Recent Developments for the Application of 3D Structured Material Nickel Foam and Graphene Foam in Direct Liquid Fuel Cells and Electrolyzers

: Platinum and platinum-based catalysts are some of the most effective catalysts used in fuel cells. However, electrocatalysts used for direct liquid fuel cells (DLFCs) and electrolyzers are high cost and suffer from several other problems, thus hindering their commercialization as power sources to produce clean energy. Common issues in electrocatalysts are low stability and durability, slow kinetics, catalyst poisoning, high catalyst loading, high cost of the catalytic materials, poisoning of the electrocatalysts, and formation of intermediate products during electrochemical reactions. The use of catalyst supports can enhance the catalytic activity and stability of the power sources. Thus, nickel foam and graphene foam with 3D structures have advantages over other catalyst supports. This paper presents the application of nickel foam and graphene foam as catalyst supports that enhance the activities, selectivity, efﬁciency, speciﬁc surface area, and exposure of the active sites of DLFCs. Selected recent studies on the use of foam in electrolyzers are also presented. phologies of a hollow structure, larger surface area, and high loading capacity. The hollow porous structure around Co 3 O 4 increases the mass transfer rate between the electrode and electrolyte as the electron resistance decreases as well as increases the number of active sites for adsorption and oxidation. Interestingly, the Co 3 O 4 supported on NF went through a pressure machine at a pressure of 10 MPa, but the catalytic activity remained the same after the pressure was introduced. Rajeshkhanna et al. [5] used a different precursor salt of Co 3 O 4 /NF to obtain Co 3 O 4 with different structures (micro-ﬂowers, nanograss, and microspheres) as shown in Figure 5, surface areas, and MOR current densities, but the onset potential of Co 3 O 4 /NF was almost similar to that of Co 3 O 4 . The microspheres give the best performance and have a BET surface area and current density of 100 m 2 /g and 36.2 A/g, respectively. In other different studies performed by Hassan et al. [68], mesoporous carbon was added on Co 3 O 4 /NF. The C/Co 3 O 4 /NF material exhibits a catalytic activity that was three times higher than that of Co 3 O 4 /NF and comparable current density retention during the stability test, which was performed with NiCo 2 O 4 with different catalyst supports.


Introduction
An economical, efficient and clean alternative energy is needed to replace the increasingly used fossil fuel due to increasing energy demands, which has caused the reservoir of fossil fuels to be depleted and high CO 2 emissions [1][2][3]. These problems have led to the use of fuel cells, an alternative which can generate electricity from chemical energy without combustion [4]. Direct liquid fuel cells (DLFCs) have many advantages, such as high energy density and efficiency, fast start-up, easy refueling, storage, and transport, low operating temperature, and environmental friendliness [5][6][7], compared to other types of fuel cells, especially the polymer electrolyte membrane fuel cells (PEMFCs) that use hydrogen as fuel.
The liquid fuels that are usually used in DLFCs are methanol, ethanol, formic acid, ethylene glycol, glycerol, urea, ammonia, hydrogen peroxide, and many others [8][9][10][11]. Each liquid fuel in DLFCs has different electrochemical reactions, energy densities, and theoretical cell potentials [8]. For example, crossover occurs a lot in Direct Methanol Fuel Cells because the methanol molecule is smaller than other type of liquid fuel such as ethanol and glycerol. The fuel crossover occurs when fuel is transported from anode to cathode through membrane and will reduce use of the fuel. However, in the fuel oxidation reaction, methanol is easier to convert to other products than ethanol and glycerol. The C-C bonds in ethanol and glycerol require higher activation energy to form another product [12,13].
The electrolyzers are used to produce a high purity of hydrogen on a large scale. Water splitting in an alkaline medium suffers from sluggish reaction because it requires an  Schematic of the synthesis of a graphene film on Ni foam using the RTA process. Inset is photographs of a 6 × 6 cm 2 Ni foam sample before and after the growth of C-based films with/without the use of PMMA. Reprinted with permission from Ref [39]. Copyright 2018 Royal Society of Chemistry.
Powdery catalysts are commonly used in DLFCs that require the involvement of a binder to make the electrode slurry [44]. The presence of the binder decreases the electrochemical activity, as the binder reduces the ion and electron transport occurring in Figure 3. Schematic illustration of the catalyst layer and the regions (in red color) of (a) triple-phase boundary, and (b) two-phase boundary. Reprinted with permission from Ref [53]. Copyright 2014 Royal Society of Chemistry.
The use of NF and GF has significantly reduced carbon monoxide's (CO's) ability to be adsorbed on the surface catalyst while further enhancing the catalytic activity, stability, and durability of the electrochemical reaction in the fuel cell. The CO molecules on the catalyst surface are reduced by improving the particle distribution, thus increasing the number of catalytic active sites for the electrochemical reactions to occur [26]. However, how the mechanism of the electrochemical reaction occurs in DLFCs using NF and GF and to reduce CO adsorption and other poisonous intermediates on the catalyst surface remains a question. There must be some interaction between the catalyst and the support to reduce the adsorption energy of CO [26,28] and other poisonous intermediates [18] and further oxidize to complete the electrochemical reaction.

