Abstract
Hollow Sn-Co nanospheres have been fabricated by galvanic replacement reaction. In particular, the hollow resultants with different shell thickness and void space can be obtained using sacrificial templates with different sizes. The structural evolution of Sn-Co hollow microspheres and structure changes during charge/discharge process were studied using XRD, SEM, and TEM. As an anodic material, the hollow resultants with thin shell and relatively large void space exhibited a good reversible capacity of 502 mAh g−1 at a current density of 100 mA g−1 and a coulomb efficiency over 99 % after 100 cycles. The contributions of the hollow structure and the inactive Co element to electrochemical performance were verified by galvanostatic charge/discharge cycling, electrochemical impedance spectroscope, and TEM measurements. A possible mechanism for hollow structure with different shell thickness to alleviate the volume change was proposed.
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Introduction
Owing to their advantages of high operation voltage, no memory effect, and high energy density, lithium ion batteries (LIBs) have been commercially used as power sources for extended applications such as portable electronic devices and electric vehicles [1, 2]. With the growing need for higher capacity and safety, numerous efforts have been made to develop novel anode materials as alternatives to graphite. Among various attractive candidates for anodes, metal tin (Sn) has emerged as a kind of promising anode for next-generation LIBs, since it has a theoretical specific capacity of as high as 993 mAh g−1 [3, 4]. However, it has been shown to be difficult to utilize pure Sn due to the severe volume variation (about 300 %) between Sn and Li4.4Sn during cycling. The volume change can cause electrode pulverization and electric disconnection, which is responsible for the poor cyclic life of Sn electrodes [5, 6]. The most common problem-solving strategy employed in the literature is to tailor the particle size of electrochemical materials to nanometer-scale [7–10] and to form intermetallic Sn-based compounds [11–14]. Though the electrochemical performance of Sn-based anodes in literature is improved, it is still not sufficient to meet the practical demands, which implies that the implement of Sn-based electrodes may not be achieved by simply introducing Sn-based alloy at nanoscale.
According to recent research studies [15–19], hollow structure has been developed to further circumvent the issue of volume change. Fang et al. [20] synthesized SnO2-Fe2O3 hollow spheres using a solid acid sphere, as the template and the hollow SnO2-Fe2O3 nanospheres showed excellent cycling performance. The enhancement of the battery performance could be attributed to the structural merit of hollow structure [21, 22]. The large surface area of the hollow structure enables better access for Li+ as a result of the increased electrode-electrolyte contact area. Moreover, the combination of exterior shell and hollow interior significantly shortens Li+ transport path, thus resulting in improved electrochemical kinetics of the hollow structure. Besides the large surface area and the reduced Li+ diffusion length, the interior cavities can enhance the specific capacity by providing extra space for the storage of Li+ and improve the cycling stability by buffering against the local mechanical strain associated with repeated Li+ insertion/extraction process [23]. As a result of the significantly mitigated electrode pulverization and polarization, exceptional electrochemical performance is thus highly anticipated for hollow Sn-based alloy anodes.
Recently, significant efforts have been devoted to the fabrication of hollow structure on the basis of template method, since the utilization of pre-grown templates allows rational design of the size and shape of the resultant hollow structure [24–26]. Nevertheless, these hard or soft template-based methods face many challenges, such as the tedious procedures for shell deposition and template removal. In contrast to the polymer and inorganic nonmetal templates, novel approaches based on sacrificial templates hold great promise in synthesizing hollow nanostructure with well-defined interiors. The sacrificial templates act as consumable resultants for shell construction and can be depleted during the hollowing process. This simple preparation process will avoid the additional problems on the product quality and process cost. Especially for the hollow structure with tiny size (<200 nm), these strategies are particularly attractive due to the convenience of growing shells on high-curvature objects [24, 27]. Generally, there are two main mechanisms using sacrificial template method to obtain hollow resultants, i.e., Kirkendall effect [28–30] and galvanic replacement [31–34]. Compared with Kirkendall effect, galvanic replacement does not require additional surface functionalization, and moreover, it provides a remarkably facile and versatile route to fabricate hollow intermetal nanostructure [27, 33]. However, previous reports are almost limited to noble metal materials. Hollow Sn-based bimetallic nanostructure for LIBs is rare. It is worth mentioning that in galvanic replacement reaction, the void space and shell thickness of the hollow resultants can be easily controlled by tuning the size of sacrificial templates, thus providing the opportunity to further optimize the performance of anode materials [35].
