Single-atom electrocatalysts (SAEs) can realize the target of low-cost by maximum atomic efficiency. However, they usually suffer performance decay due to high energy states, especially in a harsh acidic water splitting environment. Here, we conceive and realize a double protecting strategy that ensures robust acidic water splitting on Ir SAEs by dispersing Ir atoms in/onto Fe nanoparticles and embedding IrFe nanoparticles into nitrogen-doped carbon nanotubes (Ir-SA@Fe@NCNT). When Ir-SA@Fe@NCNT acts as a bifunctional electrocatalyst at ultralow Ir loading of 1.14 μg cm −2 , the required overpotentials to deliver 10 mA cm −2 are 250 and 26 mV for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in 0.5 M H 2 SO 4 electrolyte corresponding to 1370-and 61-fold better mass activities than benchmark IrO 2 and Pt/C at an overpotential of 270 mV, respectively, resulting in only 1.51 V to drive overall water splitting. Moreover, remarkable stability is also observed compared to Pt/ C-IrO 2 .

A palladium phosphide electrocatalyst supported on carbon black (PdP2@CB) shows efficient water splitting in both alkaline and neutral electrolytes. Significantly lower overpotentials are required for PdP2@CB (27.5 mV in 0.5 m H2SO4; 35.4 mV in 1 m KOH; 84.6 mV in 1 m PBS) to achieve a HER electrocatalytic current density of 10 mA cm−2 compared to commercial Pt/CB (30.1 mV in 0.5 m H2SO4; 46.6 mV in 1 m KOH; 122.7 mV in 1 m PBS). Moreover, no loss in HER activity is detectable after 5000 potential sweeps. Only 270 mV and 277 mV overpotentials are required to reach a current density of 10 mA cm−2 for PdP2@CB to catalyze OER in 1 m KOH and 1 m PBS electrolytes, which is better OER activity than the benchmark IrO2 electrocatalyst (301 mV and 313 mV to drive a current density of 10 mA cm−2). 1.59 V and 1.72 V are needed for PdP2@CB to achieve stable water splitting catalytic current density of 10 mA cm−2 in 1 m PBS and 50 mA cm−2 in 1 m KOH for 10 h, respectively.

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Two-dimensional Mo/Mo 2 C heteronanosheets (Mo/ Mo 2 C-HNS) were successfully prepared via a NaCl template-assisted synthesis route followed by a controllable simultaneous reduction and carbonization of MoO 3 nanosheets for efficient hydrogen evolution reaction (HER) catalysis under both acidic and alkaline conditions. The Mo species in the atomically thin Mo/Mo 2 C-HNS not only guarantees the rapid transport of electrons but also optimizes the electronic configuration of β-Mo 2 C. Besides, the abundant Mo/β-Mo 2 C heterointerfaces in nanodimension afford large numbers of additional heterogeneous catalytic sites. HER electrocatalytic performance with overpotential of merely 89 mV to drive a current density of 10 mA/cm 2 in 0.5 M H 2 SO 4 is therefore achieved. Strikingly, stable chronoamperometric electrolysis for 20 h and also an impressive cycling stability with negligible overpotential decay over 4000 sweeps demonstrate its considerable durability in an acidic environment. These findings highlight the promising potential of Mo/Mo 2 C-HNS catalyst as an efficient and stable noble metal-free electrocatalyst toward the HER.

The ultra-stable highly efficient HER over a wide pH range on defect-rich MoN nanosheets synthesized using a modified salt-template process.

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The design and fabrication of a highly-durable and carbon monoxide (CO) tolerant catalyst for direct methanol fuel cells (DMFCs) is highly required since the DMFCs are promising power sources in the near future. Here we describe the finding that a fuel cell catalyst composed of carbon black, poly[2,2'-(2,6-pyridine)-5,5'-bibenzimidazole] and platinum that was coated by a polymer acid, poly(vinylphosphonic acid), shows a high durability and CO tolerance in the methanol oxidation reaction, which have been revealed by electrochemical methods together with a transmission electron microscopy study.