Methanol Electro-Oxidation Reaction
Pt is the best catalyst for the electrochemical reaction in DLFCs. However, the high cost and limited resources of Pt have led to several efforts to reduce Pt loading while maintaining the electrochemical reaction activity by methods such as alloying with other metals and using catalyst supports to increase the dispersion of the Pt catalyst [30]. Using layered double hydroxides (LDHs) that have an ionic solid surface is a new strategy created for achieving electrochemical conversion with a high chemical and thermal stability [55]. Ni(OH) 2 is used together with Pt metal as a catalyst, and NF is used as catalyst support for methanol oxidation reaction (MOR), as described by Yuan et al. [56]. Ni(OH) 2 can remove any poisonous intermediates during the MOR, and the large area provided by NF aided in the reactant and product removal, thus increasing the mass transfer coefficient. The Pt/NF and Pt-doped Ni(OH) 2 /NF materials show no oxidation peak during the CO-stripping voltammetry analysis, indicating that both catalysts have high resistance towards any poisoning effect. A catalyst with a very low Pt content and a co-catalyst with MoS 2 -Ni 3 S supported on NF is synthesized by Tang et al. [32]. During the CV scan in 1.0 M KOH, the hybrid catalyst Pt with MoS 2 -Ni 3 S has an electrochemical surface area (ECSA) of 76.7 m 2 /g Pt , which is higher than that of Pt/C, with a value of only 30.3 m 2 /g Pt . The ECSA value of the NF-supported catalyst is higher than that of the commercial carbon support because the Pt catalyst is highly exposed and uniformly distributed on the surface of MoS 2 -Ni 3 S with high porosity and surface area. Zhang et al. [30] deposited Pt on a NiCo-layer double hydroxide (NiCo-LDH) on NF to increase the anti-poisoning effect (by increasing the number of active sites for OH − ) on the catalyst and stability. The stable support directly contributes to the high catalytic performance and tolerance observed during MOR. The ECSA value of Pt-NiCo-LDH/NF is 16 times higher than that of commercial Pt/C/NF; the ECSA values of Pt-NiCo-LDH/NF and commercial Pt/C/NF are 131.86 m 2 /g and 8.27 m 2 /g, respectively. Due to the advantageous high porosity of NF, Du et al. [57] produced a co-catalyst of CoSe/NiSe with a low loading of Pt, and XRD testing showed the presence of NiOOH/CoOOH on the catalyst surface. NiSe/NF helped improve water splitting and, in the presence of NiOOH/CoOOH, increased OH − adsorption, thus assisting in the oxidation of the CO that adsorbed on the surface of the Pt catalyst. This effect leads to a higher value of ECSA of 85 m 2 /g Pt when NF is used compared to Pt/C, which only has an ECSA value of 3.03 m 2 /g Pt . Palladium (Pd) metal is a promising electro-catalyst that can catalyze the fuel oxidation in DLFCs and replace the Pt catalysts [12,54]. Niu et al. [58] investigated the effect of the precursor on the deposition of Pd on NF, as well as the arrangements and coverages of Pd by using a galvanic replacement method. A 2:1 atomic ratio of Pd to Ni results in an exposed NF surface, as shown in Figure 4, and leads to a catalytic interface composed of a Pd-Ni alloy or a bi-functional effect during the MOR, leading to a mass activity that is 1.5 times higher than that obtained with other ratios. Cheng et al. investigated the combination of Pd metal with MnO 2 for the MOR and the stability of the catalyst increases when the NF is used as the catalyst support [42]. The authors found that MnO 2 reduced the poisoning effect during the MOR, as Pd-MnO 2 /NF increases the current density by three times compared to the current density increase obtained with Pd/NF, while the NF helped to stabilize the catalyst, both of which increased the MOR activity. Yu et al. [6] have compared catalyst supports prepared with NF and with indium tin oxide (ITO) electrodes using Ag nanoparticles (AgNP) as the catalyst. AgNP/NF showed a better electrical conductivity than AgNP/ITO, as the interaction of Ag-Ni creates a new electron transfer pathway, and the NF helps to increase the electrolyte diffusion rate. In the stability test, the strong interaction between Ag and NF, which was determined using an ion implantation method, showed that the current density is in a stable condition, even after 5000 s. Then, Niu et al. [59] added Pd to form PdAg/NF for the MOR, and this combination was used to build a ternary alloy of Pd-Ag-Ni using a galvanic replacement method. The atomic ratio of Pd:Ag plays an important role in increasing the mass activity by as much as 3.3 times the mass activity of the Pd/Ni binary alloy. Guo et al. [60] studied using the ion implantation method to dope Co nanoparticles (CoNPs) on NF to increase the electrical conductivity and mechanical stability of the catalyst-NF. Using this technique has increased the number of particle dislocations and defects in the CoNPs, thus increasing the number of active sites for the MOR. These factors, as well as using the free binder, have increased the mass activity and current density for the MOR. Jadhav et al. [61] used MnCo 2 O 4 as a catalyst grown on NF. The MnCo 2 O 4 material supported on the surface of NF formed a flake-like structure with a thickness of 20-22 nm. The NF increased the stability of the MOR by speeding up the ion/electron transfer rate, as proven in the stability test after 1000 cycles were performed. The current density reduced to 66% but increased back to 77% when the new electrolyte was replaced with an electrolyte containing the new methanol solution. The decrease in 66% is due to the consumption of methanol during the MOR. The Jadhav et al. group also used MgCo 2 O 4 /NF for the MOR [43], in which the Mg metal side adsorbed more OH − than the NF side and further oxidized CO to CO 2 . Meanwhile, Shi et al. [47] synthesized ZnCo 2 O 4 supported on NF using a solvothermal and calcination process. The duration of the solvothermal reaction used to form the grown catalyst sheets on NF affected the structure and porosity of ZnCo 2 O 4 and thus led to the surface area. The structure of ZnCo 2 O 4 /NF has been interlaced between the sheets of ZnCo 2 O 4 , making the diffusion of the electrolyte to the surface catalyst much easier. Not only that, but ZnCo 2 O 4 /NF also has high stability, even after the 1000th cycle in the CV analysis. The same ZnCo 2 O 4 /NF material was developed by Sreekanth et al. [46], but a different method was used to synthesize the catalyst at 180 • C and produce a cubic structure of ZnCo 2 O 4 . Another interesting study was carried out by Jadhav et al. [62], who developed mesoporous ZnCo 2 O 3 on NF. The same materials but with different morphologies still affected the electrochemical reaction in DLFCs [63,64]. Gu et al. [65] and Wang et al. [66] synthesized NiCo 2 O 4 nanosheets/NF and obtained an ECSA of 146.5 m 2 /g and 66.9 m 2 /g using different methods, respectively. Both materials have good stabilities, even after running the materials in an alkaline methanol solution after 500 and 1000 cycles.
The combination of other metals with cobalt oxide also resulted in a promising activity for the MOR and was supported on NF. ZnCo 2 O 4 and NiCo 2 O 4 supported on NF were synthesized by Tombac et al. [67] and showed a high current density, low onset potential, and strong stability. The temperature of the annealing process used to synthesize the catalyst with NF is very important, as increasing the temperature to more than 500 • C will change the NF to NiO. The formation of NiO reduced the active sites, thus reducing the reactivity of the MOR. The MCo 2 O 4 material formed nanoflower particles on the nanorod supported on NF. The anodic peak current density obtained using NF as support is higher than that obtained using the other materials such as glassy carbon, stainless steel mesh, and carbon. Both ZnCo 2 O 4 and NiCo 2 O 4 have current densities of 154 mA/cm 2 and 280 mA/cm 2 , respectively.
