Effects of Polypropylene Orientation on Mechanical and Heat Seal Properties of Polymer-Aluminum-Polymer Composite Films for Pouch Lithium-Ion Batteries

In this study, polyamide-aluminum foil-polypropylene (PA-Al-PP) composite films with different orientation status of the PP layer were prepared, and their morphology, tensile, peeling and heat seal behavior were studied. The comparative study of tensile and fracture behaviors of single-layer film of PA, Al and PP, as well as the composite films of PA-Al, PP-Al and PA-Al-PP revealed that in PA-Al-PP composite film, the PA layer with the highest tensile strength can share the tensile stress from the Al layer during stretching, while the PP layer with the lowest tensile strength can prevent further development of the small cracks on boundary of the Al layer during stretching. Moreover, the study of heat seal behavior suggested that both the orientation status and the heat seal conditions were important factors in determining the heat seal strength (HSS) and failure behavior of the sample. Four failure types were observed, and a clear correspondence between HSS and failure types was found. The results also elucidated that for the composite film, only in the cases where the tensile stress was efficiently released by each layer during HSS measurement could the composite film exhibit desired high HSS that was even higher than its tensile strength.

In summary, to meet the high performance demands for LIB packaging, the tensile behavior and the roles of each layer during the tensile process should be investigated in detail. Furthermore, the roles of each layer in the heat seal properties of the composite film are also of great importance. However, as far as we are concerned, these important points are not deeply understood.
In the present study, the tensile performances and fracture behaviors of the individual layers of PA, Al and PP, as well as the laminated films of PA-Al, PP-Al and PA-Al-PP, were investigated to explore the contributions of each layer to the tensile behavior of the PA-Al-PP composite films for pouch LIBs. Moreover, two PP layers with different orientation status were used to prepare the laminated films, so as to comparatively study the role of PP orientation in the peeling and tensile behavior of heat seal strength (HSS) of the laminated film. The related mechanism was proposed.
To benefit the discussion, the polymer-metal-polymer tri-layer laminated films used in this study were shortened to PCPF.
It should be noted that the adhesive between the layers played an important role in the tensile, peeling and even the heat seal behaviors. If alternative adhesives were used, the results and summaries may be totally different. Therefore, the selection of adhesives is carefully considered according to the commercial composite films for LIBs.

Sample Preparation
The laminated film was prepared according to industrialized manufacturing procedures as follows (Schemes 1 and 2): Step one, the surfaces of aluminum foil were washed, and then one surface was subjected to corona surface treatment to enhance its adhesion to adhesives; Step two, the BOPA film, PU adhesive and the surface-treated Al foil were laminated by dry lamination process using a Dry Compounded Machine to obtain the PA-Al laminated film. Then, a thermal aging process was applied to enhance the adhesion strength of the PU adhesive; Step three, chemical surface treatment was applied on the other side of the Al foil surface of the PA-Al laminated film to enhance its resistance to the electrolyte and solvent; Step four, the laminated film of PP-PA-Al was prepared by an extrusion coating process, as can be seen n Scheme 2. The PP and adhesive were first coextruded via the extruder die and then laminated with the PA-Al film using a set of rolls. Finally, an online annealing process was applied. Scheme 1. Schematic illustration of the process to prepare PA/PU adhesive/Al foil/Polyolefin adhesive/PP laminated film.
Scheme 2 Schematic illustration of the extrusion coating process to prepare the PA-Al-PP laminated film.

Scanning Electron Microscope (SEM)
The morphology observation (Scanning Electronic Microscopy, SEM, JEOL, Tokyo, Japan) was performed on a JSM-5900 LV environmental scanning electron microscope at an accelerating voltage of 20 kV. Before SEM characterizations, the fractured surfaces of all the samples were coated with a thin layer of gold by ion sputtering [26].

Fourier Transform Infrared Spectroscopy (FT-IR)
Fourier transform infrared spectroscopy (FTIR) (Madison, WI, USA) was performed to detect the orientation of the amorphous and crystalline phases. This method is based on the absorption of infrared light at certain frequencies corresponding to the vibration modes of atomic groups present within the molecule. A Nicolet 560 FTIR instrument from Thermo Electron was used for FTIR measurements, and the beam was polarized in two orthogonal directions, parallel and perpendicular Scheme 2 Schematic illustration of the extrusion coating process to prepare the PA-Al-PP laminated film.

Scanning Electron Microscope (SEM)
The morphology observation (Scanning Electronic Microscopy, SEM, JEOL, Tokyo, Japan) was performed on a JSM-5900 LV environmental scanning electron microscope at an accelerating voltage of 20 kV. Before SEM characterizations, the fractured surfaces of all the samples were coated with a thin layer of gold by ion sputtering [26].

Fourier Transform Infrared Spectroscopy (FT-IR)
Fourier transform infrared spectroscopy (FTIR) (Madison, WI, USA) was performed to detect the orientation of the amorphous and crystalline phases. This method is based on the absorption of infrared light at certain frequencies corresponding to the vibration modes of atomic groups present within the molecule. A Nicolet 560 FTIR instrument from Thermo Electron was used for FTIR measurements, and the beam was polarized in two orthogonal directions, parallel and perpendicular Scheme 2. Schematic illustration of the extrusion coating process to prepare the PA-Al-PP laminated film.

