A Facile Design of Solution-Phase Based VS2 Multifunctional Electrode for Green Energy Harvesting and Storage

This work reports the fabrication of vanadium sulfide (VS2) microflower via one-step solvo-/hydro-thermal process. The impact of ethylene glycol on the VS2 morphology and crystal structure as well as the ensuing influences on electrocatalytic hydrogen evolution reaction (HER) and supercapacitor performance are explored and compared with those of the VS2 obtained from the standard pure-aqueous and pure-ethylene glycol solvents. The optimized VS2 obtained from the ethylene glycol and water mixed solvents exhibits a highly ordered unique assembly of petals resulting a highly open microflower structure. The electrode based on the optimized VS2 and exhibits a promising HER electrocatalysis in 0.5 M H2SO4 and 1 M KOH electrolytes, attaining a low overpotential of 161 and 197 mV, respectively, at 10 mA.cm−2 with a small Tafel slope 83 and 139 mVdec−1. In addition, the optimized VS2 based electrode exhibits an excellent electrochemical durability over 13 h. Furthermore, the superior VS2 electrode based symmetric supercapacitor delivers a specific capacitance of 139 Fg−1 at a discharging current density of 0.7 Ag−1 and exhibits an enhanced energy density of 15.63 Whkg−1 at a power density 0.304 kWkg−1. Notably, the device exhibits the capacity retention of 86.8% after 7000 charge/discharge cycles, demonstrating a high stability of the VS2 electrode.


Introduction
Demand on renewable energy is growing impressively day-by-day. However, the heavy reliance on fossil fuels to fulfill the global energy demand has resulted many environmental issues [1]. Consequently, green and efficient energy resources for sustainable energy conversion and storage technologies are highly demandable. Hydrogen (H 2 ) is a green energy that may be produced by water-electrolysis. Moreover, the waterlysis can be powered via a renewable energy, and this route of energy production can append a large contribution to achieve the goal on future global carbon neutrality program [2,3]. To produce hydrogen, water electrolysis is commonly catalyzed by noble metal-based catalysts such as those consisting of platinum (Pt) and iridium (Ir). However, these noble metals are rare and are very expensive, resulting the water-electrolysis unaffordable commercially [4,5]. Great efforts have been made to search for noble-metal-free catalysts with high activity and durability. To date, transition metal dichalcogenides (TMDs) [6], metal phosphides [7], MXenes [8] and MOFs [9,10] have been explored as suitable alternatives of Pt for the hydrogen evolution reaction (HER). For example, non-noble metal-based compounds such as MoS 2 , WS 2 , CoS 2 , NiSe 2 , CoSe 2 [11], amorphous MoSx, VS 2 , CoP, Ni 2 P, FeP, WP, MoP|S, CoPS, NiP 1.93 Se 0.07 , and NiMo alloys have been studied as potential HER electrocatalysts [12,13]. Amongst, Vanadium disulfide (VS 2 ) has been emerging as a promising electrocatalyst due to the fact that VS 2 is a layered 2D-material with high HER catalytic activity both on the basal plane and edge [14][15][16].
On the other hand, another attractive characteristic of VS 2 is its excellent electrical charge storing ability with a suitable conductivity for charge transport, which is vital for constructing supercapacitors (SCs). Tshifhiwa et al. reported the fabrication of an asymmetric supercapacitor cell based on porous activated carbon material as negative electrode and VS 2 as positive electrode [17], Similarly, Feng et al. provided a detailed study of Metallic Few-Layered VS 2 ultrathin nanosheets with less than five S-V-S atomic layers to design practical in-plane supercapacitors for the power sources in advanced ultrathin electronics [18]. Meyer et al. also reported carbon supported VS 2 nanocomposites possessing the highest possible specific capacitance of 33 Fg −1 at a current density of 1 mA which is ascribed to the superior electrical conductivity [19]. SCs are simple electrochemical charge storing devices and have generated substantial research attention due to their facile fabrication process with less environmental concerns, and their high-power density with long cycling stability over the traditional secondary batteries [20]. As a potential SC material, VS 2 is a hexagonal graphite-like structure composed of S-V-S layers having a large interlayer distance of 5.76 Å, which is suitable to guest Na + and K + ions in the interlayer spacing without a significant structural collapse [17,21]. In addition, the VS 2 layered structure with suitable electrical conductivity also allows for their rapid electron transport during the charging/discharging cycles [14,21]. Overall, the excellent electrical conductivity, flexible interlayer interactions, high specific surface area with edge exposed atom, and a remarkably resilient, VS 2 layered structure easily satisfy the requirement basis for developing a promising candidate for electrocatalyst and charge storing electrodematerials [18,22,23].
In this study, we designed a solution phase mediated VS 2 consisting of microflowered structure, demonstrating the excellent performance on electrocatalytic HER in acidic (0.5 M H 2 SO 4 ) and alkaline (1 M KOH) electrolytes together with the electrochemical energy storage capabilities. The optimized VS 2 electrodes obtained via ethylene glycol added aqueous solvent synthetic route exhibited a highly ordered and smaller microflowered structures distributed uniformly over the larger electrode surface than the one deposited via pure aqueous or ethylene glycol mediated synthesis routes. As a result of their large surface area having abundant active sites and facile charge transport path, the optimized VS 2 film-based electrodes demonstrated an excellent electrocatalytic HER and electrochemical supercapacitor performance.

