An excess of elemental sulfur is generated annually from hydrodesulfurization in petroleum refining processes; however, it has a limited number of uses, of which one example is the production of sulfuric acid. Despite this excess, the development of synthetic and processing methods to convert elemental sulfur into useful chemical substances has not been investigated widely. Here we report a facile method (termed ‘inverse vulcanization’) to prepare chemically stable and processable polymeric materials through the direct copolymerization of elemental sulfur with vinylic monomers. This methodology enabled the modification of sulfur into processable copolymer forms with tunable thermomechanical properties, which leads to well-defined sulfur-rich micropatterned films created by imprint lithography. We also demonstrate that these copolymers exhibit comparable electrochemical properties to elemental sulfur and could serve as the active material in Li–S batteries, exhibiting high specific capacity (823 mA h g⁻¹ at 100 cycles) and enhanced capacity retention.

Stimuli-responsive polymers have been attracting great interest within the scientific community for several decades. The unique feature to respond to small changes in the environmental conditions has made this class of materials very promising for several applications in the field of nanoscience, nanotechnology and nanomedicine. So far, several different chemical, physical or biochemical stimuli have been investigated within natural or synthetic polymers. Very interesting and appealing seems to be the combination of several stimuli to tune the properties of these materials in manifold ways. Within this present review, we want to highlight the recent progress in the field of synthetic stimuli-responsive polymers combining temperature and light responsiveness.

The integration of several responsive moieties within one polymer yields smart polymers exhibiting a multifaceted responsive behaviour.

A graphical abstract is available for this content