A powdery Co 3 O 4 material was derived from a zeolitic imidazolate framework-67 (ZIF-67) and supported on NF to form a 3D skeleton for MOR, and this binder-free process was performed by Qian et al. [44]. The combination materials have the characteristic mor-phologies of a hollow structure, larger surface area, and high loading capacity. The hollow porous structure around Co 3 O 4 increases the mass transfer rate between the electrode and electrolyte as the electron resistance decreases as well as increases the number of active sites for adsorption and oxidation. Interestingly, the Co 3 O 4 supported on NF went through a pressure machine at a pressure of 10 MPa, but the catalytic activity remained the same after the pressure was introduced. Rajeshkhanna et al. [5] used a different precursor salt of Co 3 O 4 /NF to obtain Co 3 O 4 with different structures (micro-flowers, nanograss, and microspheres) as shown in Figure 5, surface areas, and MOR current densities, but the onset potential of Co 3 O 4 /NF was almost similar to that of Co 3 O 4 . The microspheres give the best performance and have a BET surface area and current density of 100 m 2 /g and 36.2 A/g, respectively. In other different studies performed by Hassan et al. [68], mesoporous carbon was added on Co 3 O 4 /NF. The C/Co 3 O 4 /NF material exhibits a catalytic activity that was three times higher than that of Co 3 O 4 /NF and comparable current density retention during the stability test, which was performed with NiCo 2 O 4 with different catalyst supports.
A powdery Co3O4 material was derived from a zeolitic imidazolate framework-67 (ZIF-67) and supported on NF to form a 3D skeleton for MOR, and this binder-free process was performed by Qian et al. [44]. The combination materials have the characteristic morphologies of a hollow structure, larger surface area, and high loading capacity. The hollow porous structure around Co3O4 increases the mass transfer rate between the electrode and electrolyte as the electron resistance decreases as well as increases the number of active sites for adsorption and oxidation. Interestingly, the Co3O4 supported on NF went through a pressure machine at a pressure of 10 MPa, but the catalytic activity remained the same after the pressure was introduced. Rajeshkhanna et al. [5] used a different precursor salt of Co3O4/NF to obtain Co3O4 with different structures (micro-flowers, nanograss, and microspheres) as shown in Figure 5, surface areas, and MOR current densities, but the onset potential of Co3O4/NF was almost similar to that of Co3O4. The microspheres give the best performance and have a BET surface area and current density of 100 m 2 /g and 36.2 A/g, respectively. In other different studies performed by Hassan et al. [68], mesoporous carbon was added on Co3O4/NF. The C/Co3O4/NF material exhibits a catalytic activity that was three times higher than that of Co3O4/NF and comparable current density retention during the stability test, which was performed with NiCo2O4 with different catalyst supports. Roy et al. [41] developed CuO/NF for the MOR through two processes, which are electrodeposition and calcination processes. The calcination temperature has been tested, and it was found that the temperature must not exceed 450 °C to prevent the instability of Roy et al. [41] developed CuO/NF for the MOR through two processes, which are electrodeposition and calcination processes. The calcination temperature has been tested, and it was found that the temperature must not exceed 450 • C to prevent the instability of NF and further transformation to NiO. The CuO/NF material showed a remarkably high current density as well as a low onset potential and overpotential due to the easy pathways of electron tunneling from the NF. Roy et al. [69] developed a binder-free and carbon-free catalyst using Co(OH) 2 /NF and compared the resulting catalyst with Co 3 O 4 /NF for MOR applications. Co(OH) 2 /NF had an onset potential of the MOR that was much lower than that obtained by other researchers. The Co(OH) 2 /NF materials have a high current density of 27 A/g due to the ability to control the intermediate kinetics at the electrode surface of Co(OH) 2 /NF, being better than that of Co 3 O 4 /NF.
To increase the poison tolerance and long-term stability of catalysts used for MOR, Yuan et al. developed a core-shell of Ni 3 S 2 with many defects that were supported on NF [70]. The result showed that the increase in the stability, activity and poison tolerance is due to the electro-catalyst being supported on the NF without any binder, thus increasing the mass transport of electrons and ions. The stability test performed using cyclic voltammetry showed that the peak current is maintained, even after 5000 cycles were performed in 0.5 M KOH and 1 M methanol at a scan rate of 50 mV/s. Another nickel-based catalyst developed by Li et al. [36] used Ni 3 B supported on NF. Usually, the Ni metal has a low activity towards the MOR, but not when using Ni 3 B with a particle size of 100-200 nm. The mechanical stability obtained when testing in 6 M KOH with 0.5 M methanol was high, and it was shown that anodic oxidation efficiency can be maintained at 87%, even after 1000 cycles. Eisa et al. [20] developed Ni/NiO nanorods grown on the NF surface that has superhydrophilic surface characteristics. The strong attraction of water molecules is important so that the decomposition of methanol and water to form protons becomes easy [71]. Another synergistic effect catalyst of nickel oxide and nickel oxalate (NiC 2 O 4 ) was developed by Zhang et al. [48] and shown to have increased activity for MOR. The comparison of the MOR activity is very significant, as the current density of NiO/NF and NF is 34 mA/cm 2 and 14 mA/cm 2 , respectively. The current density value increased by three times when the methanol concentration was increased from 0.025 M to 0.40 M. Besides, Xiao et al. [72] and Luo et al. [73] synthesized different structures of NiO films and nanosheet@nanowire arrays on NF. Xiao et al. [72] used a NiO film/NF with high stability for the MOR, which resulted in the current retention decreasing to only 92% after the stability test was performed for 500 cycles.
Cheng et al. [74] used a combination of Ni and CuS 2 with NF for the electrochemical conversion of methanol. The morphology resulting from the deposition of NiCu on NF is uniform, smooth, and compact but becomes a rough and uneven surface after sulphurization to form NiCuS 2 . The addition of sulphide is performed to increase the electrocatalytic activity of the catalyst. The NiCu 2 S 2 /NF material has a high current density and a better catalytic activity and stability than NiCu/NF; NiCu 2 S 2 /NF and NiCu/NF have current densities of 825 mA/mg and 673 mA/mg, respectively. Both electrodes can also maintain high stability after 5000 s, as the NiCu 2 S 2 /NF and NiCu/NF electrodes decay to only 76% and 74%, respectively. Hong et al. [75] investigated a hybrid NiO-CoO/NF material, in which the increase in the MOR activity is higher than that in pure NiO and CoO. However, the stability of the NiO-CoO/NF electrode decreased after 150 min, and the current density dropped from 110 to 85 µA/cm 2 .