Here, the hollow Sn-Co nanospheres are synthesized by using Co nanoparticles as sacrificial templates via galvanic replacement reaction. In particular, hollow Sn-Co nanospheres with different shell thickness were prepared to investigate the influence of shell thickness on electrochemical performance. Based on the electrochemical results, a possible mechanism for hollow structure to relieve the volume change is proposed. Benefiting from the synergetic merits of the hollow nanostructure along with the nonreactive Co element, the resulting hollow Sn-Co nanospheres could dramatically improve the electrochemical performance.
Experimental
Materials and equipments
All chemicals were of analytical grade and used as purchased without further purification. C4H6CoO4 · 4H2O (>99.5 %), SnSO4 (>99 %), poly(vinylpyrrolidone) (PVP), sodium borohydride (NaBH4, >98 %), and sodium hydroxide (NaOH, >96 %) were obtained from Kewei Chemical Reagent Co. Ltd. of Tianjin University (Tianjin, China).
The morphology and microstructure of the samples were examined by transmission electron microscopy (TEM, JEM100CXII, 5KV) and field emission scanning electron microscopy (FESEM, S-4800) with energy dispersive X-ray spectrometer. X-ray powder diffraction (XRD, Rigaku D/MAX-2500) was used to examine the alloy components.
Electrochemical measurements of the resultant samples were carried out using two-electrode cells (CR2032) in a glove box. The working electrode was prepared by coating the mixture of prepared active materials, acetylene black, and polyvinylidene fluoride (8:1:1 by weight) in n-methyl pyrrolidinone onto Cu substrates and dried at 90 °C for 12 h followed with pressing them at 10 MPa. The mass of active materials on the anode was 0.025 g. The counter/reference electrode was the lithium metal, and the electrolyte solution contained 1 M LiPF6 in a mixture of ethylene carbonate and diethyl carbonate (1:1 by volume). Celgard 2400 was used as the separator. The cell assembly was performed in an Ar-filled glovebox filled with moisture and oxygen concentrations below 1.0 ppm. Galvanostatic charge and discharge measurements were carried out at a constant current density of 100 mA g−1 in the voltage range of 0.01–2.0 V by a LAND battery tester. Cyclic voltammetry (CV) was performed on a CHI 660B electrochemical workstation at a scan rate of 0.1 mV s−1 in the potential window of 0.001–2.0 V. Electrochemical impedance spectroscopy (EIS) was performed with a frequency range of from 1 × 106 to 0.01 Hz.
Synthesis of Co nanoparticles
Co nanoparticles were synthesized by chemical reduction method. A 0.33 g C4H6CoO4 · 4H2O and 0.1 g PVP were dissolved in 30 mL glycol. Then, the pH of the solution was adjusted to 12 using 2-M NaOH solution. Afterward, 0.33 g NaBH4 as reducing agent was added into the solution with vigorous stirring at 50 °C. Finally, the mixed solution was stirred for 40 min, and the Co nanoparticles were collected and washed with distilled water and ethanol for several times. The products were obtained by vacuum drying at 200 °C for 2 h. The Co nanoparticles with larger diameters were also prepared by reducing the amount of PVP to 0.01 g. The prepared Co nanoparticles were stored in ethanol for further use.
