Experimental Investigations Conducted for the Characteristic Study of OM29 Phase Change Material and Its Incorporation in Photovoltaic Panel

: The solar photovoltaic (PV) system is emerging energetically in meeting the present energy demands. A rise in PV module temperature reduces the electrical efﬁciency, which fails to meet the expected energy demand. The main objective of this research was to study the nature of OM29, which is an organic phase change material (PCM) used for PV module cooling during the summer season. A heat transfer network was developed to minimize the experimental difﬁculties and represent the working model as an electrical resistance circuit. Most existing PV module temperature (T PV ) reduction technology fails to achieve the effective heat transfer from the PV module to PCM because there is an intermediate layer between the PV module and PCM. In this proposed method, liquid PCM is ﬁlled directly on the back surface of the PV module to overcome the conduction barrier and PCM attains the thermal energy directly from the PV module. Further, the rear side of the PCM is enclosed by tin combined with aluminium to avoid any leakages during phase change. Experimental results show that the PV module temperature decreased by a maximum of 1.2 ◦ C using OM29 until 08:30. However, after 09:00, the OM29 PCM was unable to lower the T PV because OM29 is not capable of maintaining the latent heat property for a longer time and total amount of the PCM experimented in this study was not sufﬁcient to store the PV module generated thermal energy for an entire day. The inability of the presented PCM to lower the temperature of the PV panel was attributed to the lower melting point of OM29. PCM back sheet was incapable of dissipating the stored PCM’s thermal energy to the ambient, and this makes the experimented PCM unsuitable for the selected location during summer.


