“…Finally,t he preparationo ft he 2D functional separator usually appliesf iltration, whichw ould reduce the industrial production in the future.M ore facile and scalable methods still require exploration. [43] 480 mAh g À1 at 0.67 C800 mAh g À1 after 300 cycles at 100 mA g À1 MoS 2 /3 Dg raphene [46] 600 mAh g À1 at 3Ag À1 689 mAh g À1 after 200 cycles at 0.5 Ag À1 MoS 2 /rGO [47] 615 mAh g À1 at 2C 368 mAh g À1 after 500 cycle at 1C 3D MoS 2 [49] 756 mAh g À1 at 3C 593 mAh g À1 after 600 cycles at 1C MoS 2 -PDDA-PAA [56] 766 mAh g À1 at 3C 423 mAh g À1 after 2000 cycles at 1C Thermals tability (150 8C) Sb 2 S 3 /CNT [55] 530 mAh g À1 at 2C 450 mAh g À1 after 200 cycles at 2C 1.33-2.14 eV binding energy with PS SnS 2 -modified separator [54] 700 mAh g À1 at 5C 597 mAh g À1 after the 500 cycles at 2C [28] 281.8 h, 0.2 mA cm À2 11.8 h, 0.2 mA cm À2 3D conformalGOc oated GF [29] % 320 h, 1mAcm À2 , 1mAh cm À2 % 80 h, 1mAcm À2 , 1mAh cm À2 83 %e fficiency,160 cycles, 1mAcm À2 ,1mAh cm À2 80 %e fficiency,80cycles, 1mAcm À2 ,1mAhcm À2 GO-SiO 2 coated polyolefin [30] 350 cycles( LiCoO 2 cathode, 1C)2 20 cycles N, Sd opedgraphene coated PE [32] 85 %, 350 cycles( LiNi 0.8 Co 0.15 Al 0.05 O 2 cathode,0 .5 C)…”