikov (FFLO). On étudie tout particulièrement les fluctuations supraconductrices à l'approche de la transition de phase. On montre que ces fluctuations peuvent servir de révélateur à cette phase. Notamment, la capacité calorifique et la paraconductivité divergent de façon caractéristique à la transition vers un état modulé. On décrit également comment les effets paramagnétiques modifient les fluctuations de l'aimantation, annulant la réponse diamagnétique ou produisant des oscillations entre réponse para- et dia-magnétique. La seconde partie est dévolue aux jonctions supraconducteur-ferromagnétique (S/F). Dans les jonctions Josephson S/F/S, le champ d'échange donne lieu à des oscillations du courant critique en fonction de la longueur de la jonction, charactérisées par une alternance des états 0 et . On prédit une transition entre les états 0 et induite par la température, même dans la limite ballistique. Dans cette limite ballistique, on montre également que le courant de Josephson s'atténu sous la forme de lois de puissance en fonction de la longueur de la jonction, alors que le cas diffusif présente une atténuation exponentielle. On étudie ensuite la seconde harmonique de la relation courant-phase en présence d'une faible quantité d'impuretés. La dernière partie traite des effets de proximité lorsque les deux effets paramagnétique et spin-orbite sont présents dans une jonction Josephson. On montre que l'association d'une interaction Rashba et d'un champ d'échange induit un couplage direct entre les ordres magnétique et supraconducteur. En particulier, ce couplage permet de générer toute la dynamique magnétique par l'application d'une simple tension électrique. / The superconducting state being a Cooper pair condensate built on opposite spin and momentum electrons, it can be strongly influenced by any spin effect. In this thesis, we investigate the roles of strong paramagnetic and spin-orbit effects on superconducting properties. In a first part, the interplay between paramagnetic effect and bulk superconductivity is studied, leading to the modulated Fulde, Ferrell, Larkin and Ovchinnikov phase (FFLO phase). We focus on superconducting fluctuations near to the FFLO state. We show that these fluctuations can serve as a smoking gun for this phase. Noticeably, the fluctuation heat capacity and paraconductivity diverge in a characteristic way when approaching the phase transition towards a modulated state. Moreover, the fluctuation induced magnetization is predicted to be drastically quenched or to oscillate between dia- and para-magnetic responses. The second part is devoted to superconductor-ferromagnetic (S/F) junctions. In S/F/S Josephson junctions, the exchange field is responsible for the critical current oscillation, characterized by alternative 0- and -states, with respect to the junction length. We predict a temperature induced (0-) state transition, even in the ballistic case. Moreover, the ballistic case exhibits some power law decays of the Josephson current, in contrast to the exponentially decaying current in dirty limit. The moderately dirty limit is then investigated, and the second harmonic of the current-phase relation is established. The last part deals with proximity effects when both paramagnetic and spin-orbit interactions are present in a Josephson junction. We show that the association of both Rashba interaction and exchange field induces a direct coupling between magnetic and superconducting orders. Particularly, this coupling generates the complete magnetization dynamics by applying an appropriate d.c. voltage.