Synthesis of hollow Sn-Co nanospheres
A 0.1 g of as-prepared Co nanoparticles was initially dispersed in 150 mL distilled water and sonicated to obtain a homogeneous suspension. Then, 0.364 g SnSO4 was added to the suspension at 80 °C under argon atmosphere, and the mixed solution was stirred for 10 h. The ratio of Sn2+/Co was 1:1. After cooling to room temperature, the precipitate was centrifuged and washed with distilled water and ethanol for several times. After annealing at 200 °C for 8 h, the hollow Sn-Co nanospheres were obtained (sample 1). Under the same conditions, Co nanoparticles with a larger diameter were used as sacrificial templates to prepare another type of hollow Sn-Co nanospheres (sample 2). For comparison, pure Sn nanoparticles were synthesized with an average diameter of about 63 nm according to our previous literature [36].
Results and discussion
Figure 1 shows the XRD patterns of the two types of hollow Sn-Co nanospheres utilizing different Co nanoparticles as sacrificial templates. As shown in Fig. 1, the peaks at 28.1°, 32.92°, 35.66°, 38.66°, 40.08°, 43.24°, 43.76°, 45.12°, 56.86°, 58.00°, 60.42°, 62.58°, 65.58°, 68.24°, 68.8°, 71.82°, 81.84°, 83.74°, 86.08°, and 86.34° are assigned to CoSn2 (JCPDS no. 25-0256), and peaks at 28.5°, 30.56°, 31.88°, 33.38°, 33.78°, 35.72°, 40.76°, 42.76°, 43.24°, 46.18°, 52.68°, 59.3°, 62.08°, 63.28°, 66.48°, 69.44°, 73.82°, and 75.4° are attributed to CoSn3 (JCPDS no. 48-1813). The peaks are sharp and intensive, and no residues or contaminants are detected, implying the high crystallization and purity of the samples. Although the size of Co templates is different, the component of the two types of hollow resultants is almost the same. This is attributed to the same galvanic replacement mechanism between bulk Co nanoparticles and Sn2+ in the aqueous solution.
Figure 2a, b shows the morphology of the two types of resultant hollow Sn-Co nanospheres, respectively. The inserted SEM images display the morphology of corresponding sacrificial template Co nanoparticles. As shown in Fig. 2a, the solid Co nanoparticles and the corresponding hollow Sn-Co resultants are about 83 and 150 nm in diameter, respectively. It can be also clearly seen in Fig. 2b that the diameter of Co nanoparticles is about 112 nm and that of hollow Sn-Co resultants is about 230 nm. In both cases, the final hollow Sn-Co products possess a uniform spherical shape, closely resembling that of the original template Co nanoparticles. This further confirms that the sacrificial templates directly determine the size and shape of the hollow resultants in galvanic replacement reaction. As shown in Fig. 2a, b, highly uniform hollow structure is obviously visible by the sharp contrast between the Sn-Co shells and the hollow interiors. It should be pointed out that the shell thickness of hollow Sn-Co resultants in two cases is different. The shell thickness of hollow Sn-Co resultants in Fig. 2a is about 20 nm, whereas that in Fig. 2b is about 40 nm. Here, sample 1 and sample 2 are denoted as hollow Sn-Co-20 nanospheres and hollow Sn-Co-40 nanospheres according to the shell thickness of 20 and 40 nm, respectively. Figure 2c, d shows the EDS spectrums of hollow Sn-Co-20 and Sn-Co-40 nanospheres. The weight percentage of Sn in hollow Sn-Co-20 nanospheres is measured to be 83.28 %, and that in hollow Sn-Co-40 nanospheres is 82.54 %. These results reveal that the composition of hollow Sn-Co-20 and Sn-Co-40 nanospheres is almost the same.