Introduction
The global energy demand has increased by 2.3% compared to 2010, and this increase is mainly due to modernization and industrialization [1]. Air pollution has increased significantly because of the forest to agricultural land transformation, burning of fossil fuels, dumping waste into water, burning waste, and vehicle smoke emission. This increases by 1.7% the CO 2 concentration every year, leading to a threatening global climate change [2][3][4]. To overcome this issue, renewable energy systems are widely engaged to meet energy demand [5]. Among other renewable energy sources, solar photovoltaic (PV) systems gain attention for their low maintenance and payback period. A great amount of research work is also carried out on PV materials to improve the efficiency of PV panel [6,7]. The PV system can be operated on a standalone basis or in grid connected mode [8][9][10][11][12]. Crystalline silicon solar cell converts 1/5th of the photon into electrical energy, while some is reflected, and this reflection can be controlled by coating a thin layer of Al 2 O 3 and Ta 2 O 5 [13], and the rest is almost converted into thermal energy. Excess thermal energy in the PV module results in the drop of efficiency by 0.3-0.4% for every 1 • C more than the nominal operating cell temperature [14]. Further reduction in T PV can increase the performance of the system.
Earlier PV module cooling was conducted using water or air as a cooling agent. Water has a high specific heat capacity (4.2 J/g·K), and it can absorb higher thermal energy from the PV module. Water-assisted PV modules are mostly performed as an active method by spraying water over the PV module [15] or using heat pipe behind the PV module for both the electrical and thermal applications [16,17]. Other than active method, thermosiphon concept has also been tested but the result lowers the T PV reduction [18]. Air-based PV module cooling is mostly examined for hybrid applications where hot air is used for thermal comfort and space heating [19,20]. In most cases, water and air-based T PV reductions are not convenient due to lack of resource.
In recent years, phase change material (PCM)-assisted PV module cooling has gained great attention in terms of its striking latent heat of fusion [21,22]. PCM can extract the generated thermal energy from the PV module, and it is stored in the form of specific heat capacity and latent heat of fusion; this is as expressed in Equation (1) [23]. PCM-aided PV modules are prominent and they depend on the application of cooling methods chosen, either active or passive. Q = T m T i mC p,s dT + mL + T e T m mC p,l dT (1) where T i is initial temperature, T m is melting temperature, T e is ending temperature, m is total mass of PCM, C p,s is solid specific heat capacity of PCM, C p,l is liquid specific heat capacity of PCM, L is latent heat capacity of the PCM, and Q is the total amount of energy stored in the PCM. Active cooling methods are implemented for the performance enhancement of electrical and thermal energy using working fluids [24,25]. This active method requires less PCM because it is assisted with working fluid and periodically PCM temperature is removed by working fluid, which enables the heat transfer between the PV module and PCM. Fayaz et al. performed COMSOL simulation for a photovoltaic-thermal (PVT) system with and without PCM using heat exchanger-assisted model and compared it with the PV module [26]. They found that numerical simulation results are accurate compared to the experimental result and the remarkable increase in flow rate leads to reduce the T PV maximum by 13.77 • C. Al-Waeli et al. studied a nano PCM and nanofluid-assisted PVT collector, a copper absorber tube entrenched with nano PCM, to extract the heat from PCM container by flowing nanofluid, which enhances the thermal energy transfer from PV to PCM container [27]. Silicon oil is placed between the PV module rear surfaces and the PCM container to make perfect contact. The result shows that nano PCM assisted T PV reduced from 68.46 • C to 36.04 • C with the help of nanofluid.
Modjinou et al. comparatively analyzed macro encapsulated PCM, micro-channel heat pipe (MCHP), and regular PVT with water [28]. They found that PVT-PCM and PVT-MCHP enhanced both electrical and thermal performance. Notably, PCM-based PV module maintains constant temperature whenever there is a sudden drop in ambient temperature. Acetone influenced MHCP gains higher performance than regular PVT setup since refrigerant fluid leads to enhance the heat transfer.
PCM-only (passive cooling) incorporated PV modules are widely performed to enhance electrical efficiency without using an external source, and this system is totally autonomous and maintenance-free. Sandro et al. examined RT 38 and pork fat as a PCM in Croatia. Both PCM performed well throughout the year and there was no noticeable difference in T PV reduction except in June when ambient temperature is higher [29]. Zhao et al. analyzed different melting temperatures of PCM (PCM15, PCM20, PCM25, and PCM30) using MATLAB to find the role of PCM melting temperature [30]. A higher melting range of PCM sustains a longer time in summer, and a lower melting range of PCM performs well in winter (PCM20). This study enhanced by 2.4% the annual electric energy production.
The orientation of the PV module along with PCM plays an energetic role in T PV reduction because, internally, PCM gains thermal energy by both the conduction and the convection [31]. When the PV-PCM tilt increases, PCM internal convection also increases and it helps to reduce the higher T PV . During PCM melting, thermal energy gains by convection and it activates latent heat property, and conduction occurs during PCM solid state. Thermal variation on the PV module was simulated using ANSYS fluent under different climatic conditions such as 1-5 m/s wind variation. It showed an increase in wind speed and wind azimuth angle lead to dissipate higher thermal energy from both the PV module and the PCM container, which encourages heat transfer between the PV module and the PCM. A 22.6 • C melting range of PCM extracts higher heat than a 30.6 • C melting range of PCM [32].