Au cours de cette thèse, on étudie les systèmes différents : graphène (une monocouche de carbone), graphène fonctionnalisé et les nanofils de Bismuth en induisant la supraconductivité par l’effet proximité. On montre que l’effet proximité fonctionne comme un probe sensible pour les effets des interactions, de couplage spin-orbite, etc.La structure de band de graphène a une relation dispersion linéaire au niveau de Fermi, et le band de conductance et le band de valence est lié aux six points dans l’espace réciproque, appelé le point Dirac. Autour du point Dirac, graphène occupe d’une densité d’état faible (par rapport aux métaux). Alors le niveau de Fermi dans graphene est modulable. On fabrique les jonctions S/Graphene/S avec les contacts de matériaux différents (Al, ReW, Nb). En comparant avec la théorie, on a complété le diagramme du produit R_N I_c (R_N la résistance d’état normal, I_c le courant critique dans une jonction) vs l’énergie Thouless E_Th (une énergie caractéristique intervient dans la jonction SNS longue et dépend la partie normale). Une réduction de R_N I_c globale de la jonction courte à la jonction longue, surtout dans la limite de la jonction longue, la réduction est 10 fois plus grande que celle de la jonction courte. On l’explique par une réduction d’une énergie Thouless effective à cause l’interface S/G imparfaite. Une suppression du supercourant près du point Dirac dans les jonctions longues est considérée comme une signature de la réflexion Andreev spéculaire sur les « puddles » dans le graphène. Aussi, l’injection des paires de Cooper dans les états de bord de l’effet Hall quantique du graphène est étudiée dans cette thèse.L’interaction du couplage spin-orbite et l’effet proximité peut produire les physiques très intéressantes comme le supra de triplet, jonction π, et récemment la formation des Fermions majoranas. Motivé par ces possibilités d’explorer les nouvelles physiques, on a essayé d’induire le couplage spin-orbite dans graphène dans lequel ce couplage est initialement très faible. En greffant les molécules de Pt-porphyrines, qui tiennent un atome de Pt au milieu, on espère que le couplage spin-orbite fort dans l’atome de Pt peut « diffuser » dans le graphène. Au lieu d’avoir vu le couplage spin-orbite, on a plutôt découvert un magnétisme qui dépend la grille dans le graphène induit par les molécules. Plusieurs échantillons avec les contacts normaux ou supraconducteurs sont mesurés avant et après mettant les molécules. Un transfert de charge dans deux sens (électron ou trou) est observé à la température ambiante. Il est lié à l’alignement des niveaux de Fermi des molécules et le graphène. A basse température (~70mK), les hystérésis dans la magnétorésistance (MR) et une asymétrie en B_(//) et B_⊥ impliquent un magnétisme dans graphène. Plus spectaculaire, une asymétrie en la dépendance de la grille du supercurrent est détectée. Bismuth est un élément très lourd et un matériau avec le couplage Rashba spin-orbite fort. On a connecté les nanofils de Bismuth avec tungstène (H_c∼12T) électrodes par FIB (Focused Ions Beam) et induit l’effet proximité dans les fils. Les résultats les plus étonnants sont : (1) le supercourant se tient au champ magnétique jusqu’à 11 Tesla. (2) Il y a des oscillations dans le courant critique en fonction du champ avec une période de centaine gauss qui ressemble à celui d’une structure de SQUID (composé des deux jonctions Josephson en parallèles. (3) Sur ces oscillations, nous trouvons aussi une modulation quasi-périodique lente de quelque milles gauss. Pour expliquer tous ces phénomènes, nous proposons qu’il y a quelques canaux étroites balistiques 1D se forment aux bords des certaines surfaces qui se tiennent au champ jusqu’à 11T et se construisent une interférence entre eux. L’effet Zeeman cause une modulation de phase entre les quasi-particules dans une paire d’Andreev qui module donc le supercourant en échelle de quelques milles gauss. / In this thesis we investigated graphene and Bi nanowire systems by inducing superconducting proximity effect in them. Typically the samples are realized in the form of S/N/S junction. The special properties of these systems are revealed by observing some unusual proximity effect in them. The interplay of the superconducting proximity effect and other effects (spin-orbit coupling, Zeeman effect, quantum Hall effect, impurities, etc...) at the mesoscopic scale gives rise to new physics. Some of our main results are listed below.GrapheneWe succeeded to induce superconducting proximity effect in the very long junction limit, thus completing the diagram of the superconducting proximity effect in graphene. Since by changing the gate voltage, one changes the carrier density in graphene and eventually the transport characteristic quantities (l_e, E_Th etc...). We could scan a whole range of Thouless energy. We present a diagram of eR_N I_c vs Thouless energy compared to theoretical prediction. The Thouless energy dependence of the eR_N I_c products varies from the long junction limit to the short junction limit. The discrepancy (mainly due to the imperfect S/G interface) between theory and experiment is also limit dependent: in the short junction limit, the eR_N I_c products are smaller than the theoretical prediction (with a perfect interface) by a factor of about 3-4; in the long junction limit, however, the disagreement is increased to about 100. We show that the factor deduced from the junctions in different limits is length dependent. This can be explained by the effect of finite transmission at the