Synthesis of VS 2 Microflower Structured Powder
To synthesize VS 2 , 0.1 M sodium orthovanadate and 0.5 M thioacetamide were dissolved in 30 mL DI water by ultrasonic agitation at a frequency of 38.1 kHz for 2 h to obtain a homogeneous solution. The resulting solution was then solvo-/hydro-thermally reacted for 24 h at 160 • C to obtain a black precipitate. The reaction product was naturally cooled to room temperature, then washed several times with DI water and ethanol. After that, the black products were centrifuged at 5000 rpm and finally dried under vacuum in a desiccator. This product is denoted as VS 2 -1 sample. Following a similar procedure, Nanomaterials 2022, 12, 339 3 of 15 two more VS 2 powder samples were synthesized for comparison with different solvent composition while keeping all other parameters as they were in the case of VS 2 -1 sample. The VS 2 sample obtained using pure-ethylene is denoted as VS 2 -2 and the one obtained using 20 mL ethylene glycol and 10 mL DI water mixture solution is named asVS 2 -3 sample.

VS 2 -Based Electrode Fabrication
For catalysis test, the working electrode was prepared by drop casting the catalyst-ink onto a washed NF-substrate. The ink was prepared by mixing 6 mg of the as-synthesized VS 2 powder in 0.5 mL of a mixture solution obtained from 6.93 mL of DI water-ethanol (3:1 volume ratio) and 5% Nafion (70 µL) solution via ultrasonic agitation at a frequency of 38.1 kHz in normal tap-water for 12 h to form a homogeneous ink. Following the formation of uniform ink, 285 µL was carefully loaded onto a 1 cm 2 area of the NF substrate. The freshly prepared catalyst film was dried at room temperature for 24 h at 60 • C under vacuum in an oven. The mass loading of the VS 2 was determined precisely using an inductively coupled plasma mass spectrometry (ICP-MS, NexION ® 300D, PerkinElmer, Waltham, MA, USA).
A symmetric device was assembled to study the supercapacitor performance of the as-synthesized VS 2 based electrodes. For assembly of the symmetric device, VS 2 -1, VS 2 -2, or VS 2 -3 based films on NF-substrate were utilized as positive and negative electrodes and 1 M aqueous solution of KOH was employed as electrolyte. A cellulose membrane was used as a separator, sandwiched between two the symmetric electrodes. The electrodes (VS 2 -1, VS 2 -2, and VS 2 -3) were prepared by mixing the carbon black and polyvinylidene (PVDF) with a mass ratio of 80:10:10, respectively. Then, the mixture was ground by adding a few drops of N-methyl-2-pyrrolidene (NMP) in a mortar until a uniform ink was obtained. The ink was dropped uniformly on the Ni foam and dried in a vacuum oven at 60 • C for 24 h.

Electrochemical Measurements
The multifunctional electrochemical characteristics of the VS 2 -1, VS 2 -2, and VS 2 -3 films on NF-substrates were performed using a three-electrode system (CHI 660D electrochemical instrument). HER experiments were performed in acidic (0.5 M H 2 SO 4 ) and alkaline (1 M KOH) electrolytes at a scanning speed of 5 mV·s −1 at room temperature (25 • C). Carbon rods and active ingredients (VS 2 -1, VS 2 -2, and VS 2 -3) coated nickel foams (NF) were used as the counter electrode and working electrode, respectively. The Ag/AgCl was employed as a reference electrode and a cyclic voltammetry (CV) was applied to activate the working electrode for several cycles until constant CV curves were obtained. A linear sweep voltammetry (LSV) was conducted for evaluation of HER and iR losses were compensated to the LSV data.
All the potentials were calibrated to the RHE potential scale using the Equation (1) Electrochemical impedance spectra (EIS) were measured in the frequency ranging from 0.1 Hz to 100 kHz.

Topographic, Crystal Structure and Chemical Composition Charaterization of VS 2
The synthetic process of the VS 2 microflower structured powder is schematically illustrated in Scheme 1. The VS 2 microflower morphologies (VS 2 -1, VS 2 -2, and VS 2 -3) were obtained via solvo-/hydro-thermal reaction of Na 3 VO 4 ·10H 2 O and thioacetamide (C 2 H 5 NS) at 160 • C for 24 h. The morphology of the fabricated VS 2 -1, VS 2 -2, and VS 2 -3 powder was characterized by field-emission scanning electron microscopy (FE-SEM, Hitachi SU8010, Seoul, South Korea) and the resulting images are shown in Figure 1a-f. Figure 1a,b shows randomly oriented nanosheets in a microflowered structure obtained using a pure-aqueous solvent. The diameter of these microstructures lies between 15 and 30 mm and the microstructures look similar to the assembly of flower-petals having 50 nm thick (inset Figure 1b). A similar layered nanosheet or nanoflake-structure of the VS 2 was reported by hydrothermal synthesis in pure water [17][18][19].
