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. 2022 Apr 14;15(8):2889. doi: 10.3390/ma15082889

Prediction of Exchange-Correlation Energy of Graphene Sheets from Reverse Degree-Based Molecular Descriptors with Applications

Mohammed Albadrani 1,*, Parvez Ali 1, Waleed H El-Garaihy 1,2, Hassan Abd El-Hafez 1,3,*
Editors: Jerzy P Lukaszewicz, Piotr Kamedulski
PMCID: PMC9028513  PMID: 35454580

Abstract

Over the past few years, the popularity of graphene as a potential 2D material has increased since graphene-based materials have applications in a variety of fields, including medicine, engineering, energy, and the environment. A large number of graphene sheets as well as an understanding of graphene’s structural hierarchy are critical to the development of graphene-based materials. For a variety of purposes, it is essential to understand the fundamental structural properties of graphene. Molecular descriptors were used in this study to investigate graphene sheets’ structural behaviour. Based on our findings, reverse degree-based molecular descriptors can significantly affect the exchange-correlation energy prediction. For the exchange-correlation energy of graphene sheets, a linear regression analysis was conducted using the reverse general inverse sum indeg descriptor, RGISI(p,q). From RGISI(p,q), a set of reverse topological descriptors can be obtained all at once as a special case, resulting in a model with a high correlation coefficient (R between 0.896 and 0.998). Used together, these reverse descriptors are graphed in relation to their response to graphene. Based on this study’s findings, it is possible to predict the exchange correlation energy as well as the geometric structures of graphene sheets with very little computational cost.

Keywords: exchange-correlation energy, reverse topological descriptors, graphene

1. Introduction

Carbon is a widely studied and influential element across many scientific disciplines. Many allotropes of carbon exist, each with special properties, such as graphite, diamond, and amorphous carbon as well as fullerenes, carbon nanotubes (CNTs), and graphene [1,2,3,4,5,6]. Graphene is at the forefront of research in fields such as physics, chemistry, and materials science, among many others. Researchers have been intrigued by graphene due to its great mechanical, transportable, optical, and thermal properties as well as its thermal stability and unique electronic structures [7,8,9]. Graphene is packed in a unique two-dimensional nano-carbon hexagonal lattice [10,11]. Graphene’s unique combination of characteristics strongly qualifies it for use in multiple applications, such as biosensors [9], membranes [12], drug delivery, tissue engineering, sensing applications [13], photodetectors [14], electrochemical sensors [15], and hydrogen-based energy storage [16].

A nanostructure is composed of distinct and measurable elements, known as nano-patterns. In contrast to random patterns, these patterns follow the order of chemical and physical laws. Physical and chemical laws determine how atoms and molecules form discrete and measurable geometric structures, ranging from repeating lattices to complex shapes. Rules from the chemical graph theory can be used to analyze and predict the properties of these well-defined structures [17]. In the chemical graph theory, a chemical structure is represented by a corresponding molecular graph, where vertices represent atoms and edges represent bonds [18]. Molecular descriptors are commonly used in the chemical graph theory to predict various properties of chemical structures. Among the many molecular descriptors available, the topological molecular descriptors are a prominent [19,20]. Topological molecular descriptors are used to transform molecular graphs into mathematical models as well as encrypt significant amounts of information about the molecular structure. Topological molecular descriptors can be classified into a number of groups according to their graph parameters. Some of the well-known topological descriptors include distance [21], degree [22], eccentricity [23], and spectrum-based descriptors [24]. Researchers often prefer degree-based topological descriptors due to their simplicity, and some of the most popular degree-based topological descriptors are the first and second Zagreb [25], Randić [26], sum−connectivity [27], and geometric−arithmetic descriptors [28], etc. Wei et al. [29] recently introduced many reverse degree-based topological descriptors, inspired by their work on degree-based topological descriptors.

In this article, molecular graphs are represented by Ǥ. Φu denotes the degree of a vertex u, and Δ(Ǥ) is the maximum degree of the graph Ǥ. The reverse degree [30] of a vertex u is defined as Ru=Δ(Ǥ)Φu+1.

