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Solar-driven conversion of bicarbonate (HCO3−) to carbonaceous fuels and/or chemicals provides an alternative route for the development of sustainable carbon economies. However, promoting the HCO3− reduction rate and tuning product selectivity remain significant challenges. This study reports the identification of isolated Ni/Cu atomic pairs dispersed on a BiOCl surface (Ni1/Cu1-BOC) as a promising candidate for efficient HCO3− reduction under UV-vis light irradiation. The optimized photocatalyst exhibits a high CO formation rate of 157.1 μmol g−1 h−1 with nearly 100% selectivity, even in the absence of added proton sources, sacrificial agents, or sensitizers. Experimental and theoretical investigations reveal that the atomically dispersed Ni/Cu pairs facilitate the protonation of HCO3− to CO2, which then undergoes a H+-assisted reduction pathway to produce CO, with *COOH as the intermediate. The synergistic effects of the Ni/Cu atomic pairs simultaneously promote the HCO3−-to-CO2 conversion and the subsequent CO2-to-CO reduction, providing valuable insights for the development of efficient diatomic catalysts for photocatalytic HCO3− reduction reactions. [ABSTRACT FROM AUTHOR]

The key means to improve the performance of lithium–sulfur batteries (LSBs) is to reduce the internal resistance by building an electronic/ionic pathway and to accelerate the conversion kinetics of lithium polysulfides (LiPSs) through modulation of interface functions. Herein, inspired by a grass root system, a flexible hierarchical CNF‐CNT (carbon nanofiber‐carbon nanotube) membrane decorated with Co‐doped NiS2 nanoparticles (Co‐NiS2@CNF‐CNT) is designed as an interlayer for LSBs, in which the in situ grown CNTs (root hairs) are wound on CNF (roots). Density functional theory (DFT) calculations show that Co doping introduces electron‐deficient regions at the doping sites in NiS2, thus improving chemical adsorption and catalytic activities toward LiPSs. The cell pairs with the Co‐NiS2@CNF‐CNT interlayer exhibit a high rate performance of 951.4 mAh g−1 at 3 C, a reversible capacity of 944.1 mAh g−1 after 500 cycles at 0.2 C, and a prolonged cycle life of 3000 cycles at 5 C. More importantly, an areal capacity of 7.96 mAh cm−2 is achieved with a sulfur loading of 9.6 mg cm−2. This work provides a strategy for enhancing the electrochemical performance of LSBs by combining 3D hierarchical conductive skeletons and electron‐deficient functional adsorption and catalysis materials. [ABSTRACT FROM AUTHOR]

The decay of lithium–sulfur (Li–S) batteries is mainly due to the shuttle effect caused by intermediate polysulfides (LiPSs). Herein, a multiple confined cathode architecture is prepared by filling graphitized Pinus sylvestris with carbon nanotubes and defective LaNiO3−x (LNO‐V) nanoparticles. The composite electrode with high areal sulfur loading of 11.6 mg cm−2 shows a high areal specific capacity of 8.5 mAh cm−2 at 1 mA cm−2 (0.05 C). Both experimental results and theoretical calculations reveal that this unique structure not only provides physical restriction on LiPSs within microchannels but also offers strong chemical immobilization and catalytic conversion of LiPSs attributed to the spin density around oxygen vacancies of LaNiO3−x. These oxygen vacancies elongate the SS and LiS bonds and make them easy to break. Furthermore, the lengthwise channels derived from cytoderm restrict the transverse diffusion of polysulfides, leading to a uniform areal current and thus homogeneous lithium infiltration. This suppresses the corrosion of the lithium anode due to polysulfides confinement. The discovery of the multiple confined structure that provides chemical adsorption, fast diffusion, and catalytic conversion for polysulfides can broaden the application of biomass materials and offer a new strategy to achieve robust Li–S batteries. [ABSTRACT FROM AUTHOR]

The development of Fe single‐atom catalysts (Fe SACs) with abundant, accessible Fe sites is a key step toward enhancing the efficiency of the oxygen reduction reaction (ORR) in proton exchange membrane fuel cells (PEMFCs). In this study, Zn4O(1,4‐benzenedicarboxylate)3 (MOF‐5), which has a 3D microporous cubic structure, is used as the precursor to prepare highly‐porous carbon (denoted as C‐MOF‐5) with an ultrahigh specific surface area (2751 m2 g–1) and high external surface area (1651 m2 g–1). C‐MOF‐5 is demonstrated as an effective carbon support to yield Fe SAC‐MOF‐5 with a large amount of accessible FeNx sites (2.35 wt%). Fe SAC‐MOF‐5 delivers a half‐wave potential of 0.83 V (vs RHE) in a 0.5 m H2SO4 electrolyte, and achieves a peak power density of 0.84 W cm–2 in a 0.2 MPa H2‐O2 PEMFC. This excellent performance originates from the ultrahigh specific surface area of C‐MOF‐5 for the formation of a high density of single Fe atoms, and high external surface area for the increased exposure of active sites. This work may inspire the rational design of metal single‐atom catalysts derived from a wider range of MOF precursors with ultrahigh specific area to improve the performance of the oxygen reduction reaction in PEMFCs. [ABSTRACT FROM AUTHOR]