Nanomaterials 2022, 12, x FOR PEER REVIEW 4 of 17 obtained via solvo-/hydro-thermal reaction of Na3VO4.10H2O and thioacetamide (C2H5NS) at 160 °C for 24 h. The morphology of the fabricated VS2-1, VS2-2, and VS2-3 powder was characterized by field-emission scanning electron microscopy (FE-SEM, Hitachi SU8010, Seoul, South Korea) and the resulting images are shown in Figure 1a-f. Figure 1a,b shows randomly oriented nanosheets in a microflowered structure obtained using a pure-aqueous solvent. The diameter of these microstructures lies between 15 and 30 mm and the microstructures look similar to the assembly of flower-petals having 50 nm thick (inset Figure 1b). A similar layered nanosheet or nanoflake-structure of the VS2 was reported by hydrothermal synthesis in pure water [17][18][19]. While synthesizing in pure ethylene glycol solvent, the resulting VS2 microflowers were agglomerated, and the nanosheets were stacked one above another very closely (Figure 1c,d). A similar VS2 microflowers structure has been reported by Chen et al. while synthesizing in propylene glycol and ammonia solution [24]. In contrast, the VS2-3 based electrode, which was fabricated from the corresponding power sample synthesized in a mixture solvent of ethylene glycol and water, exhibited uniformly distributed microflowered structures with a diameter of about 1~2 µm (Figure 1e,f). This flower structure was consisted of an assembly of highly ordered unique sheet-like open flower-petal structure with a thickness of ~100 nm, which can be observed at a closer microscopic examination (inset Figure 1f). This highly ordered unique assembly would be beneficial for the improvement of catalytic and supercapacitor performance. It should be noted that the microstructure in this sample was approximately 4 and 15 times smaller than those achieved in a pure-ethylene glycol and pure-water-mediated process, respectively. This is due to the fact that in comparison to the pure water-mediated reaction process, the addition of ethylene glycol lowers the solubility and mobility of the reactants, hindering the crystal formation [25]. As a result, smaller flowers were achieved, which would be beneficial to increase the concentration of active catalytic sites. Furthermore, due to the reductive nature of the alcohol moiety, ethylene glycol can help to minimize the intrinsic defect concentration of the VS2 structure, and impurity, such as vanadium oxidation, formation can be prevented during synthesis [26,27]. Remarkably, each nanosheet in VS2-3 sample is linked to the next in a highly ordered fashion, generating an open microflower-like While synthesizing in pure ethylene glycol solvent, the resulting VS 2 microflowers were agglomerated, and the nanosheets were stacked one above another very closely (Figure 1c,d). A similar VS 2 microflowers structure has been reported by Chen et al. while synthesizing in propylene glycol and ammonia solution [24]. In contrast, the VS 2 -3 based electrode, which was fabricated from the corresponding power sample synthesized in a mixture solvent of ethylene glycol and water, exhibited uniformly distributed microflowered structures with a diameter of about 1~2 µm (Figure 1e,f). This flower structure was consisted of an assembly of highly ordered unique sheet-like open flower-petal structure with a thickness of~100 nm, which can be observed at a closer microscopic examination (inset Figure 1f). This highly ordered unique assembly would be beneficial for the improvement of catalytic and supercapacitor performance. It should be noted that the microstructure in this sample was approximately 4 and 15 times smaller than those achieved in a pure-ethylene glycol and pure-water-mediated process, respectively. This is due to the fact that in comparison to the pure water-mediated reaction process, the addition of ethylene glycol lowers the solubility and mobility of the reactants, hindering the crystal formation [25]. As a result, smaller flowers were achieved, which would be beneficial to increase the concentration of active catalytic sites. Furthermore, due to the reductive nature of the alcohol moiety, ethylene glycol can help to minimize the intrinsic defect concentration of the VS 2 structure, and impurity, such as vanadium oxidation, formation can be prevented during synthesis [26,27]. Remarkably, each nanosheet in VS 2 -3 sample is linked to the next in a highly ordered fashion, generating an open microflower-like structure. This structural feature would be advantageous for free flow of charges between the structures and the electrolyte, thereby enhancing the charge transfer kinetics in electrolysis and supercapacitors. Furthermore, the VS 2 -3 sample contains a consistent distribution of microstructures of comparable size and shape. structure. This structural feature would be advantageous for free flow of charges between the structures and the electrolyte, thereby enhancing the charge transfer kinetics in elec trolysis and supercapacitors. Furthermore, the VS2-3 sample contains a consistent distri bution of microstructures of comparable size and shape. Transmission electron microscopy (TEM, JEOL-3000F, Seoul, Korea) was also used to demonstrate the formation of the microflowered structure. The TEM depiction of a VS2-3 sample obtained from an ethylene glycol/DI water solvent combination