To meet the practical demand of overall water splitting and regenerative metal–air batteries, highly efficient, low‐cost, and durable electrocatalysts for the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER) are required to displace noble metal catalysts. In this work, a facile solid‐state synthesis strategy is developed to construct the interfacial engineering of W2N/WC heterostructures, in which abundant interfaces are formed. Under high temperature (800 °C), volatile CNx species from dicyanodiamide are trapped by WO3 nanorods, followed by simultaneous nitridation and carbonization, to form W2N/WC heterostructure catalysts. The resultant W2N/WC heterostructure catalysts exhibit an efficient and stable electrocatalytic performance toward the ORR, OER, and HER, including a half‐wave potential of 0.81 V (ORR) and a low overpotential at 10 mA cm−2 for the OER (320 mV) and HER (148.5 mV). Furthermore, a W2N/WC‐based Zn–air battery shows outstanding high power density (172 mW cm−2). Density functional theory and X‐ray absorption fine structure analysis computations reveal that W2N/WC interfaces synergistically facilitate transport and separation of charge, thus accelerating the electrochemical ORR, OER, and HER. This work paves a novel avenue for constructing efficient and low‐cost electrocatalysts for electrochemical energy devices.

An oxygen vacancy-rich Au/TiO2 hybrid nanosheet is used as an electrocatalyst for NRR that delivers a high NH3 yield of 64.6 μg h−1 mg−1 cat and an faradic efficiency (FE) of 29.5% and excellent structural stability under ambient conditions.

Hierarchical vertical WO3 nanowire arrays on vertical WO3 nanosheet arrays with rich oxygen vacancies were synthesized via a simple and facile method, and the outstanding OER performance which is superior to that of most reported state-of-the-art catalysts was reported for the first time.

A kind of porous carbon coated SnO2-based composites was successfully produced under direction of a silica template. The prepared SnO2@PC anodes deliver high specific capacity, excellent cycling durability and remarkable rate capability in LIBs.

Multi-yolk–shell bismuth@porous carbon catalyst was fabricated by facile synthetic processes. The MB@PC catalyst displays deliver a NH3 yield of 28.63 μg h−1 mg−1cat., a Faraday efficiency of 10.58 % at −0.5 V versus RHE under ambient conditions.

Water electrolysis, driven by earth-abundant transition-metal-based electrocatalysts, is an important reaction for sustainable energy storage. Efficient water splitting processes at electrode are kinetically limited by the improper adsorption strengthens between...

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Simultaneously optimizing elementary steps, such as water dissociation, hydroxyl transferring, and hydrogen combination, is crucial yet challenging for achieving efficient hydrogen evolution reaction (HER) in alkaline media. Herein, Ru single atom‐doped WO2 nanoparticles with atomically dispersed Ru–W pair sites (Ru–W/WO2‐800) are developed using a crystalline lattice‐confined strategy, aiming to gain efficient alkaline HER. It is found that Ru–W/WO2‐800 exhibits remarkable HER activity, characterized by a low overpotential (11 mV at 10 mA cm−2), notable mass activity (5863 mA mg−1 Ru at 50 mV), and robust stability (500 h at 250 mA cm−2). The highly efficient activity of Ru–W/WO2‐800 is attributed to the synergistic effect of Ru–W sites through ensemble catalysis. Specifically, the W sites expedite rapid hydroxyl transferring and water dissociation, while the Ru sites accelerate the hydrogen combination process, synergistically facilitating the HER activity. This study opens a promising pathway for tailoring the coordination environment of atomic‐scale catalysts to achieve efficient electro‐catalysis.