The goal of the presented project is development a new type of direct sodium hypophosphite fuel cell (DSHFC) System, with Sodium Hypophosphite direct oxidation at the CoB2O4 based anode. Synthesized CoB2O4 was used as a catalyst of sodium hypophosphate oxidation [1,2]. CoB2O4 was annealed at 280˚C - 350˚C demonstrated best catalytic activity. In X-ray phase analysis of the sample show the X-ray diffraction pattern according to the ASTM standard of СoB2O4 (2.88,2.44, 2.03, 1.86 Å). Sodium Hypophosphite is oxidized in alkaline media. Hypophosphite-ion is adsorbed at metal oxide CoB2O4 surface, hydrogen atom, which is connected with catalyst surface by covalent bond, attenuates P-H bond and finally cleaves it; hydrogen is replaced by hydroxide-ion of water (1, 2) which causes hypophosphite transformation in phosphate. The overall anodic reaction will be (3) H2O=H++OH- (1) H2PO2 -ads + OH-ads = H2PO3 -ads+ H++ 2e- (2) NaH2PO2 + H2O = NaH2PO3 + 2H+ +2e- (3) The DSHFC anode was made by next steps: the CoB2O4 powder and carbon black XC72 powder 1:3 were mixed in isopropanol alcohol, as a binder was used polytetrafluoroethylene suspension and sonicated during 30 min. A carbon felt was used as an anode substrate and catalytic layer was covered bay spry-gun and heated at 250 oC during 5 min. the figure 1 show the DSHFC construction. The fuel Cell is undivided. As a cathode was used ordinary gas diffusion electrode for O2 reduction. The Anode and the cathode geometric surface area was 4 cm2 (2cm X 2cm) The Voltage –Ampere characteristics of the Direct Sodium Hypophosphite Fuel Cell was recorded with various concentrations of electrolyte X NaH2PO2 + Y NaOH, electrolyte was feed in to fuel cell by pump, oxygen to the cathode chamber was feed by air compressor (pressure 35-40 mm.H2O).Test were performed at room temperature. External load was changed from 10 000 Ω to 0.1 Ω. Current and voltage of DSHFC was recorded by multi-meters. In optimal conditions, electrolyte 1M NaH2PO2 + 2 NaOH, external load 1 Ω, the current density was 36 mA cm-1, the suitable power density was 13,5 mwt cm-1, open circuit potential was 1v References [1] Electroless plating: fundamentals and applications edited by G. O. Mallory, J. B. Hajdu [2] P.O. Nikoleishvili, at all, Russian Journal of Electrochemistry, 2015, Vol. 51, No. 7, pp. 665–671 Figure 1