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This paper describes the synthesis of low cost electrocatalyst for oxygen reduction reaction (ORR) from spent coffee grounds (SCGs) through heteroatom engineering and simultaneous co‐doping of N and P. The co‐doping of N and P to coffee carbon (N−P/CC) brings maximum defect sites in the catalyst which are favourable for ORR in relation to the individual heteroatom doped catalyst. Microscopic analysis confirms that N−P co‐doped coffee carbon (N−P/CC) undergoes slight structural changes by altering its porosity as well as surface area. Electrochemical studies confirm that, N−P/CC has superior catalytic activity with no effect to CO which makes it highly desirable as a metal‐free electrocatalyst for ORR. The developed catalyst is subjected to 10,000 repeated potential cycles in alkaline media and is found only ∼30 mV loss in its E 1/2 potential, while the drop in E 1/2 is about ∼180 mV from its original value even after 1000 potential cycles for the commercial Pt/C catalyst. XPS analysis for N−P/CC shows the presence of active pyridinic‐N, graphitic‐N species and active P−C and P−O bonds. Co‐existence of all these species induces maximum polarization of C−C bonds in the carbon matrix and synergistically enhances the ORR behaviour in alkaline medium.
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Akula et al. (2018) studied this question.
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