The photocatalytic CO2 reduction reaction (CRR) holds great promise for curbing anthropogenic CO2 emissions, though boosting photocatalyst activity and tuning product selectivity remain key priorities. Herein, isolated Ni single atoms dispersed on defect rich zirconia (Ni‐SA‐x/ZrO2) are identified as a very promising photocatalyst for CRR under Xe lamp irradiation, showing good activity and CO selectivity in the absence of added sacrificial agents or sensitizers. Due to an abundance of accessible nickel single atomic sites, the optimized photocatalyst affords CO at a rate of 11.8 µmol g−1 h−1 (92.5% selectivity). Experimental and theoretical investigations determine that the atomically dispersed Ni sites lower the energy barrier for CO2 to CO conversion via an adsorbed COOH intermediate, while also suppressing H2 desorption in the competing water splitting reaction. The Ni single atom sites thus simultaneously promote CO2 conversion and CO selectivity, thus offering valuable new insights for the future design of improved metal single‐atom catalysts for CRR. [ABSTRACT FROM AUTHOR]

The discovery of improved chemical processes for CO and CO2 hydrogenation to valuable hydrocarbon fuels and alcohols is of paramount importance for the chemical industry. Such technologies have the potential to reduce anthropogenic CO2 emissions by adding value to a waste stream, whilst also reducing our consumption of fossil fuels. Current thermal catalytic technologies available for CO and CO2 hydrogenation are demanding in terms of energy input. Various alternative technologies are now being developed for COx hydrogenation, with solar-driven processes over two-dimensional (2D) and 2D-related composite materials being particularly attractive due to the abundance of solar energy on Earth and also the high selectivity of defect-engineered 2D materials towards specific valuable products under very mild reaction conditions. This review showcases recent advances in the solar-driven COx reduction to hydrocarbons over 2D-based materials. Optimization of 2D catalyst performance demands interdisciplinary research that embraces catalyst electronic structure manipulation and morphology control, surface/interface engineering, reactor engineering and density functional theory modelling studies. Through improved understanding of the structure–performance relationships in 2D-related catalysts which is achievable through the application of modern in situ characterization techniques, practical photo/photothermal/photoelectrochemical technologies for CO and CO2 reduction to high-valuable products such as olefins could be realized in the not-too-distant future. [ABSTRACT FROM AUTHOR]

We present a surfactant-mediated approach to the production of single-crystal Bi3O4Br nanorings via a simple solvothermal method. The ring-like morphology is rare among bismuth oxyhalides, and the reaction pathways are superior to traditional chemical transformations. In detail, Bi3O4Br nanorings are prepared in three stages: (1) the formation of precursors, (2) selective etching and (3) Ostwald ripening. During these steps, the extra usage of templates is avoided and a series of useful intermediates are obtained. Besides, this method can be extended to fabricate other bismuth oxyhalide nanorings. Under visible-light irradiation, all of our samples are photo-activated. The Bi3O4Br nanorings exhibit an efficient oxygen-evolution rate (72.54 μmol h−1) and pollutant degradation rate (4.71 × 10−2 g min−1 m−2), which can be attributed to their unique ring structures and band potentials. Thus, the surfactant-mediated chemical conversion strategy not only paves a new way to enhance the photocatalytic activity of bismuth oxyhalides, but also provides an important large-scale route for designing other nanomaterials with ring-like structures. [ABSTRACT FROM AUTHOR]

Halide anion-doped bismuth terephthalate hybrids were synthesized using a facile solvothermal method. Four series of hybrids doped with halide anions X− (F−, Cl−, Br− and I−) were produced by varying the molar ratios ( n) of X− relative to Bi(NO3)3 ( n = 0.25, 0.5, 0.75 and 1) in dimethylformamide solution. The results indicated that 0.25 equiv. of different halide anion-doped bismuth terephthalate hybrids, especially BiBDC-Cl(0.25) and BiBDC-Br(0.25), exhibited excellent photocatalytic activity under visible light and UV light irradiation. They also exhibited excellent adsorption performance for Rhodamine B which could be attributed to high surface areas and negative charge on the surface of the catalysts. Moreover, the degradation of Rhodamine B under visible light irradiation is a photosensitization process and •O2− is the most important active species. The halide anion-doped bismuth terephthalate hybrids are promising photocatalysts for removal of organic pollutants. Copyright © 2016 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]