Kung et al. [35] applied the GF as catalyst support for MOR by anchoring the PtRu catalyst on the GF surface to enhance the active surface area. The porous structure of GF allowed for the smooth mass transfer of the reactant towards the catalyst surface. The resistance to CO adsorption increased when the ratio of the current density of the forward scan to that of the backward scan increased, and thus, the long-term stability of PtRu/GF also increased. The present reduction observed after 900 cycles of CV, performed when using PtRu/GF, is only 0.73%. In comparison, the current density of PtRu/graphene and PtRu/C decreases significantly after 900 cycles to 55% and 79%, respectively. Yi et al. [34] used a high internal phase emulsion method to synthesize the GF (denoted as GF-HIPE) due to the low cost and simplicity of the method and ability to control the void size. A GF-HIPE that has an average void size of 146 µm was used as a support for the PtRu nanoparticle catalyst. The high catalytic activity obtained using PtRu/GF-HIPE was due to the strong bonding between the catalyst and support, as the surface of GF-HIPE contains many heteroatoms of nitrogen and oxygen to anchor PtRu. In addition to that, the large surface area and the existence of graphitic layers have reduced the charge transfer resistance during the MOR.
Zhang et al. prepared and used GF as catalyst support for Pt nanoflowers by a chemical vapor deposition (CVD) method [23]. The charge transfer resistance on the catalyst and GF showed a higher charge efficiency, thus giving a fast reaction rate, with a charge transfer resistance of 11 Ω cm 2 . This also suggested that the electron transport and ion diffusion achieved using GF is very effective. Another study by Zhang et al. [22] developed Pt nanoflower/GF materials for MOR. The GF has a larger surface area than commercial carbon supports, in which the surface areas of GF and commercial carbon supports are 670 m 2 /g and 250 m 2 /g, respectively. More of the Pt (111) crystal plane is exposed to the catalyst support due to the large surface area of the GF.
Cui et al. [12] synthesized a GF using a lamellar MCM-22 zeolite as a template and deposited Pd nanoparticles (PdNPs) for the MOR. The catalytic activity for the MOR increased very significantly by 1.7-2.9 times that of the commercial Pd/C catalyst. The ECSA value of Pd/MGF is 59 m 2 /g, while that of Pd/C is only 46 m 2 /g due to the better dispersion of ultrafine PdNPs on the GF surface. Cheng et al. [29] grew a binder-free 1D cobalt sulphide nanoneedle catalyst on the GF surface. The binder-free method prevents the self-aggregation of the graphene surface on the interconnected structure of the GF. Indirectly, the binder-free method increases the catalytic activity of the site, improves the interfacial contact, reduces the resistance, and increases the transfer efficiency.
Some studies use deposit graphene on the NF surface without sacrificing the NF. Studies that used both graphene and the NF produce graphene that is highly stable in acidic/alkaline media, low cost, and has a high electronic conductivity [76]. Wang et al. deposited a graphene hydrogel in NF (G-NF), which was used as a support catalyst for Pt in MOR [45]. The rate of the MOR achieved with rGO-NF is 27 and 86 times higher compared with that achieved with glassy carbon and Pt electrodes, respectively. The poisoning effect obtained using G-NF is very low, and the I f /I b ratio is high, with a value of 18.2. Yu et al. [77] investigated using the combined G-NF material as a support for NiCo 2 O 4 catalysts used for MOR. The 1D NiCo 2 O 4 nanoneedles grown vertically on the graphene surface have features including a high capacitance, with a value of 1588 F/g at 1 A/g and are suitable for use as the current collector in DMFCs and other types of DLFCs. Thoufeeq et al. [78] studied nickel-GF (Ni-GF) prepared by a modified polyol method for use in MOR. The authors state that the activity of Ni in the electrochemical reaction is highly dependent on the structure and preparation method of Ni. There is no NiO present on the surface of Ni-GF, which has a highly stable current density as high as 4.81 mA/cm 2 , as determined by chronoamperometry analysis, which is 1.7 times higher than that of pure Ni.
Gao et al. used graphene oxide-NF as a conductive substrate for the polyoxometalate encapsulation of Pt (PPt/GO-NF) [76]. The functional groups that exist on the graphene surface prevent the mobilization of Pt nanoparticles, while polyoxometalate is used to increase the electronic transfer capacity and size of the Pt nanoparticles. The PPt/GO-NF material prevents the CO adsorption effect by having an I f /I b ratio of 5.10 and a maximum mass activity at 250.6 mA/mg. Kamyabi et al. [24] investigated combining Pt and NiO with graphene oxide (GO), which were supported on NF. NiO and GO were synthesized by using a hydrothermal method, while the Pt is electro-deposited on the NiO-GO surface. The ratio of the forward scan and backward scan (i f /i b ) during the MOR is important for determining the poisoning degree of the catalyst. In comparison with other supports, such as CNF and nanowires, which have i f /i b ratios of 1.1 and 1.22, NF showed a poisoning tolerance, with an i f /i b ratio of 1.05. Pure Ni is used in MOR as NiOOH, which becomes the determining step, while pure copper (Cu) tends to transform to Cu(OH) 2 and CuO, in which both materials result in positive outcomes in MOR. Catherin Sesu et al. [79] developed both combinations of Ni-Cu to form a 3D structured material of a Cu-Ni-rGO foam for MOR. The current density of Cu-Ni-rGO foam can retain value as high as 95% after operation for 600 s.
The gas diffusion layer (GDL) usually used in fuel cells is carbon paper and carbon cloth. The exploration of using stainless steel fiber felt (SSFF) and metal foam as the GDL has become more extensive. Zhu et al. [80] tested the use of GF as the GDL in a micro-DMFC. The fiber size is larger in GF than in the carbon paper, and the contact resistance decreased to as low as 0.259 Ω. The new GF as the GDL instead of carbon paper have also resulted in increasing the power density from 25 mW to 31.2 mW due to the shorter diffusion path of methanol toward the catalyst surface.