Figure 3a shows the high magnification TEM image of hollow Sn-Co-20 nanospheres. From the TEM image, the uniform shell of hollow Sn-Co-20 nanospheres is clearly observed. Meanwhile, Fig. 3b displays the HRTEM image of hollow Sn-Co-20 nanospheres. The lattice spacing of 0.1619 nm corresponds to the (312) plane of CoSn2, and 0.2094 nm relates to the (602) plane of CoSn3, which confirm the nanostructure of hollow Sn-Co-20 nanospheres. To further explore the structural feature, the elemental mapping study of hollow Sn-Co-20 nanospheres is carried out by EDS and presented in Fig. 3c–e. From the mappings, it is found that both Sn and Co compositions exist homogeneously along in the depth direction.
Figure 4 shows the schematic illustration of the major steps at different stages of the galvanic replacement reaction between Co nanoparticles and SnSO4 aqueous solution. In particular, the corresponding TEM images at these four stages are also displayed in Fig. 4a–d to demonstrate morphological and structural evolution in the hollowing process. The driving force for the reaction comes from the difference in reduction potential of the two metals involved. When the SnSO4 solution is added into the Co nanoparticles aqueous suspension, galvanic replacement reaction will be initiated immediately. In the initial stage, the Co atoms from the surface of the solid nanoparticles can quickly react with Sn2+ ions to release Co2+ ions and electrons into the solution. Simultaneously, the Sn2+ ions are reduced into Sn atoms by capturing electrons and then deposited on the surface of the Co templates. With the reaction proceeding, the deposition will lead to a thin and incomplete shell of Sn on the surface of each nanoparticle. As shown in step 1, the void space between exterior shell and interior solid core is visible. This structural evolution can be confirmed by the TEM image at corresponding stage as shown in Fig. 4b. Accompanying the deposition of Sn, alloying will occur between Sn and Co atoms. Further prolonging the reaction time, the Co core becomes smaller, and consequently, the interior of nanoparticle gradually becomes empty, as shown in step 2. At the same time, the shell grows complete without small holes or opening, which can be attributed to the continuous deposition of Sn on the surface and a mass-transport process [37–39]. The TEM image in Fig. 4c verifies this speculation. In the later stage of reaction (step 3), a uniform hollow void with a pine-free shell has formed, which is in agreement with the TEM image in Fig. 4d.
The galvanostatic discharge-charge profiles of hollow Sn-Co-20 and Sn-Co-40 nanospheres are evaluated over a voltage range of 0.01 to 2.00 V at a current density of 100 mA g−1, as shown in Fig. 5. In both cases, the voltage plateau at 0.3 V is observed, and the subsequent sloping regions gradually falling to 0.01 V are related to the lithiation of hollow Sn-Co nanospheres [40–44]. The irreversible capacity loss in the first cycle probably originates from the irreversible reduction of Sn-Co to Sn and the formation of solid electrolyte interface (SEI) film on the surface [42, 45].
In order to investigate the electrochemical behavior of electrodes, the first three CV curves of hollow Sn-Co-20 and Sn-Co-40 nanospheres are scanned at 0.1 mV s−1 and cycled between 0.001 and 2.0 V vs Li+/Li, as shown in Fig. 6a, b, respectively. The CV curves of hollow Sn-Co-20 electrodes show the similar outline to that of hollow Sn-Co-40 electrodes, indicating that the electrochemical reaction mechanism of hollow Sn-Co electrodes is similar to each other. In both cases, the reduction peaks at 0.25 V are due to the electrochemical reaction of Sn component in the Sn-Co alloy involving the formation of LixSn alloy [46, 47]. In contrast, the oxidation peaks are observed at 0.5 and 0.68 V, which is ascribed to a dealloying reaction from LixSn to form Li and Sn [41, 48]. These current-potential characteristics are in line with previous research studies on Sn-Co alloy anodes [49, 50]. Compared with hollow Sn-Co-40 nanospheres, the CV curves of hollow Sn-Co-20 nanospheres in the successive cycles are more overlapped, proving the better cycling stability of the electrodes consisting of hollow Sn-Co-20 nanospheres.