In the passive cooling system, PCM temperature has been dissipated naturally without using any working fluid. Mostly, PCM filled in a container that is made up of high thermal conducting material. Considering cost-effectiveness and high thermal conductivity, aluminium is more widely used as a PCM container than nickel, stainless steel, and iron. Thin aluminium is difficult to weld because of its melting temperature, which is lower than other metals. During sunny days, PCM changes its phase and, considering this phase change, PCM container is fabricated in the thickness of 4-8 mm metal [32][33][34][35][36]. In T PV reduction, low operating PCM temperature is used, which is sensitive in thermal conduction whenever the thickness of PCM container material increases. To facilitate thermal dissipation, the high conducting heatsink has been attached behind the PCM container.
Rajvikram et al. conducted a comparative analysis of PV with heatsink, PCM, and PCM-heatsink [37]. The results show that PV only and heatsink-assisted PV module maintain 1 • C reduction. PCM integrated PV module regulates better T PV than heatsink by almost 7.7 • C because PCM enables high heat transfer from PV module. Finally, PCM-heatsink controls better than only heatsink or PCM, because it dissipates the stored thermal energy to the ambient during sunshine hours, which leads to maintaining a lower PCM temperature than only PCM and this discharge helps to transfer the heat from PV module and PCM.
It was noticed that using heatsink for PCM-based passive cooling technique enhances T PV reduction [38]; however, the PV module backside (tedlar) is made up of non-metal, the whole PV module is fragile, and it is not advisable to keep the PCM container or PCM container with heat sink. To obtain perfect physical contact, PCM container is attached to the PV module back surface using high-temperature adhesive material or conducting oil, even though perfect physical contact is not justified. It was reported that total weight of the system could increase due to the thickness of PCM container material and fastening heatsink behind the PCM container. Attaching a PCM container or PCM container with heatsink reduces T PV , but it damages the PV module's physical structure.
To prevent this contact loss and physical damage, PCM is filled on the back surface of the PV module directly [39]. Nada et al. used 10-cm PCM and its rear side was sealed using a 5-mm galvanized sheet to prevent leaks [40]. The comparative study of RT55 as pure PCM and Al 2 O 3 nanoparticle composited PCM shows better T PV reduction and the result shows that pure PCM reduced a maximum of 8.1 • C and composite PCM reduced 10.6 • C. The reason behind the T PV reduction of composite PCM is its enhanced thermal conductivity. Even though PCM is an effective thermal energy storage material, it has a lack of thermal conductivity. This low thermal conductivity creates thermal conduction barrier within the PCM.
Stropnik et al. conducted TRNSYS simulation for Ljubljana location using 3.5-cm RT28HC and they validated it with experimental results [41]. Filling PCM directly behind the PV module enhances heat transfer because PV module back surface temperature is directly in contact with PCM and there is no intermediate layer. The rear side of the PCM is covered by 5-mm acrylic glass, and the direct enforcement of PCM leads to reduce the T PV by a maximum of 35.6 • C. The relative error of the simulation is less than 3.8% compared to the experimental results. Total energy production was enhanced from 242.36 to 260.17 kWh/year and, especially from March to September, better performance is achieved.
Hasan Mahamudul et al. conducted the performance analysis of RT 35 PCM under Malaysian climatic condition with a thickness of 2 cm, which is filled and fitted within the PV module frame height, and the rear side of PCM is closed by using fiber optic glass [42,43]. The results show that a maximum of 10-12 • C reduction is achieved, but this system yields T PV reduction for only 4 h because the amount of PCM used in this system is less. Some of the literature works are summarized in Table 1 for the understanding of the PCM behavior in PV module cooling under different climatic condition. Selecting appropriate melting range of PCM is one of the most crucial decisions in PV module cooling because thermal absorption of the PCM relies on its melting range and natural factors, mainly ambient temperature, humidity, and wind speed [44].
The existing literature makes clear that PCM is an effective thermal absorber and storage medium for T PV reduction. PCM only and composite PCM gains great attention because of its zero maintenance and free from external energy. Systematically, PCM stores thermal energy during sunshine hours and it discharges at night, which makes this system free from maintenance and external sources. The only drawback in this system is physical contact between the PV module and the PCM container because it could damage the physical structure of the PV module due to forging hard metal onto the soft material of the PV module. Considering contact loss and weight, filling liquid PCM behind the PV module is the most effective and safest method to reduce the T PV .
The main objective of this research was to analyze the effectiveness of the direct filling PCM on the back surface (tedlar) of the PV module for the summer season. OM29 is used as PCM for the location of Madurai, India (9.88 • N, 78.08 • E) to regulate the excess T PV . In this current work, thermal absorption and dissipation of the PCM are exclusively discussed in the following section.

