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Developing low‐cost and high‐activity pH‐universal hydrogen evolution reaction (HER) catalysts is very crucial to the industrialization of water electrolysis. However, the high price, low yield, and poor stability of current HER catalysts make them difficult to meet practical requirements. Herein, a plasma spraying technique is employed to prepare self‐supported Cu catalysts with tensile strain for the first time. The tensile strain upshifts the d‐band of Cu, improves the water dissociation and H* adsorption, eventually improves the intrinsic HER catalytic activity. As such, Cu electrode achieves overpotentials of 182 mV in 0.5 m H2SO4, 261 mV in 1 M PBS, and 121 mV in 1 M KOH at 10 mA cm–2. In addition, Cu electrode also performs well at high current densities, the overpotentials at 1 A cm–2 are much lower than those of Pt foil in acid, neutral, and alkaline solutions. [ABSTRACT FROM AUTHOR]

Catalyst support with good conductivity and stability is an eternal pursuit in the search for a high‐performance electrocatalyst. Here, an unusual catalyst support, laser‐modified boron nitride with C, O dopants (L‐BN), for the oxygen evolution reaction is reported. L‐BN exhibits unique advantages for electrocatalysis, namely, high corrosion resistance under oxidizing conditions, enhanced electrical conductivity arising from interlayer B–B dipolar interaction, and strong interaction with IrOx catalyst caused by NCN bonds. As an excellent substrate, L‐BN helps to achieve higher activity and stability than its carbon black counterpart. [ABSTRACT FROM AUTHOR]

Exploiting low-cost and high-activity catalysts is crucial for lowering energy consumption for hydrogen evolution reaction (HER). Herein, we reported a pure Nickel catalyst with high activity and long-term stability at a large current density in an alkaline medium. We employed an industrial machining technology, turning processing, to generate Ni-chips, a self-supported catalyst, with mostly close-packed planes exposed and high compressive strain. The close-packed plane and compressive strain jointly lower the d -band center of the nickel catalyst and overcome the excessive adsorption for reactive intermediates. As such, Ni-chip achieves ultralow overpotentials of 70 mV at 10 mA cm−2 and 297 mV at 1000 mA cm−2. Particularly, the catalyst exhibits outstanding stability at high current density (1 A cm−2), after working for one and a half months (ca. 1070 h), the initial current density merely declined by 7.3%. With its remarkable catalytic activity, excellent stability, ease of synthesis, and utilization of metallic scraps, the Ni-chip catalyst may serve as a promising catalyst for industrial applications. Ni-chip catalysts with high compressive strain and predominantly close-packed planes were prepared through turning processing. This combination effectively mitigated the excessive adsorption of *OH and *H on the Ni surface, enabling an ultralow overpotential of 297 mV at 1000 mA cm-2, and excellent stability at 1 A cm-2 for 1070 h, demonstrating potential as an efficient and durable electrocatalyst. [Display omitted] [ABSTRACT FROM AUTHOR]

As a cheap and earth-abundant metal, copper is known highly conductive but inactive for catalyzing hydrogen evolution reaction (HER) due to its fully filled d orbital and weak adsorption for hydrogen intermediate. Herein, we adopt a mechanical stirring process to introduce a large number of dislocations into copper plate, and retain the dislocations by the quenching effect of dry ice. Theoretical computation indicates that dislocation can cause uneven distribution of charge density, and the electron-deficient area remarkably enhances the hydrogen adsorption, turning inactive copper into active HER catalyst. The product achieves high turnover frequency, low overpotential and long-term durability. Our work bridges mechanical process and functional materials, and exploits a powerful technology on producing self-supported catalysts in a rapid way : [Display omitted] [ABSTRACT FROM AUTHOR]

Water electrolysis has been proven as an effective means to produce clean hydrogen energy, and such a process can be accelerated by active bifunctional electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Herein, we adopted a laser ablation technique to prepare a strawberry-like catalyst with Co 3 O 4 clusters embedded in Ag nanoparticles, realizing the ingenious mutual regulation of Co 3 O 4 and Ag. The Co 3 O 4 facilitates the water dissociation and optimizes the hydrogen adsorption of Ag by introducing tensile strain and low coordination number, resulting in a low HER overpotential of 51 mV at 10 mA cm−2. Meanwhile, the electron transfer from Co 3 O 4 to Ag facilitates the oxidization of Co 3 O 4 and improves the OER performance, leading to a low OER overpotential of 206 mV at 10 mA cm−2. Ultimately, an ultralow potential of 1.49 V for overall water splitting has been achieved at 10 mA cm−2, outperforming Pt/C+RuO 2 couple. [Display omitted] Utilizing the non-equilibrium synthesis method of the laser ablation, this work investigates a unique strawberry-like Co 3 O 4 -Ag composite with Co 3 O 4 clusters embedding in Ag substrate. Through the ingenious mutual regulation and synergic effect of the two components, the catalytic activity of the inactive component can be improved simultaneously, thereby achieving outstanding overall water splitting performance. • A novel strawberry-like structure with Co 3 O 4 clusters embedding in Ag substrate was prepared by laser ablation. • The embedded Co 3 O 4 clusters optimize the hydrogen adsorption of Ag, thus improving the HER performance. • The electron transfer from Co 3 O 4 to Ag facilitates the oxidization of Co 3 O 4 and then optimizes the OER performance. • Mutual regulation and synergic effect endow strawberry-like catalyst excellent water electrolysis performance. [ABSTRACT FROM AUTHOR]