Scanning Electron Microscope (SEM)
The morphology observation (Scanning Electronic Microscopy, SEM, JEOL, Tokyo, Japan) was performed on a JSM-5900 LV environmental scanning electron microscope at an accelerating voltage of 20 kV. Before SEM characterizations, the fractured surfaces of all the samples were coated with a thin layer of gold by ion sputtering [26].

Fourier Transform Infrared Spectroscopy (FT-IR)
Fourier transform infrared spectroscopy (FTIR) (Madison, WI, USA) was performed to detect the orientation of the amorphous and crystalline phases. This method is based on the absorption of infrared light at certain frequencies corresponding to the vibration modes of atomic groups present within the molecule. A Nicolet 560 FTIR instrument from Thermo Electron was used for FTIR measurements, and the beam was polarized in two orthogonal directions, parallel and perpendicular to a reference axis, by a zinc selenide wire grid polarizer. These two absorption values should be different, and their ratio is defined as the dichroic ratio, D.
The Herman orientation function of this vibration was obtained according to the method of Tabatabaei et al. [27,28]: where D is the ratio of the absorption parallel and absorption perpendicular to the machine direction. For polypropylene, absorption at the wave number of 998 cm −1 is attributed to the crystalline phase (c axis) whereas absorption at the wave number of 972 cm −1 is due to the contribution of both crystalline and amorphous phases. The orientation of crystalline phase (f c ) and average orientation function (f av ) could be calculated by Equation (1). Moreover, since the 2723 cm −1 band is the only amorphous band of PP, the orientation of the amorphous phase (f am ) could be calculated by Equation (2). The transition moment angle at 2723 cm −1 is 90 • [28].

Differential Scanning Calorimeter (DSC)
All the calorimetric experiments were performed with a Mettler Toledo DSC1 differential scanning calorimeter (DSC) (Mettler-Toledo, Zurich, Switzerland), under a nitrogen atmosphere (50 mL/min). The temperature scale calibration was performed using indium as a standard to ensure reliability of the data obtained. In order to ensure the homogeneity of samples and the good contact between sample and pan, the virgin polymer was molded at 190 • C, 10 MPa for 5 min into sheets of uniform thickness about 500 µm. Then, 5 mg round samples were punched out of the sheets.
The degree of crystallinity (X c ) of the samples was calculated by the following equation [29,30]: where ∆H m is the DSC measured value of fusion enthalpy, and ∆H 0 m is the fusion enthalpy of the completely crystalline iPP. The values of ∆H 0 m for PP and PA were selected as 209 J/g and 255 J/g, respectively.

Mechanical Properties Measurement
Tensile behavior: Rectangular strips with a width of 15 mm were carefully cut from the films along the machine direction (MD) and transverse direction (TD). The tensile testing was conducted on a universal tensile testing machine (Instron 4302, Instron Corporation, Turin, Italy) with a load range of 0-1000 N. The gauge length was 50 mm. All the tensile tests were performed at 25 • C with an elongation rate of 50 mm/min.
T-Peel test: The measurement of heat seal strength (HSS) was performed by tension peel testing on universal tensile testing machine (Instron 4302, Instron Corporation, Turin, Italy) [3]. The specimens were aligned with seal lines perpendicular to the direction of tension. All tests were conducted at about 25 • C with a strain rate of 50 mm/min. During the test, the maximum load was recorded. The HSS was defined as the maximum tensile load divided by the sample width, in units of N/15 mm. The HSS was averaged over five samples for every heat-seal condition. In addition, the failure mode of each test was carefully examined and investigated in the study.

Lamination Structure Observation
The SEM images of the cross-section of the composite film (PCPF-1 and PCPF-2) are shown in Figure 1. The five-layered structure, including three main layers and two adhesive layers, can be clearly observed. The affiliations of these layers are also added in Figure 1.

Lamination Structure Observation
The SEM images of the cross-section of the composite film (PCPF-1 and PCPF-2) are shown in Figure 1. The five-layered structure, including three main layers and two adhesive layers, can be clearly observed. The affiliations of these layers are also added in Figure 1.  Figure 1 clearly reveals the five-layer structure in the composite film, where the cross-section morphology of PCPF-1 and PCPF-2 is quite similar. The total thickness of the composite film is about 125 μm. The middle layer is aluminum foil (Al layer) with a thickness of about 40 μm, while on its two sides, the PP layer and PA layer with a thickness of about 40 μm and 30 μm, respectively, can be observed. Between the PP layer and Al foil, there is polyolefin adhesive (thickness 15 μm), which provides adhesion between PP/Al, while on the other hand, there is polyurethane adhesive (thickness 3-5 μm) between the PA layer and Al layer.
These different layers contribute to different properties, which together enable the composite film to meet the critical performance requirement for pouch LIBs: The PP layer provides heat-seal properties, certain resistance of electrolyte and mechanical properties, while the PA layer contributes its superior mechanical properties. The Al layer in the middle gives the laminated film superior gas and water barrier properties. In this way, the easily sealable laminated film with high barrier property and superior mechanical properties for pouched LIB application is obtained.