Figure 7 highlights the better cycling performance of the two types of hollow Sn-Co nanospheres than the pure ultra fine Sn nanoparticles at a current density of 100 mA g−1, wherein hollow Sn-Co-20 nanospheres show the highest specific capacity. As shown in Fig. 7, the initial discharge capacity of ultra fine Sn nanoparticles is 1090 mAh g−1, and the capacity decreases sharply in the following cycles and fades to only 200 mAh g−1 after 30th cycle. The abrupt degradation of capacity is the typical behavior for the pure Sn electrodes, which can be attributed to the electrical isolation of Sn from the current collector caused by the pulverization associated with extreme volume change in Sn during lithiation/delithiation [41, 51, 52]. By comparison with pure Sn, the hollow Sn-Co nanospheres show an enhanced electrochemical performance. For hollow Sn-Co-40 nanospheres, the initial discharge capacity is 900 mAh g−1, and the reversible capacity drops to 613 mAh g−1 in the second cycle, with the first coulomb efficiency being 83.3 %. The capacity for the first ten cycles was even higher than 613 mAh g−1 and then gradually decreases. Finally, the hollow Sn-Co-40 nanospheres maintain a reversible capacity of 430 mAh g−1 after 100th cycle, with the coulomb efficiency being about 98 %. These results demonstrate that introduction of inactive Co element and hollow structure could partially alleviate the pulverization induced by the volume change of Sn [23, 24, 53, 54]. However, hollow Sn-Co-20 nanospheres with thin shell thickness show better cycling properties. The hollow Sn-Co-20 nanospheres exhibit a reversible capacity of 808 and 632 mAh g−1 in the first and second cycle, with the initial coulomb efficiency being 91.6 %. In addition, an increase in capacity in the subsequent several cycles can be observed. The hollow Sn-Co-20 nanospheres exhibit a steady reversible capacity of 502 mAh g−1 after 100th cycle, significantly higher than that of these counterparts. It is worth noting that the hollow Sn-Co-20 electrodes perform significantly better than recently reported tin-based electrodes [55–59] in terms of specific capacity and cycling stability. Abundant research has confirmed that the most stable electrochemical performance is found in Sn1-xCox alloy for 0.28 < x < 0.43 [6, 50]. In the as-prepared hollow Sn-Co samples, CoSn2 phase plays a more important role in the improvement of electrochemical performance than CoSn3 phase.
The electrochemical performance of hollow Sn-Co-20 nanospheres is superior to hollow Sn-Co-40 nanospheres, which can be attributed to the smaller size, thinner shell thickness and relatively large void volume of hollow Sn-Co-20 nanospheres. Firstly, the decrease in size and shell thickness provides short diffusion length and large contact area between liquid electrolyte and electrode, which are beneficial for the diffusion of the Li+ during insertion/extraction process [23, 24]. Secondly, the hollow volume-occupying rate in hollow Sn-Co-20 nanospheres is about 48.6 %, whereas that of hollow Sn-Co-40 nanospheres is about 31.7 %. This suggests that hollow Sn-Co-20 nanospheres offer relatively large vacancy for the volume expansion and recovery in the lithiated/delithiated state, reinforcing the integrity of electrodes [21–24].
EIS measurement of the working electrodes is carried out to further investigate the contribution to superior electrochemical performance of hollow Sn-Co-20 nanospheres. As shown in Fig. 8, the Nyquist plots in both cases exhibit two distinct parts including a semicircle in the high and middle frequency region and a sloped line in the low frequency region. It is clear that the diameter of the depressed semicircle of hollow Sn-Co-20 nanospheres is much smaller than that of hollow Sn-Co-40 nanospheres, which reveals that hollow Sn-Co-20 nanospheres have lower contact and charge transfer resistance [60]. Moreover, hollow Sn-Co-20 nanospheres possess more straight inclined line in comparison to hollow Sn-Co-40 nanospheres, indicating that the Li+ diffusion of hollow Sn-Co-20 nanospheres is faster [61]. These results imply that the combination of thin shell thickness and relatively large void space can facilitate the charge and Li+ transfer.
