Graphene-based Nanomaterials Research Articles

Novel Concepts for Graphene-Based Nanomaterials Synthesis for Phenol Removal from Palm Oil Mill Effluent (POME).

In recent years, the global population has increased significantly, resulting in elevated levels of pollution in waterways. Organic pollutants are a major source of water pollution in various parts of the world, with phenolic compounds being the most common hazardous pollutant. These compounds are released from industrial effluents, such as palm oil milling effluent (POME), and cause several environmental issues. Adsorption is known to be an efficient method for mitigating water contaminants, with the ability to eliminate phenolic contaminants even at low concentrations. Carbon-based materials have been reported to be effective composite adsorbents for phenol removal due to their excellent surface features and impressive sorption capability. However, the development of novel sorbents with higher specific sorption capabilities and faster contaminant removal rates is necessary. Graphene possesses exceptionally attractive chemical, thermal, mechanical, and optical properties, including higher chemical stability, thermal conductivity, current density, optical transmittance, and surface area. The unique features of graphene and its derivatives have gained significant attention in the application of sorbents for water decontamination. Recently, the emergence of graphene-based adsorbents with large surface areas and active surfaces has been proposed as a potential alternative to conventional sorbents. The aim of this article is to discuss novel synthesis approaches for producing graphene-based nanomaterials for the adsorptive uptake of organic pollutants from water, with a special focus on phenols associated with POME. Furthermore, this article explores adsorptive properties, experimental parameters for nanomaterial synthesis, isotherms and kinetic models, mechanisms of nanomaterial formation, and the ability of graphene-based materials as adsorbents of specific contaminants.

Graphene oxide worsens copper-mediated embryo-larval toxicity in the pacific oyster while reduced graphene oxide mitigates the effects

Due to their properties, graphene-based nanomaterials (GBMs) are triggering a great interest leading to an increase of their global production and use in new applications. As a consequence, their release into the environment is expected to increase in the next years. When considering the current knowledge in the evaluation of GBMs ecotoxic potential, studies aiming to evaluate the hazard associated to these nanomaterials towards marine species and particularly considering potential interactions with other environmental pollutants such as metals are scarce. Here we evaluated the embryotoxic potential of GBMs, which include graphene oxide (GO) and its reduced form (rGO), both individually and in combination with copper (Cu) as a referent toxicant, towards early life stages of the Pacific oyster through the use of a standardized method (NF ISO 17244). We found that following exposure to Cu, dose-dependent decrease in the proportion of normal larvae was recorded with an Effective Concentration leading to the occurrence of 50% of abnormal larvae (EC50) of 13.85 ± 1.21 μg/L. Interestingly, the presence of GO at a non-toxic dose of 0.1 mg/L decreased the Cu EC50 to 12.04 ± 0.85 μg/L while it increased to 15.91 ± 1.57 μg/L in presence of rGO. Based on the measurement of copper adsorption, the obtained results suggest that GO enhances Cu bioavailability, potentially modifying its toxic pathways, while rGO mitigates Cu toxicity by decreasing its bioavailability. This research underscores the need to characterize the risk associated to GBMs interactions with other aquatic contaminants and supports the adoption of a safer-by-design strategy using rGO in marine environments. This would contribute to minimize the potential adverse effects on aquatic species and to reduce the risk for economic activities associated to coastal environments.

Intelligent cyclic fire warning sensor based on hybrid PBO nanofiber and montmorillonite nanocomposite papers decorated with phenyltriethoxysilane

An abundance of early warning graphene-based nano-materials and sensors have been developed to avoid and prevent the critical fire risk of combustible materials. However, there are still some limitations that should be addressed, such as the black color, high-cost and single fire warning response of graphene-based fire warning materials. Herein, we report an unexpected montmorillonite (MMT)-based intelligent fire warning materials that have excellent fire cyclic warning performance and reliable flame retardancy. Combining phenyltriethoxysilane (PTES) molecules, poly(p-phenylene benzobisoxazole) nanofiber (PBONF), and layers of MMT to form a silane crosslinked 3D nanonetwork system, the homologous PTES decorated MMT-PBONF nanocomposites are designed and fabricated via a sol–gel process and low temperature self-assembly method. The optimized nanocomposite paper shows good mechanical flexibility (good recovery after kneading or bending process), high tensile strength of ∼81 MPa and good water resistance. Furthermore, the nanocomposite paper exhibits high-temperature flame resistance (almost unchanged structure and size after 120 s combustion), sensitive flame alarm response (∼0.3 s response once exposure onto a flame), cyclic fire warning performance (>40 cycles), and adaptability to complex fire situations (several fire attack and evacuation scenarios), showing promising applications for monitoring the critical fire risk of combustible materials. Therefore, this work paves a rational way for design and fabrication of MMT-based smart fire warning materials that combine excellent flame shielding and sensitive fire alarm functions.