is displayed in Figure 2a, which reveals the petal-shaped sheet. The high-resolution TEM image the cor responding inverse FFT spectrum (Figure 2b,c) generated using the ImageJ computer-pro gram (1.8.0_172, Seoul, Korea) indicates a lattice spacing of 0.15 nm, which correspond to the characteristic (111) crystal-line lattice fringes of VS2. Furthermore, the polycrystal line character of the sample is shown by the selected area electron diffraction (SAED) pat tern in Figure 2d. The scanning transmission electron microscopy (STEM) image and ele mental mapping demonstrate that the V and S elements were distributed consistently throughout the microflowered structure, with no signs of V or S aggregation (Figure 2e,f) Transmission electron microscopy (TEM, JEOL-3000F, Seoul, Korea) was also used to demonstrate the formation of the microflowered structure. The TEM depiction of a VS 2 -3 sample obtained from an ethylene glycol/DI water solvent combination is displayed in Figure 2a, which reveals the petal-shaped sheet. The high-resolution TEM image the corresponding inverse FFT spectrum (Figure 2b,c) generated using the ImageJ computerprogram (1.8.0_172, Seoul, Korea) indicates a lattice spacing of 0.15 nm, which corresponds to the characteristic (111) crystal-line lattice fringes of VS 2 . Furthermore, the polycrystalline character of the sample is shown by the selected area electron diffraction (SAED) pattern in Figure 2d. The scanning transmission electron microscopy (STEM) image and elemental mapping demonstrate that the V and S elements were distributed consistently throughout the microflowered structure, with no signs of V or S aggregation (Figure 2e Furthermore, Figure 3a shows the XRD spectra of the as-fabricated VS2-1, VS2-2, and VS2-3 powder samples along with the reference patterns of VS2 imported from the JCPDS file no. 01-089-1640. The XRD spectra are well matched to the reference patterns and display various diffraction peaks of the polycrystalline nature. This finding confirms the existence of the hexagonal phase of VS2. Based on the standard powder diffraction card, the diffraction peaks (black and blue spectrum) at 2θ = 15.3°, 31.9°, 35.7°, 45.5°, and 47.31° can be indexed to the reflection of (001), (100), (011), (012), and (003) planes of VS2, respectively [23]. In addition, the VS2-3 sample (magenta color spectrum) also shows two additional different peaks at 58.3° and 59.8 that can be associated with the (103), and (111) planes. These additional VS2 phases could further enhance the catalytic site densities in sample VS2-3. The corresponding hexagonal crystal phase structure of VS2 in a space-filling model is displayed in Figure 3b. Raman analysis was conducted for the VS2-1, VS2-2, and VS2-3 electrodes in the range of 200-800 cm −1 as shown in Figure 3c. The three well-defined peaks located at 280 and 404 cm −1 can be ascribed to the Eg vibration (S dumbbells librational) mode and the out-of-plane (Ag) vibration mode of the VS2, respectively, while the peak at 685 cm −1 corresponds to the rocking and stretching vibrations of V-S bonds or their combination [28]. The binding states of the constitutional elements in the optimized VS2-3 sample were studied using X-ray photoelectron spectroscopy (XPS), as illustrated in Figure  3d-f. A typical XPS survey spectrum of the VS2-3 sample shows that the VS2 nanoflower is mostly constituted of V and S, with a small O 1s peak resulting from surface oxidation of VS2 in air. The high-resolution spectra of V 2p and S 2p are displayed in Figure 3e,f, respectively. The high-resolution V 2p XPS spectrum can be deconvoluted into a doublet with peaks located at the binding energies of 524.8 eV and 517 eV, respectively, for the V 2p1/2 and V 2p3/2. This suggests that vanadium in the +4 oxidation state. Similarly, the highresolution S 2p spectra can be deconvoluted to a doublet with the centers located at the binding energies of 163.6 eV and 162.4 eV, which correspond to the S 2p1/2 and S 2p3/2, respectively. This reveals the divalent sulfide (S 2− ), and the XPS finding further confirms the VS2 (1:2) composition of the sample [29]. In Figure S1, the related EDX spectrum also demonstrates that the V and S stoichiometry is about 1:2, confirming that the synthesized microflower is constituted of VS2. Moreover, the VS2 particle loading on the NF substrate  [23]. In addition, the VS 2 -3 sample (magenta color spectrum) also shows two additional different peaks at 58.3 • and 59.8 that can be associated with the (103), and (111) planes. These additional VS 2 phases could further enhance the catalytic site densities in sample VS 2 -3. The corresponding hexagonal crystal phase structure of VS 2 in a space-filling model is displayed in Figure 3b. Raman analysis was conducted for the VS 2 -1, VS 2 -2, and VS 2 -3 electrodes in the range of 200-800 cm −1 as shown in Figure 3c. The three welldefined peaks located at 280 and 405 cm −1 can be ascribed to the Eg vibration (S dumbbells librational) mode and the out-of-plane (Ag) vibration mode of the VS 2 , respectively, while the peak at 688 cm −1 corresponds to the rocking and stretching vibrations of V-S bonds or their combination [28]. The binding states of the constitutional elements in the optimized VS 2 -3 sample were studied using X-ray photoelectron spectroscopy (XPS), as illustrated