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In this work, we report a facile method to prepare P, N co‐doped porous carbon (PNPC) by the carbonization of covalent organic polymer (COP) used as efficient metal‐free electrocatalyst for hydrogen evolution reaction (HER), oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Overpotential is only 150 mV for the PNPC electrocatalyst to reach 10 mA cm−2 in the acidic medium due to the heteroatom dopants in the carbon matrix; meanwhile, stable HER activity is recorded during 5000 potential cycles. Additionally, overpotential is 343 mV for PNPC electrocatalyst to drive OER catalysis with 10 mA cm−2, which is comparable to the benchmarked IrO2 (320 mV). Similarly, PNPC electrocatalyst can achieve a Pt‐like ORR catalytic activity. The power density of the assembled rechargeable zinc‐air battery (ZAB) is 1.8 times higher than that of the commercial system (Pt/C−IrO2) and charge‐discharge voltage gap is well maintained during 20 h test, implying the high stability of the formed PNPC electrocatalyst. [ABSTRACT FROM AUTHOR]

As well known, heteroatom doped carbon material served as metal‐free electrocatalyst for hydrogen evolution (HER) and oxygen reduction reactions (ORR) particularly relies on the heteroatom doping level. Here, we report a 3D porous nitrogen doped carbon (PNC) electrocatalyst with superior HER and ORR electrocatalytic activities derived from the calcination of the discarded cigarette butt and dicyandiamide possessing a high nitrogen content (20 at%). PNC electrocatalyst only demands 143 mV versus RHE to achieve 10 mA cm−2 ascribed to the high nitrogen percentile in PNC electrocatalyst favorable for constructing successive active centers contributing to efficiently catalyzing HER. Ignorable degradation in HER activity observed after 10000 potential cycles as well as undetectable decay in HER performance recorded after 12 h operation indicate high stability of PNC electrocatalyst. Meanwhile, half‐wave potential of PNC electrocatalyst reaches 0.81 V versus RHE in 1 M KOH electrolyte. Additionally, stable ORR activity attained after 1000 potential cycles is indicative of high stability. A comparably high zinc‐air battery performance with maximum power density of 66 mW cm−2 is achieved by PNC electrocatalyst. This study highlights the importance of nitrogen doping level in metal‐free electrocatalyst for boosting HER and ORR activities. What? No metal! A 3D porous nitrogen doped carbon (PNC) electrocatalyst with superior HER and ORR electrocatalytic activities derived from the calcination of the discarded cigarette butt and dicyandiamide possessing a high nitrogen content (20 at%). [ABSTRACT FROM AUTHOR]

Constructing high-performance catalyst for hydrogen evolution reaction (HER) is the effective way to eliminate energy crisis. Reasonable engineering of heterointerfaces can effectively create more active sites and promote electron transfer resulting in improvement in the catalytic activity. In this work, we synthesize the well-defined molybdenum carbides and tungsten carbides nano-heterostructure (Mo 2 C/W 2 C) by carbonization with CH 4 /H 2 at 800 °C showing excellent HER activity, fast kinetics and electrochemical stability in both alkaline and acidic electrolytes. Mo 2 C/W 2 C requires only 140 and 132 mV overpotentials to reach catalytic current density of 10 mA cm−2 in 0.5 M H 2 SO 4 and 1 M KOH electrolyte, respectively. Tafel slope is as low as 51 and 76 mV dec−1 in 0.5 M H 2 SO 4 and 1 M KOH comparable to the benchmarked Pt/C. Moreover, Mo 2 C/W 2 C exhibits a superior stability with slight deterioration in HER performance after 5000 potential cycles. This work elucidates that the rational construction of heterointerfaces is favorable for design of efficient non-noble metal electrocatalyst for HER catalysis. Image 1 • Mo 2 C/W 2 C heterogeneous electrocatalyst is successfully synthesized. • The overpotential is 140 mV for Mo 2 C/W 2 C to deliver 10 mA cm−2 in acidic medium. • Mo 2 C/W 2 C requires 132 mV overpotential to reach 10 mA cm−2 in alkaline medium. [ABSTRACT FROM AUTHOR]

Highly active and stable electrocatalysts at low cost for hydrogen evolution reaction are essential for large scale hydrogen production. The Ni 3 P-Ni heterostructure confined in 3D networks of carbon nanotube (CNT) has been successfully prepared as the hydrogen evolution reaction (HER) electrode. The morphology and phase composition of Ni 3 P-Ni heterostructure are tunable by varying the acid pickling time. The Ni 3 P-Ni/CNT composite electrode with optimized Ni:Ni 3 P ratio of 22.29 wt% demonstrate high catalytic activity and excellent stability for HER. It demonstrates a comparable HER activity to the standard Pt electrode in alkaline solution, i.e., overpotentials of 116 vs 67 mV at 10 mA·cm−2 and Tafel slops of 59 vs 37 mV·dec−1. No degradation is observed after 1000 cyclic voltammetry (CV) cycles or 50 h operation under constant 0.3 V overpotential. • Pickling affects the morphology of heterogeneous structure and the content of Ni. • The Ni 3 P-Ni heterostructure was anchored to the carbon nanotube network by ball milling. • The electrode was prepared by mixing with PTFE and pressing. • The results show that Ni 3 P-Ni/CNT electrode has the best hydrogen evolution activity when the Ni/Ni 3 P ratio is 22.29 %. [ABSTRACT FROM AUTHOR]