DSC Analysis
The DSC cooling curves after elimination of thermal history, as well as the subsequent melting curves of each layer are plotted as shown in Figure 2. The obtained crystallization and melting parameters are listed in Table 1.  Figure 1 clearly reveals the five-layer structure in the composite film, where the cross-section morphology of PCPF-1 and PCPF-2 is quite similar. The total thickness of the composite film is about 125 µm. The middle layer is aluminum foil (Al layer) with a thickness of about 40 µm, while on its two sides, the PP layer and PA layer with a thickness of about 40 µm and 30 µm, respectively, can be observed. Between the PP layer and Al foil, there is polyolefin adhesive (thickness 15 µm), which provides adhesion between PP/Al, while on the other hand, there is polyurethane adhesive (thickness 3-5 µm) between the PA layer and Al layer. These different layers contribute to different properties, which together enable the composite film to meet the critical performance requirement for pouch LIBs: The PP layer provides heat-seal properties, certain resistance of electrolyte and mechanical properties, while the PA layer contributes its superior mechanical properties. The Al layer in the middle gives the laminated film superior gas and water barrier properties. In this way, the easily sealable laminated film with high barrier property and superior mechanical properties for pouched LIB application is obtained.

DSC Analysis
The DSC cooling curves after elimination of thermal history, as well as the subsequent melting curves of each layer are plotted as shown in Figure 2. The obtained crystallization and melting parameters are listed in Table 1.   As can be seen from Figure 2 and Table 1, the crystallization peak temperatures Tc of the PP layer and PA layer after elimination of the thermal history are 110.2 °C and 180.5 °C, respectively. For the polyolefin adhesive, its crystallization peak can hardly be observed, indicating that its isotacticity is very low [24,30]. No crystallization peak can be observed for the PU adhesive, since it is already crosslinked and cannot crystallize.
From the aspect of melting, the melting points Tm and degrees of crystallinity Xc of PP and PA are 159.3 °C and 216.2 °C, 34.2% and 36.1%, respectively. The Tm and Xc of polyolefin adhesive are only 85.4 °C and 7.8%, respectively, reflecting the very poor crystallizability of the polyolefin elastomer [31,32]. Moreover, no melting peak of the PU adhesive can be found, indicating that it cannot crystallize.

Tensile Properties of the Laminated Films
Although the gas and water barrier properties of aluminum foil are extremely high, suffering from its poor ductility, permanent deformation and even fracture will easily take place when the aluminum foil is under even slight scraping or stretching [3]. Therefore, it must be laminated with polymer films to enhance its ductility and to give it the heat seal property.
To deeply investigate the relationship between the multi-layer structure and final properties of the composite film and to clarify the contribution of each layer to the mechanical properties of the composite film, in this section, we carefully prepared the composite films with different constitutions, including PP/Al, PA/Al and PA/Al/PP. Their tensile behaviors are investigated. Figure 3a represents the stress-strain curves of PCPF-1 at both MD (machine direction) and TD (transverse direction), and Figure 3b shows the stress-strain curves of samples in the MD direction, including single-layer PP, Al, PA films, and the composite films of PA-Al, PP-Al, PP-Al-PA. From Figure 3a, the tensile strength and elongation at the breakage points of the specimens are shown in Table 2.  Table 1. Crystallization and melting parameters of the materials involved in composite film.

Sample
Cooling Process Subsequent Heating Process As can be seen from Figure 2 and Table 1, the crystallization peak temperatures T c of the PP layer and PA layer after elimination of the thermal history are 110.2 • C and 180.5 • C, respectively. For the polyolefin adhesive, its crystallization peak can hardly be observed, indicating that its isotacticity is very low [24,30]. No crystallization peak can be observed for the PU adhesive, since it is already crosslinked and cannot crystallize.
From the aspect of melting, the melting points T m and degrees of crystallinity X c of PP and PA are 159.3 • C and 216.2 • C, 34.2% and 36.1%, respectively. The T m and X c of polyolefin adhesive are only 85.4 • C and 7.8%, respectively, reflecting the very poor crystallizability of the polyolefin elastomer [31,32]. Moreover, no melting peak of the PU adhesive can be found, indicating that it cannot crystallize.