in Figure 3d-f. A typical XPS survey spectrum of the VS 2 -3 sample shows that the VS 2 nanoflower is mostly constituted of V and S, with a small O 1s peak resulting from surface oxidation of VS 2 in air. The high-resolution spectra of V 2p and S 2p are displayed in Figure 3e,f, respectively. The high-resolution V 2p XPS spectrum can be deconvoluted into a doublet with peaks located at the binding energies of 524.8 eV and 517 eV, respectively, for the V 2p 1/2 and V 2p 3/2 . This suggests that vanadium in the +4 oxidation state. Similarly, the high-resolution S 2p spectra can be deconvoluted to a doublet with the centers located at the binding energies of 163.6 eV and 162.4 eV, which correspond to the S 2p 1/2 and S 2p 3/2 , respectively. This reveals the divalent sulfide (S 2− ), and the XPS finding further confirms the VS 2 (1:2) composition of the sample [29]. In Figure S1, the related EDX spectrum also demonstrates that the V and S stoichiometry is about 1:2, confirming that the synthesized microflower is constituted of VS 2 . Moreover, the VS 2 particle loading on the NF substrate

HER Performance of VS2 Electrodes in Acidic and Alkaline Electrolyte
The electrocatalytic performances of the VS2 based electrodes were assessed for HER using the LSV in a standard three-electrode cell containing 0.5 M H2SO4 or 1 M KOH aqueous solution as acidic and alkaline electrolyte, respectively. The LSV data were measured at a scan rate of 5 mVs −1 and the LSV curves were iR-corrected using the solution resistance acquired from the EIS measurement. Figure 4a, shows the polarization curves of the VS2-1, VS2-2, and VS2-3 samples in a 0.5 H2SO4 aqueous electrolyte. The VS2-1 electrode shows the HER overpotential of 227 mV at a current density of 10 mA cm −2 . The overpotential is lower for the VS2-2 electrode obtained from the pure-ethylene glycol-based synthesis route, displaying HER overpotential of 222 at 10 mAcm −2 . In contrast, the catalyst fabricated utilizing ethylene glycol and water solvent (VS2-3) exhibits a relatively lower overpotential of 161 mV at 10 mAcm −2 . This illustrates that the addition of ethylene into water to synthesize VS2-3 catalyst substantially boosted its intrinsic activity. As explained in the earlier section, this is owing to the fact that the addition of ethylene glycol hinders crystal formation and prevents oxide formation when compared to a pure aqueous-mediated process. This led to the highly ordered unique sheet-like open flower-petal microstructure (Figure 1f), thereby boosting the concentration of active catalytic sites. For the

HER Performance of VS 2 Electrodes in Acidic and Alkaline Electrolyte
The electrocatalytic performances of the VS 2 based electrodes were assessed for HER using the LSV in a standard three-electrode cell containing 0.5 M H 2 SO 4 or 1 M KOH aqueous solution as acidic and alkaline electrolyte, respectively. The LSV data were measured at a scan rate of 5 mVs −1 and the LSV curves were iR-corrected using the solution resistance acquired from the EIS measurement. Figure 4a, shows the polarization curves of the VS 2 -1, VS 2 -2, and VS 2 -3 samples in a 0.5 H 2 SO 4 aqueous electrolyte. The VS 2 -1 electrode shows the HER overpotential of 227 mV at a current density of 10 mA cm −2 . The overpotential is lower for the VS 2 -2 electrode obtained from the pure-ethylene glycol-based synthesis route, displaying HER overpotential of 222 at 10 mAcm −2 . In contrast, the catalyst fabricated utilizing ethylene glycol and water solvent (VS 2 -3) exhibits a relatively lower overpotential of 161 mV at 10 mAcm −2 . This illustrates that the addition of ethylene into water to synthesize VS 2 -3 catalyst substantially boosted its intrinsic activity. As explained in the earlier section, this is owing to the fact that the addition of ethylene glycol hinders crystal formation and prevents oxide formation when compared to a pure aqueous-mediated process. This led to the highly ordered unique sheet-like open flower-petal microstructure (Figure 1f), thereby boosting the concentration of active catalytic sites. For the performance evaluation, the Nanomaterials 2022, 12, 339 8 of 15 overpotential was obtained by subtracting the thermodynamic potential of HER (i.e., 0.00 V vs. RHE) from that of the experimentally obtained potential of the working electrode at a given current density. Figure 4b displays a comparative HER overpotential profiles vs. current densities. The VS 2 -3 based electrode, as shown in Figure 4b, has a lower overpotential of 161 and 386 mV at 10, and 50 mAcm −2 , respectively. This implies that a relatively lower driving energy is needed to drive the HER for the VS 2 -3 sample. In addition, the Tafel plots, presented in Figure 4c, revealed a reasonably low Tafel slope of 88 mV dec −1 with a higher exchange current density (J 0 ) of 7.294 × 10 −5 . This finding reveals the facile HER kinetic for the VS 2 -3 electrode and a smaller amount of driving energy was required towards HER, which is lower than the VS 2 -2 (93 mVdec −1 , J 0 = 1.640 × 10 −5 ) and VS 2 -1 (103 mVdec −1 , J 0 = 3.863 × 10 −6 ) based electrodes, respectively. The charge transport nature of the electrodes was evaluated using electrochemical impedance spectroscopy (EIS), and the resulting Nyquist plot fitted with an analogous circuit is shown in Figure 