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One-step synthesis of nanowoven ball-like NiS-WS2 for high-efficiency hydrogen evolution
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Lanfang Wang1,*, Jiangnan Lv1, Yujia Li1, Yanqing Hao, Wenjiao Liu, Hui Zhang, Xiaohong Xu*
Chinese Chemical Letters | 2025, 36(1) : 109597
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Chinese Chemical Letters | 2025, 36(1): 109597
• Communication •
One-step synthesis of nanowoven ball-like NiS-WS2 for high-efficiency hydrogen evolution
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Lanfang Wang1,*, Jiangnan Lv1, Yujia Li1, Yanqing Hao, Wenjiao Liu, Hui Zhang, Xiaohong Xu*
Affiliations
  • Key Laboratory of Magnetic Molecules and Magnetic Information Materials of Ministry of Education, School of Chemical and Material Science, Shanxi Normal University, Taiyuan 030032, China
Published: 2025-01-15 doi: 10.1016/j.cclet.2024.109597
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Exploring transition metal sulfide electrocatalysts with high-efficiency for hydrogen evolution reaction (HER) is essential to produce H2 fuel through water splitting. Herein, novel nickel tungsten sulfide heterojunction (NiS-WS2) with a nanowoven ball-like structure were directed synthetized by a facile hydrothermal method. The hierarchical NiS-WS2 exhibited excellent HER activity with a relatively small overpotential of 142 and 137 mV at 10 mA/cm2 in 0.5 mol/L H2SO4 and 1 mol/L KOH, which is much better than that of single NiS and WS2. The impressive performance of NiS-WS2 heterojunction is owed to the collective synergy of special morphological and more exposed active sites between the crystal interfacial of NiS and WS2. In addition, the hierarchical NiS-WS2 can facilitate the transport of charge/mass by optimized electronic structure, which further improves the HER activity of electrocatalysts. These outcomes provide a simple method to prospect towards the design and application of heterostructures as efficient electrocatalysts, shedding some light on the development of functional materials in energy chemistry.

Nanowoven ball-like  /  Hierarchical  /  NiS-WS2  /  Hydrogen evolution reaction  /  Synergy
Lanfang Wang, Jiangnan Lv, Yujia Li, Yanqing Hao, Wenjiao Liu, Hui Zhang, Xiaohong Xu. One-step synthesis of nanowoven ball-like NiS-WS2 for high-efficiency hydrogen evolution[J]. Chinese Chemical Letters, 2025 , 36 (1) : 109597 - . DOI: 10.1016/j.cclet.2024.109597
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With the continuous progress of science and technology and the rapid growth of global economy, energy crisis has become worldwide issues. Hydrogen energy has received extensive attention because of its high efficiency, cleanliness and renewability [1–4]. For sustainable hydrogen production, electrochemical water splitting is a promising technology, and has been widely studied. As an important reaction for water splitting, hydrogen evolution reaction (HER) usually required additional overpotentials to overcome the slow water decomposition kinetics and unfavorable thermodynamics [5–8]. Therefore, effective HER electrocatalysts with high reaction rates are required to afford high current at low overpotential. Among many hydrogen evolution catalysts, transition metal sulfide (such as WS2) has received growing attention due to its low price, environmental friendliness and Pt-like electron configuration [9–12]. However, their performance is still inferior to that of Pt-based catalysts for HER [13,14].
To improve the HER catalytic activity of WS2, several strategies, including morphology engineering and electron structure modulation, have been proposed to overcome the intrinsic activity limitation [15–18]. For example, higher conductivity and more catalytic active sites can be obtained by combining WS2 with other metal sulfides (such as FeS2, CoS2 and Ni3S2) to form heterojunction [19–23]. This heterointerface engineering can modulate the electronic properties, as well as chemisorption behavior and composition of catalysts, thereby improving the catalytic efficiency. More importantly, the heterointerface effect can generate new catalytic active centers and charge carriers, which not only increase the number of catalytic active sites, but also promote the mass transport involved in the catalytic reaction. Finally, the kinetic characteristics and adsorption conversion of reactants on the multiphase catalysts were optimized.