To derive a set of reverse degree-based topological descriptors, we first define the reverse general inverse sum indeg descriptor, denoted by RGISI(p,q)(Ǥ), as follows: RGISI(p,q)(Ǥ)=uvE(G)[ΦuΦv]p [Φu+Φv]q  where p and q are any real numbers.

Table 1 Some reverse degree-based topological descriptors derived from the reverse general inverse sum indeg descriptor by assigning specific values to the parameters p and q.

Table 1.

Some reverse degree-based topological descriptors derived from the reverse general inverse sum indeg descriptor.

(p,q) RGISI(p,q) Corresponding Reverse
Topological Descriptors
(0,1) RGISI(0,1)=RM1(Ǥ) Reverse first Zagreb descriptor
(1,0) RGISI(1,0)=RM2(Ǥ) Reverse second Zagreb descriptor
(12,0) RGISI(12,0)=RR1/2(Ǥ) Reverse Randić descriptor
(0, 12) RGISI(0,12)=RSCI(Ǥ) Reverse sum−connectivity descriptor
(0,1) 2RGISI(0,1)=RH(Ǥ) Reverse harmonic descriptor
(0,2) RGISI(0,2)=RHZ(Ǥ) Reverse hyper Zagreb descriptor
(12,1) 2RGISI(12,1)=RGA(Ǥ) Reverse geometric−arithmetic descriptor
(12,1) 12RGISI(12,1)=RAG(Ǥ) Reverse arithmetic−geometric descriptor
(1,1) RGISI(1,1)=RISI(Ǥ) Reverse inverse sum indeg descriptor
(1,1) RGISI(1,1)=RReZG1(Ǥ) Reverse redefined first Zagreb descriptor
(1,1) RGISI(1,1)=RReZG3(Ǥ) Reverse redefined third Zagreb descriptor

Our main objective is to offer an alternate method, with high accuracy, for computing the exchange-correlation energies of graphene sheets. The DFT calculations of the exchange-correlation energies of graphene sheets have the advantage of being accurate, but they also have the disadvantage of being computationally expensive. Therefore, Section 2 provides a relationship between the exchange-correlation energy of graphene sheets and reverse degree-based topological descriptors. Section 3 contains detailed analytical results for graphene using reverse degree topological descriptors and polynomial as well as numerical comparisons.

2. Relationship between the Exchange-Correlation Energy and the Reverse General Inverse Sum Indeg Descriptor of Graphene Sheets

A wide range of molecular descriptors have been proposed in the current literature, but many of them show little evidence that they correlate with any of the physical or chemical properties of the chemical structure. This section highlights the inquiry that was undertaken to determine whether reverse general inverse sum indeg descriptors possess any predictive power and whether or not they should be used in any chemical applications. In order to achieve this, we selected ten graphene sheets from one cycle to ten cycles. The molecular structures of these graphene sheets are provided in Table 2. The exchange-correlation energies (ECE) of these graphene sheets were obtained from the literature [31] and have been listed in Table 2.

Table 2.

Graphene sheets from C6 to C32 with their exchange-correlation energy and reverse general inverse sum indeg descriptors.

Graphene Sheets EC Energy RGISI(p,q)(Ǥ)=uvE(G)[ΦuΦv]p [Φu+Φv]q
graphic file with name materials-15-02889-i001.jpg 278.3728274 RGISI(p,q)(C6)=6[2]q
graphic file with name materials-15-02889-i002.jpg 582.3543 RGISI(p,q)(C10)=[2]q+[2]p+2[3]q+6[4]p+q
graphic file with name materials-15-02889-i003.jpg 870.9878 RGISI(p,q)(C13)=3[2]q+[2]p+1[3]q+1+6[4]p+q
graphic file with name materials-15-02889-i004.jpg 1165.387066 RGISI(p,q)(C16)=5[2]q+[2]p+3[3]q+6[4]p+q
graphic file with name materials-15-02889-i005.jpg 1512.946726 RGISI(p,q)(C19)=7[2]q+5[2]p+1[3]q+6[4]p+q
graphic file with name materials-15-02889-i006.jpg 1868.115158 RGISI(p,q)(C22)=5[2]q+1+[2]p[3]q+2+2[4]p+q+1
graphic file with name materials-15-02889-i007.jpg 2129.987845 RGISI(p,q)(C24)=3[2]q+2+[2]p+2[3]q+1+6[4]p+q
graphic file with name materials-15-02889-i008.jpg 2698.081041 RGISI(p,q)(C28)=15[2]q+[2]p+2[3]q+1+2[4]p+q+1
graphic file with name materials-15-02889-i009.jpg 2951.482056 RGISI(p,q)(C30)=17[2]q+7[2]p+1[3]q+7[4]p+q
graphic file with name materials-15-02889-i010.jpg 3253.425639 RGISI(p,q)(C32)=19[2]q+[2]p+4[3]q+6[4]p+q