4d. The relatively low solution resistance (R s = 1.8) and charge-transfer resistance (R ct = 2.41 Ω) experienced by the VS 2 -3 electrode indicates the close contact between the VS 2 -3 active species and NF substrate, and a facile charge transport between the electrolyte and electrode with compared to the VS 2 -1 (R s = 1.9 Ω, R ct = 2.91 Ω) and VS 2 -2 (R s = 2.1 Ω, R ct = 3.08 Ω) based electrodes. The detailed EIS parameters including constant phase element (CPE) and diffusion impedance (Zw) are shown in Table S1. The electrochemical surface area (ECSA) of the catalyst is one of the key factors in electrocatalysis and was computed in terms of the commonly used double-layer charging currents in the non-Faradic regions. The VS 2 -1 (4.0 mFcm −2 ) and VS 2 -2 (4.1 mFcm −2 ) samples showed similar double-layer capacitance while the VS 2 -3 (10 mFcm −2 ) sample exhibited a significantly higher doublelayer capacitance ( Figure S2). The computed double-layer capacitance is directly related to the ECSA, which is further related directly to the available active electrocatalytic sites. This implies that the VS 2 -1 sample had significantly higher catalytic HER sites compared with the other two samples. As a result, the VS 2 -1 based electrode offered the lower overpotential and faster HER kinetics. Apart from the overpotential and HER kinetic, long-term electrochemical stability of the catalyst-based electrode is also a key factor determining the practical applicability of the catalyst. The long-term electrochemical durability of the VS 2 -3 catalyst-based electrode, which demonstrated a high HER performance amongst other catalyst-based electrodes, was examined via chronoamperometry (j vs. t measurement). The HER current density remains fairly stable for a long run over 13 h and has shown the retention of about 85% of the initial current density at the end of 13.43 h. Beyond this, the electrode started to degrade as shown in Figure 5.
In addition, as shown in Figure 6a, the HER performance of the catalyst was also investigated in 1 M KOH aqueous electrolyte. In line with the HER performance in acidic electrolyte, amongst all, the VS 2 -3 based electrode demonstrated a lower HER overpotential of 197 mV to achieve the current density of −10 mAcm −2 . As revealed by Figure 6a, this HER activity is relatively lower than that of the VS 2 -1 and VS 2 -2 based electrodes. This finding implies that the solvents used in the synthesis of VS 2 microstructures play a key role in determining the HER activity via manipulation of microstructure of the catalyst, which can favor for enhancement of the catalytic active sites. Figure 6b depicts a comparative HER overpotential profiles vs. current densities. The VS 2 -3 based electrode, as shown in Figure 6b, has a relatively lower overpotential of 197, 265, and 329 mV at 10, 25, and 50 mAcm −2 , respectively. Furthermore, the Tafel slope exhibited by the VS 2 -3 based electrode is 139 mVdec −1 , which is lower than that exhibited by the VS 2 -1 (146 mVdec −1 ) and VS 2 -2 (158 mVdec −1 ) based electrodes (Figure 6c). This finding implies that the HER kinetics on the VS 2 -3 electrode is faster than on the other electrodes. Tables S2 and S3 demonstrate a comparison of HER performance of the VS 2 -3/NF electrode with other previously published representative transition metal-based electrocatalysts. To further support this finding on HER kinetics, EIS was measured in 1 M KOH electrolyte, and the resulting Nyquist plot is shown in Figure 6d. In comparison to the VS 2 -1 and VS 2 -2 based electrodes, the VS 2 -3 based electrode exhibited a relatively smaller charge-transfer resistance (R ct ) as shown by the smaller semicircle in Figure 6d. This implies the facile charge transfer between the VS 2 -3 based electrode and electrolyte indicating the faster HER kinetic.  In addition, as shown in Figure 6a, the HER performance of the catalyst was also investigated in 1 M KOH aqueous electrolyte. In line with the HER performance in acidic electrolyte, amongst all, the VS2-3 based electrode demonstrated a lower HER overpotential of 197 mV to achieve the current density of −10 mAcm −2 . As revealed by Figure 6a, this HER activity is relatively lower than that of the VS2-1 and VS2-2 based electrodes. This finding implies that the solvents used in the synthesis of VS2 microstructures play a key

Supercapacitor Performance of VS2 in Symmetric Device-Configuration
A symmetric device is employed for the evaluation of the electrochemical performance of VS2 electrodes. For this, the as-prepared electrodes were utilized as cathode and anode with 1 M KOH as electrolyte. Cyclic voltammetry (CV) was examined at the voltage ranging between −0.3 to 0.6 V, as shown in Figure 7a-d. The CV curves for the device prepared from the VS2-1, VS2-2, VS2-3 based electrodes are depicted in Figure 7a. The VS2-3 electrode-based device clearly exhibited a high current response which was an about 2folds integral area compared with the VS2-1 and VS2-2 electrode-based devices. The CV curves of all the VS2 based devices exhibited a notably similar shape resembling to the rectangular nature of an electric double layer capacitor (EDLC). However. It should be noted that the CV curves are not ideally rectangular. Although, no distinctive redox peaks