New insight into the biocompatibility/toxicity of graphene oxides and their reduced forms on Chlamydomonas reinhardtii

Graphene oxides (GOs) and their reduced forms are often discussed both positively and negatively due to the lack of information about their chemistry and structure. This study utilized GOs with two sheet sizes that were further reduced by two reducing agents (sodium borohydride and hydrazine) to obtain two different degrees of reduction. The synthesized nanomaterials were characterized using scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), elemental analysis (EA), Fourier transform infrared (FTIR) spectroscopy, and Raman spectroscopy (RA) to understand their chemistry and structure. The second focus of our investigation included in vitro testing of the biocompatibility/toxicity of these materials on a model organism, the freshwater microalga Chlamydomonas reinhardtii. The effects were studied on the basis of biological endpoints complemented by biomass investigation (FTIR spectroscopy, EA, and atomic absorption spectrometry (AAS)). The results showed that the biocompatibility/toxicity of GOs is dependent on their chemistry and structure and that it is impossible to generalize the toxicity of graphene-based nanomaterials.

Synthesis, characterization, and application of graphene oxide and reduced graphene oxide and its influence on rheology, microstructure, and mechanical strength of cement paste

The present study is an attempt in disseminating the influence of graphene-based nanomaterials such as graphene oxide (GO) and reduced graphene oxide (rGO) in cement composites. The improved Hummer's approach was employed to synthesise the GO and rGO. Various characterization techniques involving XRD, FTIR, TGA, TEM, and SEM were utilized to understand the crystalline structure, interlayer spacing, functional groups, and microstructure of GO and rGO nanoparticles and further nanomaterial-doped cement composites. Both GO and rGO were used as 0.01%, 0.02%, 0.03%, 0.04%, and 0.05% by weight of cement. The influence of GO and rGO on rheology, workability, microstructure and mechanical strength were determined. The compressive test results indicated an improvement of compressive strength by 21.72% and 30.26% in 0.03% GO and 0.04% rGO cement composites respectively. The enhancement in physicochemical properties is attributed to the densification of microstructure with the GO and rGO usage in cement composites. Concrete workability, pumpability, and printability depend on rheological parameters such yield stress, viscosity, and thixotropy. The research paper highlights the significance of critical rheological parameters of cement with the addition of nanomaterials. The incorporation of graphene oxide and reduced graphene oxide into cement paste represents a promising avenue for enhancing the material's rheology, microstructure, and mechanical strength, with the potential to revolutionize the construction industry and pave the way for a new generation of high-performance, sustainable building materials.

Multifunctional Concrete with Graphene-Based Nanomaterials and Superabsorbent Polymer

This study reports on the development of a multifunctional concrete using graphene nanoplatelet (GnP) and sodium polyacrylate (SP) superabsorbent polymer. A combination of concrete functionalities was convened to improve, i.e., high strength and durability along with smart properties such as self-healing and self-sensing. GnP (0.05% by weight of cement) and SP (0.11% by weight of cement) were dispersed in concrete. Compared to the control concrete mix (no GnP and SP), the compressive strength increased 14% by GnP and decreased 9% by SP, and their combination resulted in a 6% enhancement in strength. The durability performance of concrete samples under coupled degradation mechanisms of freeze-thaw and chloride ion ingress suggested that SP in concrete has a better performance than GnP in concrete. SP in concrete shows self-sealing abilities resulting in less chloride ion penetration. However, the combined effect of both GnP and SP in concrete resulted in the maximum reduction in chloride ion penetration depth under freeze-thaw, a 42% reduction compared to the control mix. Microstructural analysis was conducted and found to resist the effects of freeze-thaw and reduce chloride ion penetration in modified concrete compared to the control concrete mix. GnP developed self-sensing abilities in concrete, resulting in about 12.7% fractional change of electrical resistance under 10 KN of cyclic compressive loading. The synergic impact of GnP and SP possesses a new prospect for developing highly efficient multifunctional concrete.