S/G interface in both the critical current I_c and the induced mini-gap in the graphene. In another hand, a suppression of supercurrent near the Dirac point is observed in long junctions which is attributed to the indication of the specular Andreev reflection upon the puddles in graphene. Also the injection of the Cooper pairs into the QHE edge states is investigated in this thesis.Graphene grafted with Pt-porphyrinsBy grafting the Pt-porphyrins onto graphene, we observed a charge transfer between molecules and the graphene both for electrons and holes. One of the important consequences of the charge transfer is that when the molecules are ionized, a collective magnetic order can be formed by the long range RKKY interaction: the magnetic moments interact via the carrier in graphene. This effect is detected by a hysteretic magnetoresistance of the graphene in a perpendicular field and the asymmetric magnetoresistance in parallel field. Even more striking, the observation of a unipolar supercurrent in S/G/S junction implies that this magnetism induced by porphyrins is gate dependent. The theoretical calculations by Uchoa et al. using the Anderson model indeed find that the gate voltage should tune the impurities in graphene between non-magnetic state and magnetic state.Bi nanowireThe observation of a SQUID-like oscillations persisting up to 10 T and thousands Gauss range modulation in I_c hints to a complex physic in the W-Bi nanowire-W junctions. The results are consistent with a SQUID structure consisting of 2 edges channels which could have an I_c oscillation with period defined by the area between the two edges, typically the size of the nanowire. The origin of the edge states formation is attributed to the strong spin-orbit coupling in Bi that leads to the quantum spin Hall (QSH) state. The thousands Gauss range modulation is the consequence of the interplay between the Zeeman effect and the proximity effect. The phase accumulation in an Andreev quasiparticle pair is Δϕ=g_eff⋅μ_B⋅B_(//) (ℏv_F/L) which is of the order of few thousands Gauss. In one particular sample, a full modulation of the critical current with about 1 T range is observed. This is similar to the proximity effect in S/F/S junctions which suggests a 0-π junction transition.

Neste trabalho foram estudadas as fases topológicas não triviais presentes em sistemas formados pela deposição de átomos de grafeno. Encontramos que quando um átomo hibridiza fortemente com o grafeno, apresenta um momento magnético e um forte spin-órbirta é possível a formação de uma rede hexagonal de baricentros que efetivamente gera uma estrutura de bandas característica de um efeito hall quântico anômalo. Especificamente, determinamos que o Ru satisfaz estas características. Quando este metal é depositado em uma configuração triangular no grafeno ocorrem picos na densidade de estados localizados no centro geométrico (baricentro) dos triângulos formados pelos Ru. Estes picos estão distribuídos de forma hexagonal e efetivamente geram uma estrutura de bandas que nas proximidades do nível de Fermi apresenta uma configuração de spin característica do efeito Hall quântico anômalo. Adicionalmente, encontramos que o sistema composto pela absorção de Ba ou Sr no grafeno favorece a formação do efeito Hall quântico de spin. Neste sistema, o acoplamento spin-órbita (SOC) gera um gap mais de 1000 vezes maior ao período no grafeno prístino. Para o estudo destes sistemas, implementamos no código SIESTA a aproximação on-site do acoplamento spin-órbita via o formalismo dos pseudopotenciais relativísticos de norma conservada. Nossa implementação foi testada a partir do estudo de fenômenos já conhecidos: i) o strong spin-splitting gerado no grafeno pela adsorção de Au, ii) o efeito hall quântico de spin no poço quântico de HgTe/CdTe e, iii) a formação de estados topológicos na superfície do Bi2Se3 e as fases magnéticas deste material com átomos de Mn adsorvidos. / In this work, were studied the non-trivial topological phases present in systems formed by deposition of atoms in graphene. We found that when an atom hybridizes strongly with grapheme, has a magnetic moment and a strong spin-orbit it is possible the formation of a hexagonal network of barycentres that effectively generates a structure band characteristic of a quantum anomalous Hall effect. Specifically, we determined that Ru satisfies these characteristics. When this metal is deposited in a triangular configuration in grapheme, peaks occur in the density of localized states in the geometric center (centroid) of the triangles formed by Ru. These peaks are distributed in a hexagonal structure and effectively generates a band structure that near the Fermi level has a spin configuration characteristic of the spin quantum Hall effect anomalous. Additionally, we found that the system composed by the adsorption of Ba or Sr in grapheme, promotes the formation of spin quantum Hall effect. In this system, the spin-orbit coupling (SOC) generates a gap more than 1000 times grater that predicted in pristine praphene. To study these systems, wu implemented in the code SIESTA the on-site approach of the spin-orbit coupling throught the formalism of norm conserved relativistic pseudo potentials. Our implementation was tested from the study of phenomena already known: i) the strong spin-splitting generated in graphene by adsorption of Au, ii) the quantum spin Hall effect in quantum well of HgTe / CdTe and, iii) formation of topological states in the surface of Bi2Se3 and the magnetic of this material with Mn atoms adsorved.