Supercapacitor Performance of VS 2 in Symmetric Device-Configuration
A symmetric device is employed for the evaluation of the electrochemical performance of VS 2 electrodes. For this, the as-prepared electrodes were utilized as cathode and anode with 1 M KOH as electrolyte. Cyclic voltammetry (CV) was examined at the voltage ranging between −0.3 to 0.6 V, as shown in Figure 7a-d. The CV curves for the device prepared from the VS 2 -1, VS 2 -2, VS 2 -3 based electrodes are depicted in Figure 7a. The VS 2 -3 electrode-based device clearly exhibited a high current response which was an about 2-folds integral area compared with the VS 2 -1 and VS 2 -2 electrode-based devices. The CV curves of all the VS 2 based devices exhibited a notably similar shape resembling to the rectangular nature of an electric double layer capacitor (EDLC). However. It should be noted that the CV curves are not ideally rectangular. Although, no distinctive redox peaks in the CV curves can be observed, the curves are, in fact, deviated from the pure-EDLC derived ideal rectangular shape. This indicates the possibility of occurrence of reversible redox reactions within the voltage window under study. In general, the charge storage mechanism can be classified into the diffusion-controlled faradaic components originated from the pure redox reactions taking place by the diffusion of active ions from electrolyte to the electrode, surface-bound rapid faradaic components originated from the redox reaction of the surface adsorbed active ions on the electrode surface, and the surface-bound rapid non-faradaic components resulting from the material's EDLC behavior [30,31].
in the CV curves can be observed, the curves are, in fact, deviated from the pure-EDLC derived ideal rectangular shape. This indicates the possibility of occurrence of reversible redox reactions within the voltage window under study. In general, the charge storage mechanism can be classified into the diffusion-controlled faradaic components originated from the pure redox reactions taking place by the diffusion of active ions from electrolyte to the electrode, surface-bound rapid faradaic components originated from the redox reaction of the surface adsorbed active ions on the electrode surface, and the surface-bound rapid non-faradaic components resulting from the material's EDLC behavior [30,31].  Further, the CV curves at various sweep rates (10 mVs −1 to 60 mVs −1 ) are recorded in Figure 7b-d. Based on the highly ordered and open petal assembled microflower-like structures of VS 2 in VS 2 -3 sample, a rapid to-and-fro trafficking of K + ions facilitated by the 2D multi-layered VS 2 nanosheets can be assumed in the VS 2 -3 based symmetric device. As a consequence, the CV curve of the VS 2 -3 based symmetric device maintains a similar shape even at the higher scan rates such as 60 mVs −1 , indicating the excellent reversibility of the symmetric device. In contrast, the VS 2 -1 and VS 2 -2 based symmetric devices exhibited the CV curves deviated largely from the rectangular shape, showing severe polarization when the scan rate was increased from 10 to 60 mVs −1 . The deviation in the shape of CV curves is attributed to the redox reaction across the electrode-electrolyte interface, which corresponds to the contribution from the typical characteristics of the pseudo-capacitance. Notably, when the CV loops were repeated for 100 cycles at the 10 mVs −1 , unperturbed shape of the CV curve even after a colossal number of cycles were obtained in the VS 2 -3 based symmetric device, exhibiting an about of 98% cyclic retentions. This preliminary finding reveals a long-term stability and higher rate capability of the VS 2 -3 based symmetric device.
For in-depth evaluation of the device performance, galvanostatic charging discharging (GCD) has been analyzed at 0.7 Ag −1 and the results are presented in Figure 8a. The VS 2 -3 based symmetric device exhibited longest discharging time compared with the others, thereby leading to the higher specific capacitance (Cs), which is consistent with the CV curves. The symmetric device shows smaller iR drops particularly at the lower current density of 0.7 Ag −1 , implying the low internal resistance of the symmetric device. Moreover, the GCD curves for the VS 2 -1, VS 2 -2 and VS 2 -3 based devices were examined at the various current densities, and are depicted in Figure 8b-d. Here, Cs was determined through GCD curve using the following Equation (2).
wherein, I dis is the discharging current density, ∆t dis is the discharging time, and ∆V is the voltage window. The VS 2 -3 symmetric device shows Cs of 139 Fg −1 which is higher than that of VS 2 -2 (120 Fg −1 ) and VS 2 -1 (54 Fg −1 ) at the discharging current density of 0.7 Ag −1 (Figure 9a). The long-term stability of the symmetric device is a key parameter for practical application of the supercapacitors, which was investigated by the repeated GCD measurements at a current density of 0.7 Ag −1 for 7000 cycles, as presented in Figure 9b. The capacity retention was almost 100% at the end of 1000 cycles, beyond which it decreased gradually. Notably, the VS 2 -3 based symmetric device showed remarkable capacity retentions of 86% even at the end of 7000 cycles revealing the capacitance degradation of only about 14%, which is lower than that of VS 2 -2 (17%) and VS 2 -1 (18%) based devices.