A review on energy conversion applications of graphene-based nanomaterials and environmental remediation

Graphene is popular for its striking physicochemical properties. Conversely, the application of pure graphene is greatly limited inert owing to its inert nature. Therefore, one of the greatest approaches to investigate graphene's intrinsic features is by functionalization. The highly conductive rGO (reduced graphene oxide) sheet is generally used as a suitable solid support for catalysts that not only inhibit carrier recombination but also improve carrier mobility to power a variety of solar energy conversion applications. According to various studies, the photocatalytic H2 production rate was found to be significantly increased by the potential electron storing and transferring characteristics of the rGO sheet, going from 16656 mol/h for Cu2O-TiO2 to 110968 mol/h for Cu2O-TiO2/rGO, or an increase of at least 7 times. The Cu2O-rGO-C3N4 photocatalyst 139 considerably enhanced the photocatalytic 4-nitrophenol reduction in comparison to the Cu2O-C3N4 photocatalyst alone. The oxygen reduction reaction, photocatalytic water splitting, photocatalytic degradation of organic contaminants, and polymer solar cells were only a few of the applications that rGO-based nanocomposites were used for in the current study.

Functionalization of graphene-based nanomaterials for energy and hydrogen storage

Graphene and its derivatives are attractive solid-state candidates to meet the needs of next-generation energy and hydrogen storage technologies. Although impressive storage capacities have been demonstrated, materials meeting all targets established by the United States Department of Energy have yet to be identified. In this review, we provide an overview of recent developments in functionalized graphene-based nanomaterials for energy and hydrogen storage systems. First, considerations for the most common synthetic approaches to graphene-based nanomaterials are briefly summarized. Then, the effects of traditional functionalization strategies on the structural characteristics and properties of pristine graphene are discussed. Lastly, recent advances and progress in energy applications using functionalized graphene-based nanomaterials including supercapacitors, batteries and hydrogen storage are highlighted, and new directions are discussed.

Effect of electrolytes on the performance of graphene oxide anode material for ultracapacitor, Li-ion capacitor, and Li-ion battery: three-in-one approach

Graphene-based 2D nanomaterials are gaining much interest in energy storage systems, specifically in ultracapacitors. Various electrolytes increase the performance of ultracapacitor (UC), Li-Ion capacitor (LIC), and Li-Ion battery (LIB). In the present work, we have successfully designed a "three-in-one" artificial method to engineer anode from a single precursor for high-performance UC, LIC, and LIB. In the present investigation, graphene oxide (GO) slurry was developed using the modified Hummers’ method. The effect of KOH, H2SO4, and KCl electrolytes on electrochemical performance of UC was demonstrated. The LiPF6 organic electrolyte solution on electrochemical performance of LIC and LIB is demonstrated. The GO deposited on stainless steel electrode achieved its highest specific capacitance of 422 F/g, energy density of 45.50 kWh/kg, and power density of 10,000 W/kg in 3.0 M in KCl, whereas GO as an anode material delivered a first discharge capacity of 456 mAh/g at 0.05 A/g current density with the efficiency of 100%.

Transformation of graphene oxide affects photodegradation of imidacloprid in the aquatic environment: Mechanism and implication

Graphene oxide (GO) is a representative novel carbonaceous nanomaterial, and neonicotinoid insecticides (NEOs) are currently the insecticides with the highest market share in the world. Their widespread application deservedly leads to their release to the environment. Thus, the complex interactions of these two types of organic compounds have attracted extensive attention. In this study, the effects of GO and its derivatives, reduced GO (RGO) and oxidized GO (OGO), on the photolysis of imidacloprid (IMD) (a typical NEO) under ultraviolet (UV) irradiation were systematically investigated. The results showed that the presence of the graphene-based nanomaterials (GNs) largely depressed the photodegradation of IMD, and the inhibition degree followed the order of RGO > GO > OGO. This was because the sp2 π-conjugated structure in the GNs caused light-shielding effect and attenuated the direct photolysis of IMD, even though the GNs-generated reactive oxygen species (ROS) promoted the indirect photodegradation of IMD to a certain extent. Additionally, the rich O-functionalized GO and OGO altered the photolysis pathway of IMD and induced more toxic intermediate products. These results highlight the implication of carbonaceous nanomaterials on the behavior, fate and potential risk of NEOs in aqueous systems.

Impact of Environmental Stresses on the Antibacterial Activity of Graphene Oxide (GO) Nanoparticles against P. putida Biofilms.