Ethanol Electro-Xxidation Reaction
Ethanol produced from abundant and renewable agricultural products and biomass substrates has been applied to DLFCs [37]. Pd metal and Pd-based metals have high catalytic activity and are more abundant, less expensive, and less poisoning than Pt during the ethanol oxidation reaction (EOR) in DLFCs [33,81]. Wang et al. [82], Mikolajczyk et al. [37], Li et al. [53], Pierozynski et al. [40], and Verlato et al. [54] used different preparation methods to support Pd metal on NF to form a 3D structured catalyst. Pd/NF has a large surface area and produces a higher ECSA than the Pd film electrode, Pd/C, and Pd bulk catalyst. The developed Pd/NF material is also durable and has a catalytic activity that is eight times higher than that of the Pd film [82]. Li et al. [53] developed a thin and porous Pd sponge structure on an interconnected NF structure, with few aggregates forming. There are three advantages of this method, which were discovered by the authors, in terms of the catalytic activity of the EOR: the increased ECSA, reduced loss of chemical precursors, and more uniform Pd-sponge structures on NF. Mikolajczyk et al. [37] and Pierozynski et al. [40] investigated using Pd/NF for EOR and their effect when the reaction temperature was changed (20-60 • C). As the temperature increases, the current density also increases, and the oxidation potential tends to move towards more positive potentials. Meanwhile, Verlato et al. [54] found that the factors of the concentration and the duration of the electrodeposition method have changed the size of Pd, thus leading to different mass densities for EOR, including reactions with other alcohols, such as methanol, ethylene glycol, and glycerol. The surface of NF is modified by replacing the pure nickel with hydroxide to reduce the poisoning of carbonaceous adsorption on the Pd surface and further increase the oxidation rate of the reaction. However, Chen et al. [83] found that the morphologies and growth rate of the modified Ni(OH) 2 material greatly affects water dissociation and results in the high insulating property of hydroxide, which will lower the electron conductivity of the materials.
Other than Pd and Pd-based metal, Pt and Pt-based metal were also tested to improve the EOR developed by Pierozynski et al. [84,85], which used Pt/NF [84] and PtSn/Ni(OH) 2 /NF [85]. Sn was added to PtSn/Ni(OH) 2 /NF to prevent the dissolution of Pt during the electro-oxidation reaction. Although Pt formed and was non-uniformly distributed on the NF surface, the charge transfer resistance of the /Ni(OH) 2 /NF was lower than that of Pt/NF. The advantages of the Sn in PtSn and the hydroxide layer on NF have increased the reactivity of the EOR and reduced the charge transfer resistance in the catalyst. The slow rate of the EOR achieved using nickel led to the study by Hatamie et al. [86], which compared the EOR resulting from using NF and Au/NF. The performance of Au nanoparticles with an average size of 37 nm increased by 253% relative to that of NF. The authors also studied the effects of the concentration of ethanol and mixing rate, but the mixing rate did not affect electro-oxidation, because the diffusion-controlled processes are not effective. Although other studies showed that the rate of the reaction using NF was slow, Zhang et al. [48] and Eisa et al. [20] used NiO/NF and Ni nanorods (NNR)/NF, which show a high reactivity for the EOR, respectively. The NiO derived from the NiC 2 O 4 precursor and the presence of NiC 2 O 4 on the NiO/NF surface have advantages because the presence of NiC 2 O 4 improves the cycling performance and specific capacitance [48]. While, the small size of the nanorod morphology, with the wettability and hydrophilic properties of the NNR surface, has increased the surface area by 18 times compared to the surface area of NF [20].
Kung et al. [35] have used PtRu/GF, which had a higher EOR reactivity than other catalyst supports, such as graphene, carbon black and PtRu without a support. In terms of the stability, GF has a higher stability than PtRu/graphene after being tested in the stability cycle. Xu et al. [87] have emphasized the importance of obtaining the monolithic 3D GF structure, which helps to enhance the EOR performance of PdCo alloy and other metal and metal oxide catalysts. This is because developing the GF using NF as a template will lower the volume and specific surface area of GF and lead to a low volumetric loading and energy capacity. The monolithic 3D GF can be produced using the chemical vapour deposition (CVD) method. Liu et al. [88] used carbon foam (CF), used as a support on Pt skin and PtCo nanowires, to prevent the Ostwald ripening of Pt and dissolution and aggregation of the nanoparticles during the electro-oxidation reaction in fuel cells run for a long time. Li et al. [81] produced PdNi/CF with various atomic ratios of Pd:Ni. XPS revealed that the presence of NiO from the PdNi alloy has helped to increase the EOR rate in alkaline media. There have been numerous studies showing the high reactivity of NiO in EOR. Authors have also suggested that PdNi/CF can be used as a direct electrode in DEFC without using conventional carbon paper or carbon cloth.
Zhang et al. [89] argue that using GF-NF provides several advantages over using the CVD method to produce GF. Combining solution casting and electrochemical reduction methods gives the advantage of the synergistic interaction of nickel-Pd, which enhances the EOR. Tsang et al. [90] deposited a graphene aerogel (GA) on NF, found that an increase in the Pd loading from 0.8 wt.% to 7.65 wt.% increased the EOR rate and obtained an I f /I b ratio of 2.72. Based on the potential demonstrated by GA/NF, the Tsang group [91,92] added Pd to the PdPt alloy and applied the current-collector-free electrode into the DEFC. The power density generated using the PdPt alloy is 3.6 mW/cm 2 at room temperature. At 60 • C, the performance of the single cell DEFC was tested by Sun et al. [49] using an ultra-low loading Pd/C-NF, with a value of 202 mW/cm 2 . Jiang et al. [33] produced a Pd distribution on GNF using a metal atomic layer deposition technique and found that an ultra-low Pd loading (50 µg/cm 2 ) in GNF increased the current density by 2.64 times compared to the current density of a commercial Pd catalyst. This technique has the advantage of controlling the atomic layer thickness, which can lead to highly dispersed nanoparticles. In addition, Dogan et al. [93] deposited Pd on the reduced graphene oxide (rGO) at the NF surface, also resulting in remarkable activity that was comparable to that achieved by researchers using GNF as the catalyst support.

Borohydride Electro-Oxidation Reaction
Borohydride (NaBH 4 ) is used as a fuel in DLFC because it has many hydrogen carriers. The specific capacity of NaBH 4 , with a value of 5.7 Ah/g, is higher than that of methanol, and NaBH 4 also has other advantages, which include its high gravimetric energy density (7100 Wh/kg), high volumetric energy density (7314 Wh/L) and high cell voltage (1.64 V). The electro-oxidation of NaBH 4 (BOR) does not cause problems, such as catalyst poisoning, does not release CO 2 , is non-flammable, and possesses many hydrogen carriers. Catalyst poisoning did not occur because no carbon element was involved in the BOR. The complete oxidation of BOR produces 8-electrons, as shown in Equation (1), but the hydrolysis of NaBH 4 also occurs concurrently, as shown in Equation (2). However, the main problem with the BOR is the conversion efficiency, and the selectivity requires that a catalyst can reduce the hydrolysis reaction that occurs in the BOR [94].