<p>The main focus of this thesis is the investigation of the dissociation dynamics of aryl halides using femtosecond pump-probe spectroscopy. In the monohalogenated aryl halides, iodo-, bromo- and chlorobenzene, the rate of dissociation following excitation at 266 nm in the gas phase increased with increasing mass of the halogen atom. This process was assigned to predissociation of the initially excited singlet (π, π*) state via a repulsive triplet (n, σ*) state due to spin-orbit interaction. In addition to the predissociative mechanism, a direct dissociation channel was observed in iodobenzene. The rate of the predissociation in bromobenzene was found to be faster in the condensed phase than in the gas phase, which can be explained by solvent-induced symmetry perturbations. <i>Ab initio</i> calculations of the potential energy surfaces of the ground state and several low lying excited states in bromobenzene have been performed in order to verify the suggested mechanism. Substituting one of the hydrogen atoms in bromobenzene affected the predissociation rate significantly. In o-, m- and p-dibromobenzene the predissociation rate increased with decreasing distance between the bromine atoms in accordance with an increased spin-orbit interaction introduced by the bromine substituent. The fastest predissociation rate was observed in 1,3,5-tribromobenzene. With chlorine and fluorine substitution, inductive and conjugative effects were found to be of importance. In the o- and m-isomers of the dihalogenated aryl halides, an additional faster dissociation channel was observed. Guided by <i>ab initio</i> calculations of the potential energy surfaces in the dibromobenzene isomers, we ascribed the fast dissociation pathway to predissociation of an initially excited triplet state. Upon methyl group substitution in bromobenzene, the decreased lifetime of the initially excited state was attributed to an incresaed density of coupled states.</p><p>Another system which has been studied in the condensed phase is diiodomethane. Using Car-Parrinello molecular dynamics simulations we observed a prompt dissociation and subsequent recombination to the isomer, iso-diiodomethane, in acetonitrile solution.</p><p>Vibrational wavepacket dynamics in the C (¹Σ⁺) state of NaK were studied using a direct ionization probing scheme. A simple analytical expression for the pump-probe signal was developed in order to see what factors that govern direct ionization of the vibrational wavepacket. Our experimental data was consistent with a photoionization transition dipole moment that varies with internuclear distance.</p>

The main focus of this thesis is the investigation of the dissociation dynamics of aryl halides using femtosecond pump-probe spectroscopy. In the monohalogenated aryl halides, iodo-, bromo- and chlorobenzene, the rate of dissociation following excitation at 266 nm in the gas phase increased with increasing mass of the halogen atom. This process was assigned to predissociation of the initially excited singlet (π, π*) state via a repulsive triplet (n, σ*) state due to spin-orbit interaction. In addition to the predissociative mechanism, a direct dissociation channel was observed in iodobenzene. The rate of the predissociation in bromobenzene was found to be faster in the condensed phase than in the gas phase, which can be explained by solvent-induced symmetry perturbations. Ab initio calculations of the potential energy surfaces of the ground state and several low lying excited states in bromobenzene have been performed in order to verify the suggested mechanism. Substituting one of the hydrogen atoms in bromobenzene affected the predissociation rate significantly. In o-, m- and p-dibromobenzene the predissociation rate increased with decreasing distance between the bromine atoms in accordance with an increased spin-orbit interaction introduced by the bromine substituent. The fastest predissociation rate was observed in 1,3,5-tribromobenzene. With chlorine and fluorine substitution, inductive and conjugative effects were found to be of importance. In the o- and m-isomers of the dihalogenated aryl halides, an additional faster dissociation channel was observed. Guided by ab initio calculations of the potential energy surfaces in the dibromobenzene isomers, we ascribed the fast dissociation pathway to predissociation of an initially excited triplet state. Upon methyl group substitution in bromobenzene, the decreased lifetime of the initially excited state was attributed to an incresaed density of coupled states. Another system which has been studied in the condensed phase is diiodomethane. Using Car-Parrinello molecular dynamics simulations we observed a prompt dissociation and subsequent recombination to the isomer, iso-diiodomethane, in acetonitrile solution. Vibrational wavepacket dynamics in the C (1Σ+) state of NaK were studied using a direct ionization probing scheme. A simple analytical expression for the pump-probe signal was developed in order to see what factors that govern direct ionization of the vibrational wavepacket. Our experimental data was consistent with a photoionization transition dipole moment that varies with internuclear distance.