The reverse general inverse sum indeg descriptors of these graphene sheets were obtained through direct calculations using the edge partition technique. For example, the reverse general inverse sum indeg descriptor for the graphene sheet C24 (RGISI(p,q)(C24)), shown in Table 2, was obtained by the following way: The molecular graph of C24 had 24 vertices, 30 edges, and Δ(C24)=3. Based on the reverse degrees of each of the vertices, the edges set of C24 was partitioned into three sets: rm11(C24),rm12(C24),rm22(C24) with cardinalities |rm11(C24)|=12, |rm12(C24)|=12, |rm22(C24)|=6. From the definition of a reverse general inverse sum indeg descriptor, we used the following:

RGISI(p,q)(C24)=uvE(C24)[ΦuΦv]p [Φu+Φv]q  =12[(1)(1)]p[1+1]q+12[(1)(2)]p[1+2]q+[(2)(2)]p[2+2]q

After simplification, we arrived at RGISI(p,q)(C24)=3[2]q+2+[2]p+2[3]q+1+6[4]p+q.

Table 3 lists 11 reverse topological descriptors: the reverse first and second Zagreb descriptor, the reverse Randić descriptor, the reverse sum−connectivity descriptor, the reverse harmonic descriptor, the reverse hyper Zagreb descriptor, the reverse geometric−arithmetic descriptor, the reverse arithmetic−geometric descriptor, the reverse inverse sum indeg descriptor, the reverse redefined first Zagreb descriptor, and the reverse redefined third Zagreb descriptor. These descriptors were obtained by setting specific values of p and q, such as the following:

Table 3.

Values of the reverse topological descriptors from C6 to C32.

(p,q) (0,1) (1,0) (1   2,0) (0, 1   2) (0,1) (0,2) (12,1) (1   2,1) (1,1) (1,1) (1,1)
Graphene Sheets RM1 RM2 RR12 RSCI RH RHZ RGA RAG RISI RReZG1 RReZG3
C6 12 6 6 4.2426 6 24 6 6 3 12 12
C10 38 33 6.8284 6.0165 6.6667 136 10.771 11.243 9.1667 14 122
C13 48 39 10.243 8.5855 10 162 14.657 15.364 11.5 21 138
C16 58 45 13.657 11.154 13.333 188 18.542 19.485 13.833 28 154
C19 68 51 17.071 13.723 16.667 214 22.428 23.606 16.167 35 170
C22 79 60 20.364 16.267 20 249 26.485 27.546 19 41.5 202
C24 84 60 23.485 18.414 23 252 29.314 30.728 20 48 192
C28 98 71 27.485 21.534 27 296 34.314 35.728 23.5 56 230
C30 104 73 30.399 24.104 30.33 306 37.199 38.849 24.833 62 230
C32 110 75 33.314 25.673 32.667 316 40.97 41.97 26.167 68 230

(0,1),(1,0),(1 2,0),(0, 1 2),(0,1),(0,2),(12,1), (1 2,1),(1,1),(1,1),(1,1) in the reverse general inverse sum indeg descriptors (Table 1) for each graphene sheet from C6 to C24.

To predict the exchange-correlation energy of the graphene sheets, the following linear regression model was used:

ECE=α(RGISI(p,q))+β,

where ECE is the exchange-correlation energy of the graphene sheets from C6 to C32, β is the regression model constant, α is the reverse topological descriptor coefficient, and RGISI(p,q) is any predictor from Table 1. This linear regression model was used in compiling Table 4, which used SPSS software to show the regression equations of the 11 reverse topological descriptors, the correlation coefficient between the exchange-correlation energy of the graphene sheets, and the reverse topological descriptors from the data obtained from Table 2 and Table 3. Statistical quantities, such as the standard error (SE) and the F-test, were used to check the reliability of the predictive models listed in Table 4. Based on Table 2 and Table 3, we found that the reverse topological descriptors and the exchange-correlation energy exhibit similar trends and Figure 1 and Figure 2 illustrates this similarity. Figure 3 shows the linear relationship between the exchange-correlation energy while Figure 4 graphically depicts the predictive potential of the reverse topological descriptors via the square of the correlation (R2) with the help of the reverse topological descriptors of the studied graphene sheets using the regression model presented in Table 4.

