The direct dehydrogenation of alkanes to olefins under mild conditions is challenging due to the inert nature of alkyl C─H bonds. Herein, an efficient photocatalytic system is developed for propane direct dehydrogenation (PDH) to propylene, consisting of ≈1.30 nm sized PtO clusters immobilized on a layered double hydroxide -derived ZnO/AlO support (LD-Pt).
View Article and Find Full Text PDFLithium (Li) metal batteries (LMBs) are promising for high-energy-density rechargeable batteries. However, Li dendrites formed by the reaction between highly active Li and non-aqueous electrolytes lead to safety concerns and rapid capacity decay. Developing a reliable solid-electrolyte interphase is critical for realizing high-rate and long-life LMBs, but remains technically challenging.
View Article and Find Full Text PDFCarbon nanomaterials show outstanding promise as electrocatalysts for hydrogen peroxide (HO) synthesis via the two-electron oxygen reduction reaction. However, carbon-based electrocatalysts that are capable of generating HO at industrial-level current densities (>300 mA cm) with high selectivity and long-term stability remain to be discovered. Herein, few-layer boron nanosheets are in-situ introduced into a porous carbon matrix, creating a metal-free electrocatalyst (B-C) with HO production rates of industrial relevance in neutral or alkaline media.
View Article and Find Full Text PDFHerein, conductive polyaniline (PANI) was chemically polymerized on the surface of a bismuth-based metal-organic framework (Bi-MOF) to form conductive PANI@Bi-MOF composites. FT-IR and PXRD measurements verified the successful production of PANI@Bi-MOF, whereas SEM, TEM, and EDAX mapping demonstrated that PANI was uniformly coated on the surface of Bi-MOF. The resulting PANI@Bi-MOF composites were characterized by cyclic voltammetry (CV and electrochemical impedance spectroscopy (EIS), then used to develop a sensitive electrochemical sensor for the detection of lead ions based on differential pulse anodic stripping voltammetry (DPASV).
View Article and Find Full Text PDFElectrochemical activation of dinitrogen (N) is notoriously challenging, typically yielding very low ammonia (NH) production rates. In this study, we present a continuous flow plasma-electrochemical reactor system for the direct conversion of nitrogen from air into ammonia. In our system, nitrogen molecules are first converted into a mixture of NO species in the plasma reactor, which are then fed into an electrochemical reactor.
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