This work comprises two main parts. The first part outlines our efforts to expand on the recent work of Gütlich et.al. by synthesizing Co(II) based spin crossover systems within a dendritic framework. We wanted to investigate the possibility of synthesizing different first generation, triazole containing dendrimers using “click” type reactions and their coordination ability with Co(II) ions. To this end we have had limited success mainly due to the numerous challenges in synthesizing a pure dendrimer product. The second part details our efforts in the synthesis of a mononuclear Co(II) based single molecule magnet. This comes as an extension to recent reports by Chang and Long where they have successfully obtained mononuclear Fe(II) single molecule magnets by inducing structural distortions within the complexes to amplify the spin-orbit coupling. We postulated that the use of Co(II) in conjunction with a bulky ligand framework would lead to desirable magnetic properties. We chose the known bis(imino)pyridine ligand scaffold due to its rich chemistry and its interesting and unexpected coordination behaviour, as we have seen in previous research efforts by our lab. To this end we were successful in isolating and characterizing 4 compounds, and we have carried out detailed magnetic measurements on the two most magnetically interesting species.

This work comprises two main parts. The first part outlines our efforts to expand on the recent work of Gütlich et.al. by synthesizing Co(II) based spin crossover systems within a dendritic framework. We wanted to investigate the possibility of synthesizing different first generation, triazole containing dendrimers using “click” type reactions and their coordination ability with Co(II) ions. To this end we have had limited success mainly due to the numerous challenges in synthesizing a pure dendrimer product. The second part details our efforts in the synthesis of a mononuclear Co(II) based single molecule magnet. This comes as an extension to recent reports by Chang and Long where they have successfully obtained mononuclear Fe(II) single molecule magnets by inducing structural distortions within the complexes to amplify the spin-orbit coupling. We postulated that the use of Co(II) in conjunction with a bulky ligand framework would lead to desirable magnetic properties. We chose the known bis(imino)pyridine ligand scaffold due to its rich chemistry and its interesting and unexpected coordination behaviour, as we have seen in previous research efforts by our lab. To this end we were successful in isolating and characterizing 4 compounds, and we have carried out detailed magnetic measurements on the two most magnetically interesting species.

During the last decades the specific manipulation of matter on the (sub-) nanometer scale, also known as nanoscience, became possible by technologies such as the scanning tunneling microscope. Nanocatalysts, i.e. catalytic active structures of up to a few nanometers in size, belong to this rather new class of materials. Unlike ordinary ’macroscopic’ catalytic materials, the performance of nanocatalysts does not simply scale, for instance, with the surface to volume ratio of the active material. In this Thesis model nanocatalysts are investigated by means of ab-initio density functional theory calculations. In paper I, we explain the experimentally observed catalytic characteristics of small gold clusters, Au1-4, on a regular magnesium oxide terrace towards the oxidation of carbon monoxide by thoroughly studying the adsorption of CO and O2 on these clusters. In the subsequent paper II, we study the feasibility of a catalytic water-mediated CO oxidation reaction on Au1-4/MgO and find that this reaction mechanism is not assessable for Au2,4/MgO and unlikely for Au1,3/MgO. Papers III and IV concentrate on the reactivity of clusters in the gas phase. Particularly, we focus on the relative stability of Au13 isomers and its potential for O2 dissociation (paper III). We find the lowest energy isomers, which contain a triangular prism at their center surrounded by a ring of the remaining seven atoms, to be generally stable upon O2 adsorption. The dissociation of O2 at certain sites of Au13 is found to be exothermic. In paper IV we performed scans of the Born-Oppenheimer potential energy surfaces of neutral and charged Cu3, Ag3, and Au3 to explore the thermally excited vibrations of these trimers. While the Born-Oppenheimer surface of Cu3 exhibits one fairly deep energy minimum, it is comparatively flat with two shallow minima in the case of Ag3. Hence for Ag3 there exist many thermally accessible geometries in a wide range of angles and bond lengths. For Au3, two