the 2D multi-layered VS2 nanosheets can be assumed in the VS2-3 based symmetric device. As a consequence, the CV curve of the VS2-3 based symmetric device maintains a similar shape even at the higher scan rates such as 60 mVs −1 , indicating the excellent reversibility of the symmetric device. In contrast, the VS2-1 and VS2-2 based symmetric devices exhibited the CV curves deviated largely from the rectangular shape, showing severe polarization when the scan rate was increased from 10 to 60 mVs −1 . The deviation in the shape of CV curves is attributed to the redox reaction across the electrode-electrolyte interface, which corresponds to the contribution from the typical characteristics of the pseudo-capacitance. Notably, when the CV loops were repeated for 100 cycles at the 10 mVs −1 , unperturbed shape of the CV curve even after a colossal number of cycles were obtained in the VS2-3 based symmetric device, exhibiting an about of 98% cyclic retentions. This preliminary finding reveals a long-term stability and higher rate capability of the VS2-3 based symmetric device. For in-depth evaluation of the device performance, galvanostatic charging discharging (GCD) has been analyzed at 0.7 Ag −1 and the results are presented in Figure 8a. The VS2-3 based symmetric device exhibited longest discharging time compared with the others, thereby leading to the higher specific capacitance (Cs), which is consistent with the CV curves. The symmetric device shows smaller iR drops particularly at the lower current density of 0.7 Ag −1 , implying the low internal resistance of the symmetric device. Moreover, the GCD curves for the VS2-1, VS2-2 and VS2-3 based devices were examined at the various current densities, and are depicted in Figure 8b-d. Here, Cs was determined through GCD curve using the following Equation (2).  The energy and power density of the symmetric devices were determined utilizing the following equation: where, E and P are energy and power density, respectively. The energy density as a function of power density of the symmetric VS 2 based devices is shown in Figure 9c. The VS 2 -3 based device exhibited a maximum energy density of 15 Whkg −1 at a power density of 0.304 kWkg −1 . Furthermore, EIS was measured to investigate the charge transfer behaviors of the VS 2 -1, VS 2 -2, and VS 2 -3 electrodes in the frequency ranging from 100 mHz to 200 kHz under an open circuit potential (Figure 9d). The variables R s and R ct represent the electrochemical system resistance (i.e., all resistances including electrolyte ionic resistance, substrate intrinsic resistance, and contact resistance between the active material and current collector) and charge transfer resistance, respectively. The R s and R ct of the VS 2 -3 devicebased electrodes are smaller than those of VS 2 -1, VS 2 -2 based devices (Table S4), indicating that the VS 2 -3 based material in the device transport current fluently to the current collector than the other VS 2 materials. This EIS data supports the higher performance of the VS 2 -3 based symmetric device.

Conclusions
A solvo-/hydro-thermal route was employed to design a solution-phase mediated layered VS2 microflower structured materials in a mixture of ethylene glycol and water as the reaction media. The optimized VS2-3 based electrode obtained from the ethylene glycol and water mixed solvent-mediated synthesis route demonstrated a high catalytic performance for HER in both acidic and alkaline electrolytes containing 0.5 M H2SO4 or 1 M KOH. This finding demonstrates the ability of the VS2 to catalyze HER in a wide pH range of electrolyte. In addition, the optimized VS2-3 electrode-based symmetrical supercapacitor exhibited a specific capacitance of 139 Fg −1 with an energy density of 15 Whkg −1 . Moreover, the device showed an excellent capacity retention of 86.8% of the initial value at the end of 7000 charge/discharge cycles, demonstrating a high stability of the VS2 electrode. The strong electrocatalytic and supercapacitor performance is attributed to the crystalline microflower structure of VS2 consisting of highly ordered nanosheet layers. This study proposes a straightforward construction technique for green hydrogen energy production and green energy storage devices which can contribute to the future global carbon neutrality program.

Conclusions
A solvo-/hydro-thermal route was employed to design a solution-phase mediated layered VS 2 microflower structured materials in a mixture of ethylene glycol and water as the reaction media. The optimized VS 2 -3 based electrode obtained from the ethylene glycol and water mixed solvent-mediated synthesis route demonstrated a high catalytic performance for HER in both acidic and alkaline electrolytes containing 0.5 M H 2 SO 4 or 1 M KOH. This finding demonstrates the ability of the VS 2 to catalyze HER in a wide pH range of electrolyte. In addition, the optimized VS 2 -3 electrode-based symmetrical supercapacitor exhibited a specific capacitance of 139 Fg −1 with an energy density of 15 Whkg −1 . Moreover, the device showed an excellent capacity retention of 86.8% of the initial value at the end of 7000 charge/discharge cycles, demonstrating a high stability of the VS 2 electrode. The strong electrocatalytic and supercapacitor performance is attributed to the crystalline microflower structure of VS 2 consisting of highly ordered nanosheet layers. This study proposes a straightforward construction technique for green hydrogen energy production and green energy storage devices which can contribute to the future global carbon neutrality program.