Phase Change Material
OM29 is a commercial organic PCM purchased from Pluss [43], India, and it is a combination of several fatty acids. The physical appearance of OM29 is a white wax at 25 • C (solid-state). OM29 was tested by PLUSS T-History method, resulting in 29 • C onsets melting temperature with high latent heat of fusion, which makes this PCM able to store thermal energy effectively. In addition, OM29 is chemically and thermally stable for 2000 cycles, which means OM29 can perform effectively for 2000 days. It is considered that every single day T PV reduction is equivalent to a single thermal cycle. The experimental location is rich in strong sunshine of approximately 300 days per year, which means OM29 can perform effectively for 6.5 years without degrading its thermal property and performance. The thermophysical properties of OM29 are listed in Table 2. Thermal stability (No.) ∼2000 12 Maximum operating temperature 120

Experimental Setup
Two identical 20 Wp polycrystalline PV modules (Loom solar with the dimension 450 mm × 350 mm × 22 mm) were used in this experiment, one for PV without PCM and another for PV with PCM, as shown in Figure 1. Without further processing, 2.8 kilograms of liquid OM29 PCM was filled on the backside of the PV module with 5% space left for volume change during phase transition or volume expansion. Over the PCM layer, the rear side of the PCM was enclosed by using a 0.5-mm tin combined with aluminium sheet and, thus, leakages were protected during phase change. The experiment was conducted in summer (6 July 2019) at the location of 9.88 N, 78.08 E. To make an effective comparison of OM29, which was incorporated for the PV module cooling, the front and back surface of the PV module temperature was captured using FLIR thermal imaging camera every 30 min for PV without PCM. For the PV with PCM front surface was captured, but it was difficult to capture the back surface of the PV module because PV module back surface was not exposed to the camera as it was incorporated with the PCM. Thus, PCM back sheet temperature was captured to analyze the thermal dissipation of the PCM.

Heat Transfer Model for PV without PCM
Conventional PV module thermal characteristics are represented in the form of a heat transfer model, as shown in Figure 2. In the conventional system, the PV module generated thermal energies and they are mostly dissipated to the surrounding, depending on the ambient temperature (T amb ) and wind speed. In hot region, less thermal dissipation occurs because of high T amb and low wind speed, which increases the T PV because excess thermal energy has been dissipated by radiation (R rad, PV→ sky and R rad, PV→surr ) and natural convection (R conv, PV→amb and R conv, PV→surr ) on both the top and the bottom surface of the PV module.
Thermal energy dissipations are exclusively represented in the form of an energy balance equation in the following subsection.

Energy Balance for PV without PCM
The solar PV module is a specific heat storage material, and it stores thermal energy during the photovoltaic effect. Equation (2) denotes the total amount of thermal energy stored in the PV module corresponding to the solar irradiance, which is absorbed and transmitted to the solar cell for the energy conversion process, and during that time the PV module generates thermal energy. That energy is transferred to the ambient and sky by the mode of convection and radiation over the flat surface of the PV module, respectively. The rear side of the PV module transfers thermal energy to the surrounding by natural convection and radiation. PV module electrical efficiency is directly correlated with the T PV .
where m PV is the weight of the PV module; C PV is the specific heat capacity of the PV module; α g is the absorbance of the PV module glass; τ g is the transmittance of the PV module; I is the solar irradiance in W/m 2 ; t is the time in s; h conv,g→amb is the convection heat transfer between PV module glass and ambient (W/m 2• C); h rad,g→sky is the radiation heat transfer between PV module glass and sky (W/m 2• C); h conv,t→surr is the convection heat transfer between PV module tedlar and surrounding (W/m 2• C); h rad,t→surr is the radiation heat transfer between PV module tedlar and surrounding (W/m 2• C); T PV,g is the PV module glass temperature in • C; T amb is the ambient temperature in • C; T sky is the sky temperature in • C; T PV,t is the PV module tedlar temperature in • C, T surr is the surrounding temperature in • C, η PV is the efficiency of the PV module in %; β is the packing factor; and A PV is the area of the PV module.
Convection over the PV module majorly occurs with the influence of wind (v) and an increase in wind speed over the surface of the PV module dissipates higher thermal energy to the ambient, as represented by Equation (3).
PV module front surface radiates thermal energy to the sky and this radiation truly depends on the emissivity of the solar PV module glass [55]. It is represented by Equation (4). h rad,g→sky = g σ T PV,g + T sky T PV,g + T sky 2 (4) where σ is the Stefan-Boltzmann constant and g is the emissivity of the PV module glass.
Long-range thermal radiation to the sky is calculated using Equation (5) The backside of the PV module dissipates thermal energy to the surroundings. Usually, this convection is poor due to the thermal resistance. PV module dissipated thermal energy stagnates in the area between the PV module backsurface and the ground. Especially the hot and low wind area suffers in thermal stagnation. This stagnation leads to reduce the thermal conductivity of air because convection depends on the surrounding air thermal conductivity, as expressed in Equation (6), and the increase in air temperature causes to reduce the thermal conductivity of the air. h conv,t→surr = K air L PV Nu air (6) where K air is the thermal conductivity of air; L PV is the PV module length; and Nu air is Nusslets Number. The rear side of the PV module Nusselt number is calculated using Equation (7) and radiation to the surrounding using Equation (8 where R a is the Rayleigh number; P r is the Prandtl number; and t is the Emissivity of the PV module tedlar. Electrical efficiency of the PV module is calculated using Equation (9) [57], where η PV is the Efficiency of the PV module in %; η STC is the PV module efficiency at standard test condition in %; T PV is the PV module temperature in • C; T STC is the Standard test condition temperature in • C; and β STC is the Temperature Coefficient.