As the production of graphene-based nanomaterials such as GO is increasing, it is expected that a large amount of GO waste will be generated. The environment (i.e., soil and aquatic systems) will be amongst the final repositories of these wastes which means important natural microbial communities in such environments will be at risk of GO exposure. However, little is known about how these communities respond to environmental stresses in synergy with the presence of GO. In this study, the effect of three different stress conditions: temperature (5, 25 and 40 °C); pH (5 to 9) and osmotic stress (51, 219 and 320 mM NaCl) in addition to GO treatment was investigated on the viability and physiology of biofilms and planktonic cells of soil bacterium P. putida. It was found that planktonic cells were more resistant to GO alone compared to biofilms. However, the cells were sensitive to GO when exposed to pH or osmotic stresses. Temperature was not found to influence the survival of biofilm with or without exposure to GO. However, low pH caused a reduction in colony-forming units (CFU) at pHs 5 and 6 for the pre-treated samples, while biofilms at pH 7-9 did not show any decrease. Interestingly, the post-treatment of planktonic cells or biofilms with GO showed a significant reduction in CFU at all pH ranges. The effect of higher osmotic stress in combination with GO resulted in a significant reduction in biofilms. These results show that the effect of stresses naturally occurring in the environment can be affected and changed when in combination with GO and can potentially affect the balance of natural biofilms.

Effects of sunlight on the fate of graphene oxide and reduced graphene oxide nanomaterials in the natural surface water

Graphene nanomaterials have been commercialized for use in the electronic and biomedical industries, increasing their dissemination into surface waters and subsequent transformation in natural aquatic environment. While the photodegradation of graphene oxide nanomaterials has been investigated in the past, previous research did not consider actual natural aquatic environment and also focused on primarily graphene oxide nanomaterials. In this study, photodegradation of graphene nanomaterials with varying oxidation levels, including graphene oxide (GO) and partially reduced graphene oxide (rGO-2 h) are evaluated in Columbia River Water and compared with each other. Our results indicate that both direct and indirect photolysis of graphene-based nanomaterials will occur simultaneously in natural surface water. However, environmentally relevant concentrations of photosensitizers in surface water are not capable of producing sufficient ·OH to initiate degradation of GO via indirect photolysis. For all conditions tested, GO showed more rapid photodegradation compared to rGO. Overall, direct and indirect photodegradation of graphene oxide nanomaterials in natural surface water is minimal and slow indicating that phototransformation of graphene-based nanomaterials will be insignificant in natural surface water.

Pore Perforation of Graphene Coupled with In Situ Growth of Co3 Se4 for High-Performance Na-Ion Battery.

Graphene-based nanomaterials have sprung up as promising anode materials for sodium-ion batteries due to the intriguing properties of graphene itself and the synergic effect between graphene and active materials. However, the 2Dgraphene sheet only allows the rapid diffusion of sodium ions along the parallel direction while that of the vertical direction is difficult, limiting the rate capability of graphene-based electrode materials. To tackle this problem, pore-forming engineering has been employed to perforate graphene and concurrently achieve the in situ growth of Co3 Se4 nanoparticles. The generation of in-plane nanohole breaks through the physical barriers of the graphene nanosheets, enabling the fast diffusion of electrolyte ions in the longitudinal direction. In addition, this design limits the aggregation of Co3 Se4 nanoparticles because of the high affinity of Co3 Se4 on graphene. Benefiting from the high conductivity and fast ion transport bestowed by the ingenious architecture, the Co3 Se4 /holey graphene exhibits a remarkable rate performance of 519.5 mAh g-1 at 5.0 A g-1 and desirable cycle stability. Conclusions drawn from this investigation are that the transport of sodium inside the graphene-based composites is crucial for rate performance enhancement and this method is effective in modifying graphene-based nanomaterials as potential anode materials.

