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Page 12 of 30                                                      Yoon et al. Energy Mater 2024;4:400063  https://dx.doi.org/10.20517/energymater.2023.146

               Table 2. Li-storage properties of Sb-based LIB anodes
                                                          Electrolyte                                                             Rate capability
                                                                                                       Cyclability after the Xth cycle   Current  Reversible
                Material                                                               Binder  ICE (%)      -1                                   Ref.
                                      Salt      Solvent                                                (mAh g )                 rate   capacity
                                                                                                                                            -1
                                                                                                                                   -1
                                                                                                                                (A g )  (mAh g )
                Micro-sized Sb        1.0 M LiPF 6  PC with 10 vol% FEC                CMC     81.0    540 (X = 150)            5.0    575       [72]
                Bulk Sb               1.2 M LiFSI  TEP:HFE = 1:3 mol%                  PAA/CMC  87.5   648 (X = 50)             0.5    604       [73]
                Pristine Sb           3.0 M LiFSI +    DOL:DME = 1:1 vol%              PAA/CMC  82.5   624 (X = 100)            3.3    487       [74]
                                      0.4 M LiNO
                                             3
                Spherical Sb/C        1.0 M LiPF 6  EC:DMC = 1:1 vol% with 5 vol% FEC  Alginate  86.7  590 (X = 80)             1.2    535       [75]
                Sb/CNT composite film  1.0 M LiPF  EC:DEC = 3:7 vol%                   Binder-free  78.7  340 (X = 100)         3.2    300       [76]
                                            6
                Nanorod-in-nanotube Sb/N-C  1.0 M LiPF 6  EC:DMC:EMC = 1:1:1 vol% with 10 wt% FEC  CMC  78.3  346 (X = 3,000)   20.0   343       [77]
                Sb/carbon nanosheets  1.0 M LiPF  EC:DMC = 1:1 vol%                    PVDF    62.5    598 (X = 100)            2.0    449       [78]
                                            6
                NiSb/N-C nanosheets   1.0 M LiPF 6  EC:DMC = 1:1 vol%                  PTFE    71.8    401 (X = 1,000)          5.0    252       [79]
                Sb/CTHNs              1.0 M LiPF  EC:DEC = 1:1 vol% with 5 vol% FEC    PVDF    52.4    607 (X = 100)            5.0    435       [80]
                                            6
                CS/NPC                1.0 M LiPF 6  EC:DEC:DMC = 1:1:1 vol%            CMC     52      833 (X = 3,000)          10.0   343       [81]
                ZnSnSb 2              1.0 M LiPF 6  PC:EC:DMC = 1:1:3 vol% with 5 vol% FEC + 1 vol% VC  CMC  83.0  615 (X = 200)  0.63  650      [82]
                NiSb/C                1.0 M LiPF  EC:DEC = 1:1 vol% with 5 vol% FEC    Alginate  68.5  500 (X = 200)            2.0    426       [83]
                                            6
                NiSb/C nanosheets     1.0 M LiPF 6  EC:DEC = 1:1 vol%                  PVDF    64.1    405 (X = 1,000)          2.0    305       [84]
                Sb/rGO                1.0 M LiPF  EC:DMC = 1:1 vol%                    PVDF    52.3    798 (X = 200)            0.43   563       [85]
                                            6
                silica-reinforce Sb/CNF  1.0 M LiPF 6  EC:DMC = 1:1 vol%               PAA     66.4    700 (X = 400)            1.0    468       [86]


                                                       [90]
               system using XPS and electrochemical testing . Sb was detected in the Sb 3d XPS spectrum of the Sb-carboxymethyl cellulose (CMC) anode in the fully
               desodiated state, consistent with the partial redissolution of the SEI layer (dissolution of Na O/NaOH). In contrast, Sb was not detected on the Sb-PVDF anode
                                                                                            2
               in the fully desodiated state because the SEI layer covering the Sb anode was more than 5 nm thick. Therefore, a more uniform and thinner SEI layer was
               formed in the case of the Sb-CMC anode compared to the Sb-PVDF anode, resulting in superior electrochemical performance [Figure 9C].


               Nanostructural design and low-dimensional engineering aimed at accelerating reaction kinetics are considered the most efficient strategies for addressing the
               abovementioned drawbacks, including the sluggish rate capability and rapid capacity decay associated with the excessive volume change experienced by
               Sb [67,91-96] . Liu et al. fabricated highly uniform Sb nanotubes (NTs) using a galvanic replacement approach using a Cu Sb-mediated formation mechanism . The
                                                                                                                                              [91]
                                                                                                                2
               Sb NT anode delivered a reversible capacity of 546 mAh g  after 100 cycles with a capacity retention of 98.7% at 0.1 A g  and excellent long-term cycling
                                                                                                                       -1
                                                                  -1
                               -1
                                          -1
               stability at 1.0 A g  (342 mAh g  after 6,000 cycles with a capacity retention of 74%) [Figure 10A]. The excellent Na-storage performance of the Sb NTs was
               attributed to the one-dimensional hollow structure, which effectively relieves structural deformation and shortens the ion-diffusion path, thereby improving
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