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Preparation of NASICON-Type Nanosized Solid Electrolyte Li1.4Al0.4Ti1.6(PO4)3 by Evaporation-Induced Self-Assembly for Lithium-Ion Battery


A simple and practicable evaporation-induced self-assembly (EISA) method is introduced for the first time to prepare nanosized solid electrolyte Li1.4Al0.4Ti1.6(PO4)3 (LATP) for all-solid-state lithium-ion batteries. A pure Na+ super ion conductor (NASICON) phase is confirmed by X-ray diffraction (XRD) analysis, and its primary particle size is down to 70 nm by optimizing evaporation rate of the solvent. Excellent room temperature bulk and total lithium-ion conductivities of 2.09 × 10−3 S cm−1 and 3.63 × 10−4 S cm−1 are obtained, with an ion-hopping activation energy as low as 0.286 eV.


All-solid-state batteries using ceramic electrolytes have attracted great interests due to their good chemical stability, high ionic conductivity, and superior safety which have been considered as the ultimate safe batteries [1]. Li1+x Al x Ti2−x (PO4)3 (LATP) is one of the fastest lithium-ion-conducting ceramics with a Na+ super ion conductor (NASICON) type structure [2], offering great potential as solid electrolytes applied in all-solid-state lithium-ion batteries (LIBs) [3].

Particle size plays an important role on conductivity of crystalline electrolytes, and usually reduction on particle size favors improved ionic conductivity [4, 5]. There are various methods to synthesize LATP such as solid state reaction, co-precipitation, sol-gel, and melting-quenching methods [69]. High temperature approaches including solid state reaction and melting-quenching usually involve high energy consumption and loss of stoichiometric lithium associated with impurities in the final product. In addition, among the above methods, sol-gel method is the only way to obtain nanocrystalline LATP at a moderate temperature. However, as a crucial step of sol-gel method, controlling hydrolysis of titanium salt is relatively complex and time-consuming. Therefore, in this contribution, we investigated a simple evaporation-induced self-assembly (EISA) method suitable for large-scale production of nanosized LATP (X = 0.4) with high ionic conductivity, which employs ethanol (EtOH) as solvent to avoid the hydrolysis of titanium salt. This work may also offer a new strategy for fabrication of other LATP solid electrolytes with varying x values.


Ethanol soluble LiNO3•H2O, AlCl3, TiCl4, and H3PO4 were used as starting materials. All chemicals were of analytical grade and used as received, without further purification. They were accurately weighed with the stoichiometric ratio as in Li1.4Al0.4Ti1.6(PO4)3. TiCl4 and AlCl3 were first dissolved in EtOH and magnetically stirred for 30 min. Then LiNO3•H2O and H3PO4 were added to the solution under vigorous stirring for another 2 h. The homogenous sol solution was poured into open Petri dishes and heated at various temperatures (30, 50, and 70 °C) in air allowing the solvent to evaporate until viscous sol-gel was formed. We therefore denominated the samples by evaporation temperature, e.g., LATP-30 meaning EtOH evaporated at 30 °C. The sol-gel was further aged at 100 °C for 6 h to become the dry LATP precursor. Such dried gel was subsequently pyrolyzed in air at 300 °C for 3 h, followed by annealing at 800 °C for 2 h.

Thermogravimetric analysis (TGA) was performed on the dried gel (LATP precursors) at a heating rate of 10 °C min−1 in a temperature range of 30–800 °C under air atmosphere. The crystal structures of LATP powders prepared with various evaporation rate of EtOH were investigated by powder X-ray diffraction (XRD) on a Rigaku (SmartLab III) using Cu Kα radiation within 2θ = 10–70° with a step width of 0.06°. The microstructure and morphology were observed by field emission scanning electron microscopy (FESEM) (Quanta FEI, America). The as-prepared powders were pelletized by cold pressing at 200 MPa to a diameter and thickness of 13 and 1.3 mm, respectively. The pellets were sintered at 950 °C for 6 h in air and sputtered with Au on both sides as blocking electrodes for ionic conductivity measurements. AC impedance measurements were performed using an AutoLab 302–N impedance analyzer with an AC voltage of 5 mV over a frequency range of 10−1–105 Hz.

Results and Discussion

Figure 1 displays the TGA curve of the dried gel for LATP precursors. A sharp weight loss of about 35% occurs between 100 and 300 °C, as a result of decomposition of volatile components such as NO3 −1, Cl−1, and H2O. While with increasing temperature, no further weight loss is observed. Therefore, based on the TGA result, in order to obtain final LATP powders, the dried gel was devised to a heat treatment procedure as described in the experimental section.

