Seawater is one of the most abundant natural resources on our planet. Electrolysis of seawater is not only a promising approach to produce clean hydrogen energy, but also of great significance to seawater desalination. The implementation of seawater electrolysis requires robust and efficient electrocatalysts that can sustain seawater splitting without chloride corrosion, especially for the anode. Here we report a three-dimensional core-shell metal-nitride catalyst consisting of NiFeN nanoparticles uniformly decorated on NiMoN nanorods supported on Ni foam, which serves as an eminently active and durable oxygen evolution reaction catalyst for alkaline seawater electrolysis. Combined with an efficient hydrogen evolution reaction catalyst of NiMoN nanorods, we have achieved the industrially required current densities of 500 and 1000 mA cm⁻² at record low voltages of 1.608 and 1.709 V, respectively, for overall alkaline seawater splitting at 60 °C. This discovery significantly advances the development of seawater electrolysis for large-scale hydrogen production.

Developing highly active and low-cost electrocatalysts with superior durability for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is a grand challenge to produce hydrogen by electrolysis of water. Here, we report on a facile and scalable approach to fabricate highly efficient three-dimensional (3D) bulk catalysts of core–shell nanostructures, in which few-layer NiFe layered double hydroxide (LDH) nanosheets are grown on Cu nanowire cores supported on Cu foams, toward overall water splitting. Remarkably, benefiting from the 3D hierarchical nanoarchitecture with large surface areas, fast electron transport, and open-channels for effective gas release, the resulting 3D self-standing catalysts exhibit outstanding OER activity as well as excellent HER performance in an alkaline medium. Using them as bifunctional catalysts for overall water splitting, a current density of 10 mA cm⁻² was achieved at a voltage of 1.54 V, and 100 mA cm⁻² at 1.69 V with excellent durability, which is much better than the benchmark of IrO₂(+)//Pt(−) electrodes. Our 3D core–shell electrocatalysts significantly advance the research towards large-scale practical water electrolysis.

Water electrolysis is an advanced energy conversion technology to produce hydrogen as a clean and sustainable chemical fuel, which potentially stores the abundant but intermittent renewable energy sources scalably. Since the overall water splitting is an uphill reaction in low efficiency, innovative breakthroughs are desirable to greatly improve the efficiency by rationally designing non-precious metal-based robust bifunctional catalysts for promoting both the cathodic hydrogen evolution and anodic oxygen evolution reactions. We report a hybrid catalyst constructed by iron and dinickel phosphides on nickel foams that drives both the hydrogen and oxygen evolution reactions well in base, and thus substantially expedites overall water splitting at 10 mA cm⁻² with 1.42 V, which outperforms the integrated iridium (IV) oxide and platinum couple (1.57 V), and are among the best activities currently. Especially, it delivers 500 mA cm⁻² at 1.72 V without decay even after the durability test for 40 h, providing great potential for large-scale applications.

Developing energy- and time-saving methods to synthesize active and stable oxygen evolving catalysts is of great significance to hydrogen production from water electrolysis, which however remains a grand challenge. Here we report a one-step approach to grow highly porous S-doped Ni/Fe (oxy)hydroxide catalysts on Ni foam in several minutes under room temperature. This ultrafast method effectively engineers the surface of Ni foam into a rough S-doped Ni/Fe (oxy)hydroxide layer, which has multiple levels of porosity and good hydrophilic features and exhibits extraordinary oxygen evolution reaction (OER) performance in both alkaline salty water and seawater electrolytes. Specifically, the S-doped Ni/Fe (oxy)hydroxide catalyst requires low overpotentials of 300 and 398 mV to deliver current densities of 100 and 500 mA cm⁻², respectively, when directly used as an OER catalyst in alkaline natural seawater electrolyte. Using this OER catalyst together with an efficient hydrogen evolution reaction catalyst, we have achieved the commercially demanded current densities of 500 and 1000 mA cm⁻² at low voltages of 1.837 and 1.951 V, respectively, for overall alkaline seawater electrolysis at room temperature with very good durability. This work affords a cost-efficient surface engineering method to steer commercial Ni foam into robust OER catalysts for seawater electrolysis, which has important implications for both the hydrogen economy and environmental remediation.

Thrifty thermoelectric cooling: Currently available thermoelectric devices for cooling rely on expensive bismuth telluride. Mao et al. systematically developed a far less expensive n-type magnesium-bismuth–based material with good thermoelectric properties. They built a device that could generate a temperature difference of up to 90 kelvin when coupled with a commercially available p-type material. Such materials should provide an excellent basis for cost-effective thermoelectric cooling technology. Science , this issue p. 495