Tensile Properties of the Laminated Films
Although the gas and water barrier properties of aluminum foil are extremely high, suffering from its poor ductility, permanent deformation and even fracture will easily take place when the aluminum foil is under even slight scraping or stretching [3]. Therefore, it must be laminated with polymer films to enhance its ductility and to give it the heat seal property.
To deeply investigate the relationship between the multi-layer structure and final properties of the composite film and to clarify the contribution of each layer to the mechanical properties of the composite film, in this section, we carefully prepared the composite films with different constitutions, including PP/Al, PA/Al and PA/Al/PP. Their tensile behaviors are investigated. Figure 3a represents the stress-strain curves of PCPF-1 at both MD (machine direction) and TD (transverse direction), and Figure 3b shows the stress-strain curves of samples in the MD direction, including single-layer PP, Al, PA films, and the composite films of PA-Al, PP-Al, PP-Al-PA. From Figure 3a, the tensile strength and elongation at the breakage points of the specimens are shown in Table 2.   Figure 3 and Table 1 reveal that for the single-layer films, PA exhibits the highest tensile strength of more than 144 MPa, and its elongation at breakage lies between 50-70%; PP has the lowest tensile strength of about 23 MPa; however, it exhibits the highest elongation at a breakage of more than 600%; Al foil has high tensile strength of about 80 MPa, but its elongation at breakage is as low as 9-11%.
After lamination, elongation at breakage of PA-Al is evidently enhanced compared with single Al foil, indicating that using PU adhesive, PA and Al foil are closely bonded, and the poor ductility of Al foil is evidently reinforced. Meanwhile, its tensile strength is also increased, indicating that the tensile stress is released from Al to PA. With respect to the PP-Al composite film, its tensile strength and elongation at breakage are very low compared with PA-Al, which might be attributed to the very low tensile strength of PP. When the tensile stress is applied, the "soft" PP layer cannot efficiently share the tensile stress in Al layer; therefore, the deformation and rupture of each layer mainly occur in their own way, and the final tensile property of PP-Al can hardly be significantly enhanced.
For the PA-Al-PP laminated film, its tensile strength and elongation at break are higher compared with PA-Al, indicating that the addition of the PP layer can further reinforce the tensile properties of the laminated film.
On the other hand, considering the tensile results in MD and TD, only slight differences in their tensile properties can be seen.
To further explore the contributions of the PP layer and PA layer to the PA-Al-PP laminated film, the morphology evolution of PP-Al, PA-Al and PA-Al-PP during the tensile process are further studied. The results are shown in Figure 4.   Figure 3 and Table 1 reveal that for the single-layer films, PA exhibits the highest tensile strength of more than 144 MPa, and its elongation at breakage lies between 50-70%; PP has the lowest tensile strength of about 23 MPa; however, it exhibits the highest elongation at a breakage of more than 600%; Al foil has high tensile strength of about 80 MPa, but its elongation at breakage is as low as 9-11%.
After lamination, elongation at breakage of PA-Al is evidently enhanced compared with single Al foil, indicating that using PU adhesive, PA and Al foil are closely bonded, and the poor ductility of Al foil is evidently reinforced. Meanwhile, its tensile strength is also increased, indicating that the tensile stress is released from Al to PA. With respect to the PP-Al composite film, its tensile strength and elongation at breakage are very low compared with PA-Al, which might be attributed to the very low tensile strength of PP. When the tensile stress is applied, the "soft" PP layer cannot efficiently share the tensile stress in Al layer; therefore, the deformation and rupture of each layer mainly occur in their own way, and the final tensile property of PP-Al can hardly be significantly enhanced.
For the PA-Al-PP laminated film, its tensile strength and elongation at break are higher compared with PA-Al, indicating that the addition of the PP layer can further reinforce the tensile properties of the laminated film.
On the other hand, considering the tensile results in MD and TD, only slight differences in their tensile properties can be seen.
To further explore the contributions of the PP layer and PA layer to the PA-Al-PP laminated film, the morphology evolution of PP-Al, PA-Al and PA-Al-PP during the tensile process are further studied. The results are shown in Figure 4. As can be seen from Figure 4, the deformation and rupture processes of these three types of laminated films are quite different. For PA-Al, when the tensile stress is applied, the PA layer and Al layer deform simultaneously at the beginning, and the width of the specimen decreases gradually, indicating that plastic deformation takes place. As the strain increases, the tensile stress concentrates, which cannot be efficiently dispersed, and the ruptures of the PA layer and Al layer take place simultaneously in the boundaries. The elongation at breakage and the tensile strength of the PA-Al film are 41.2% and 87.5 MPa, respectively, both higher compared with the single Al layer, which can be explained as follows: PA has higher tensile strength compared with Al, which can share a large amount of stress from Al during stretching, resulting in the coordination deformation of PA and Al with the characteristic of plastic deformation.
On the other hand, for PP-Al, when tensile stress is applied, the width of the specimen remains almost unchanged before the rupture of the Al layer. When the strain increases to more than 10%, the Al foil is broken in a brittle rupture manner, while the elongation and plastic deformation of PP layer continue.
For the PA-Al-PP composite film, it can be observed that during the tensile process, the characteristic of plastic deformation is observed, and all the layers deform simultaneously in the same manner; the decrease of width and necking can be seen as the strain increases. At higher strain, many tiny cracks can be seen from the boundary of the Al layer, as indicated by arrows in Figure 4d. Surprisingly, with the help of the PA and PP layers, the further enlargement of these cracks are restrained, resulting in higher tensile tolerance of the laminated films. Finally, as the strain further increases, the sample is fractured, exhibiting high elongation at a breakage of 53.2% and a high tensile strength of 61.5 MPa.
Based on the experimental results above, we proposed the following mechanism describing the roles of the PA and PP layers in the final tensile behavior of the PA-Al-PP composite film, as shown in Figure 5. As can be seen from Figure 4, the deformation and rupture processes of these three types of laminated films are quite different. For PA-Al, when the tensile stress is applied, the PA layer and Al layer deform simultaneously at the beginning, and the width of the specimen decreases gradually, indicating that plastic deformation takes place. As the strain increases, the tensile stress concentrates, which cannot be efficiently dispersed, and the ruptures of the PA layer and Al layer take place simultaneously in the boundaries. The elongation at breakage and the tensile strength of the PA-Al film are 41.2% and 87.5 MPa, respectively, both higher compared with the single Al layer, which can be explained as follows: PA has higher tensile strength compared with Al, which can share a large amount of stress from Al during stretching, resulting in the coordination deformation of PA and Al with the characteristic of plastic deformation.
On the other hand, for PP-Al, when tensile stress is applied, the width of the specimen remains almost unchanged before the rupture of the Al layer. When the strain increases to more than 10%, the Al foil is broken in a brittle rupture manner, while the elongation and plastic deformation of PP layer continue.
For the PA-Al-PP composite film, it can be observed that during the tensile process, the characteristic of plastic deformation is observed, and all the layers deform simultaneously in the same manner; the decrease of width and necking can be seen as the strain increases. At higher strain, many tiny cracks can be seen from the boundary of the Al layer, as indicated by arrows in Figure 4d. Surprisingly, with the help of the PA and PP layers, the further enlargement of these cracks are restrained, resulting in higher tensile tolerance of the laminated films. Finally, as the strain further increases, the sample is fractured, exhibiting high elongation at a breakage of 53.2% and a high tensile strength of 61.5 MPa.
Based on the experimental results above, we proposed the following mechanism describing the roles of the PA and PP layers in the final tensile behavior of the PA-Al-PP composite film, as shown in Figure 5.  As is illustrated in Figure 5, for PP-Al, since the tensile strength of the PP layer is too low compared with Al, PP cannot efficiently share tensile stress from Al and cannot reinforce the ductility of Al. During stretching, PP and Al are broken individually in their own manner.
For PA-Al, owing to the high tensile strength and plastic film nature of the PA layer, it can share a large amount of stress from the Al layer, helping the Al layer to deform in the plastic deformation manner. However, when cracks appear on the Al layer, PA can hardly restrain the further enlargement of these cracks. The Al layer and PA layer break together.
For the PA-Al-PP laminated film, it can be seen that not only the tensile strength can be efficiently shared from Al layer, but also the small cracks can be restrained with the help of the PP layer (compared with Figure 5b). In this way, the laminated PA-Al-PP film with balanced tensile strength and elongation at break is obtained.
In summary, in the PA-Al-PP laminated film, PA with high tensile strength can release a large amount of tensile stress from the Al layer during stretching, while the PP layer can restrain the further development of the small cracks on the boundary of the Al layer, preventing the final rupture of the laminate. It should also be noted that the adhesives between the PP-Al and PA-Al layers also play a determining role in the final properties of the laminated film. Tight and even bonding between each layer is a prerequisite and the foundation for obtaining the laminated PA-Al-PP with desired tensile properties [4,5].