Yang et al. [50] synthesized Au nanosheets (AuNSs) and nanoparticles (AuNPs), which were to be supported on NF. The catalytic activity of the outstanding AuNS/NF material was 278% higher than that of AuNP/NF, and also, the H 2 gas produced by AuNS/NF diffused freely without blocking the active surface sites, thanks to the high porosity of NF. Song et al. [51] synthesized the nanosheets of PtCo/Co 3 O 4 on the NF surface. The presence of Co metal and Co 3 O 4 make it easy to break the B-H bond in the BOR. Due to the advantages of Co metal breaking the B-H bond, Guo et al. [95] produced a low cost Ni-Co alloy/NF to further enhance the catalytic activity of the BOR as a result of the synergistic effect of Ni-Co. Song et al. [31] synthesized nanoneedles of ternary Pd alloys on NF by increasing the amount of CuNi to reduce the cost of loading the Pd catalyst without reducing the catalytic activity of BOR. Altering the pure electronic conductivity of the Pd metal and the unique structure of the NF and nanoneedles have resulted in an activation energy and number of transferred electrons during the BOR of 18.42 kJ/mol and 4.9 e − , respectively. Ma et al. [94] found that the fuel conversion efficiency in DBFCs was dependent on the catalytic activity. In addition, the CoSn x -B/NF catalyst developed by Ma et al. [94] also demonstrated the importance of the Co:Sn ratio in influencing the power density, which increased by 1.58 times compared to the power density of Co-B/NF (only 100 mW/cm 2 ).
Santos et al. [96] and Gouveia et al. [97] used various metal foam for applications in DBFCs. Santos et al. [96] used Ni-Cu foam to increase the amount of BH 4 − oxidized per unit volume and subsequently improved the single cell performance of a DBFC. Gouveia et al. [97] states that Co metal tends to promote the hydrolysis reaction, while the Ni metal is more preferable to proceeding with the BOR pathway. In addition, the research proved that the atomic ratio of Ni, Cu, Co and Fe in the foam plays an important role in DBFCs, either to proceed with the BOR or the hydrolysis reaction. As shown by Santos et al. [96], a certain Ni-Cu atomic ratio showed that the BOR is the preferred reaction pathway in DBFCs. However, the Li et al. group [98][99][100] used Co-based and Au-based catalysts deposited on reduced-graphene oxide foam (rGoF), in which all the catalysts reacted by a first-order reaction. Pure Au/rGoF [98] as shown in Figure 6 has a high electron transfer rate, with value of 7.2 e − , because pure Au/rGoF has a lower activation energy and smaller charge transfer impedance than CoAu/rGoF [100] and CoNi/rGoF [100], in which the electron transfer is only 6.9 e − and 6.7e − , respectively.

Urea Electro-Oxidation Reaction
Urea (CO(NH) 2 ) has advantages as a fuel in DLFC, as it is abundant and low cost, has high energy density, is non-flammable, is a harmless product of electro-oxidation in DLFCs (nitrogen and carbonate), is non-toxic, and has a lot of hydrogen carriers [101,102]. A fuel cell that uses urea as a fuel is called a direct urea fuel cell (DUFC) [48], while the cathode of DUFCs that uses hydrogen peroxide (H 2 O 2 ) as the oxidant is called a direct hydrogen peroxide fuel cell (DUPFC) [102]. The urea can be obtained from fertilizer, wastewater, and urine, which can be applied as fuel in DUFC [101,102]. The advantages of the DUFC can not only produce the hydrogen gas but also can reduce the water pollution [103] and can be applied as a spaceship power source [102]. However, a major problem with the urea electro-oxidation reaction (UER) is the sluggish reaction kinetics [104], and thus, an efficient, stable, and low cost catalyst is needed [105].
Guo et al. [101] supported a Ni-Co alloy with different ratios as low as 0% Ni and as high as 100% on NF for the urea electro-oxidation reaction (UER) in DUFCs. Ni-Co/NF is tested on a DUFC, and among the factors that play a role in achieving the best single DUFC performance at a temperature of 70 • C, with a performance output of 31.5 mW/cm 2 , are the urea concentration, operation temperature, and flow rate. The authors also tested pure human urine, but the power output was as low as 7.5 mW/cm 2 , which is lower than the power output of artificial urea, with a value of 17.4 mW/cm 2 , due to the various chemical compounds in human urine. Qian et al. [106] used the unalloyed state of Ni-Rh supported on NF, in which the presence of Rh that reduces the poisoning at the Ni surface and facilitates the UER. However, the authors also stated that the adsorption of CO 2 on Rh is still unknown.
Ye et al. [102] developed LDH on the Ni surface on the NF by controlling the temperature reaction to reduce the usage of noble metal catalysts. The rate of hydrogen bubbling during the UER is fast and produces a power density as high as 19.7 mW/cm 2 at a temperature of 20 • C. In addition, the synergistic effect of metallic NF with the many defects of Ni(OH) 2 from the Ni 2+ ions and oxygen vacancies, as prepared by Yan et al. [107], showed the long-term stability of the UER. Tang et al. [105] added Se on the LDH Ni and investigated the nanowire structure of Se-Ni(OH) 2 on the NF surface. The addition of Se as well as the LDHs to create more active sites reduces the amount of CO 2 adsorbed/desorbed. The synergistic effect on both metals has further increased the reaction kinetics. Zhang et al. [48] developed low cost NiO/NF by a chemical bath deposition method to prevent the formation of non-active sites for UERs. Zhan et al. [108] controlled the height and thickness of NiO nanowalls (NiO-NW)/NF by changing the amount of ammonia fluoride. The morphology of the NiO-NW/NF material affects the reactivity and stability in which the NiO-NW/NF is produced in the presence of ammonia fluoride is stable even after 12 h, while the NiO-NW/NF that prepared without ammonia fluoride is not stable after 12 h. To improve the electronegativity of Ni, Sha et al. [104,109] synthesized efficient NiCo 2 S 4 nanowire catalysts on NF, resulting in a low onset potential and high activity during the UER as well as an NF with good stability and high electronic conductivity. The increased activity is due to the many active sites on Co with a high-density defect structure.

