Lithium–sulfur
(Li–S) batteries are among the most
promising candidates for next-generation high-energy-density batteries;
however, the polysulfide shuttle represents a major drawback in their
application. Here, we report on sulfurized poly(norbornadiene) (S/pNBD)
and its analogue, sulfurized poly(dicyclopentadiene) (S/pDCPD), two
polysulfide shuttle-free and cheap cathode materials with good performance
in Li–S battery technology. Both S/pNBD and S/pDCPD can be
prepared in a straightforward two-step procedure. Time-of-flight secondary
ion mass spectrometry, X-ray photoelectron spectroscopy measurements,
and cyclic voltammetry indicate that all sulfur in S/pNBD and S/pDCPD
is covalently bound to the polymer matrix in the form of C–S
x
–C units. Li–S cells based
on an S/pNBD cathode exhibit a high discharge capacity up to 1050
mA h/g sulfur at 1 C with a good capacity retention of 62 % after
1900 cycles. The structurally similar analogue S/pDCPD shows comparable
electrochemical performance, again with excellent capacity retention.
The high reversibility and ultra-long cycle life of both, S/pNBD and
S/pDCPD, are attributed to the covalent binding of sulfur to the polymer
backbone.