Fourier Transform Infrared Spectroscopy Analysis on PP Layer
To explore the role of PP orientation in the final properties of the laminated film, we have prepared two PP layers with different orientation status, and thus two laminated films, PCPF-1 and PCPF-2. The FT-IR spectrums of the PP layers of PCPF-1 and PCPF-2 in two directions are shown in Figure 3. The calculation results of the orientation factors of crystalline phase, amorphous phase and average are listed in Table 3. Figure 6 and Table 3 reveal that the IR spectrum of the PP layer of PCPF-1 at two different directions is almost the same, and its orientation factors are zero; on the other hand, for the PP layer of PCPF-2, it can be seen that its fc, fam and fav are 0.294, 0.350 and 0.309, respectively, indicating that As is illustrated in Figure 5, for PP-Al, since the tensile strength of the PP layer is too low compared with Al, PP cannot efficiently share tensile stress from Al and cannot reinforce the ductility of Al. During stretching, PP and Al are broken individually in their own manner.
For PA-Al, owing to the high tensile strength and plastic film nature of the PA layer, it can share a large amount of stress from the Al layer, helping the Al layer to deform in the plastic deformation manner. However, when cracks appear on the Al layer, PA can hardly restrain the further enlargement of these cracks. The Al layer and PA layer break together.
For the PA-Al-PP laminated film, it can be seen that not only the tensile strength can be efficiently shared from Al layer, but also the small cracks can be restrained with the help of the PP layer (compared with Figure 5b). In this way, the laminated PA-Al-PP film with balanced tensile strength and elongation at break is obtained.
In summary, in the PA-Al-PP laminated film, PA with high tensile strength can release a large amount of tensile stress from the Al layer during stretching, while the PP layer can restrain the further development of the small cracks on the boundary of the Al layer, preventing the final rupture of the laminate. It should also be noted that the adhesives between the PP-Al and PA-Al layers also play a determining role in the final properties of the laminated film. Tight and even bonding between each layer is a prerequisite and the foundation for obtaining the laminated PA-Al-PP with desired tensile properties [4,5].

Fourier Transform Infrared Spectroscopy Analysis on PP Layer
To explore the role of PP orientation in the final properties of the laminated film, we have prepared two PP layers with different orientation status, and thus two laminated films, PCPF-1 and PCPF-2. The FT-IR spectrums of the PP layers of PCPF-1 and PCPF-2 in two directions are shown in Figure 3. The calculation results of the orientation factors of crystalline phase, amorphous phase and average are listed in Table 3. Figure 6 and Table 3 reveal that the IR spectrum of the PP layer of PCPF-1 at two different directions is almost the same, and its orientation factors are zero; on the other hand, for the PP layer of PCPF-2, it can be seen that its f c , f am and f av are 0.294, 0.350 and 0.309, respectively, indicating that although a thermosetting process is performed, the PP layer of PCPF-2 retains a certain degree of orientation along the machine direction. although a thermosetting process is performed, the PP layer of PCPF-2 retains a certain degree of orientation along the machine direction.  Samples fc fav fam PP layer (PCPF-1) 0.000 0.000 0.000 PP layer (PCPF-2) 0.294 0.309 0.350

Peeling Behavior of PCPF-1 and PCPF-2
The peeling test is performed on the PP-Al layer of PCPF-1 and PCPF-2 to explore the impact of PP orientation in this process. The obtained peeling curves and morphology image are shown in Figure 7.