Fig. 1
figure 1

TGA curve of the dried gel for LATP precursors prepared by EISA method (heating rate 10 °C min−1, air atmosphere)

X-ray diffraction patterns of the LATP powders prepared at various evaporation temperatures are shown in Fig. 2. The standard diffraction peaks of LiTi2(PO4)3 (JCPDS card No. 35-0754) are also indicated. Pure NASICON structured LATP is successfully obtained in all cases and there is no obvious difference on the crystal phase between these samples by varying the evaporation temperature. The lattice constants calculated from the XRD data are a = 0.8471 nm and c = 2.0763 nm, respectively, belonging to R-3c space group.

Fig. 2
figure 2

XRD patterns of LATP prepared with various evaporation rate of EtOH

However, the SEM images clearly demonstrate that the evaporation rate of EtOH is crucial in determining the particle size of the LATP nanoparticles. As shown in Fig. 3, the average particle size of LATP-30, LATP-50, and LATP-70 are 70, 90, and 100 nm, respectively. The synthesizing process via the EISA method is schematically illustrated in Fig. 4. The so-called EISA process is an efficient approach to tune inorganic “polymerization” with the formation of a mesostructured template during the solvent evaporation, which has been widely applied to production of ordered porous materials or nanocomposites in the form of films, fibers, or powders [10, 11]. In this work, EISA is first developed to prepare nanocrystals of ceramic electrolyte LATP. When TiCl4 and AlCl3 are dissolved in EtOH, the metal chlorides react vigorously with EtOH to form complexes M(OR) x Cl nx (n = 3−4, x = 1−3), which can further self-assemble or polymerize to inorganic oligomers or even frameworks when the solvent EtOH is gradually removed. At the meanwhile, the Li+, PO4 3− ions dispersed in the sol solution deposit onto the M(OR) x Cl nx aggregates, which will be converted to LATP precursors after aging. Therefore, increase on the evaporation temperature promotes the crosslinking of M(OR) x Cl nx , resulting in growth of the precursors thus bigger particle size of the final LATP powders.

Fig. 3
figure 3

FESEM images of a LATP-30, b LATP-50, and c LATP-70 prepared with various evaporation rate of EtOH

Fig. 4
figure 4

Schematic illustration of the synthesizing processes for LATP via EISA method

The room temperature Nyquist plots of LATP prepared with various evaporation rate of EtOH are demonstrated in Fig. 5a. Only one semi-circle at high frequencies along with an inclined spike at low frequencies is observed for all samples. As using blocking electrodes, the semi-circle corresponds to the transportation properties of Li+ in the ceramic electrolyte. The bulk resistance (R b) and total resistance (R t = R b + R gb) (R gb refers to the grain boundary resistance) can be calculated from the left and right intercepts of the semi-circle with the real axis, respectively [12]. Thus, one can obtain the bulk conductivity (σ b) and total conductivity (σ t) using equation: σ = l/R · S, where l and S are thickness and area of the disk, respectively. As shown in Fig. 5a, both the σ b and σ t increase as the evaporation temperature decreases from 70 to 30 °C. The bulk and total conductivities of different LATPs at room temperature are summarized in Table 1. As can be seen, LATP-30 has the maximum room temperature σ b and σ t of 2.09 × 10−3 S cm−1 and 3.63 × 10−4 S cm−1, respectively.

Fig. 5
figure 5

a Room temperature AC impedance plots of LATP prepared with various evaporation rate of EtOH (sputtered Au electrodes). b Arrhenius plots of total conductivity of the pelletized LATP-30 electrolyte

Table 1 Average particle size and room temperature conductivities of LATP prepared with various evaporation rate of EtOH

The temperature dependence of the total conductivity of LATP-30 in the temperature range of 30–110 °C is shown in Fig. 5b. The plots of log(σ) against 1000/T are linear and well fitted by the Arrhenius equation as σT = Aexp(−Ea/kT), where A is the pre-exponential parameter, k is the gas constant, and Ea represents the ion-hopping activation energy of the ceramic electrolyte [13]. The Ea of LATP-30 sample calculated from the slope of linear fitted line is 0.286 eV. NASICON-structured lithium electrolytes usually have a constant Ea of about 0.3 eV for the bulk, but the Ea value at the grain boundary varies depending on the M3+ content and the degree of densification [14, 15]. The relative densities of the pressed sample disks determined by the Archimedes method with ethanol as the immersion medium are about 97, 96.7, and 96.4% for LATP-30, LATP-50, and LATP-70, respectively. These values are similar to those of the samples prepared by conventional sol-gel or melting-quenching methods [13]. The replacement of Ti4+ by Al3+ (x = 0.4) and the relatively high density of LATP-30 might decrease the Ea value at the grain boundary, which is beneficial to ion hopping in the electrolyte.


To summarize, we have developed an evaporation-induced self-assembly (EISA) method for fabrication of nanosized fast lithium-ion conductor LATP (x = 0.4) with high ionic conductivity for the first time. This method is simple, applicable for large-scale production, and avoids the difficulty of controlling hydrolysis of titanium salt that conventional sol-gel method has to encounter. The particle size greatly depends on the evaporation rate of the solvent EtOH, which increases gradually with increasing evaporation temperature from 30 to 70 °C. LATP-30 with an average particle size of 70 nm and a relative density of 97% shows a high total lithium-ion conductivity of 3.63 × 10−4 S cm−1 at room temperature and a low activation energy of 0.286 eV, which will be a promising solid electrolyte for all-solid-state LIBs.



