The Li–S battery has emerged
as a promising next-generation
system for advanced energy storage. Notwithstanding the recent progress,
the problematic polysulfide shuttling, retarded sulfur redox, and
low output of volumetric capacity remain daunting challenges toward
its practicability. In response, this work demonstrates herein a universal
approach to in situ craft MO
x
-MXene (M: Ti, V, and Nb) heterostructures
as heavy and multifunctional hosts to harvest good battery performances
with synchronous polysulfide immobilization and conversion. Theoretical
calculations indicate that the in situ implanted
oxides boost the reaction kinetics of polysulfide transformation without
affecting the intrinsic conductivity of MXene. As a result, the representative
VO
x
-V2C/S
electrode enables a high volumetric capacity (offering 1645.98 mAh
cm–3 at 0.2 C) and cycling stability (retaining
631.17 mAh cm–3 after 1500 cycles at 2.0 C with
a capacity decay of 0.03% per cycle). More encouragingly, 3D-printed
sulfur electrodes harnessing VO
x
-V2C hosts readily harvest an areal capacity
of 9.74 mAh cm–2 at 0.05 C under an elevated sulfur
loading of 10.78 mg cm–2, holding promise for the
development of practically viable Li–S batteries.