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Conductive porous materials having a high surface reactivity offer great promise for a broad range of applications. However, a general and scalable synthesis of such materials remains challenging. In this work, the facile synthesis of catalytic metal nanoparticles (NPs) embedded in 2D metal–organic frameworks (MOFs) is reported as highly active and conductive porous materials. After the assembly of 2D conductive MOFs (C‐MOFs), i.e., Cu3(hexahydroxytriphenylene)2 [Cu3(HHTP)2], Pd or Pt NPs are functionalized within the cavities of C‐MOFs by infiltration of metal ions and subsequent reduction. The unique structure of Cu3(HHTP)2 with a cavity size of 2 nm confines the bulk growth of metal NPs, resulting in ultra‐small (≈2 nm) and well‐dispersed metal NPs loaded in 2D C‐MOFs. The Pd or Pt NPs‐loaded Cu3(HHTP)2 exhibits remarkably improved NO2 sensing performance at room temperature due to the high reactivity of catalytic metal NPs and the high porosity of C‐MOFs. The catalytic effect of Pd and Pt NPs on NO2 sensing of Cu3(HHTP)2, in terms of reaction rate kinetics and activation energy, is demonstrated. [ABSTRACT FROM AUTHOR]

Single-crystal nanocrystals of catalytic metals and oxides are essential for understanding chemical interactions on well-defined catalyst surfaces. However, a comprehensive understanding of the crystallographic origins for such enhancement has been lacking. This work provides formal evidence of the structure–property relationship through a model study on single-crystal TiO 2. Our approach involves transient pulse heating to manipulate porosity and phase in epitaxially-grown TiO 2 nanosheets along the (0 0 1) plane. Furthermore, we could introduce high-entropy alloy nanoparticles into the system, which exhibited excellent catalytic activity toward CO oxidation, achieving T 90 at 143 °C. This improved performance is attributed to the interplay between the catalytic nanoparticles and the multiphase support, facilitating CO and O 2 adsorption. Our study contributes to a fundamental understanding of structure–property relationships in heterogeneous catalyst systems. Overall, our thermal shock synthesis approach shows much promise for developing single crystal-based advanced nanocatalysts with broad practical implications. [ABSTRACT FROM AUTHOR]

The lack of bifunctional features of perovskite oxide toward the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) significantly limits its use as a cathode catalyst for rechargeable Zn–air batteries (ZABs). Thus far, numerous techniques to disperse additional catalysts on a perovskite host have been suggested to overcome this problem; however, cost-effectiveness and catalyst lifespan remain unsatisfactory. Herein, we present cobalt-based-nanoparticle-decorated Sr 0.95 Nb 0.1 Co 0.7 Fe 0.2 O 3–δ (S0.95NCF) by a simple ex-solution method and use it as a novel air-electrode catalyst. We successfully implemented the socketed nanoparticles with various compositions at different reduction temperatures, achieving notably enhanced activity towards OER and ORR. More importantly, the newly designed catalyst exhibits record-high charge/discharge durability over 500 h (or 1500 consequent cycles) when used as the ZABs cathode. Our findings provide essential guidelines for designing heterostructured electrocatalysts for future energy devices, in which multifunctionality is desirable. [Display omitted] • Ex-solution is applied to Sr 0.95 Nb 0.1 Co 0.7 Fe 0.2 O 3 –δ at various reduction temperatures. • The exsolved metals are elaborately explored depending on ex-solution conditions. • CoFe-nanoalloy ex-solution enhances electrochemical performances for OER and ORR. • The designed catalyst exhibits record-high durability for the Zinc-air batteries. [ABSTRACT FROM AUTHOR]