High-Affinity-Assisted Nanoscale Alloys as Remarkable Bifunctional Catalyst for Alcohol Oxidation and Oxygen Reduction Reactions.

A key challenge in developing fuel cells is the fabrication of low-cost electrocatalysts with high activity and long durability for the two half-reactions, i.e., the methanol/ethanol oxidation reaction (MOR/EOR) and the oxygen reduction reaction (ORR). Herein, we report a conductivity-enhanced bifunctional electrocatalyst of nanoscale-coated Pt-Pd alloys on both tin-doped indium (TDI) and reduced graphene oxide (rGO), denoted as Pt-Pd@TDI/rGO. The mass activities of Pt in the Pt-Pd@TDI/rGO hybrid toward MOR, EOR, and ORR are 2590, 1500, and 2690 mA/mg, respectively. The ORR Pt specific activity and mass activity of the electrocatalyst are 17 and 28 times larger, respectively, than commercial Pt/C catalysts. All these remarkable catalytic performances are attributed to the role of TDI in enhancing the catalytic activity by protecting Pt from oxidation as well as rapid mass/charge transfer due to the synergistic effect between surface Pt-Pd alloys and TDI/rGO.

Accelerated Bone Regeneration by Two-Photon Photoactivated Carbon Nitride Nanosheets.

Human bone marrow-derived mesenchymal stem cells (hBMSCs) present promising opportunities for therapeutic medicine. Carbon derivatives showed only marginal enhancement in stem cell differentiation toward bone formation. Here we report that red-light absorbing carbon nitride (C3N4) sheets lead to remarkable proliferation and osteogenic differentiation by runt-related transcription factor 2 (Runx2) activation, a key transcription factor associated with osteoblast differentiation. Accordingly, highly effective hBMSCs-driven mice bone regeneration under red light is achieved (91% recovery after 4 weeks compared to 36% recovery in the standard control group in phosphate-buffered saline without red light). This fast bone regeneration is attributed to the deep penetration strength of red light into cellular membranes via tissue and the resulting efficient cell stimulation by enhanced photocurrent upon two-photon excitation of C3N4 sheets near cells. Given that the photoinduced charge transfer can increase cytosolic Ca2+ accumulation, this increase would promote nucleotide synthesis and cellular proliferation/differentiation. The cell stimulation enhances hBMSC differentiation toward bone formation, demonstrating the therapeutic potential of near-infrared two-photon absorption of C3N4 sheets in bone regeneration and fracture healing.

Efficient CO Oxidation by 50-Facet Cu2O Nanocrystals Coated with CuO Nanoparticles.

As carbon monoxide oxidation is widely used for various chemical processes (such as methanol synthesis and water-gas shift reactions H2O + CO ⇄ CO2 + H2) as well as in industry, it is essential to develop highly energy efficient, inexpensive, and eco-friendly catalysts for CO oxidation. Here we report green synthesis of ∼10 nm sized CuO nanoparticles (NPs) aggregated on ∼400 nm sized 50-facet Cu2O polyhedral nanocrystals. This CuO-NPs/50-facet Cu2O shows remarkable CO oxidation reactivity with very high specific CO oxidation activity (4.5 µmolCO m-2 s-1 at 130 °C) and near-complete 99.5% CO conversion efficiency at ∼175 °C. This outstanding catalytic performance by CuO NPs over the pristine multifaceted Cu2O nanocrystals is attributed to the surface oxygen defects present in CuO NPs which facilitate binding of CO and O2 on their surfaces. This new material opens up new possibilities of replacing the usage of expensive CO oxidation materials.