Table 4.

Linear prediction models with statistical parameters of the exchange-correlation energy of graphene sheets from C6 to C32.

Regression Equation r SE F
ECE=123.542+24.198(RM1) 0.980475724 213.8003228 198.893
ECE=123.542+24.198(RM2) 0.945489731 354.0705116 67.437
ECE=22.043+3.584(RR12) 0.997953668 69.52114251 1948.719
 ECE=4.057+3.371(RSCI) 0.998617364 57.15508183 2887.026
ECE=4.057+3.371(RH) 0.997778424 72.43364998 1794.526
ECE=4.057+3.371(RHZ) 0.947685472 347.0617000 70.514
ECE=4.057+3.371(RGA) 0.997280715 80.12777418 1464.977
ECE=4.057+3.371(RAG) 0.980655201 95.36092088 1031.971
ECE=4.057+3.371(RISI) 0.980655201 212.8250165 200.793
ECE=123.542+24.198(RReZG1) 0.998037144 68.08980614 2031.849
ECE=123.542+24.198(RReZG3) 0.896497248 481.7127938 32.755

Figure 1.

Figure 1

Variation of reverse topological descriptors and ECE.

Figure 2.

Figure 2

ECE and reverse descriptors.

Figure 3.

Figure 3

Figure 3

Plot between the reverse topological descriptors and ECE of graphene sheets from C6 to C32.

Figure 4.

Figure 4

Predictive potential of the reverse topological descriptors via square of the correlation coefficient R2.

3. Reverse General Inverse Sum Indeg Descriptor of Graphene

This section covers graphene systems, which have gained a lot of research interest across a wide range of applications due to their fascinating properties. There are numerous studies [32,33,34,35,36,37,38,39,40] dedicated to the computation of topological descriptors of graphene systems in recent years. Most of these studies are devoted to obtaining an individual formula for each topological descriptor. This article presents a general reverse degree-based topological descriptor, namely, a reverse general inverse sum indeg descriptor from which 11 other reverse degree-based topological descriptors can be obtained. To compute the general reverse inverse sum indeg descriptor for the molecular structure of the graphene under study, we considered four different cases based on the number of rows (l) and the number of benzene rings in each row (k). Initially, the case in which the number of rows and the number of rings in each row were both greater than one was considered, as shown in Figure 5 and Figure 6 as 3D plots. For the second case, the graphene structure had only one row and more than one benzene ring. Figure 7 shows such a situation. In the third case, there was more than one row with only one benzene ring in each column, as shown in Figure 8 and Figure 9 as 3D plots. Figure 10 represents the last case where there was only one benzene ring. Using these four cases and edge partitioning as well as degree counting and graph structure analysis, the reverse general inverse sum indeg descriptor of graphene (Ǥ) was derived as follows:

Figure 5.

Figure 5

Graphene structure with l>1,k>1.

Figure 6.

Figure 6

Figure 6

3D Plots when ( l>1,k>1).

Figure 7.

Figure 7

Graphene structure with l=1,k>1.

Figure 8.

Figure 8

Graphene structure with l>1,k=1.

Figure 9.

Figure 9

Figure 9

3D plots when ( l=1,k>1) and ( l>1, k=1).

Figure 10.

Figure 10

Graphene structure with l=1,k=1.

Theorem 1.

The reverse general inverse sum indeg descriptor RGISI(p,q)(Ǥ)of graphene is as follows:

RGISI(p,q)(Ǥ)={(3lk2kl1)[1]p[2]q+(4k+2l4)[2]p[3]q+(l+4)[4]p+q,

           if l>1,k>1

and RGISI(p,q)(Ǥ)=(k1)[1]p[2]q+(4k4)[2]p[3]q+(6)[4]p+q,if l=1,k>1
and RGISI(p,q)(G)=(2l3)[1]p[2]q+(2l)[2]p[3]q+(l+4)[4]p+q, if l>1, k=1
and RGISI(p,q)(G)=(6)[2]q, if l=1, k=1

Proof. 

