Graphitic carbon is a valuable material that can be utilized in many fields, such as electronics, energy storage and wastewater filtration. Due to the high demand for commercial graphite, an alternative raw material with lower costs that is environmentally friendly has been explored. Amongst these, an agricultural bio-waste material has become an option due to its highly bioactive properties, such as bioavailability, antioxidant, antimicrobial, in vitro and anti-inflammatory properties. In addition, biomass wastes usually have high organic carbon content, which has been discovered by many researchers as an alternative carbon material to produce graphite. However, there are several challenges associated with the graphite production process from biomass waste materials, such as impurities, the processing conditions and production costs. Agricultural bio-waste materials typically contain many volatiles and impurities, which can interfere with the synthesis process and reduce the quality of the graphitic carbon produced. Moreover, the processing conditions required for the synthesis of graphitic carbon from agricultural biomass waste materials are quite challenging to optimize. The temperature, pressure, catalyst used and other parameters must be carefully controlled to ensure that the desired product is obtained. Nevertheless, the use of agricultural biomass waste materials as a raw material for graphitic carbon synthesis can reduce the production costs. Improving the overall cost-effectiveness of this approach depends on many factors, including the availability and cost of the feedstock, the processing costs and the market demand for the final product. Therefore, in this review, the importance of biomass waste utilization is discussed. Various methods of synthesizing graphitic carbon are also reviewed. The discussion ranges from the conversion of biomass waste into carbon-rich feedstocks with different recent advances to the method of synthesis of graphitic carbon. The importance of utilizing agricultural biomass waste and the types of potential biomass waste carbon precursors and their pre-treatment methods are also reviewed. Finally, the gaps found in the previous research are proposed as a future research suggestion. Overall, the synthesis of graphite from agricultural bio-waste materials is a promising area of research, but more work is needed to address the challenges associated with this process and to demonstrate its viability at scale.

Two different phases of alumina (Al2O3) nanoparticles (γ-alumina and α-alumina) have successfully been synthesized by using a sol-gel method. During the process a mixture of aluminum nitrate and citric acid (C/N=0.5) was heated at 60°C followed by 80°C until a gel was formed. The amorphous gel structure then was dried and sintered from 600°C to 1200°C. From the X-ray diffraction (XRD) analysis, crystalline structure of γ-alumina started to form at 800°C with average crystallite size of 11.5 nm, followed by the formation of the mixture phase of γ-alumina and α-alumina at 1000°C. The transformation from γ- to α-alumina occured at 1100°C of sintering temperature and above with the average crystallite size of 49 nm. The efficiency of the synthesized alumina nanoparticles as an adsorbents was tested by immersing the powder into the copper ions solution. The percentage of the copper removal was measured by using atomic absorption spectroscopy (AAS). It was found that, the efficiency of the alumina nanoparticles as an adsorbent was not depending on their phases, but might due to the increased of the particle size at higher sintering temperature. The highest percentage of removal 82.1% was obtained when using the alumina sintered at 1200°C.

A silver sulfide (Ag₂S) semiconductor photocatalyst film has been successfully synthesized using a solution casting method. To produce the photocatalyst films, two types of Ag₂S powder were used: a commercialized and synthesized powder. For the commercialized powder (CF/comAg₂S), the Ag₂S underwent a rarefaction process to reduce its crystallite size from 52 nm to 10 nm, followed by incorporation into microcrystalline cellulose using a solution casting method under the presence of an alkaline/urea solution. A similar process was applied to the synthesized Ag₂S powder (CF/syntAg₂S), resulting from the co-precipitation process of silver nitrate (AgNO₃) and thiourea. The prepared photocatalyst films and their photocatalytic efficiency were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and UV-visible spectroscopy (UV-Vis). The results showed that the incorporation of the Ag₂S powder into the cellulose films could reduce the peak intensity of the oxygen-containing functional group, which indicated the formation of a composite film. The study of the crystal structure confirmed that all of the as-prepared samples featured a monoclinic acanthite Ag₂S structure with space group P₂₁/C. It was found that the degradation rate of the methylene blue dye reached 100% within 2 h under sunlight exposure when using CF/comAg₂S and 98.6% for the CF/syntAg₂S photocatalyst film, and only 48.1% for the bare Ag₂S powder. For the non-exposure sunlight samples, the degradation rate of only 33–35% indicated the importance of the semiconductor near-infrared (NIR) Ag₂S photocatalyst used.

Despite the increasing trend of n-type silicon wafer utilization in the manufacturing of high-efficiency heterojunction solar cells due to the superior advantages over p-type counterparts, its high manufacturing cost remains to be one of the most crucial factors, which impedes its market share growth with state-of-the-art silicon heterojunction (SHJ) solar cells demonstrating high conversion efficiencies from various configurations, the prospect of using an n-type wafer is debatable from a cost-efficiency point of view. Hence, a systematic comparison between p- and n-type SHJ solar cells was executed in this work using AFORS-HET numerical software. Front and rear-emitter architectures were selected for each type of wafer with ideal (without defects) and non-ideal (with defects) conditions. For ideal conditions, solar cells with p-type wafers and a front-emitter structure resulted in a maximum conversion efficiency of 28%, while n-type wafers demonstrated a maximum efficiency of 26% from the rear-emitter structure. These high-performance devices were possible due to the optimization of the bandgap and electron-affinity for all passivating and doping layers with values ranging from 1.3 to 1.7 eV and 3.9 to 4 eV, respectively. The correlation between the device structure and the type of wafers as demonstrated here will be helpful for the development of both types of solar cells with comparable performance.

Dye-sensitized solar cells (DSSCs) were developed by exploiting the photovoltaic effect to convert solar energy into electrical energy. The photoanode layer thickness significantly affects the semiconductor film’s ability to carry electronic charges, adsorb sensitizing dye molecules, and lower the recombination of photo-excited electrons injected into the semiconductor. This study investigated the dependence of the zinc oxide (ZnO) photoanode thin-film thickness and the film soaking time in N719 dye on the photocurrent–voltage characteristics. The ZnO photoanode was applied to glass using the doctor blade method. The thickness was varied by changing the scotch tape layers. The ZnO-based DSSC attained an efficiency of 2.77% with three-layered photoanodes soaked in the dye for three hours, compared to a maximum efficiency of 0.68% that was achieved with three cycles using the dip-coating method in other research. The layer thickness of the ZnO photoanode and its optimal adsorption time for the dye are important parameters that determine the efficiency of the DSSC. Therefore, this work provides important insights to further improve the performance of DSSCs.

Dye sensitized solar cell (DSSC) is a promising candidate for a low cost solar harvesting technology as it promised a low manufacturing cost, ease of fabrication and reasonable conversion efficiency. Basic structure of DSSC consists of photoanode, dye, electrolyte and counter electrode. Photoanode plays an important role for a DSSC as it supports the dye molecules and helps in the electron transfer that will determine the energy conversion efficiency. This paper emphasizes the various improvements that had been done on the TiO2 and ZnO photoanode nanostructures synthesized through thermal method. For overall comparisons, ZnO nanoflowers photoanode had achieved the highest energy conversion efficiency of 4.7% due to its ability of internal light scattering that had increased the electron transportation rate. This has made ZnO as a potential candidate to replace TiO2 as a photoanode material in DSSC.