Evaporation-induced self-assembly


Li1+x Al x Ti2−x (PO4)3


Lithium-ion battery


  1. Hayashi A, Konishi T, Tadanaga K et al (2006) Formation of electrode–electrolyte interface by lithium insertion to SnS–P2S5 negative electrode materials in all-solid-state cells. Solid State Ionics 177(26):2737–2740

    Article  Google Scholar 

  2. Kakihana M, Tada M, Shiro M et al (2001) Structure and stability of water soluble (NH4)8[Ti4(C6H4O7)4(O2)4] · 8H2O. Inorg Chem 40(5):891–894

    Article  Google Scholar 

  3. Kotobuki M, Isshiki Y, Munakata H et al (2010) All-solid-state lithium battery with a three-dimensionally ordered Li1.5Al0.5Ti1.5(PO4)3 electrode. Electrochimica Acta 2010 55(22):6892–6896

  4. Thokchom JS, Kumar B (2006) Microstructural effects on the superionic conductivity of a lithiated glass-ceramic. Solid State Ionics 177(7):727–732

    Article  Google Scholar 

  5. Maier J (2000) Point-defect thermodynamics and size effects. Solid State Ionics 131(1):13–22

    Article  Google Scholar 

  6. Xu X, Wen Z, Yang X et al (2008) Dense nanostructured solid electrolyte with high Li-ion conductivity by spark plasma sintering technique. Mater Res Bull 43(8):2334–2341

    Article  Google Scholar 

  7. Huang L, Wen Z, Wu M et al (2011) Electrochemical properties of Li1.4Al0.4Ti 1.6(PO4)3 synthesized by a co-precipitation method. J Power Sources 196(16):6943–6946

    Article  Google Scholar 

  8. Wolfenstine J, Foster D, Read J et al (2008) Rate-controlling species for the sintering of LiTi2(PO4)3. J Power Sources 182(2):626–629

    Article  Google Scholar 

  9. Kotobuki M, Koishi M (2013) Preparation of Li1.5Al0.5Ti1.5(PO4)3 solid electrolyte via a sol-gel route using various Al sources. Ceram Int 39(4):4645–4649

    Article  Google Scholar 

  10. Brinker CJ, Lu Y, Sellinger A, Fan H (1999) Evaporation-induced self-assembly: nanostructures made easy. Adv Mater 11(7):579–585

    Article  Google Scholar 

  11. Soler-Illia G, Louis A, Sanchez C (2002) Synthesis and characterization of mesostructured titania-based materials through evaporation-induced self-assembly. Chem Mater 14(2):750–759

    Article  Google Scholar 

  12. Arico AS, Bruce P, Scrosati B et al (2005) Nanostructured materials for advanced energy conversion and storage devices. Nat Mater 4(5):366–377

    Article  Google Scholar 

  13. Xu X, Wen Z, Wu J et al (2007) Preparation and electrical properties of NASICON-type structured Li1.4Al0.4Ti1.6(PO4)3 glass-ceramics by the citric acid-assisted sol-gel method. Solid State Ionics 178(1):29–34

    Article  Google Scholar 

  14. Adachi G, Imanaka N, Aono H (1996) Fast Li+ conducting ceramic electrolytes. Adv Mater 8(2):127–135

    Article  Google Scholar 

  15. Aono H, Sugimoto E, Sadaoka Y et al (1990) Electrical properties of sintered lithium titanium phosphate ceramics (Li1+xMxTi2-x (PO4)3, M3+ = Al3+, Sc3+, or Y3+). Chem Lett 10:1825–1828

    Article  Google Scholar 

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This work was financially supported by the National Basic Research Program of China (973 program, No. 2013CB934700), National Natural Science Foundation of China (No. 51222305), and Program for New Century Excellent Talents in University (No: NCET-12-0386).

Authors’ Contributions

XL performed the synthesis and characterization of nano-LATP, JF participated in the characterization, and CZ supervised the conceptual framework and drafted the manuscript. All authors read and approved the final manuscript.

Competing Interests

The authors declare that they have no competing interests.

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Correspondence to Chuhong Zhang.

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Liu, X., Fu, J. & Zhang, C. Preparation of NASICON-Type Nanosized Solid Electrolyte Li1.4Al0.4Ti1.6(PO4)3 by Evaporation-Induced Self-Assembly for Lithium-Ion Battery. Nanoscale Res Lett 11, 551 (2016).

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  • Nano-LATP
  • Evaporation-induced self-assembly (EISA)
  • Solid electrolyte
  • Lithium-ion battery