In this work, for the first time, we synthesize a SnO 2 nanomaterial through the calcination of tin metal-organic framework (MOF) precursors. X-ray diffraction, field emission scanning electron microscope, transmission electron microscopy, and the Brunauer-Emmett-Teller specific surface area are used to characterize the phases and to observe surface morphologies. This anode material exhibits good electrochemical performance in LIBs with high reversible capacity and cycling stability. The good electrochemical properties could be ascribed to the short transport/diffusion path of electrons and lithium ions and the high contact area between the electrode and electrolyte that results from the nanostructured SnO 2 . This is low-cost, 3 templates to synthesize nanoparticles and high specific surface area materials. There have also been many reports of the synthesis of metal oxide nanoparticles by direct calcination of MOFs, which exhibit excellent electrochemical performance. [19][20][21] 23 Nevertheless, to the best of our knowledge, there has been no report on synthesis of SnO 2 nanoparticles with homogeneous morphology using MOFs as template. Herein we report a simple, scalable and low-cost synthesis of SnO 2 nanoparticles via the conversion of the Sn-MOF. When evaluated as an anode material for LIB, the as-prepared SnO 2 nanoparticles exhibit good electrochemical performance of a high reversible capacity and excellent stability of up to 100 charge/discharge cycles.
Experimental details2.1 Reagents and Chemicals. Tin (II) sulfate (SnSO 4 ) and p-Phthalic acid (C 8 H 6 O 4 ) were purchased from Sinopharm Chemical Reagent Co. Ltd. Sodium hydroxide (NaOH, AR) was purchased from Aladdin Chemistry Co. Ltd. All chemicals were used as received without further purification.
Synthesis of Sn-MOF.In a typical procedure, 0.012 mol C 8 H 6 O 4 and 0.024 mol NaOH were dissolved in a 300 ml deionized water under stirring. After that, 60 mL of a 0.25 M SnSO 4 aqueous solution was simultaneously added dropwise into the above solution under constant stirring. The mixture was stirred for 5 h at room temperature until MOF precipitation was formed. The product was collected and washed with ethanol and deionized water for several times. At last, the white powder of Sn-MOF was dried in vacuum at 50 ℃.
SnO 2 nanoparticles synthesis.The Sn-MOF was thermally treated at 400 ℃ for 2 h under air atmosphere with a ramping rate of 5 ℃ min -1 and then naturally cooled down to room temperature. Finally, the product was taken out and it was found that the color of the material changed from white to gray. 7 formation of a SEI film, which disappeared under the subsequent cycles, 30 and finally the alloying reaction between Sn and Li + , respectively. In the case of the first anodic process, two broader anodic peaks at 0.48 and 0.60 V corresponded to the extraction of lithium ion from Li-Sn alloys. Note that another oxidation peak at 1.25 V was also observed, which was most likely due to the partially reversible reaction of SnO 2 to Sn and Li 2 O. 31 C...