Effect of graphene-based nanomaterials on corneal wound healing in vitro

Graphene-based nanomaterials (GBNs) are widely used due to their chemical and physical properties for multiple commercial and environmental applications. From an occupational health perspective, there is concern regarding the effects of inhalation on the respiratory system, and many studies have been conducted to study inhalation impacts on lung. Similar to the respiratory system, the eyes may also be exposed to GBNs and thus impacted. In this study, immortalized human corneal epithelial (hTCEpi) cells and rabbit corneal fibroblasts (RCFs) were used to investigate the toxicity of eight types of GBN: graphene oxide (GO; 400 nm), GO (1 μm), partially reduced graphene oxide (PRGO; 400 nm), reduced graphene oxide (RGO; 400 nm), RGO (2 μm), graphene (110 nm), graphene (140 nm), and graphene (1 μm). We next examined the effects of these GBNs on hTCEpi cell migration. We also determined whether the expression of α-smooth muscle actin (αSMA), a myofibroblast marker, is altered by the GBNs using RCFs. We found that RGO (400 nm) and RGO (2 μm) were highly toxic to hTCEPi cells and RCFs meanwhile, PRGO (400 nm) was toxic only to hTCEpi cells. In addition, PRGO (400 nm), RGO (400 nm), and RGO (2 μm) inhibited hTCEpi cell migration and significantly increased αSMA mRNA expression. Further study in vivo is required to determine if RGO nanomaterials delay corneal epithelial healing and induce scar formation.

Graphene-based nanomaterials for stimuli-sensitive controlled delivery of therapeutic molecules.

Stimuli-responsive drug delivery has attracted tremendous attention in the past decades. It provides a spatial- and temporal-controlled release in response to different triggers, thus enabling highly efficient drug delivery and minimizing drug side effects. Graphene-based nanomaterials have been broadly explored, and they show great potential in smart drug delivery due to their stimuli-responsive behavior and high loading capacity for an extended range of drug molecules. These characteristics are a result of high surface area, mechanical stability and chemical stability, and excellent optical, electrical, and thermal properties. Their great and infinite functionalization potential also allows them to be integrated into several types of polymers, macromolecules, or other nanoparticles, leading to the fabrication of novel nanocarriers with enhanced biocompatibility and trigger-sensitive properties. Thus, numerous studies have been dedicated to graphene modification and functionalization. In the current review, we introduce graphene derivatives and different graphene-based nanomaterials utilized in drug delivery and discuss the most important advances in their functionalization and modification. Also, their potential and progress in an intelligent drug release in response to different types of stimuli either endogenous (pH, redox conditions, and reactive oxygen species (ROS)) or exogenous (temperature, near-infrared (NIR) radiation, and electric field) will be debated.

Development of Thiol-Maleimide hydrogels incorporating graphene-based nanomaterials for cancer chemo-photothermal therapy

Nano-sized materials have been widely explored in the biomedicine field, especially due to their ability to encapsulate drugs intended to be delivered to cancer cells. However, systemically administered nanomaterials face several barriers that can hinder their tumor-homing capacity. In this way, researchers are now focusing their efforts in developing technologies that can deliver the nanoparticles directly into the tumor tissue. Particularly, hydrogels assembled using Thiol-Maleimide Michael type additions are emerging for this purpose due to their capacity to incorporate high nanoparticles’ doses in a compact 3D structure as well as good chemical selectivity, biocompatibility, and straightforward preparation. Nevertheless, such hydrogels have been mostly prepared using synthetic polymers, which is not ideal due to their poor biodegradability. In this work, a novel natural polymer-based Thiol-Maleimide hydrogel was produced for application in breast cancer chemo-photothermal therapy. To obtain natural polymers compatible with this crosslinking chemistry, Hyaluronic acid was endowed with Thiol groups and deacetylated Chitosan was grafted with Maleimide groups. Parallelly, Doxorubicin loaded Dopamine-reduced graphene oxide (DOX/DOPA-rGO) was prepared for attaining Near Infrared (NIR) light responsive chemo-photothermal nanoagents. By simply mixing Hyaluronic Acid-Thiol, deacetylated Chitosan-Maleimide and DOX/DOPA-rGO, Thiol-Maleimide crosslinked hydrogels incorporating this nanomaterial could be assembled (DOX/DOPA-rGO@TMgel). When breast cancer cells were incubated with DOPA-rGO@TMgel and exposed to NIR light (photothermal therapy), their viability was reduced to about 59 %. On the other hand, DOX/DOPA-rGO@TMgel (chemotherapy) reduced cancer cells’ viability to 50 %. In stark contrast, the combined action of DOX/DOPA-rGO@TMgel and NIR light decreased breast cancer cells’ viability to just 21 %, highlighting its chemo-photothermal potential.