Glucose Electro-Oxidation Reaction
Glucose is renewable fuel energy generated from agricultural activity. The application of glucose in DLFCs has advantages; for instance, glucose has a high theoretical energy density (4430 Wh/kg) and is abundant in nature, easy to handle and produce, non-toxic, and cheap. Glucose is also used in enzymatic and microbial fuel cells, in which these fuel cells use enzymes and microorganisms to break down the bonds in glucose, respectively. The main problem with using microorganisms as the catalyst is the sluggish reaction kinetics of the glucose electro-oxidation reaction (GluOR) and difficulty transferring the electrons from the catalyst surface to the electrode surface. Meanwhile, using enzymes is highly costly, has a limited lifetime and limited stability, and only reacts with partial electrooxidation. These deficiencies lead to the application of direct glucose fuel cell (DGluFC), and subsequently, producing an efficient catalyst is a challenge to reduce the sluggish fuel oxidation reaction kinetics, substrate crossover, and low catalytic activity for the GluOR due to the high concentration of hydroxyl ions and reaction intermediates [110,111]. Equation (4) showed the GluOR at the anode side, in which a total of 24 electrons were generated, but usually, the GluOR can only harvest two electrons.
Chen et al. [112] used Ag metal as a catalyst, and NF acted as catalyst support and an electrode in the DGFC. The 3D NF with a high porosity facilitated the diffusion of glucose, which has a larger molecular structure than other fuels used in the DLFC. This study found that heating the electrolyte increased the performance of the DGluFC by 2.03 mW/cm 2 at 80 • C. The problem of slow electron transfer during the glucose electro-oxidation reaction (GER) has led to the use of methyl viologen and NF by Liu et al. [110] as an electron mediator and electrode, respectively. However, Yang et al. [111] also used the same electron mediator and electrode and tested them in a DGluFC with different operating conditions, such as different types of membranes, concentration mediators, KOH, and glucose. Varying all the factors has resulted in the optimum performance of the DGluFC at 25 • C with 5.20 W/cm 2 . Li et al. [113] investigated the different types of mediators with the NF as the electrode. The mediators used in this study were anthraquinone (AQ), methyl viologen (MV), neutral red (NR), methylene blue (MB), 2-hydroxy-1,4-naphthoquinone (NQ), and 1,5-dichloroanthraquinone (DA). The NQ mediator showed the highest performance, with a peak power density of 16.10 W/m 2 , with advantages of lower toxicity and high catalytic activity in GluOR. Chen et al. [114] tested the various operating parameters of the DGluFC using Au/NF and identified the role of the temperature, concentration glucose, KOH and medium to obtain a power of as high as 26.6 mW/cm 2 .
Tsang et al. [115] investigated by applying a graphene aerogel on NF (GE-NF) as a catalyst support for Pd-Pt alloys with different Pt:Pd ratios. A Pt:Pd ratio resulted in a high performance at 1.25 mW/cm 2 with a total loading of only 8.13 wt.%, which is a better performance than observed in other studies using high metal loading and carbon as the catalyst support. Zhao et al. [116] used Ni-rGO/NF and compared it with an NQ mediator/activated carbon. The results suggest that Ni-rGO/NF is an alternative to costly NQ and Ni-rGO/NF and can enhance the OCV of the single DGluFC. Wu et al. [117] added ZnO to the G-NF support to increase the sensitivity and selectivity for glucose detection and the initiation of the GluER. Wu et al. detected glucose at concentrations as low as 5 µM with a sensitivity of 129.44 µA/mM.cm 2 . Thoufeeq et al. [78] also tested the glucose sensitivity using rGO-NF, but rGO-NF only detected concentrations as low as 10 µM. In addition to NF and GF, copper foam [118] was used with metal-doped-Cu 2 O for GluORs. Cu nanoparticles that have a low mechanical stability and durability have led to the use of CF by El-Nagar et al. [119]. The metals used with 4% loading are nickel, cobalt, and iron and are doped on the surface of Cu 2 O. The number of active sites of Cu 3+ is increased after the deposition of nickel, cobalt, and iron atoms.

Hydrogen Peroxide Electro-Oxidation and Electro-Reduction Reaction
Hydrogen peroxide (H 2 O 2 ) is used as a fuel in DLFC because it has the advantage of being an energy carrier, being carbon free and having a low cost as well as being workable without water. The H 2 O 2 electro-oxidation reaction (H 2 O 2 OR) is fast, does not poison the intermediate at the anode side, as shown in Equation (5), and does not need the costly Pt catalyst. However, a strong oxidant such as H 2 O 2 requires a very stable catalyst such as a noble metal [120]. In addition, the binder gradually degraded in the harsh environment of H 2 O 2 and KOH and needs the strength and high mechanical stability of catalyst support. The concentration of H 2 O 2 also needs to be studied, because the use of H 2 O 2 leads to chemical decomposition in DLFC.
The strong oxidant of H 2 O 2 is suitable to be used in DLFC at the cathode side for the H 2 O 2 electro-reduction reaction (H 2 O 2 RR), as shown in Equation (6), due to its advantages: H 2 O 2 is easier to store and handle than gaseous oxygen and fast reduction reaction kinetics. The high energy density and cell potential [120,121] increased the theoretical cell voltage of DLFC [122,123] due to the electrochemical reaction having a lower activation barrier than O 2 [120,124] and no intermediate by-products. The O 2 bubbles that form after the H 2 O 2 RR need to efficiently diffuse without impeding the electrochemical reaction. Therefore, NF and GF are seen to better help reduce these problems than the use of carbon cloth and carbon paper [52].
Song et al. [120], Yang et al. [121,125], and Xiao et al. [122] investigated the H 2 O 2 OR using Ni micro-particles supported on NF. Ni can produce LDHs on the Ni surface give a power density of 19.4 mW/cm 2 at 20 • C using H 2 O 2 instead of oxygen gases. The function of Ni(OH) 2 on the catalyst surface helps to break the H 2 O 2 bond, and their mechanism is presented as shown in Figure 7. Xiao et al. [126]   Another combination of both rGO and NF was prepared by Song et al. [120] through a hydrothermal method and used as Pd catalyst support in a DLFC. Fast electron transfer occurs due to the plentiful channels for H 2 O 2 diffusion in the rGO-NF, and the electrons reached the Pd surface. Pd/rGO-NF produced a low activation barrier for the H 2 O 2 RR, with a value of 8.202 kJ/mol. Ye et al. [52] used a carbonization method to produce a carbon foam from polyurethane foam. Co and Pt metals are used to prepare a binary alloy catalyst by an electrodeposition method and a chemical deposition method to achieve H 2 O 2 RR, respectively. The high use of a catalyst leads to high catalytic performance and the quick release of the produced bubbled gas derived from the carbon foam.