Nowadays, prominent progress has been made on the electron structure modulation of Ni-based and W-based sulfide catalysts by heterointerface means [24–28]. And the catalytic performance of multiphase catalysts is superior to their single-component counterpart. However, most of the geometric structures for Ni-based and W-based sulfide catalysts are concentrated in nanosheets, nanorods, nanospheres, as well as their composites [29–31]. Some novel morphologies with more catalytic active sites are neglected. In addition, the Ni-based sulfide with different phase were usually integrated together to enhance their electrochemical properties, and the incorporation of Ni into sulfide catalysts can lead to a distorted structure [1,8,32]. However, the fabrication of these Ni-based and W-based multiphase sulfides required multisteps, and even desired sulfidation process with poisonous sulfurcontaining gas [33–35]. Therefore, to maximize the catalytic performance of Ni-based and W-based multiphase sulfides, a simple and cost-effective method for the integration of morphology engineering and electronic modulation is highly needed. Especially, the synthesis of nanowoven ball-like polymetallic sulfides for HER remains a significant challenge.
In this paper, a novel nanowoven ball-like NiS-WS2 with more catalytic active sites were prepared by a simple and cost-effective hydrothermal and annealing treatment. The influence of Ni content on the morphology and catalytic performance of NiS-WS2 was studied, and the possible catalytic mechanism of the sample was explored. This nanowoven ball-like catalyst has both abundant catalytic active sites and low charge transfer resistance by optimized electronic structure, which further improves the electrocatalytic performance for HER. This work will provide important experimental and theoretical support for revealing the relationship between HER catalytic activity and morphology of the catalyst.
The fabrication process of nanowoven ball-like NiS-WS2 by one-step hydrothermal method is schematically shown in Fig. 1a. The synthesized samples by the same route with different amount of NiC4H6O4·4H2O (0.15, 0.3, 0.45, 0.6 g) were named as NB1-NiS-WS2, NB2-NiS-WS2, NB3-NiS-WS2 and NB4-NiS-WS2, respectively. This process does not require complicated equipment and conditions. The crystal structure of WS2, NiS and NB3-NiS-WS2 composite was analyzed by X-ray powder diffraction (XRD). As shown in Fig. 1b, the diffraction peaks of WS2 and NB3-NiS-WS2 at 28.8°, 33.3°, 39.5°, 43.5°, 48.9°, 58.4°, 60.6° and 69.1° assign to the 2H WS2 phase (PDF#08–0237). The XRD pattern of NiS and NB3-NiS-WS2 composite shows diffraction peak at 30.2°, 32.2°, 35.6°, 37.4°, 40.4°, 48.8°, 52.5°, 56.2°, 57.4°, 59.6° and 67.3°, which can be indexed to the β-NiS phase (PDF#12–0041, space group: R3m, a = b = 9.62 Å and c = 3.15 Å). Besides, several diffraction peaks of NiS and NB3-NiS-WS2 composite at 34.4°, 45.9° and 53.4° match well with the crystal planes of α-NiS phase (PDF#02–1280, space group: P63/mmc, a = b = 3.41 Å and c = 5.32 Å), confirming the formation of a mixed phase (α-NiS and β-NiS). The XRD patterns of NiS-WS2 with different Ni precursor were also examined (Fig. S1 in Supporting information). The characteristic peaks of NiS-WS2 revealed the formation of mixed phase (α-NiS and β-NiS). The excessive Ni precursor gave rise to the increased intensity of NiS phase. For comparison, the Fe-WS2 and Co-WS2 were also synthesized by the same route (Supporting information). The incorporation of Fe precursor into WS2 formed the WS2-Fe1-xS and WS2-Fe3S4, named as Fe-WS2 (Fig. S1). And the incorporation of Co precursor formed WS2CoS2 and WS2CoS, named as Co-WS2.