Peeling Behavior of PCPF-1 and PCPF-2
The peeling test is performed on the PP-Al layer of PCPF-1 and PCPF-2 to explore the impact of PP orientation in this process. The obtained peeling curves and morphology image are shown in Figure 7. although a thermosetting process is performed, the PP layer of PCPF-2 retains a certain degree of orientation along the machine direction.  Samples fc fav fam PP layer (PCPF-1) 0.000 0.000 0.000 PP layer (PCPF-2) 0.294 0.309 0.350

Peeling Behavior of PCPF-1 and PCPF-2
The peeling test is performed on the PP-Al layer of PCPF-1 and PCPF-2 to explore the impact of PP orientation in this process. The obtained peeling curves and morphology image are shown in Figure 7.    mm, indicating that the peeling force is mainly determined by the situation of bonding, not the orientation of the PP layer. When the samples are bonded under the same condition, the final peeling forces are quite similar, too. Interestingly, at a small displacement of less than 20 mm, it can be seen that the slopes of the peeling curves of PCPF-1 and PCPF-2 are quite different; the slope of PCPF-2 is obviously higher than that of PCPF-1.
On the other hand, Figure 7b reveals that after the PP layer is peeled from the Al layer, a smooth surface of the Al layer without PO adhesive can be observed. During the peeling process, the plastic deformation of the PP layer and the separation between the PO adhesive and Al layer take place simultaneously. Meanwhile, the peeling frontier is not linear, indicating that the stress applied on the frontier is not uniformly distributed.

Heat Seal Properties
Since the heat seal properties of the laminated film are directly related to its PP layer, the orientation status of the PP layer might play an important role in the process. Therefore, in this section, the heat seal properties of PCPF-1 and PCPF-2 are investigated, and the roles of heat seal temperature (T H ) and dwell time in the heat seal strength (HSS) and failure behavior are studied.

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Effects of heat seal temperature The experiment is performed at the heat seal temperature (T H ) of 170-230 • C, dwell time of 3 s and heat seal pressure of 1 MPa. The obtained heat seal strength (HSS) is plotted as a function of T H as shown in Figure 8. On the other hand, Figure 7b reveals that after the PP layer is peeled from the Al layer, a smooth surface of the Al layer without PO adhesive can be observed. During the peeling process, the plastic deformation of the PP layer and the separation between the PO adhesive and Al layer take place simultaneously. Meanwhile, the peeling frontier is not linear, indicating that the stress applied on the frontier is not uniformly distributed.

Heat Seal Properties
Since the heat seal properties of the laminated film are directly related to its PP layer, the orientation status of the PP layer might play an important role in the process. Therefore, in this section, the heat seal properties of PCPF-1 and PCPF-2 are investigated, and the roles of heat seal temperature (TH) and dwell time in the heat seal strength (HSS) and failure behavior are studied.

