Hydrophobic TaOx Species Overlayer Tuning Light-Driven Methane Chlorination with Inorganic Chlorine.

Halogenated methane serves as a universal platform molecule for building high-value chemicals. Utilizing sodium chloride solution for photocatalytic methane chlorination presents an environmentally friendly method for methane conversion. However, competing reactions in gas-solid-liquid systems leads to low efficiency and selectivity in photocatalytic methane chlorination. Here, an in situ method is employed to fabricate a hydrophobic layer of TaOx species on the surface of NaTaO3. Through in-situ XPS and XANES spectra analysis, it is determined that TaOx is a coordination unsaturated species. The TaOx species transforms the surface properties from the inherent hydrophilicity of NaTaO3 to the hydrophobicity of TaOx/NaTaO3, which enhances the accessibility of CH4 for adsorption and activation, and thus promotes the methane chlorination reaction within the gas-liquid-solid three-phase system. The optimized TaOx/NaTaO3 photocatalyst has a good durability for multiple cycles of methane chlorination reactions, yielding CH3Cl at a rate of 233 µmol g-1 h-1 with a selectivity of 83%. In contrast, pure NaTaO3 exhibits almost no activity toward CH3Cl formation, instead catalyzing the over-oxidation of CH4 into CO2. Notably, the activity of the optimized TaOx/NaTaO3 photocatalyst surpasses that of reported noble metal photocatalysts. This research offers an effective strategy for enhancing the selectivity of photocatalytic methane chlorination using inorganic chlorine ions.

Construction of Co1-xZnxFe2xGa2-2xO4 (02 Reduction by H2O Vapour.

Solid solutions are garnering substantial attention in the realm of solar energy utilization due to their tunable electronic properties, encompassing band edge positions and charge-carrier mobilities. In this study, we designed and synthesized Co1-xZnxFe2xGa2-2xO4 (0

Enhancing Photocatalytic Activities for Sustainable Hydrogen Evolution on Structurally Matched CuInS2/ZnIn2S4 Heterojunctions.

Effective charge separation and migration pose a critical challenge in the field of solar-driven hydrogen production. In this work, a Z-scheme structured CuInS2/ZnIn2S4 heterojunction was successfully fabricated through a two-step hydrothermal synthesis method to significantly enhance the efficiency of solar-to-hydrogen energy conversion. Structural characterization revealed that the lattice-matched CuInS2/ZnIn2S4 heterojunction exhibits an enlarged interfacial contact area, which facilitates the transfer and separation of photogenerated charges. Microscopic analysis indicated that the CuInS2/ZnIn2S4 composite material has a tightly interwoven interface and a morphology resembling small sugar cubes. Photoelectrochemical spectroscopy analysis demonstrated that the heterojunction structure effectively enhances visible light absorption and charge separation efficiency, leading to an improvement in photocatalytic activity. Hydrogen production experimental data indicated that the CuInS2/ZnIn2S4 heterojunction photocatalyst prepared with a CuInS2 content of 20 wt% exhibits the highest hydrogen evolution rate, reaching 284.9 µmol·g-1·h-1. Moreover, this photocatalyst maintains robust photocatalytic stability even after three consecutive usage cycles. This study demonstrated that the Z-scheme CuInS2/ZnIn2S4 heterojunction photocatalyst exhibits enhanced hydrogen evolution efficiency, offering an effective structural design for harnessing solar energy to obtain hydrogen fuel. Therefore, this heterojunction photocatalyst is a promising candidate for practical applications in solar hydrogen production.

The Synergistic Effect in CdS/g-C3N4 Nanoheterojunctions Improves Visible Light Photocatalytic Performance for Hydrogen Evolution Reactions.