The microstructure of WS2, NiS-WS2 and NiS catalyst was observed by scanning electron microscopy (SEM). The SEM image (Fig. 1c) shows that the flower-like WS2 consist of nanosheets with lengths of microns. While the NiS-WS2 (Figs. 1d-g and Fig. S2 in Supporting information) with an average size of around 1.2 µm show a semblable spherical appearance, like a nanowoven ball (inset of Fig 1d). Obviously, the spherical structures inherit well while the surface consist of convex prismatic fringes, and many small-sized nanosheets are vertically arranged and closely interconnected with each other to form the convex prismatic fringes. This prismatic fringes on spherical structures provide abundant adhesion points to grow more small-sized nanosheets. These nanosheets exposes more edges active sites on the same volume of nanospheres. As exhibited in Figs. 1d-g, the amount of Ni precursors can effectively control the number and size of small-sized nanosheets. The EDS analysis (Fig. S3 in Supporting information) confirms the presence of Ni, W and S elements in NiS-WS2, and the ratio of Ni: W has been influenced by the quantity of Ni precursors. By contrast, the surface morphology of NiS in Fig. 1h becomes loose and the irregular structure on the surface stack together. The SEM images of Fe-WS2 and Co-WS2 in Fig. S4 (Supporting information) verifies the Ni element are conducive to form nanowoven ball-like structure. Therefore, the nanowoven ball-like NiS-WS2 heterostructures with highly exposed small-sized nanosheets and abundant edges active sites were successfully synthetized through in situ self-organized strategy.
In order to further investigate the microstructures and compositions of nanowoven ball-like NiS-WS2, transmission electron microscopy (TEM) was performed. Fig. 2a shows that the NB3-NiS-WS2 have spherical morphology with some nanosheets on the surface. In the high-resolution TEM (HRTEM) image in Fig. 2b, the lattice spacing of 0.611 nm can be clearly observed, which is assigned to (003) plane of WS2. The lattice fringe with a distance of 0.2511 nm can be assigned to the (021) plane of NiS. The legible interface marked with a white dashed line indicate the existence of a heterointerface between NiS and WS2. The corresponding selected area electron diffraction (SAED) is displayed in Fig. 2c, the diffraction circles are clearly indexed to NiS and WS2. Furthermore, the elemental mapping was employed to analyze the atomic arrangement of NB3-NiS-WS2 catalyst (Figs. 2d-g). The S, W and Ni elements are dispersed homogeneously on the sample. All these results reflect that the incorporation of the Ni and W species modulates the micromorphology of NiS-WS2 heterostructure to form a uniform nanowoven ball-like NiS-WS2.
The surface elemental compositions and chemical states of WS2, NiS and NB3-NiS-WS2 composite were investigated using X-ray photoelectron spectroscopy (XPS). Fig. 3a exhibits the XPS survey spectra of WS2, NiS and NB3-NiS-WS2. The signal of C and O is attributed to CO2 and oxygen impurities adsorbed on the surface of sample. The high-resolution W 4f spectra of WS2 and NiS-WS2 composites (Fig. 3b) displays two sets of spin-split peaks, indicating the presence of W4+ and W6+ peaks. Here the W6+ could be derived from the oxidation of W caused by exposure under the air atmosphere. The different peak positions of W between WS2 and NB3-NiS-WS2 suggest that the Ni influences the electronic structure of W, resulting in richer valence states and a negative shift in binding energy. The Ni 2p XPS spectra of NiS and NB3-NiS-WS2 composite in Fig. 3c is fitted with three sets of peaks, which displays two valence species of Ni3+ and Ni2+. Compared to NiS, NB3-NiS-WS2 exhibits higher energy shifts in the Ni2+ and Ni3+ peaks, suggesting a decrease in electron density for Ni. Additionally, the S 2p spectrum (Fig. 3d) of NB3-NiS-WS2 mainly exhibits four different peaks, the peak at 162.1/163.3 eV attributes to S2−, the peak at 169.2/170.4 eV attributes to the peak of S-O. These peaks exhibit a significantly negative shift compared to WS2 and NiS, implying higher charge density at S sites. These findings suggest a strong interfacial interaction between WS2 and NiS is generated, leading to the electron transfer from Ni to WS2. This modifies the electronic properties of the electrocatalyst and optimizes the adsorption and desorption abilities of active species at active sites, consequently improving their HER catalytic activity [36].