Effects of heat seal temperature
The experiment is performed at the heat seal temperature (TH) of 170-230 °C, dwell time of 3 s and heat seal pressure of 1 MPa. The obtained heat seal strength (HSS) is plotted as a function of TH as shown in Figure 8. As can be seen from Figure 8, for both PCPF-1 and PCPF-2, the HSS increases gradually with the increase of TH. Meanwhile, a critical transition heat seal temperature Tcrit can be observed: when the heat seal temperature is higher than Tcrit, the HSS reaches a plateau region and does not increase evidently with the further increase of TH.
Comparing the results of PCPF-1 and PCPF-2, it can be seen that the HSS values in the MD and TD directions are quite similar. At the same TH, the HSS of PCPF-1 in MD direction is slightly higher than that in TD, and the corresponding Tcrit in MD and TD directions is 195 °C and 200 °C, respectively. However, for PCPF-2, the HSS in MD direction is obviously higher than its counterpart in the TD direction in all the heat seal temperature ranges studied, and its Tcrit in the MD and TD directions is 185 °C and 215 °C respectively. Moreover, the HSS values of the samples above the plateau region are also quite different. Generally, from the highest to lowest, the ranking is PCPF-2 MD > PCPF-1 MD > PCPF-1 TD > PCPF-2 TD.
The results above indicate that unlike PCPF-1, the heat seal properties of PCPF-2 in the MD and TD directions are quite different from each other, which should be related to its orientation in the As can be seen from Figure 8, for both PCPF-1 and PCPF-2, the HSS increases gradually with the increase of T H . Meanwhile, a critical transition heat seal temperature T crit can be observed: when the heat seal temperature is higher than T crit , the HSS reaches a plateau region and does not increase evidently with the further increase of T H .
Comparing the results of PCPF-1 and PCPF-2, it can be seen that the HSS values in the MD and TD directions are quite similar. At the same T H , the HSS of PCPF-1 in MD direction is slightly higher than that in TD, and the corresponding T crit in MD and TD directions is 195 • C and 200 • C, respectively. However, for PCPF-2, the HSS in MD direction is obviously higher than its counterpart in the TD direction in all the heat seal temperature ranges studied, and its T crit in the MD and TD directions is 185 • C and 215 • C respectively. Moreover, the HSS values of the samples above the plateau region are also quite different. Generally, from the highest to lowest, the ranking is PCPF-2 MD > PCPF-1 MD > PCPF-1 TD > PCPF-2 TD.
The results above indicate that unlike PCPF-1, the heat seal properties of PCPF-2 in the MD and TD directions are quite different from each other, which should be related to its orientation in the PP layer.
To understand fully, the failure behavior of the heat sealed samples during tensile stretching is also determined. Generally, the failure behavior can be summarized into four failure types (Types A-D) as shown in Figure 9: Type A: When the tensile stress is applied, the heat seal frontier remains unchanged. Meanwhile, the adhesion between PP layer and Al foil is broken. With the further increase of the strain, only the plastic deformation of freestanding PP layer takes place; Type B: The failure first takes place in the heat seal frontier, which is split into two pieces. With a further increase in the tensile stress, the separation between the PP layer and Al layer, as well as the failure of PP layer take place at the same time; Type C: Similar to Type B, the failure first takes place in the heat sealed frontier. Interestingly, with a further increase n the tensile stress, the PP layer is split into many tiny pieces, accompanied with the separation between PP and Al; Type D: At the beginning of the tensile stress, no evident failure is observed. Instead, evident necking in the laminate film near the heat seal frontier takes place (as indicated by arrows in Figure 9D), and the width of the laminate film decreases gradually. Meanwhile, the width of the heat seal frontier remains unchanged. With the increase of tensile stress, the strain of the laminate film along the tensile direction increases evidently, and finally, failure takes place in the heat seal frontier or in the laminate film nearby. This type of failure usually happens when HSS reaches 90 MPa or higher, reflecting that all the layers are tightly laminated, and the two PP layers are perfectly sealed.
As can be clearly seen from Figure 9 and Table 4, the failure behavior of the specimen is closely related to HSS. Generally, when HSS ≤ 70 MPa, mainly the failure mode of Type A occurs, supplemented with Type B; when 70 MPa ≤ HSS ≤ 90 MPa, the mixed failure types of Type B and Type C take place; for HSS higher than 90 MPa, only the failure mode of Type D can be observed. In summary, it is found that the failure type is an indicator of the HSS of the sample. In fact, the HSS value can be far higher than the tensile strength of the PP layer, which can be even higher than the tensile strength of the laminate film, only if each layer is tightly laminated and shares the tensile stress efficiently. Type A: When the tensile stress is applied, the heat seal frontier remains unchanged. Meanwhile, the adhesion between PP layer and Al foil is broken. With the further increase of the strain, only the plastic deformation of freestanding PP layer takes place; Type B: The failure first takes place in the heat seal frontier, which is split into two pieces. With a further increase in the tensile stress, the separation between the PP layer and Al layer, as well as the failure of PP layer take place at the same time; Type C: Similar to Type B, the failure first takes place in the heat sealed frontier. Interestingly, with a further increase n the tensile stress, the PP layer is split into many tiny pieces, accompanied with the separation between PP and Al; Type D: At the beginning of the tensile stress, no evident failure is observed. Instead, evident necking in the laminate film near the heat seal frontier takes place (as indicated by arrows in Figure 9D), and the width of the laminate film decreases gradually. Meanwhile, the width of the heat seal frontier remains unchanged. With the increase of tensile stress, the strain of the laminate film along the tensile direction increases evidently, and finally, failure takes place in the heat seal frontier or in the laminate film nearby. This type of failure usually happens when HSS reaches 90 MPa or higher, reflecting that all the layers are tightly laminated, and the two PP layers are perfectly sealed.
As can be clearly seen from Figure 9 and Table 4, the failure behavior of the specimen is closely related to HSS. Generally, when HSS ≤ 70 MPa, mainly the failure mode of Type A occurs, supplemented with Type B; when 70 MPa ≤ HSS ≤ 90 MPa, the mixed failure types of Type B and Type C take place; for HSS higher than 90 MPa, only the failure mode of Type D can be observed. In summary, it is found that the failure type is an indicator of the HSS of the sample. In fact, the HSS value can be far higher than the tensile strength of the PP layer, which can be even higher than the tensile strength of the laminate film, only if each layer is tightly laminated and shares the tensile stress efficiently.     AAAAB  AAAAB  BBBCC  BCCCD  BBCCD  BBDDD  DDDDD  PCPF-1 TD  AAAAB  AAAAB  BBBBC  BBCCC  BBCCD  BCDDD  DDDDD  PCPF-2 MD  AAABB  BBBCC  CDDDD  DDDDD  DDDDD  DDDDD  DDDDD  PCPF-2 TD  AAAAA  AAABB  AAAAB  AAABB  ABBBC  BBBCC  BBCCD • Effects of dwell time The HSS values of samples heat sealed at different dwell times are measured and plotted as a function of heat seal temperature as shown in Figure 10. To benefit comparison, the Y-axis scales of Figure 10a-d are the same.