This study focuses on the development of heterojunction photocatalysts for the efficient utilization of solar energy to address the energy crisis and reduce environmental pollution. Cadmium sulfide (CdS)/graphite-type carbon nitride (g-C3N4) nanocomposites were synthesized using a hydrothermal method, and their photoelectrochemical properties and photocatalytic performance for hydrogen evolution reaction (HER) were characterized. Scanning electron microscope images showed the intimate interface and caviar-like nanoheterojunction of the CdS nanoparticles on g-C3N4 nanospheres, suggesting their potential involvement in the photocatalytic process. Electrochemical and spectroscopic analyses were conducted to confirm the roles of CdS in the nanoheterojunction. The results showed that 10 wt% CdS/g-C3N4 nanospheres exhibited higher photocatalytic activity than pure g-C3N4 under visible light irradiation. A HER rate of 655.5 µmol/g/h was achieved after three photocatalytic cycles, signifying good photocatalytic stability. The synergistic effect of the Z-scheme heterojunction formed by g-C3N4 and CdS was identified as the main factor responsible for the enhanced photocatalytic performance and stability. The interface engineering effect of CdS/g-C3N4 facilitated the separation of photogenerated electrons and holes. This study provides insights into the design and fabrication of efficient HER photocatalysts.

Molecular Dipole-Induced Photoredox Catalysis for Hydrogen Evolution over Self-Assembled Naphthalimide Nanoribbons.

D-π-A type 4-((9-phenylcarbazol-3-yl)ethynyl)-N-dodecyl-1,8-naphthalimide (CZNI) with a large dipole moment of 8.49 D and A-π-A type bis[(4,4'-1,8-naphthalimide)-N-dodecyl]ethyne (NINI) with a negligible dipole moment of 0.28 D, were smartly designed and synthesized to demonstrate the evidence of a molecular dipole as the dominant mechanism for controlling charge separation of organic semiconductors. In aqueous solution, these two novel naphthalimides can self-assemble to form nanoribbons (NRs) that present significantly different traces of exciton dissociation dynamics. Upon photoexcitation of NINI-NRs, no charge-separated excitons (CSEs) are formed due to the large exciton binding energy, accordingly there is no hydrogen evolution. On the contrary, in the photoexcited CZNI-NRs, the initial bound Frenkel excitons are dissociated to long-lived CSEs after undergoing ultrafast charge transfer within ca. 1.25 ps and charge separation within less than 5.0 ps. Finally, these free electrons were injected into Pt co-catalysts for reducing protons to H2 at a rate of ca. 417 µmol h-1 g-1 , correspondingly an apparent quantum efficiency of ca. 1.3 % can be achieved at 400 nm.

One-Pot Fabrication of Pd Nanoparticles@Covalent-Organic-Framework-Derived Hollow Polyamine Spheres as a Synergistic Catalyst for Tandem Catalysis.

Facile fabrication of nanocatalysts consisting of metal nanoparticles (NPs) anchored on a functional support is highly desirable, yet remains challenging. Covalent organic frameworks (COFs) provide an emerging materials platform for structural control and functional design. Here, a facile one-pot in situ reduction approach is demonstrated for the encapsulation of small Pd NPs into the shell of COF-derived hollow polyamine spheres (Pd@H-PPA). In the one-pot synthetic process, the nucleation and growth of Pd NPs in the cavities of the porous shell take place simultaneously with the reduction of imine linkages to secondary amine groups. Pd@H-PPA shows a significantly enhanced catalytic activity and recyclability in the tandem dehydrogenation of ammonia borane and selective hydrogenation of nitroarenes through an adsorption-activation-reaction mechanism. The strong interactions of the secondary amine linkage with borane and nitroarene molecules afford a positive synergy to promote the catalytic reaction. Moreover, the hierarchical structure of Pd@H-PPA allows the accessibility of active Pd NPs to reactants.

Visible-Light Driven Overall Conversion of CO2 and H2O to CH4 and O2 on 3D-SiC@2D-MoS2 Heterostructure.

A marigold-like SiC@MoS2 nanoflower with a unique Z-scheme structure efficiently achieves the overall conversion of gas phase CO2 with H2O (CO2 (g) + 2H2O (g) = CH4 + 2O2) without any sacrificial reagents under visible light (λ ≥ 420 nm) irradiation. The CH4 and O2 evolution are 323 and 621 µL·g-1·h-1, and stable throughout 5 cycle reactions of total 40 h. This work demonstrates a breakthrough in artificial photosynthesis with the Z-scheme 1D heterojunction constructed by combining 2D semiconductor and 3D semiconductor based on the transfer balance of photogenerated electron and hole.

Quaternary Layered Semiconductor Ba2Cr4GeSe10: Synthesis, Crystal Structure, and Thermoelectric Properties.