distinct energy minima appear, being well-separated by a barrier of 180 meV. Already at room temperature, we find bond lengths changes of up to 5% for the studied trimers. Choosing Au3 as a case study for the changed reactivity of thermally excited modes, we find CO to bind up to 150 meV stronger to the excited cluster. Gold deposited on graphene and graphite was observed to form larger aggregates. In paper V, we study the electronic structures, high mobility, and substrate-mediated clustering processes of Au1-4 on graphene. Already in the 1970s is was speculated that dispersion forces, i.e. van der Waals forces, significantly contribute to the adsorption energies of gold atoms on graphite. We accounted for van der Waals interactions in our density functional theory calculations (paper VI) and investigated the influence of these dispersion forces on the binding of copper, silver, and gold adatoms on graphene. While copper and gold show a mixed adsorption mechanism, i.e. chemical binding plus attraction due to the van der Waals forces, silver is purely physisorbed on graphene. / Felaktigt tryckt som Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 719

This work comprises two main parts. The first part outlines our efforts to expand on the recent work of Gütlich et.al. by synthesizing Co(II) based spin crossover systems within a dendritic framework. We wanted to investigate the possibility of synthesizing different first generation, triazole containing dendrimers using “click” type reactions and their coordination ability with Co(II) ions. To this end we have had limited success mainly due to the numerous challenges in synthesizing a pure dendrimer product. The second part details our efforts in the synthesis of a mononuclear Co(II) based single molecule magnet. This comes as an extension to recent reports by Chang and Long where they have successfully obtained mononuclear Fe(II) single molecule magnets by inducing structural distortions within the complexes to amplify the spin-orbit coupling. We postulated that the use of Co(II) in conjunction with a bulky ligand framework would lead to desirable magnetic properties. We chose the known bis(imino)pyridine ligand scaffold due to its rich chemistry and its interesting and unexpected coordination behaviour, as we have seen in previous research efforts by our lab. To this end we were successful in isolating and characterizing 4 compounds, and we have carried out detailed magnetic measurements on the two most magnetically interesting species.

Les carbures et oxydes des métaux de transition sont d'une importance capitale dans le domaine industriel voir catalytique. Le carbure de tungstène WC a été identifié comme un bon substituant des métaux nobles tel que le platine dans le domaine catalytique. Le but de ce travail de thèse est d'appliquer des méthodes de chimie quantique les plus poussées pour déterminer la structure électronique, la stabilité et la nature de liaison chimique des diatomiques WC et WC2+. Notre recherche préliminaire est motivée par les données spectroscopiques disponibles sur W, W+, W2+, WC et WC2+. La méthodologie adoptée, CASSCF/MRCI/MRCI+Q/aug-cc-pV5Z(-PP) implémentée dans le code MOLPRO, consiste à réaliser des calculs quantique tenant en compte des effets de corrélation et relativistes avec un traitement spécifique du couplage spin−orbite pour la recherche des courbes d'énergie potentielle de l'état fondamental et des états excités de plus basses énergies de WCn+ (n=0-2) tout en utilisant une base suffisamment étendue. Les résultats de ce travail sont en bon accord avec ceux disponibles dans la littérature. En outre, dans ce travail nous avons confirmé pour la première fois que le carbure diatomique dicationique WC2+ est thermodynamiquement stable / Metal carbides and oxides are more interesting in catalytic and industrial domains. Tungsten carbide WC has been detected as serious substituent of platinum Pt catalytic. The ultimate goal of this thesis is theoretical studies of electronic structure, stability and the bound nature on WC, WO and its cations. Our preliminary research were motiving by the available spectroscopic data on W, W+, W2+, WC et WC2+. We used the methodology (CASSCF/MRCI/MRCI+Q/aug-cc-pV5Z(-PP)) implemented on MOLPRO package to perform quantum calculations with high accuracy taking into account the correlation and relativistic effects with a specific treatment of spin orbit coupling for some low lying excited electronic states of WCn+, (n=0, 1 et 2). Our results are shown in good agreement with those available in the literature. Furthermore, in this work for the first time we demonstrated that a carbide dication (WC2+) is thermodynamically stable