The HER activities of the as-prepared catalysts were investigated in 0.5 mol/L H2SO4 electrolyte using a standard three-electrode system without iR compensation. Fig. 4a displays linear sweep voltammetry (LSV) curves of different catalysts with a scan rate of 5 mV/s. Clearly, the HER activity of carbon fiber cloth (CF) substrate was low. The various NiS-WS2 composite catalyst exhibit significant enhancements in the HER (Fig. 4a and Fig. S5 in Supporting information). The polarization curve of the NB3-NiS-WS2 catalyst exhibits the best HER activity among these catalysts, requiring a low overpotential of 142 mV to achieve the current density of 10 mA/cm2. This is superior to that of NiS (197 mV) and WS2 (318 mV). The Tafel slope is used to reflect the kinetic characteristics of the electrocatalyst in HER. As shown in Fig. 4b, Pt/C has the smallest Tafel slope of 47.1 mV/dec, which is attributed to its optimal kinetic advantage. The NB3-NiS-WS2 composite displays a Tafel slope of 78.6 mV/dec, exhibiting a more rapid HER kinetics than that of NiS (106.3 mV/dec) and WS2 (141.3 mV/dec) electrocatalysts. The Electrochemical impedance spectroscopy (EIS) measurement was used to evaluate the electrocatalytic kinetics between the interface of electrolyte and electrocatalyst. As exhibited in Fig. S6 (Supporting information), a smaller charge transfer resistance (the diameter of the semicircle) of NB3-NiS-WS2 imply a faster electron transport kinetic in the hierarchical heterostructure. These results confirm that the Ni doping play an important role in promoting the HER activity of WS2. Moreover, as exhibited in Fig. 4c, the catalytic performance of NB3-NiS-WS2 composite surpasses most of the W-based and Ni-based electrocatalysts reported [22,23,37-40].
The electrochemical surface areas (ECSA) of electrocatalysts were evaluated by means of electrochemical double layer capacitance (Cdl) tests. The cyclical voltammetry (CV) measurement with different scan rate was used to calculate the Cdl (Fig. 4d and Fig. S7 in Supporting information). As displayed in Fig. 4e, the NB3-NiS-WS2 electrocatalyst exhibits a Cdl value of 45.3 mF/cm2, higher than those of WS2 (8.5 mF/cm2), NiS (1.9 mF/cm2), and CF (0.22 mF/cm2). This suggests the electrochemical active area of the prepared NB3-NiS-WS2 catalyst is the largest, which is consistent with the N2 adsorption–desorption result in Fig. S8 (Supporting information) and the HER catalytic activity in Fig. 4a. Fig. 4f shows the LSV curves of NB3-WS2NiS before and after 300 cycles. It can be observed that the sample almost has no HER current loss, suggesting a good stability. These results suggest that the smaller charge transfer resistance and larger ECSA of the special nanowoven ball-like structure account for the excellent HER performance of NB3-NiS-WS2.