A quaternary narrow-band-gap semiconductor, Ba2Cr4GeSe10, has been discovered by solid-state reaction. It features a new structure type and crystallizes in the triclinic space group P1̅ (No. 2). The featured 2D anionic layers are constructed by condensed CrSe6 octahedra that are stacking along the c axis, with dispersed GeSe4 tetrahedra and located Ba2+ cations forming these layers. The energy-band structure shows a clear separation between the region of electronic conduction and the zone of electronic insulation. Significantly, an undoped Ba2Cr4GeSe10 sample shows a desirable low thermal conductivity κT (0.51-0.87 W/m·K) and a high Seebeck coefficient S (351-404 µV/K) and reaches a ZT ≈ 0.08 at 773 K.

Concerted Rattling in CsAg5 Te3 Leading to Ultralow Thermal Conductivity and High Thermoelectric Performance.

Thermoelectric (TE) materials convert heat energy directly into electricity, and introducing new materials with high conversion efficiency is a great challenge because of the rare combination of interdependent electrical and thermal transport properties required to be present in a single material. The TE efficiency is defined by the figure of merit ZT=(S(2) σ) T/κ, where S is the Seebeck coefficient, σ is the electrical conductivity, κ is the total thermal conductivity, and T is the absolute temperature. A new p-type thermoelectric material, CsAg5 Te3 , is presented that exhibits ultralow lattice thermal conductivity (ca. 0.18 Wm(-1) K(-1) ) and a high figure of merit of about 1.5 at 727 K. The lattice thermal conductivity is the lowest among state-of-the-art thermoelectrics; it is attributed to a previously unrecognized phonon scattering mechanism that involves the concerted rattling of a group of Ag ions that strongly raises the Grüneisen parameters of the material.

Supercubooctahedron (Cs6Cl)2Cs5[Ga15Ge9Se48] Exhibiting Both Cation and Anion Exchange.

A novel type of supertetrahedral connectivity is exhibited by the 72-atom discrete supercubooctahedron in (Cs6Cl)2Cs5[Ga15Ge9Se48] (1), which undergoes both cation and anion exchange, as revealed by unambiguous single-crystal X-ray diffraction data. Electronic-structure studies helped to understand the Ge/Ga distribution.

Superionic adjustment leading to weakly temperature-dependent ZT values in bulk thermoelectrics.

Thermoelectric (TE) materials are of worldwide interest for energy sustainability through direct waste-heat-to-electricity conversion. Practically, a TE power generator requires a large working temperature gradient; to achieve high efficiency, key TE materials with high ZT values are necessary and, furthermore, their ZT values should decline as little as possible over the imposed temperature range. Unfortunately, sharp ZT declines in all of the known materials are inevitable. Here we found the bulk superionic α-Ag(1-x)CuSe material exhibits unusual weakly temperature-dependent ZT values in the range of 480-693 K with the smallest ZT-T slope known to date. These result from the Seebeck coefficient balance of the countercontributions of holes and electrons and the weakly temperature-dependent thermal conductivity.

Syntheses, Characterization, and Optical Properties of Centrosymmetric Ba3(BS3)1.5(MS3)0.5 and Noncentrosymmetric Ba3(BQ3)(SbQ3).

The most advanced UV-vis and IR NLO materials are usually borates and chalcogenides, respectively. But thioborates, especially thio-borometalates, are extremely rare. Here, four new such compounds are discovered by solid state reactions representing 0D structures constructed by isolated BQ3 trigonal planes and discrete MQ3 pyramids with Ba(2+) cations filling among them, centrosymmetric monoclinic P21/c Ba3(BS3)1.5(MS3)0.5 (M = Sb, Bi) 1, 2 with a = 12.9255(9), 12.946(2) Å; b = 21.139(2), 21.170(2)Å; c = 8.4194(6), 8.4207(8) Å; ß = 101.739(5), 101.688(7)°; V = 2252.3(3), 2259.9(3) Å(3) and noncentrosymmetric hexagonal P6̅2m Ba3(BQ3)(SbQ3) (Q = S, Se) 3, 4 with a = b = 17.0560(9), 17.720(4) Å; c = 10.9040(9), 11.251(3) Å; V = 2747.1(3), 3060(2) Å(3). 3 exhibits the strongest SHG among thioborates that is about three times that of the benchmark AgGaS2 at 2.05 µm. 1 and 3 also show an interesting structure relationship correlated to the size mismatching of the anionic building units that can be controlled by the experimental loading ratio of B:Sb. Syntheses, structure characterizations, and electronic structures based on the density functional theory calculations are reported.