The proof was built by taking the four cases into account. □

Case 1. 

From the graph structure analysis, the reverse edge partition of graphene whenl>1,k>1containedrm1,1=3lk2kl1edges, rm1,2=4k+2l4edges, andrm2,2=l+4edges.

Then, applying the definition of the reverse general inverse sum indeg descriptor, RGISI(p,q)(Ǥ), we arrived at RGISI(p,q)(Ǥ)=uvE(Ǥ)[ΦuΦv]p [Φu+Φv]q

RGISI(p,q)(Ǥ)=uvE1(Ǥ)[ΦuΦv]p [Φu+Φv]q+uvE2(Ǥ)[ΦuΦv]p [Φu+Φv]q
+uvE2(Ǥ)[ΦuΦv]p [Φu+Φv]q
=rm1,1[(1)(1)]p[1+1]q+rm1,2[(1)(2)]p[1+2]q+rm2,2[(2)(2)]p[2+2]q
=(3lk2kl1)[1]p[2]q+(4k+2l4)[2]p[3]q+(l+4)[4]p+q (1)

Using Table 1, in Equation (1), the following 11 reverse topological descriptors for the graphene when l>1,k>1 were obtained.

Remark 1.

  • (i)
    RGISI(0,1)=RM1(Ǥ)=(3lk2kl1)[2]1+(4k+2l4)[3]1+(l+4)[4]1
    RM1(Ǥ)=6lk+8k+8l+2
  • (ii)
    RGISI(1,0)=RM2(Ǥ)=(3lk2kl1)[1]1+(4k+2l4)[2]1+(l+4 )[4]1
    RM2(Ǥ)=3lk+6k+7l+7
  • (iii)

    RGISI(1 2,0)=RR(Ǥ)=(3lk2kl1)+(4k+2l4)12+(l+4)12 

  • (iv)

    RGISI(0,1 2)=RSCI(Ǥ)=(3lk2kl1)12+(4k+2l4)13+(l+4)12

  • (v)
    2RGISI(0,1)=RH(Ǥ)=2(3lk2kl1)[2]1+2(4k+2l4)[3]1+2(l+4)[4]1
    RH(Ǥ)=(3lk2kl1)+(4k+2l4)23+(l+4)12
  • (vi)
    RGISI(0,2)=RHZ(G)=(3lk2kl1)[2]2+(4k+2l4)[3]2+(l+4)[4]2 
    RHZ(Ǥ)=12lk+28k+30l+24
  • (vii)
     2RGISI(12,1)=RGA(G)=2(3lk2kl1)[1]12[2]1+2(4k+2l4)[2]12[3]1+2(l+4)[4]12[4]1 
    RGA(Ǥ)=(3lk2kl1)+(4k+2l4)223+(l+4)
  • (viii)
    12RGISI(1 2,1)=RAG(Ǥ)=(3lk2kl1)+(4k+2l4)12[2]12[3]1+(l+4)12[4]12[4]1
    RAG(Ǥ)=(3lk2kl1)+(4k+2l4)322+(l+4)
  • (ix)
     RGISI(1,1)=RISI(Ǥ)=(3lk2kl1)[1]1[2]1+(4k+2l4)[2]1[3]1+(l+4)[4]1[4]1
    RISI(Ǥ)=(3lk2kl1)12+(4k+2l4)23+(l+4)
  • (x)
    RGISI(1,1)=RReZG1(Ǥ)=(3lk2kl1)[1]1[2]1+(4k+2l4)[2]1[3]1+(l+4)[4]1[4]1
    RReZG1(Ǥ)=(3lk2kl1)2+(4k+2l4)32+(l+4)
  • (xi)
    RGISI(1,1)=RReZG3(Ǥ)=(3lk2kl1)[1]1[2]1+(4k+2l4)[2]1[3]1+(l+4 )[4]1[4]1
    RReZG3(Ǥ)=6lk+20k+26l+38

Case 2. 

