Advances and challenges in biocathode microbial electrolysis cells for chlorinated organic compounds degradation from electroactive perspectives.

Microbial electrolysis cell (MEC) is a promising in-situ strategy for chlorinated organic compound (COC) pollution remediation due to its high efficiency, low energy input, and long-term potential. Reductive dechlorination as the most critical step in COC degradation which takes place primarily in the cathode chamber of MECs is a complex biochemical process driven by the behavior of electrons. However, no information is currently available on the internal mechanism of MEC in dechlorination from the perspective of the whole electron transfer procedure and its dependent electrode materials. This review addresses the underlying mechanism of MEC on the fundamental of the generation (electron donor), transmission (transfer pathway), utilization (functional microbiota) and reception (electron acceptor) of electrons in dechlorination. In addition, the vital role of varied cathode materials involved in the entire electron transfer procedure during COC dechlorination is emphasized. Subsequently, suggestions for future research, including model construction, cathode material modification, and expanding the applicability of MECs to removal gaseous COCs have been proposed. This paper enriches the mechanism of COC degradation by MEC, and thus provides the theoretical support for the scale-up bioreactors for efficient COC removal.