Heat Transfer Model for PV with PCM
Excess thermal energy from the PV module is absorbed by PCM, which is filled up on the back surface. The conventional PV module rear surface dissipates thermal energy to the surrounding with the help of temperature difference and wind. In this model, PCM plays a major role during energy conversion time by absorbing the excess thermal energy and, simultaneously, it is expected to discharge. The rear surface of the PV module thermal energy is transferred to the PCM by conduction (R cond, PV→PCM ) and it is stored in it. Stored PCM thermal energy is transferred to the PCM back-sheet by conduction (R cond, PCM→Al ). From PCM back sheet, thermal energy is dissipated to the surrounding by natural convection (R conv, Al→surr ) and radiation (R rad, Al→surr ). Default front side of the PV module dissipates thermal energy by convection (R conv, PV→amb ) and radiation (R rad, PV→sky ). The working principle of the PCM integrated PV module is represented in the form of a heat transfer model, as shown in Figure 3. Heat transfer model for PV with PCM. R conv,PV→amb is the convection resistance between the PV front side and ambient; R rad,PV→sky is the radiation resistance between the PV front side PV and sky; R conv,PV→surr is the convection resistance between the PV rear side and ambient; R rad,PV→surr is the radiation resistance between the PV rear side and surrounding; R cond,PV→PCM is the conduction resistance between the PV rear side and PCM; R cond,PCM→Al is the conduction resistance between the PCM rear side and PCM back sheet; R conv,Al→surr is the convection resistance between the rear side of the PCM back sheet and surrounding; and R rad,Al→surr is the radiation resistance between the rear side of the PCM back sheet and surrounding.

Energy Balance for PCM Integrated PV Module
Equation (10) denotes the amount of thermal energy stored in the PV module after PCM absorption. The front side of the PV module absorbs and transmits the solar irradiance to the PV module for energy conversion. During that time, the PV module generates thermal energy, and it is absorbed by the PCM, which is incorporated on the back surface by direct conduction. The rest is dissipated to the sky and the ambient the same as for PV without PCM. In this case, the electrical efficiency of the PV module is directly correlated with the amount of thermal energy absorbed by PCM. m PV C PV dT PV dt = [α g τ g I (t) − h conv,g→amb T PV,g − T amb −h rad,g→sky T PV,g − T sky − h cond,t→PCM (T PV,t − T PCM ) − η PV I (t) ]βA PV (10) where h cond,t→PCM is the conduction heat transfer between PV module tedlar and PCM (W/m 2• C) and T PCM is the PCM temperature in • C. Moreover, regulating T PV for longer and effectively depends on the ratio of PCM thermal conductivity and PCM thickness, as expressed in Equation (11).
where K PCM is the PCM thermal conductivity and ∆ X PCM is the PCM thickness.

