Performance breakthrough of MoSe2 -based hydrogen evolution reaction (HER) electrocatalysts largely relies on sophisticated phase modulation and judicious innovation on conductive matrix/support. In this work the controllable synthesis of phosphate ion (PO43- ) intercalation induced-MoSe2 (P-MoSe2 ) nanosheets on N-doped mold spore carbon (N-MSC) forming P-MoSe2 /N-MSC composite electrocatalysts is realized. Impressively, a novel conductive N-MSC matrix is constructed by a facile mold fermentation method. Furthermore, the phase of MoSe2 can be modulated by a simple phosphorization strategy to realize the conversion from 2H-MoSe2 to 1T-MoSe2 to produce biphase-coexisted (1T-2H)-MoSe2 by PO43- intercalation (namely, P-MoSe2 ), confirmed by synchrotron radiation technology and spherical aberration-corrected TEM (SACTEM). Notably, higher conductivity, lower bandgap and adsorption energy of H+ are verified for the P-MoSe2 /N-MSC with the help of density functional theory (DFT) calculation. Benefiting from these unique advantages, the P-MoSe2 /N-MSC composites show superior HER performance with a low Tafel slope (≈51 mV dec-1 ) and overpotential (≈126 mV at 10 mA cm-1 ) and excellent electrochemical stability, better than 2H-MoSe2 /N-MSC and MoSe2 /carbon nanosphere (MoSe2 /CNS) counterparts. This work demonstrates a new kind of carbon material via biological cultivation, and simultaneously unravels the phase transformation mechanism of MoSe2 by PO43- intercalation.
Keywords: hydrogen evolution reaction; mold spore carbon; molybdenum selenide; phase modulation; phosphate ion intercalation.
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