Peatland fires induced changes in electron transfer properties
and relevant electroactive structures of peat soil organic matter
(PSOM) remain ambiguous, impeding comprehension of postfire biogeochemical
processes. Here, we revealed temperature-dependent electron exchange
capacity (EEC) of PSOM dynamics through simulated peat soil burning
(150–500 °C), which extremely changed postfire microbial
Fe-nanoparticles reduction and methanogenesis. EEC diminished significantly
(60–75% loss) due to phenolic-quinone moieties depletion with
increasing temperature, regardless of oxygen availability. The final
EEC in oxic burning surpassed that of anoxic burning by 1.5 times,
attributed to additional quinones from oxygen incorporation. Notably,
EEC exhibited heat resistance up to 200 °C and stabilized above
350 °C. Additionally, fire reshaped the EEC-relevant redox-active
moieties. Heterocyclic-N generated from burning predominantly contributed
to the electron-accepting capacity (EAC) alongside quinones, while
phenolic moieties and bonded Fe(II) enhanced the electron-donating
capacity (EDC). However, the preferential binding of heterocyclic-N
to Fe(II) restricted the EDC of Fe(II). Interestingly, the decrease
in EAC declined its electron-shuttling effects in microbial Fe nanoparticle
reduction, but fire-induced graphitic carbon formation increased the
electrical conductivity (EC) of PSOM, promoting electron transfer.
Further, enhanced EC may facilitate methanogenesis in postfire peatlands.
These findings advance our understanding of elemental biogeochemical
cycles and greenhouse emission mechanisms in postfire peatlands.