Energy Balance for Conduction Sourced PCM
Equation (12) denotes the amount of thermal energy stored in the PCM during energy conversion. Excess thermal energy from the PV module is transferred to the PCM by conduction and this energy is stored in three different phases, as expressed in Equation (13). During charging and off sunshine hours, PCM thermal energy is transferred to the PCM back sheet by conduction. Thus, dissipating PCM thermal energy to the surrounding leads to enhance the heat transfer from the PV module to PCM. PCM back sheet transfers thermal energy to the surrounding by natural convection and radiation because the PCM backside is not insulated. PCM should discharge the stored thermal energy before the next sunshine (overnight), else the next day PCM would not be able to initiate the absorption effectively.
where m PCM is the mass of PCM; C PCM is the storage capacity of PCM; h cond,PCM→Al is the conduction heat transfer between PCM and PCM back sheet (W/m 2• C); h conv,Al→surr is the convection heat transfer between PCM back sheet and surrounding (W/m 2• C); h rad,Al→surr is the radiation heat transfer between PCM back sheet and surrounding (W/m 2• C) ; T PCM is the PCM temperature ( • C); T Al is the PCM back sheet temperature ( • C); and T surr is the surrounding temperature ( • C). Equation (13) represents three different phases of PCM during thermal energy storage. When the PCM temperature is less than the melting point, thermal energy stores in the form of solid specific heat capacity. When it is equal to the melting point, PCM stores thermal energy in the form of latent heat of fusion. It is recommended to maintain the PCM to be in latent heat of fusion state because the liquid specific heat capacity of the PCM is not effective in storing thermal energy and thus thermal conductivity of the liquid PCM is low.
solid specific heat capacity, T PCM < T melt latent heat of fusion, T PCM = T melt liquid specific heat capacity, T PCM > T melt where T melt is the melting temperature.