Chemical modification and energetically favorable atomic disorder of a layered thermoelectric material TmCuTe2 leading to high performance.

Thermoelectric (TE) materials have continuously attracted interest worldwide owing to their capability of converting heat into electricity. However, discovery and design of new TE material system remains one of the greatest difficulties. A TE material, TmCuTe2 , has been designed by a substructure approach and successfully synthesized. The structure mainly features CuTe4 -based layers stacking along the c axis that are separated by Tm(3+) cations. Such an intrinsic Cu site vacancy structure undergoes a first-order phase transition at around 606 K driven by the energetically favorable uniform Cu atom re-distribution on the covalent CuTe4 -based layer substructure, as shown by crystal structure simulations and variable-temperature XRD data. Featured with very low thermal conductivity (ca. 0.6 W m(-1) K(-1) ), large Seebeck coefficient (+185 µV K(-1) ), and moderate electrical conductivity (220 S cm(-1) ), TmCuTe2 has a maximum ZT of 0.81 at 745 K, which is nine times higher than the value of 0.09 for binary Cu2 Te, thus making it a promising candidate for mid-temperature TE applications. Theoretical studies uncover the electronic structure modifications from the metallic Cu2 Te to the narrow gap semiconductor TmCuTe2 that lead to such a remarkable performance enhancement.

Electron-deficient telluride Cs3Cu20Te13 with sodalite-type network: syntheses, structures, and physical properties.

The first sodalite-type telluride, Cs3Cu20Te13, has been successfully synthesized by solid-state reactions. The single-crystal X-ray diffraction data reveal its cubic symmetry and lattice parameters of a = 14.7557(6) Å, V = 3212.8(2) Å(3), and Z = 4. The three-dimensional network is constructed by (CuTe)12 tetrakaidecahedra centered by different guest species (either a Cs(+) or a Te(2-)@Cu8 cube) extending in a 2 × 2 × 2 supercell with respect to the conventional sodalite. Density functional theory analysis uncovers the unique feature of the p-type metallic sodalite framework accommodating anionic guest species, which agrees well with the experimental metallic electrical conductivity and Pauli paramagnetism.

A ferrimagnetic Zintl phase Pr4MnSb9: synthesis, structure, and physical properties.

A new valence precise Zintl phase, Pr4MnSb9, has been successfully synthesized by solid-state reaction at high temperature. The single-crystal X-ray diffraction data reveal its monoclinic symmetry in the space group C2/m (No. 12) with a = 24.12(2) Å, b = 4.203(3) Å, c = 15.67(2) Å, ß = 98.05(1)°, and Z = 4. The structure is characterized by the covalent three-dimensional network constructed by two types of five-atom-wide Sb5(7-) ribbons that are joined by 6-fold coordinated Mn(3+) cations, through which the narrower three-atom-wide Sb3(5-) ribbons are attached as a tag, and interstitial Pr(3+) cations and single Sb(3-) anions locate within the tunnels. Its magnetic susceptibility and isothermal hysteresis suggest ferrimagnetic behavior. The electrical conductivity and Seebeck coefficient of the cold-pressed pellet suggest a semimetal feature that agrees with the spin-polarized calculation results using the tight-binding linear muffin-tin orbital (TB-LMTO) method.

Quaternary supertetrahedra-layered telluride CsMnInTe3: why does this type of chalcogenide tilt?

Dark-red CsMnInTe3 is synthesized by a solid-state approach using CsCl as the reactive flux. This layered compound is constructed by T3 supertetrahedra and crystallizes in the space group C2/c with a = 12.400(7) Å, b = 12.400(7) Å, c = 24.32(2) Å, ß = 97.31(2)°, and V = 927.07(6) Å(3). The electrostatic interactions cause tilting of the supertetrahedra layers, and the value of the tilting angle is fixed by a structure index, ß' = 180° - arccos(a/4c). Such an index is valid for all of the members in this family known to date.

