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Dipayan Chakraborty

Publications and source records attributed to Dipayan Chakraborty.

30 records · Page 2Linked to original sources

On locating and neighbor-locating colorings of sparse graphs

A proper $k$-coloring of a graph $G$ is a \emph{neighbor-locating $k$-coloring} if for each pair of vertices in the same color class, the two sets of colors found in their respective neighborhoods are different. The \textit{neighbor-locating chromatic number} $χ_{NL}(G)$ is the minimum $k$ for which $G$ admits a neighbor-locating $k$-coloring. A proper $k$-vertex-coloring of a graph $G$ is a \emph{locating $k$-coloring} if for each pair of vertices $x$ and $y$ in the same color-class, there exists a color class $S_i$ such that $d(x,S_i)\neq d(y,S_i)$. The locating chromatic number $χ_{L}(G)$ is the minimum $k$ for which $G$ admits a locating $k$-coloring. Our main results concern the largest possible order of a sparse graph of given neighbor-locating chromatic number. More precisely, we prove that if $G$ has order $n$, neighbor-locating chromatic number $k$ and average degree at most $2a$, where $2a\le k-1$ is a positive integer, then $n$ is upper-bounded by $\mathcal{O}(a^2(k^{2a+1}))$. We also design a family of graphs of bounded maximum degree whose order is close to reaching this upper bound. Our upper bound generalizes two previous bounds from the literature, which were obtained for graphs of bounded maximum degree and graphs of bounded cycle rank, respectively. Also, we prove that determining whether $χ_L(G)\le k$ and $χ_{NL}(G)\le k$ are NP-complete for sparse graphs: more precisely, for graphs with average degree at most 7, maximum average degree at most 20 and that are $4$-partite. We also study the possible relation between the ordinary chromatic number, the locating chromatic number and the neighbor-locating chromatic number of a graph.

math.CO↗

On three domination-based identification problems in block graphs

The problems of determining the minimum-sized \emph{identifying}, \emph{locating-dominating} and \emph{open locating-dominating codes} of an input graph are special search problems that are challenging from both theoretical and computational viewpoints. In these problems, one selects a dominating set $C$ of a graph $G$ such that the vertices of a chosen subset of $V(G)$ (i.e. either $V(G)\setminus C$ or $V(G)$ itself) are uniquely determined by their neighborhoods in $C$. A typical line of attack for these problems is to determine tight bounds for the minimum codes in various graphs classes. In this work, we present tight lower and upper bounds for all three types of codes for \emph{block graphs} (i.e. diamond-free chordal graphs). Our bounds are in terms of the number of maximal cliques (or \emph{blocks}) of a block graph and the order of the graph. Two of our upper bounds verify conjectures from the literature - with one of them being now proven for block graphs in this article. As for the lower bounds, we prove them to be linear in terms of both the number of blocks and the order of the block graph. We provide examples of families of block graphs whose minimum codes attain these bounds, thus showing each bound to be tight.

math.CO↗

A linear algorithm for radio $k$-coloring of powers of paths having small diameters

The radio $k$-chromatic number $rc_k(G)$ of a graph $G$ is the minimum integer $λ$ such that there exists a function $ϕ: V(G) \to \{0,1,\cdots, λ\}$ satisfying $|ϕ(u)-ϕ(v)| \geq k+1 - d(u,v)$, where $d(u,v)$ denotes the distance between $u$ and $v$. A considerable amount of attention has been given to find the exact values or providing polynomial time algorithms to determine $rc_k(G)$ for several basic graph families such as paths, cycles, trees, and powers of paths, usually for some specific values of $k$. In this article, we find the exact values of $rc_k(G)$ where $G$ is a power of a path with diameter strictly less than $k$. Our proof readily provides a linear time algorithm for assigning a radio $k$-coloring of $G$. Furthermore, our proof technique is a potential tool for solving the same problem for other classes of graphs having ``small'' diameters.

math.CO↗

Structural rearrangements and fragmentation pathways induced by a low-energy electron attachment to ethyl acetate

Exploring the molecular fragmentation dynamics induced by low-energy electrons offers compelling insights into the complex interplay between the projectile and target. In this study, we investigate the phenomenon of dissociative electron attachment to ethyl acetate. The recorded yields of various fragment anions within an incident electron energy range of 1 to 13 eV reveal a diverse array of products with six different mass numbers. Examples include (M$-$H)$^-$, CH$_3^-$, C$_2$H$_5$O$^-$, CH$_3$CO$^-$, CH$_2$CHO$^-$, and CH$_3$COO$^-$, formed through the fracture of single bonds. Interestingly, the generation of other fragments, such as HCCO$^-$, suggests a more intricate structural rearrangement of the nuclei, adding a layer of complexity to the observed dissociation dynamics.

physics.atm-clus↗

Location-Domination Type Problems Under the Mycielski Construction

We consider the following variants of the classical minimum dominating set problem in graphs: locating-dominating set, locating total-dominating set and open locating-dominating set. All these problems are known to be hard for general graphs. A typical line of attack, therefore, is to either determine the minimum cardinalities of such sets in general or to establish bounds on these minimum cardinalities in special graph classes. In this paper, we study the minimum cardinalities of these variants of the dominating set under a graph operation defined by Mycielski in~\cite{Mycielski1955} and is called the Mycielski construction. We provide some general lower and upper bounds on the minimum sizes of the studied sets under the Mycielski construction. We apply the Mycielski construction to stars, paths and cycles in particular, and provide lower and upper bounds on the minimum cardinalities of such sets in these graph classes. Our results either improve or attain the general known upper bounds.