Temperature Profile of PV Module
The experimental setup of the PV with and without PCM was developed and examined in the summer (6 July 2019) under the direct sunlight to observe the thermal behavior. During every 30 min interval, thermal images of the PV module and PCM back sheet were taken. Figures 4 and 5 show the meteorological data of solar irradiance and ambient temperature on the corresponding experimental day.  The examined OM29 organic PCM enabled thermal energy transfer from PV module to PCM by conduction. Figure 6a shows a thermal image of the PV module at 8:00. There was a noticeable T PV reduction of 0.4 • C because, during that time, PCM had solid specific heat capacity as well semi mushy region.
PCM absorbed the T PV effectively when the PCM attained its melting point. The results show that PCM utilized its thermal absorbing and storing capability until 8:30 because T PV reduction achieved up to 8:30 maximum of 1.2 • C. From 9:00, T PV started to rise slightly less than the PV without PCM, as shown in Figure 6b,c. Even though the latent heat capacity of the PCM was high, T PV reduction sustained for a lower period due to its low melting point, which is inappropriate for the selected location for the summer season. Further following this, T PV was not achieved during the peak sunshine hours, as shown in Figures 7 and 8. After 9:00, PCM was completely liquid completely, as listed in Table 3. Liquid specific heat capacity was not effective for storing the thermal energy such as latent heat of fusion (mushy state).  Secondly, in this experiment, PCM failed to discharge the stored thermal energy during sunshine hours, because thermal conductivity of the PCM was low, increasing the thermal conduction resistance within the liquid PCM, and the PCM back sheet (tin combined with aluminium) was not an effective thermal dissipater as compared to pure aluminium [39]. Increasing the thickness of PCM enhanced the heat transfer between the PV module and the PCM [58][59][60]. In this system, 2-cm PCM was used, which melted completely within 1 h from and, during the rest of the period, T PV increased to a maximum of 7 • C, which was more than the conventional PV module (PV without PCM), as shown in Figures 8 and 9.  The reason behind this T PV rise is that the PCM integrated PV module back surface was not interacting with the ambient and wind. Since PCM was filled on the back surface of the PV module, the PCM integrated PV module thermal dissipation depended on the PCM and PCM container material. For PV without PCM, thermal energy could be easily dissipated to the surrounding because there was no storage medium between the PV module back surface and the surrounding. However, PCM integration reduced T PV effectively when the PCM sustained the mushy state for a longer time, but, once it became liquid, PCM acted as an insulating material compared to PV without PCM. Thus, PV without PCM had a lower T PV than PV with PCM. Since the back surface of the PV module had PCM, it had stored thermal energy in it. Note that the experimental day ambient temperature was higher than the PCM melting temperature.
The 2.2-cm PCM layer contained only 2.8 kilograms of PCM. It could not maintain the mushy state for a long time and had difficulty reducing the PCM temperature lower than the melting temperature using passive cooling because it depended on the natural factor. If the PCM back sheet also had a good thermal dissipating material, PCM would not reach its melting point or mushy state again during the experimental day, because ambient temperature was higher than the PCM melting point. Thus, the only possible way is active cooling method, which could lower the PCM temperature forcibly and help to maintain the mushy state for longer time. Many researchers addressed this ineffective T PV reduction by categorizing inappropriate PCM melting temperature selection [44], PCM thickness [61], and PCM thermal conduction barrier [35]. Existing experimental investigation states that PCM selection is the crucial term in the whole process of the PV module cooling; selecting a lower or higher melting range of PCM will make the T PV reduction ineffective because T PV reduction is only achieved when the PCM reaches its melting point. Lower melting range of PCM will utilize its latent heat property before the peak sunshine hours and higher melting range of PCM will not use its latent heat property during peak sunshine hours. The only solution for this issue is to select PCM with melting range 2-3 • C higher than the peak ambient temperature so that the PCM will not gain thermal energy from ambient during sunshine hours.
During the experimental day, the recorded high ambient temperature was 33.5 • C. If the selected PCM melting range were 35-36 • C, a better T PV reduction would have been achieved. A general rule of thumb indicates that an increase in the thickness of PCM leads to sustainability of the T PV reduction for longer time, as well as creates the thermal conduction barrier during thermal absorption. To overcome this issue, several researchers have incorporated thermal additives to enhance the thermal conductivity of the PCM by adding metal foam [62], metal scrap [63], copper powder [64], graphite [64], expandable graphite [65], and nanoparticles [48].

Temperature Corrected Electrical Efficiency
The electrical efficiency of the PV module was directly correlated with the T PV ; the increase in T PV led to reduce electrical efficiency by −0.43%/ • C. However, this experiment enhanced the electrical efficiency until 8:30; afterwards, PCM integrated PV module electrical efficiency was lower than PV without PCM, as shown in Figure 10. The corresponding increase in T PV in the PCM integrated PV module reduced the electrical efficiency by a maximum of 0.38%, which shows that PCM acted as a thermal source to the PV module when it turned completely liquid.

Conclusions
The heat transfer capability from the PV module to the PCM can be greatly enhanced by the direct filling of PCM behind the PV panel without the use of an intermediate layer. It is an efficient way of keeping the temperature of the PV panel within a reasonable limit by means of passive cooling methodology. However, f an OM29 PCM tends to behave differently in the summer season because of the atmospheric condition. On the day of experimentation, T PV dropped up to 8:30; after that, the OM29 was unable to absorb the PV module generated thermal energy due to the impact of a lower melting range of the PCM. The experimental results reveal that the OM29 PCM was not capable of PV module cooling, especially for a hot and humid region such as India. Many researchers addressed this issue because selecting PCM melting temperature is the most challenging task for the module cooling for an entire year. The selected OM29 PCM performed well in winter, while, in summer, it did not dissipate the stored thermal energy; in addition, OM29 lost its latent heat property within 8:30 and after that PCM started to act as an insulating material for the PV module. Hence, it was concluded that OM29 was not a suitable PCM for cooling the PV module in the summer season. Further, it is recommended to select an appropriate PCM for this desired location. In addition, it is necessary to increase the thickness of the PCM and thermal conductivity in order to attain better absorption and dissipation.

Conflicts of Interest:
The authors declare no conflict of interest.