Rational engineering of atomically scaled metalnitrogen-carbon (M-N-C) moieties has been the topic of recent research interest because of their potential application as an electrochemical oxygen reduction reaction (ORR) catalyst. Despite numerous efforts on M-N-Cs, attaining both adequate activity and a satisfactory stability simultaneously is a principal issue. Herein, we demonstrated the synthesis of a single-atom tungsten catalyst supported on the N-doped carbon matrix (W-N-C) and its application as an ORR catalyst. W-N-C was synthesized using the economically viable, simple, one-step pyrolysis of dicyandiamide and tungsten(VI) chloride at moderate temperature (700 °C). The synthesis of W-N-C avoids any post acid treatment as it does not require any subsidiary sacrificial metal like Zn and, hence, does not induce any burden associated with chemical waste management. The atomic dispersion of W atoms stabilized by N-doped porous carbon and the formation of WN 2 C 2 were confirmed by high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption spectroscopy. Interestingly, as-synthesized WN 2 C 2 exhibited unprecedented electrocatalytic activity with a half-wave potential of 764 mV vs reversible hydrogen electrode (RHE) as well as significantly enhanced stability (retaining >99% diffusion-limited current density and the loss in activity is 10.5% at 0.84 V after 10,000 potential cycles), which is much better than the stability limit set by the US Department of Energy in an alkaline medium. Overall, the activity of W-N-C surpasses that of Pt/C after 5000 cycles. The excellent stability is believed to be due to the symmetric coordination of the metal active site (W 2 N 2 C 2 ).

M-N-C centers have garnered tremendous research attention due to a potential replacement to the Pt- group metal based cathode catalysts and is expected to be the integral part of the...

The properties and, hence, the application of materials are dependent on the way their constituent atoms are arranged. Here, we report a facile approach to produce body-centered cubic (bcc) and face-centered cubic (fcc) phases of bimetallic FeCo crystalline nanoparticles embedded into nitrogen-doped carbon nanotubes (NCNTs) with equal loading and almost similar particle size for both crystalline phases by a rational selection of precursors. The two electrocatalysts with similar composition but different crystalline structures of the encapsulated nanoparticles have allowed us, for the first time, to account for the effect of crystal structure on the overall work function of electrocatalysts and the concomitant correlation with the oxygen reduction reaction (ORR). This study unveils that the electrocatalysts with lower work function show lower activation energy to facilitate the ORR. Importantly, the difference between the ORR activation energy on electrocatalysts and their respective work functions are found to be identical (∼0.2 eV). A notable decrease in the ORR activity after acid treatment indicates the significant role of encapsulated FeCo nanoparticles in influencing the oxygen electrochemistry by modulating the material property of overall electrocatalysts.

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