When l=1,k>1, the reverse edge partition of graphene contained rm1,1=k1 edges, rm1,2=4k4 edges, and rm2,2=6 edges.

Applying the definition of the reverse general inverse sum indeg descriptor, RGISI(p,q)(Ǥ),

RGISI(p,q)(Ǥ)=uvE(Ǥ)[ΦuΦv]p [Φu+Φv]q
RGISI(p,q)(Ǥ)=uvE1(Ǥ)[ΦuΦv]p [Φu+Φv]q+uvE2(Ǥ)[ΦuΦv]p [Φu+Φv]q
+uvE3(Ǥ)[ΦuΦv]p [Φu+Φv]q
=rm1,1[(1)(1)]p[1+1]q+rm1,2[(1)(2)]p[1+2]q+rm2,2[(2)(2)]p[2+2]q
=(k1)[1]p[2]q+(4k4)[2]p[3]q+(6)[4]p+q (2)

Using Table 1, in Equation (2), we noted the following 11 reverse topological descriptors for the graphene when l=1,k>1

Remark 2.

  • (i)
    RGISI(0,1)=RM1(Ǥ)=(k1)[1]0[2]1+(4k4)[2]0[3]1+(6)[4]0[4]1 
    RM1(G)=14k+10
  • (ii)
    RGISI(1,0)=RM2(Ǥ)=(k1)[1]1[2]0+(4k4)[2]1[3]0+(6)[4]1[4]0
    RM2(Ǥ)=9k+15
  • (iii)
    RGISI(1 2,0)=RR(Ǥ)=(k1)[1]1 2[2]0+(4k4)[2]1 2[3]0+(6)[4]1 2[4]0
    RR(Ǥ)=(1+22)k+(342)
  • (iv)
    RGISI(0,1 2)=RSCI(Ǥ)=(k1)[1]0[2]1 2+(4k4)[2]0[3]1 2+(6)[4]0[4]1 2
    RSCI(Ǥ)=(12+43)k+(31243)
  • (v)
    2RGISI(0,1)=RH(Ǥ)=(k1)[1]0[2]1+(4k4)[2]0[3]1+(6)[4]0[4]1
    RH(Ǥ)=113k23
  • (vi)
    RGISI(0,2)=RHZ(Ǥ)=(k1)[1]0[2]2+(4k4)[2]0[3]2+(6)[4]0[4]2
    RHZ(Ǥ)=40k+56
  • (vii)
     2RGISI(12,1)=RGA(Ǥ)=2(k1)[1]12[2]1+2(4k4)[2]12[3]1+2(6)[4]12[4]1
    RGA(Ǥ)=(3+823)k+(5823). 
  • (viii)
    12RGISI(1 2,1)=RAG(Ǥ)= 12(k1)[2]1+ 12(4k4)[2]1 2[3]1+ 12(6 )[4]1 2[4]1
    RAG(Ǥ)=(1+32)k+(532)
  • (ix)
     RGISI(1,1)=RISI(Ǥ)=(k1)[1]1[2]1+(4k4)[2]1[3]1+(6)[4]1[4]1
    RISI(Ǥ)=196k+176
  • (x)
    RGISI(1,1)=RReZG1(Ǥ)=(k1)[1]1[2]1+(4k4)[2]1[3]1+(6)[4]1[4]1
    RReZG1(Ǥ)=8k12
  • (xi)
    RGISI(1,1)=RReZG3(Ǥ)=(k1)[1]1[2]1+(4k4)[2]1[3]1+(6)[4]1[4]1
    RReZG3(Ǥ)=26k+70

Case 3. 

Forl>1, k=1,the reverse edge partition of the graphene containsrm1,1=2l3edges, rm1,2=2ledges, andrm2,2=l+4edges.

Using the definition of the reverse general inverse sum indeg descriptor, RGISI(p,q)(Ǥ),

GISI(p,q)(Ǥ)=uvE(Ǥ)[ΦuΦv]p [Φu+Φv]q
RGISI(p,q)(Ǥ)=uvE1(Ǥ)[ΦuΦv]p [Φu+Φv]q+uvE2(Ǥ)[ΦuΦv]p [Φu+Φv]q
+uvE3(Ǥ)[ΦuΦv]p [Φu+Φv]q
=rm1,1[(1)(1)]p[1+1]q+rm1,2[(1)(2)]p[1+2]q+rm2,2[(2)(2)]p[2+2]q
=(2l3)[1]p[2]q+(2l)[2]p[3]q+(l+4)[4]p+q (3)

Using Table 1, in Equation (3), we noted the following reverse topological descriptors for the graphene when l>1,k=1

Remark 3.