Effects of dwell time
The HSS values of samples heat sealed at different dwell times are measured and plotted as a function of heat seal temperature as shown in Figure 10. To benefit comparison, the Y-axis scales of Figure 10a-d are the same.  Figure 10 suggests that for all the samples, at given TH, the HSS value increases with the increase in dwell time, and the critical transition heat seal temperature Tcrit decreases gradually.
However, the increase margin of HSS and decrease rate of Tcrit of the samples are quite different from each other. For PCPF-2 MD, when the dwell time is 6 s, the HSS value will not increase significantly with a further increase in dwell time. For PCPF-1 MD, 9 s and higher dwell time has a similar effect on the HSS value; for PCPF-1 TD and PCPF-2 TD, the HSS value increases continuously with the increase in dwell time. Moreover, when the dwell time is 12 s, the HSS values of the samples can be ordered from high to low as: PCPF-2 MD > PCPF-1 MD > PCPF-1 TD > PCPF-2 TD, indicating that given sufficient dwell time and heat seal temperature, the HSS value that the samples can achieve is still related to its orientation status of the PP layer.
On the other hand, for PCPF-1 MD and PCPF-1 TD, the critical transition heat seal temperature (Tcrit) decreases gradually from around 205 °C to 190 °C with an increase in dwell time from 3 s to 12 s, while for PCPF-2 MD and TD, the Tcrit decreases from 185 °C and 210 °C to 180 °C and 205 °C, respectively, indicating that the variation of Tcrit of the specimens is also closely related to its orientation in the PP layer.
With respect to the failure behavior, an evident relationship between HSS and failure type is clearly observed again in this section, which is in accordance with the observation above.
In summary, the important heat seal properties of the laminated film are closely related to the orientation status of the PP layer. The qualitative variation of the heat seal properties with the increase  Figure 10 suggests that for all the samples, at given T H , the HSS value increases with the increase in dwell time, and the critical transition heat seal temperature T crit decreases gradually.
However, the increase margin of HSS and decrease rate of T crit of the samples are quite different from each other. For PCPF-2 MD, when the dwell time is 6 s, the HSS value will not increase significantly with a further increase in dwell time. For PCPF-1 MD, 9 s and higher dwell time has a similar effect on the HSS value; for PCPF-1 TD and PCPF-2 TD, the HSS value increases continuously with the increase in dwell time. Moreover, when the dwell time is 12 s, the HSS values of the samples can be ordered from high to low as: PCPF-2 MD > PCPF-1 MD > PCPF-1 TD > PCPF-2 TD, indicating that given sufficient dwell time and heat seal temperature, the HSS value that the samples can achieve is still related to its orientation status of the PP layer.
On the other hand, for PCPF-1 MD and PCPF-1 TD, the critical transition heat seal temperature (T crit ) decreases gradually from around 205 • C to 190 • C with an increase in dwell time from 3 s to 12 s, while for PCPF-2 MD and TD, the T crit decreases from 185 • C and 210 • C to 180 • C and 205 • C, respectively, indicating that the variation of T crit of the specimens is also closely related to its orientation in the PP layer.
With respect to the failure behavior, an evident relationship between HSS and failure type is clearly observed again in this section, which is in accordance with the observation above.
In summary, the important heat seal properties of the laminated film are closely related to the orientation status of the PP layer. The qualitative variation of the heat seal properties with the increase of orientation degree in the MD direction is listed in Table 5. Table 5. Variation of the heat seal parameters with the increase of orientation degree in the MD direction of the PP layer.

Heat Seal Parameters MD TD
HSS + − Dwell time needed to obtain desired HSS − + Critical transition heat seal temperature (T crit ) − + Highest HSS value on the platform + − Difference of HSS between MD and TD + Since the PP layer is directly related to the heat seal properties of the laminate film, its orientation status is a determining factor of the heat seal properties, i.e., the HSS, the dwell time needed to obtain the desired HSS, the critical transition heat seal temperature (T crit ), the highest HSS value on the platform and the difference of HSS between MD and TD.
A higher orientation degree of the PP layer in the MD direction leads to a higher difference in HSS between the MD and TD direction. With the increase of the orientation degree in MD, the HSS increases, the time needed to obtain the desired HSS decreases, and both the critical transition heat seal temperature (T crit ) and the highest HSS value on the platform increase; while in TD, as the orientation degree in MD increases, the HSS decreases, the time needed to obtain the desired HSS increases, and both the critical transition heat seal temperature (T crit ) and the highest HSS value on the platform decrease.

Conclusions
In this study, the tensile performances and fracture behaviors of the single layers of PA, Al and PP, as well as the laminated films of PA-Al, PP-Al and PA-Al-PP, were investigated to explore the contributions of each layer to the tensile behavior of the PA-Al-PP composite films for pouch lithium-ion batteries. The results revealed that in the PA-Al-PP composite film, the PA layer with the highest tensile strength can release a large amount of tensile stress from the Al layer during stretching, while the PP layer with the lowest tensile strength can restrain the further development of the small cracks on the boundary of the Al layer under tensile stress; in this way, the high tensile strength and plastic deformation of the composite film are obtained.
Moreover, two PP layers with different orientation status were used to prepare the laminated films to explore the role of PP orientation in the peeling and tensile behavior of heat seal strength (HSS) of the laminated film. The results revealed that the orientation status of the PP layer has little influence on the peeling force of the sample; however, it influences the slope of the peeling curve. Both the orientation status and the heat seal conditions were important factors in determining the HSS and failure behavior of the sample. A higher heat seal temperature (T H ) leads to higher HSS and less dwell time to achieve the relatively high HSS, while with under an increase in dwell time, HSS increases gradually and the onset heat seal temperature T crit (above which the plateau region of the HSS value is reached) decreases. Four failure types of the heat sealed samples were observed, and a clear correspondence between HSS and failure types was found. From the aspect of the PP layer orientation, it was found that in the case of the PP layer without orientation, its HSS in MD and TD are quite similar; while in the case of PP with orientation, a significant difference in heat seal behavior in MD and TD was found: in MD, the composite film exhibit higher HSS, lower T crit and less time to achieve high HSS, while in TD, lower HSS, higher T crit and more time to obtain high HSS were observed; the related mechanism was proposed based on the oriented molecules in the PP layer. In general, the PP orientation status was very important in the heat seal behavior of the composite film. The results in this study also elucidated that for the PP-Al-PA composite film, only if the tensile stress was released by each layer efficiently during the HSS measurement could the composite film exhibit the desired high HSS that was even higher than its tensile strength. Therefore, adequate lamination of each layer is very important for the final properties of the film.