We further evaluated the HER performance of BN3-NiS-WS2 and the control catalysts in alkaline media (1 mol/L KOH). Fig. 5a shows that BN3-NiS-WS2 exhibits excellent electrocatalytic behavior for HER (η10 = 137 mV), exceeding NiS (η10 = 241 mV), WS2 (η10 = 381 mV) and other WS2-based catalysts (Fig. 5a and Fig. S9 in Supporting information). The dynamic process related with the Tafel slope can also be used to reveal the improved HER performance. As shown in Fig. 5b, the NB3-NiS-WS2 catalyst displays a Tafel slope of 81 mV/dec, much smaller than that of NiS (134 mV/dec), WS2 (214 mV/dec), indicating the largest catalytic reaction kinetics. The interfacial charge-transfer kinetics was elucidated by means of EIS measurements. As exhibited in Fig. 5c, the four curves have similar changing trends and are all composed of semi-circles in the high frequency region. The low charge transfer resistance of NB3-NiS-WS2 suggests the rapid catalytic reaction kinetics for HER at the electrocatalyst/electrolyte interface. Therefore, the excellent HER performance of NB3-NiS-WS2 is mainly due to the abundant edge active sites and interfaces on the special nanowoven ball-like structure, which improving the intrinsic electronic conductivity. The stability of the NB3-NiS-WS2 is finally elucidated by using the LSV curves (Fig. 5d) before and after 500 cycle CV measurement. The LSV curve remains almost the same as the initial curve. These results indicate that the NB3-NiS-WS2 electrocatalyst exhibits an outstanding and robustness HER performance in the alkaline solution.
In conclusion, a novel nanowoven ball-like NiS-WS2 were successfully prepared through a simple and scalable hydrothermal process. The surface of the as-prepared NB3-NiS-WS2 catalyst consists of convex prismatic fringes, and many small-sized nanosheets are vertically arranged and closely interconnected with each other to form the convex prismatic fringes. This NB3-NiS-WS2 catalyst exhibited an excellent HER activity and stability in both acid and alkaline solutions. The excellent HER activity is mainly due to the abundant edge active sites and interfaces on the same volume of nanospheres, which improving the intrinsic electronic conductivity. This facile and scalable method can open the door for the discovery of low-cost electrocatalyst.
Declaration of competing interest
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The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgments
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The work is financially supported by the National Natural Science Foundation of China (No. 52202340), the Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi (No. 2021L266), the Applied Basic Research Project of Shanxi Province (No. 20210302124425) and the Graduate Science and Technology Innovation Project Foundation of Shanxi Normal University (No. 2023XSY065).
Supplementary materials
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Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.cclet.2024.109597.
References
Less
[1]
T. Sun, Z. Tang, W. Zang, et al., Nat. Nanotechnol. 18 (2023) 763–771.
[2]
J. Baek, M.D. Hossain, P. Mukherjee, et al., Nat. Commun. 14 (2023) 5936.
[3]
G. Li, H. Jang, S. Liu, et al., Nat. Commun. 13 (2022) 1270.
[4]
Z. Lei, W. Cai, Y. Rao, et al., Nat. Commun. 13 (2022) 24.
[5]
J. Ge, D. Zhang, Y. Qin, et al., Appl. Catal. B: Environ. 298 (2021) 120557.
[6]
J. Li, Y. Zhang, C. Liu, et al., Adv. Funct. Mater. 32 (2021) 2108316.
[7]
B. Fei, Z. Chen, J. Liu, et al., Adv. Energy Mater. 10 (2020) 2001963.
[8]
W. Xu, R. Zhao, Q. Li, et al., Adv. Energy Mater. 13 (2023) 2300978.
[9]
Y. Yang, H. Yao, Z. Yu, et al., J. Am. Chem. Soc. 141 (2019) 10417–10430.
[10]
X. Ma, J. Li, C. An, et al., Nano Res. 9 (2016) 2284–2293.
[11]
A. Han, X. Zhou, X. Wang, et al., Nat. Commun. 12 (2021) 709.
[12]
Y. Jing, X. Mu, C. Xie, et al., Int. J. Hydrog. Energy 44 (2019) 809–818.
[13]
L. Sun, M. Gao, Z. Jing, et al., Chem. Eng. J. 429 (2022) 132187.
[14]
M. Ma, J. Xu, H. Wang, et al., Appl. Catal. B: Environ. 297 (2021) 120455.
[15]
L. Liu, C. Zhang, M. Chen, et al., Appl. Surf. Sci. 573 (2022) 151606.
[16]
S. Peng, L. Li, J. Zhang, et al., J. Mater. Chem. A 5 (2017) 23361–23368.
[17]
L. Wang, R. Yang, J. Fu, et al., Rare Metals 42 (2023) 1535–1544.
[18]
J. Tan, S. Li, B. Liu, et al., Small Struct. 2 (2020) 2000093.
[19]
H.L. Chen, Y.Q. Li, H.Y. Huang, et al., Energy Fuel 36 (2022) 4888–4894.