  • (i)
    RGISI(0,1)=RM1(Ǥ)=(2l3)[1]0[2]1+(2l)[2]0[3]1+(l+4)[4]0[4]1
    RM1(Ǥ)=14l2
  • (ii)
    RGISI(1,0)=RM2(Ǥ)=(2l3)[1]1[2]0+(2l)[2]1[3]0+(l+4)[4]1[4]0
    RM2(Ǥ)=10l+13
  • (iii)
    RGISI(1 2,0)=RR(Ǥ)=(2l3)[1]1 2[2]0+(2l)[2]1 2[3]0+(l+4)[4]1 2[4]0
    RR(Ǥ)=(5+222)l1
  • (iv)
    RGISI(0,1 2)=RSCI(Ǥ)=(2l3)[1]0[2]1 2+(2l)[2]0[3]1 2+(l+4)[4]0[4]1 2
    RSCI(Ǥ)=(2+23+12)l+(232)
  • (v)
    2RGISI(0,1)=RH(Ǥ)=2(2l3)[1]0[2]1+2(2l)[2]0[3]1+2(l+4)[4]0[4]1
    RH(Ǥ)=236l1
  • (vi)
    RGISI(0,2)=RHZ(Ǥ)=(2l3)[1]0[2]2+(2l)[2]0[3]2+(l+4)[4]0[4]2
    RHZ(Ǥ)=42l+52
  • (vii)
    2RGISI(12,1)=RGA(Ǥ)=2(2l3)[1]12[2]1+2(2l)[2]12[3]1+2(l+4)[4]12[4]1
    RGA(Ǥ)=(3+423)l+1
  • (viii)
    12RGISI(1 2,1)=RAG(Ǥ)=12(2l3)[1]1 2[2]1+12(2l)[2]1 2[3]1+12(l+4)[4]1 2[4]1
    RAG(Ǥ)=(3+32)l+1
  • (ix)
    RGISI(1,1)=RISI(Ǥ)=(2l3)[1]1[2]1+(2l)[2]1[3]1+(l+4)[4]1[4]1
    RISI(Ǥ)=103l+52
  • (x)
    RGISI(1,1)=RReZG1(Ǥ)=(2l3)[1]1[2]1+(2l)[2]1[3]1+(l+4)[4]1[4]1
    RReZG1(Ǥ)=8l2
  • (xi)
    RGISI(1,1)=RReZG3(Ǥ)=(2l3)[1]1[2]1+(2l)[2]1[3]1+(l+4)[4]1[4]1
    RReZG3(Ǥ)=32l+58

Case 4. 

Whenl=1, k=1,the reverse edge partition of the graphene contained onlyrm1,1=6edges, and by the definition of reverse general inverse sum indeg descriptor, RGISI(p,q)(Ǥ),

RGISI(p,q)(Ǥ)=uvE1(Ǥ)[ΦuΦv]p [Φu+Φv]q=rm1,1[(1)(1)]p[1+1]q=(6)[1]p[2]q

In this case, we noted the following 11 reverse topological descriptors for the graphene as follows:

Remark 4.

  • (i)

    RM1(Ǥ)=(6)[1]0[2]1=12, (ii). RM2(Ǥ)=(6)[1]1[2]0=6

  • (ii)

    RR(Ǥ)=(6)[1]1 2[2]0=6, (iv). RRSCI(Ǥ)=(6)[1]0[2]1 2=62

  • (iii)

    RH(Ǥ)=2(6)[1]0[2]1=6, (vi). RHZ(Ǥ)=(6)[1]0[2]2=24

  • (iv)

    RGA(Ǥ)=2(6)[1]12[2]1=6, (viii). RAG(Ǥ)=12(6)[1]1 2[2]1=6

  • (v)

    RISI(Ǥ)=(6)[1]1[2]1=3, (x). RReZG1(Ǥ)=(6)[1]1[2]1=12

  • (vi)

    RReZG3(Ǥ)=(6)[1]1[2]1=12

In Table 5, the numerical values of the 11 reverse topological descriptors calculated with graphene’s analytical expressions when l>1,k>1 are presented. From Table 5, it is possible to see how individual reverse topological descriptor differ and how they are similar. The computational results show that reverse topological descriptors are highly dependent on the values of l and k. As these values increase, the magnitude of all reverse descriptors also increases, and this can be visualized by the 3D graphical representation in Figure 11.