math.CO↗

Contracting edges to destroy a pattern: A complexity study

Given a graph G and an integer k, the objective of the $Π$-Contraction problem is to check whether there exists at most k edges in G such that contracting them in G results in a graph satisfying the property $Π$. We investigate the problem where $Π$ is `H-free' (without any induced copies of H). It is trivial that H-free Contraction is polynomial-time solvable if H is a complete graph of at most two vertices. We prove that, in all other cases, the problem is NP-complete. We then investigate the fixed-parameter tractability of these problems. We prove that whenever H is a tree, except for seven trees, H-free Contraction is W[2]-hard. This result along with the known results leaves behind three unknown cases among trees.

cs.DS↗

On clique numbers of colored mixed graphs

An (m,n)-colored mixed graph, or simply, an (m,n)-graph is a graph having m different types of arcs and n different types of edges. A homomorphism of an (m,n)-graph G to another (m,n)-graph H is a vertex mapping that preserves adjacency, the type thereto and the direction. A subset R of the set of vertices of G that always maps distinct vertices in itself to distinct image vertices under any homomorphism is called an (m,n)-relative clique of G. The maximum cardinality of an (m,n)-relative clique of a graph is called the (m,n)-relative clique number of the graph. In this article, we explore the (m,n)-relative clique numbers for various families of graphs.

math.CO↗

Catalytic Transformations in Coherence Theory

In 2016, A. Winter et al.(Physical Review Letters 116 (12) (2016) 120404) provided an operational meaning to relative entropy of coherence and coherence of formation by introducing coherence distillation and dilation protocol in asymptotic setup. Though relative entropy of coherence introduced in 2014 by T. Baumgratz ( Physical Review Letters 113 (14) (2014) 140401) as a coherence measure but it's operational meaning in single copy setup was unknown so far. Here we have provided relative entropy of coherence (via IO (Incoherent Operations)) and coherence of formation (via IO) and quantum incoherent relative entropy (via LQICC(Local Quantum Incoherent Operations with Classical Communications)) a clear operational significance in single copy setup using the concept of catalyst. We have proved an existential correspondence between asymptotic and catalytic state transformation using IO, LICC(Local Incoherent Operations with Classical Communications) and LQICC. We have also discussed two very important protocols, assisted distillation and quantum incoherent state merging, in single copy setup using catalyst. Monotone property of relative entropy of coherence, coherence of formation and quantum incoherent relative entropy under the catalytic transformation are also discussed here.

quant-ph↗

Necessary and Sufficient Condition for the Equivalence of Two Pure Multipartite States under Stochastic Local Incoherent Operations and Classical Communications

Resource theory of quantum coherence originated like entanglement in quantum information theory. However, still now proper classification of quantum states is missing under coherence. In this work, we have provided a classification of states under local incoherent operations. We have succeeded in deriving the necessary and sufficient condition for which two pure multipartite states are equivalent under stochastic local incoherent operations and classical communications (SLICC) and local incoherent operations and classical communications (LICC). In particular, we have succeeded in characterizing three qubit pure states under SLICC. Our result reveals the existence of infinite number of SLICC inequivalent classes for three qubit systems.

quant-ph↗

Dissociation dynamics in the dissociative electron attachment to ammonia molecule

Complete dissociation dynamics of low energy electron attachment to ammonia molecule has been studied using velocity slice imaging (VSI) spectrometer. One low energy resonant peak around 5.5 eV and a broad resonance around 10.5 eV incident electron energy has been observed. The resonant states mainly dissociate via H$^-$ and NH$_2^-$ fragments, though for the upper resonant state, signature of NH$^-$ fragments are also predicted due to three body dissociation process. Kinetic energy and angular distributions of the NH$_2^-$ fragment anions are measured simultaneously using VSI technique. Based on our experimental observations, we find the signature of A$_1$ symmetry in the 10.5 eV resonance energy whereas, the 5.5 eV resonance is associated with the well known A$_1$ symmetry.

physics.atm-clus↗

Absolute cross-sections of fragment negative ions in electron collisions with difluoromethane

Dissociative electron attachment (DEA) and ion-pair dissociation (IPD) processes of Difluoromethane (CH$_2$F$_2$) have been studied in the incident electron energy range 0 to 45 eV. Three different fragment anions (F$^-$, CHF$^-$ and F$_2^-$) are detected in the DEA range and two anions (F$^-$ and CHF$^-$) are detected in IPD range. Absolute cross-section of the F$^-$ fragment ion is measured for the first time. Three different resonances for both F$^-$ and CHF$^-$ ions and one single resonance peak for the F$_2^-$ ions are observed. Constant increase in ion counts above 8 eV incident electron energy indicates the involvement of IPD process. From the experimental observation, it is speculated that near 11 eV incident electron energy both DEA and IPD processes occur simultaneously.

physics.atm-clus↗

Dipolar dissociation dynamics in electron collisions with carbon monoxide

Dipolar dissociation processes in the electron collisions with carbon monoxide have been studied using time of flight (TOF) mass spectroscopy in combination with the highly differential velocity slice imaging (VSI) technique. Probing ion-pair states both positive and/or negative ions may be detected. The ion yield curve of negative ions provides the threshold energy for the ion-pair production. On the other hand, the kinetic energy distributions and angular distributions of the fragment anion provide detailed dynamics of the dipolar dissociation process. Two ion-pair states have been identified based on angular distribution measurements using VSI technique.

physics.atm-clus↗