Based on these experimental results, the discharge and charge mechanism for the solid Sn nanoparticles and hollow Sn-Co nanospheres with different shell thickness is displayed in Fig. 9. As observed in Fig. 9a, the large volume expansion from Sn to LixSn will result in the aggregation of Sn or LixSn particles, which will destroy spherical structure of the electrodes. In the case of hollow Sn-Co nanospheres configuration, small quality of inactive Co nanoparticles dispersed in Sn or LixSn can buffer the volume change and avoid the grain growth, shown in Fig. 9b, c. In addition, the hollow structure plays a more important role in accommodating the volume change. The interior void space allows the volume change to expand inward and outward rather than outward only.
The speculation above can be verified by the TEM images of hollow Sn-Co-20 and Sn-Co-40 nanospheres after cycling, as shown in Fig. 10. From Fig. 10a, c, similar structural evolution of hollow Sn-Co-20 and Sn-Co-40 nanospheres in the lithiated state can be observed. Due to the volume change of active materials, the shell becomes thicker and the void becomes smaller in the lithiated state. This is in agreement with the illustrations in Fig. 9b, c, further confirming that the hollow structure could accommodate the volume change. As displayed in Fig. 10b, the microstructure of hollow Sn-Co-20 nanospheres in the delithiated state shows less variation compared with the pristine samples, except for the slight increase in diameter. However, for hollow Sn-Co-40 nanospheres in the delithiated state, as shown in Fig. 10d, the void space is not as clear as the pristine samples. This suggests that the recovering process from the expanded state is not fully reversible for hollow Sn-Co-40 nanospheres. The discrepancy in both cases may be explained by the different volume-occupying rate in hollow Sn-Co-20 and Sn-Co-40 nanospheres. These results imply that a relatively large hollow volume-occupying rate in hollow configuration is favorable, especially for the anodes subjecting severe volume change.
The morphology of hollow Sn-Co-20 and Sn-Co-40 nanospheres after 100 cycles is shown in Fig. 11. For hollow Sn-Co-40 nanospheres, as shown in Fig. 11b, the slight aggregation and pulverization can be observed on the surface. This structural damage could lead to the decay of capacity upon cycling. Contrarily, the microstructure of hollow Sn-Co-20 nanospheres after 100 cycles is remained, due to the limited volume change. The well-defined morphology of hollow Sn-Co-20 nanospheres is consistent with their good electrochemical cycling performance.
Conclusion
Hollow Sn-Co nanospheres with different shell thickness and void size have been prepared by using Co nanoparticles as sacrificial templates via galvanic replacement reaction. Such a hollow structure offers sufficient void space, in which Sn-Co nanoparticles will experience a volume change without a collapse. In addition, the inactive Co element plays a role of matrix to accommodate the volume expansion and prevents the agglomeration of Sn nanoparticles. As anodes for LIBs, the hollow Sn-Co-20 nanospheres with thin shell exhibit a high capacity of 502 mAh g−1 after 100 cycles, which is superior to the corresponding counterparts. The enhancement is probably attributed to the small shell thickness and the relatively large void space of hollow Sn-Co-20 nanospheres as compared to hollow resultants with large shell thickness. Due to the facile synthesis and improved performance, it can be expected that the novel hollow Sn-Co alloy electrodes will pave the way for the development of the next generation of LIBs.
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This work was financially supported by the National Natural Science Foundation of China (No. 51143009 and 51273145).
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Jiang, A., Fan, X., Zhu, J. et al. Hollow structured Sn-Co nanospheres by galvanic replacement reaction as high-performance anode for lithium ion batteries. Ionics 21, 2137–2147 (2015). https://doi.org/10.1007/s11581-015-1420-4
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DOI: https://doi.org/10.1007/s11581-015-1420-4