Other Electro-Oxidation Reaction in DLFC
Other DLFCs have shown promising and rapid research development in electrocatalysts. However, the use of NF and GF as catalyst supports for electro-oxidation in direct glycerol fuel cell (DGFC), direct ethylene glycol fuel cell (DEGFC), direct hydrazine fuel cell (DHFC), and direct ammonia fuel cell (DAFC) is still limited. Cui et al. [12] used ultra-small Pd/GF for glycerol and ethylene glycol electro-oxidation reactions in DLFC. Ultra-thin nanosheets of graphene were formed on the MCM-22 zeolite as a template. The resulting mass activity showed the effect using GF as a support, with a value of 4.056 A/mg Pd , while the carbon support produced a value of 1.438 A/mg Pd in the ethylene glycol electrooxidation reaction. Shih et al. [128] investigated Ni(OH) 2 /NiOOH supported on NF for the ammonia electro-oxidation reaction in a DLFC. Two challenges need to be addressed in ammonia electro-oxidation are the dimerization reaction and the complicated selectivity caused by the multiple electron transfers. To increase the selectivity, Shih et al. [128] used Ni(OH) 2 /NiOOH/NF as an anode with the consideration of several factors, including the pH of the solution, temperature, current density, and initial NH 3 -N concentration. The result showed that the presence of Ni in the anode made the oxidation reaction process from NH 3 to NO 3 − and N 2 easy. Nickel-phosphate nanowires (NP) were grown on NF, as developed by Wen et al. [129] through a one-step phosphorization method for direct hydrazine fuel cell (DHFC). The NP/NF material is modelled using a first-principle calculation, which showed that the NPs have a high density of active sites and an electrical conductivity due to the addition of phosphate atoms, thus increasing the number of active sites and improving the morphology of the nanowires, respectively. Feng et al. [130] then alloyed the Ni metal with Zn and formed a nanosheet of Ni-Zn supported on NF for DHFC. The complete electro-oxidation of hydrazine produced a 4-electron pathway, and Ni-Zn/NF was 100% selective for the complete hydrazine electro-oxidation reaction. Table 1 showed the summarized application of NF and GF as catalyst supports and their performance in DLFCs. This table shows the types of metal that have been used and supported by nickel foam and graphene foam. The reaction medium plays an important role in increasing the rate of the electrochemical reaction. Resistance to catalyst poisoning can be measured through a ratio of I f /I b value where a high value indicates the catalyst can reduce catalyst poisoning. Not all catalysts are tested in a single cell performance test, but almost all catalysts supported by NF and GF show good stability and durability after being tested for a long time.    The current density has 93.4% retention of the first cycle after 500 cycles. [77]

Selected Application of Foam in the Electrolyzers
Lin et al. [15] put forward the idea of adding phosphide to the binary alloy of NiFe and support on NF. The advantage of ruthenium (Ru) metal in increasing the reaction rate has led to super-low loading of Ru in NiFe-P/NF due to Ru's cost as a precious metal that provides highly catalytic activity in all pH media. The authors also claimed that the addition of Ru increases electron interaction and ultrasmall of overpotential. Zhao et al. [131] also use almost the same material without the presence of phosphate. Cheng et al. [132] also produced the Fe-Ni-based electrocatalyst for OER. To increase the capability of the water dissolution, robust stability, and ultra-high current density, the hybrid r-FeOOH and α-Ni(OH) 2 are produced on NF surfaces having amorphous and crystalline properties, respectively. Yang et al. has created ternary metal Co 1−x V x P with nanoneedle structures supported on NF to increase the hydrogen evolution reaction (HER) [14]. The uniqueness of the structure made in this study has increased catalyst stability in the long run and has reduced overpotential and increased current density of 46 mV at 10 mA/cm 2 and 226 mV at 400 mA/cm 2 , respectively. In the theoretical study by Park et al., the use of Co 1−x V x P catalyst reduced the activation energy during the dissociation of water. Nanosheets of Co 3 S 4 directly synthesize on the NF surface through electrodeposition and sulfurization and create a more active site and accessible surface reactant for HER [133]. The authors also studied the effect of time in the sulfurization process on the formation of Cobalt sulfide on the NF surface. The optimized catalyst has produced excellent durability without overpotential and in single-cell changes in 220 h and 720 min, respectively. Metal oxide also has the advantage of increasing the current density produced by Wang et al. [134]. Wang et al. [134] synthesized the MoO 2 at surface NF, doping with phosphorus (P) and tungsten (W). Authors claim the addition of P and W's heteroatoms accelerated the charge transfer, facilitated the electron interaction, and tuned the electron environment.

Conclusions
The demand for energy consumption is on the rise. Therefore, a more consistent, active, and productive study of the high activity of the electro-oxidation reaction in DLFCs is essential to address the issues that have been mentioned in this paper. Common problems in electrocatalysts are low stability and durability, slow kinetics, catalyst poisoning, high catalyst loading, high cost of the catalytic materials, poisoning of the electrocatalysts, and formation of the intermediate products during the electrochemical reactions. One way to increase activity is by using appropriate support materials such as carbon black, carbon aerogels, carbon nanotubes, mesoporous carbon, graphene oxide, and graphene nanosheets. Support material should have characteristics such as large surface area, low surface poisoning, high porosity, multiple active sites for the reaction to occur, high activity, good conductivity, and long-term stability. Commonly used support materials face problems; namely, their corrosion resistance leads to particle detachment, Ostwald ripening, and agglomeration. The selection of Nickel foam and graphene foam is seen to reduce the problems faced by other support materials. The 3D network structure in the nickel foam and graphene foam has high conductivity, controllable electrochemical properties, excellent mechanical strength, high surface area, high porosity, and low cost, and are suitable for use as catalyst supports. Powdery catalysts are commonly used in DLFCs that require a binder's involvement to make the electrode slurry. The binder's presence decreases the electrochemical activity, as the binder reduces the ion and electron transport occurring in the electrode and at the electrode/electrolyte interface by blocking the catalyst active sites. Therefore, the use of the 3D structured materials NF and GF can improve the performance when a binder is not required in the electrode. Besides, NF and GF's use has significantly reduced CO's ability to be adsorbed on the surface catalyst while further enhancing the catalytic activity, stability, and durability of the electrochemical reaction in the fuel cell. The CO molecules on the catalyst surface are reduced by improving the particle distribution, thus increasing the number of catalytic active sites for the electrochemical reactions. Exploring various types of catalyst structures supported on NF and GF in future research, such as nanofilm, should be carried out in DLFCs because the layered structure has unique features that can increase electrochemical active surface area, most of which have been applied in other fields.

Conflicts of Interest:
The authors declare that they have no conflict of interest.