[20]
D.R. Paudel, U.N. Pan, R.B. Ghising, et al., Nano Energy 102 (2022) 107712.
[21]
Z.Q. Zhang, X.F. Lin, S.L. Tang, et al., Int. J. Hydrog. Energy 47 (2022) 33643–33651.
[22]
J. Wu, T. Chen, C. Zhu, et al., ACS Sustain. Chem. Eng. 8 (2020) 4474–4480.
[23]
L. Sun, J. Geng, M. Gao, et al., Chem. Eur. J. 27 (2021) 10998–11004.
[24]
W.J. Jiang, T. Tang, Y. Zhang, et al., Acc. Chem. Res. 53 (2020) 1111–1123.
[25]
E. Meza, R.E. Diaz, C.W. Li, ACS Nano 14 (2020) 2238–2247.
[26]
P.V. Sarma, A. Kayal, C.H. Sharma, et al., ACS Nano 13 (2019) 10448–10455.
[27]
W. Xu, C. Zhang, H. Shen, et al., ACS Sustain. Chem. Eng. 10 (2022) 14396–14406.
[28]
W. Han, Z. Liu, Y. Pan, et al., Adv. Mater. 32 (2020) 2002584.
[29]
Q. Fu, J. Han, X. Wang, et al., Adv. Mater. 33 (2021) 1907818.
[30]
R. He, C. Wang, L. Feng, Chin. Chem. Lett. 34 (2023) 107241.
[31]
K. Zhang, Y. Duan, N. Graham, et al., Appl. Catal. B: Environ. 323 (2023) 122144.
[32]
H. Wei, J. Si, L. Zeng, et al., Chin. Chem. Lett. 34 (2023) 107144.
[33]
H. Wang, J. Xu, Q. Zhang, et al., Adv. Funct. Mater. 32 (2022) 2112362.
[34]
W. Hong, E. Meza, C.W. Li, J. Mater. Chem. A 9 (2021) 19865–19873.
[35]
B. Qiu, Y. Zhang, X. Guo, et al., J. Mater. Chem. A 10 (2022) 719–725.
[36]
W. Antink, S. Lee, H. Lee, et al., Adv. Funct. Mater. 34 (2023) 2309438.
[37]
J. Li, Z. Yang, Y. Lin, et al., New J. Chem. 44 (2020) 8578–8586.
[38]
Q. Qin, L. Chen, T. Wei, et al., Small 15 (2019) 1803639.
[39]
X. Zhang, P. Yang, S.P. Jiang, Carbon 175 (2021) 176–186.
[40]
S.R. Kadam, A.N. Enyashin, L. Houben, et al., J. Mater. Chem. A 8 (2020) 1403–1416.
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Year 2025 volume 36 Issue 1
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doi: 10.1016/j.cclet.2024.109597
  • Receive Date：2023-12-26
  • Online Date：2025-11-12
  • Published：2025-01-15
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  • Received：2023-12-26
  • Revised：2024-01-23
  • Accepted：2024-01-29
Affiliations
    Key Laboratory of Magnetic Molecules and Magnetic Information Materials of Ministry of Education, School of Chemical and Material Science, Shanxi Normal University, Taiyuan 030032, China
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表12种不同金属材料的力学参数
科
Family		 属数
Number of
genus		 种数
Number of
species		 占总种数比例
Percentage of
total species (%)		 属
Genus		 种数
Number of
species		 占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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