Table 5.

Numerical values of the graphene for l>1,k>1.

(l, k) RM1 RM2 RR RSCI RH RHZ RGA RAG RISI RReZG1 RReZG3
(1, 1) 24 23 2.9142 2.9476 2.8333 94 5.8856 6.1213 5.8333 6 90
(2, 2) 58 45 13.657 11.154 13.333 188 18.542 19.485 13.833 28 154
(3, 3) 104 73 30.339 23.604 27.833 306 37.199 38.849 24.833 62 230
(4, 4) 162 107 53.142 40.295 52.333 448 61.856 64.213 38.833 108 318
(5, 5) 232 147 81.885 61.231 80.833 614 92.512 95.577 55.833 166 418
(6, 6) 314 193 116.63 86.408 115.33 804 129.17 132.94 75.833 236 530
(7, 7) 408 245 157.11 115.83 155.83 1018 171.83 176.30 98.833 318 654
(8, 8) 514 303 204.11 149.50 202.83 1256 220.48 225.67 124.83 412 790
(9, 9) 632 367 256.86 187.40 254.83 1518 275.14 281.03 153.83 518 938
(10, 10) 762 437 315.60 229.54 313.33 1804 335.80 342.40 185.83 636 1098

Figure 11.

Figure 11

An interactive visualization of Table 5.

4. Conclusions

In this paper, we presented a reverse general inverse sum inverse degree descriptor RGISI(p,q) from which one can derive a set of reverse degree-based topological descriptors. In order to assess the predictive potential of RGISI(p,q), we selected the exchange-correlation energy of the graphene sheets as a data example. Based on the results obtained in this article, we can summarize them as follows:

  • The regression models (Table 4) derived from reverse topological descriptors in the present article were extremely accurate for predicting the exchange-correlation energies in the graphene sheets.

  • The reverse sum−connectivity descriptor with R2=0.997 was the best predictor among the 11 studied descriptors. Meanwhile, the reverse redefined first Zagreb descriptor performed poorly.

  • The density functional theory (DFT) calculations of the electronic structure, such as the exchange-correlation energies of the graphene sheets, were precise; however, they were computationally expensive while the reverse topological descriptors models presented herein required minimal computations and provided high levels of accuracy.

  • Analytical expressions of the reverse first and second Zagreb descriptor, reverse Randić descriptor, reverse sum−connectivity descriptor, reverse harmonic descriptor, reverse hyper Zagreb descriptor, reverse geometric−arithmetic descriptor, reverse inverse sum indeg descriptor, and reverse redefined first and third Zagreb descriptors have been obtained for graphene structures.

  • Researchers who are trying to better understand the behaviour of graphene are likely to find the numerical values and graphical representations presented in this article helpful.

Acknowledgments

Authors would like to thank the Deanship of Scientific Research, Qassim University, for funding publication of this project.

Author Contributions

Conceptualization, M.A., P.A., W.H.E.-G. and H.A.E.-H.; methodology, M.A., P.A., W.H.E.-G. and H.A.E.-H.; software, M.A. and P.A.; validation, W.H.E.-G. and H.A.E.-H.; formal analysis, P.A. and H.A.E.-H.; investigation, P.A., W.H.E.-G. and H.A.E.-H.; data curation, M.A., P.A., W.H.E.-G. and H.A.E.-H.; writing—original draft preparation, P.A.; writing—review and editing, M.A. and W.H.E.-G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All the raw data supporting the conclusion of this paper were provided by the authors.

Conflicts of Interest

The authors declare that they have no competing interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Associated Data

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Data Availability Statement

All the raw data supporting the conclusion of this paper were provided by the authors.


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