R-curve evaluation of 3YTZP/graphene composites by indirect compliance method

This work addresses the crack growth resistance of 3 mol% Yttria-doped Tetragonal Zirconia Polycrystalline (3YTZP) spark-plasma sintered (SPS) composites containing two types of graphene-based nanomaterials (GBN): exfoliated graphene nanoplatelets (e-GNP) and reduced graphene oxide (rGO). The crack growth resistance of the composites is assessed by means of their R-Curve behavior determined by three-point bending tests on single edge “V” notched beams (SEVNB), in two different orientations of the samples: with the crack path perpendicular or parallel to the pressure axis during the SPS sintering. The sharp edge notches were machined by ultrashort laser pulsed ablation (UPLA). The compliance and optical-based methods for evaluating the crack length are compared on the basis of the experimental R-Curve results in composites with 2.5 vol% rGO tested in the perpendicular orientation. Moreover, the activation of reinforcement mechanisms is evaluated by both the fracture surface inspection by Scanning Electron Microscopy and a compliance analysis. It is shown that the indirect compliance method is relevant and reliable for calculating the R-Curve of 3YTZP/GBN composites. The effect of the type and content of GBN on the crack growth resistance of the composites is also discussed.

Optical Properties of Reduced Graphene Oxide-Coated Tellurite Glass Doped at Different Erbium Composition

Graphene-based nanomaterials have significant potential to be used as coating materials for glass performance. In this work, reduced graphene oxide (rGO)-coated tellurite glass was synthesized via melt-quenching and low-cost spray coating techniques for improving the optical properties in the glassy matrix. The structural properties investigated using X-Ray Diffraction (XRD) confirmed the structural arrangement of an amorphous nature phase meanwhile, Scanning Electron Microscopy (SEM) analysis proved the morphological structure images of rGO onto the tellurite glass surface. The refractive index value of rGO-coated glass was found higher in the range of 2.402 - 2.775 due to the graphene-based effects. The optical bandgap energy value of rGO-coated glass was improved from 1.913 - 2.980 eV which correlated to the changes in rGO absorption characteristics. The Urbach energy showed a high number of defects in absorption with the presence of rGO structures. By virtue of improved optical properties, the rGO-coated glass may be beneficial to be used as a glass coating material for high optical performance of fiber optics.

Emerging Trends and Future Direction of Graphene Family of Materials as Potential Antimicrobials: A Critical Review

Graphene research has progressed at an unprecedented rate since 2004 when Novoselov and Geim isolated and described a single sheet of graphene. In fact, the relentless progress in graphene literature over the past decades makes it challenging to diversify research efforts in varied directions. The superior optical, electrical, thermal, and mechanical properties of graphene usher in a broad spectrum of applications that attracts the interest of various scientific domains, including material scientists, physicists, chemists, and biologists. These exceptional properties of the graphene family of materials (Gfam) have inspired researchers to explore a cornucopia of potential applications surrounding graphene and its derivatives in the realm of bacterial, fungal, and viral cells. Herein, we provide an exhaustive discussion of the antimicrobial mechanism of Gfam against different pathogen types: bacteria, fungi, and viruses. In addition, we present the physicochemical differences among members of Gfam and the correlation of their germicidal activities to material properties. A comparative analysis of Gfam’s activities pertaining to bare metals and the enhanced broad-spectrum antimicrobial action of graphene family-based nanocomposites as well as surface coatings are also described. The review analyzes and discusses the present constraints and anticipated future directions that would enable graphene-based nanomaterials to advance as high-performance antimicrobial structures. Thus, Gfam as a robust biocidal material of interest can effectively bridge the gap between academia and industry.

Phosphorous- and Boron-Doped Graphene-Based Nanomaterials for Energy-Related Applications.

Doping is a great strategy for tuning the characteristics of graphene-based nanomaterials. Phosphorous has a higher electronegativity as compared to carbon, whereas boron can induce p-type conductivity in graphene. This review provides insight into the different synthesis routes of phosphorous- and boron-doped graphene along with their applications in supercapacitors, lithium- ions batteries, and cells such as solar and fuel cells. The two major approaches for the synthesis, viz. direct and post-treatment methods, are discussed in detail. The former synthetic strategies include ball milling and chemical vapor discharge approaches, whereas self-assembly, thermal annealing, arc-discharge, wet chemical, and electrochemical erosion are representative post-treatment methods. The latter techniques keep the original graphene structure via more surface doping than substitutional doping. As a result, it is possible to preserve the features of the graphene while offering a straightforward handling technique that is more stable and controllable than direct techniques. This review also explains the latest progress in the prospective uses of graphene doped with phosphorous and boron for electronic devices, i.e., fuel and solar cells, supercapacitors, and batteries. Their novel energy-related applications will continue to be a promising area of study.