Metal to non-metal sites of metallic sulfides switching products from CO to CH4 for photocatalytic CO2 reduction.

The active center for the adsorption and activation of carbon dioxide plays a vital role in the conversion and product selectivity of photocatalytic CO2 reduction. Here, we find multiple metal sulfides CuInSnS4 octahedral nanocrystal with exposed (1 1 1) plane for the selectively photocatalytic CO2 reduction to methane. Still, the product is switched to carbon monoxide on the corresponding individual metal sulfides In2S3, SnS2, and Cu2S. Unlike the common metal or defects as active sites, the non-metal sulfur atom in CuInSnS4 is revealed to be the adsorption center for responding to the selectivity of CH4 products. The carbon atom of CO2 adsorbed on the electron-poor sulfur atom of CuInSnS4 is favorable for stabilizing the intermediates and thus promotes the conversion of CO2 to CH4. Both the activity and selectivity of CH4 products over the pristine CuInSnS4 nanocrystal can be further improved by the modification of with various co-catalysts to enhance the separation of the photogenerated charge carrier. This work provides a non-metal active site to determine the conversion and selectivity of photocatalytic CO2 reduction.

Fabrication of 2H/3C-SiC heterophase junction nanocages for enhancing photocatalytic CO2 reduction.

The morphology and structure of photocatalyst play an important role in photocatalytic activity. SiC semiconductor is considered as a promising material for the photocatalytic CO2 reduction due to its negative conduction band position. Herein, SiC nanocages is creatively synthesized by simple low-temperature molten-salt-mediated magnesiothermic reduction method with using SiO2 as template. The morphology and phase composition of SiC nanocages can be controlled by magnesium dosage and reaction temperature. The 2H and 3C crystal phase in SiC nanocage can form heterophase junctions uniformly to effectively accelerate the photogenerated electron transfer, and plays a key role in improving the photocatalytic activity of 2H/3C-SiC samples. The optimal SiC nanocage sample possesses a CO generation rate of 4.68 µmol g-1h-1 for photocatalytic CO2 reduction, which is 3.25 times higher than that of commercial SiC.

Self-assembly of Ni2P/γ-Ga2O3 nanosheets for efficient photocatalytic water splitting hydrogen production.

The development of photocatalysts enabling stable and highly efficient water splitting hydrogen production remains an open challenge in the field of energy photocatalysis. Herein, Ni2P/γ-Ga2O3 nanosheets have been reported as excellent water splitting photocatalysts. Ni2P particles and γ-Ga2O3 nanosheets were synthesized by a facile hydrothermal process. The Ni2P/γ-Ga2O3 samples were prepared by an electrostatic self-assembly method with Ni2P particles and γ-Ga2O3 nanosheets as precursors. The 0.5 wt% Ni2P/γ-Ga2O3 sample shows a photocatalytic H2-production activity as high as 2.7 mmol g-1 h-1 in pure water and 12 mmol g-1 h-1 in an aqueous methanol solution under a 125 W high pressure mercury lamp, respectively, which are much higher than those of pure γ-Ga2O3 and Pt/γ-Ga2O3 nanosheets modified with a comparable Pt content. The Ni2P component plays a role as an electron collector that promotes efficient separation of photogenerated electrons and holes, and thereby improves the efficiency of photocatalytic hydrogen production. The effects of inorganic and organic sacrificial reagents on the reaction efficiency and stability were observed and discussed. This work shows that Ni2P as a cocatalyst substituting noble metals can greatly improve the photocatalytic hydrogen production efficiency of γ-Ga2O3 compared to that in pure water and a methanol-water solution.

Photochemistry of Nitrate Ion: Reduction by Formic Acid under UV Irradiation.

Mutual transformations of various nitrogen compounds and their reaction mechanisms have been a subject of great concern to the chemical, ecological and environmental communities. In the paper, the reactions of NO 3 - ion with small organic acids such as formic acid (HCOOH), acetic acid (CH3 COOH) and lactic acid (C3 H6 O3 ) under ultraviolet illumination were investigated systematically. It was found that NO 3 - ion is easily reduced into NO 2 - and NOx and then further into N2 and NH3 (in the form of NH 4 + ) in the process. The carboxyl anion radicals and hydrogen formed by photodecomposition of formic acid are responsible for the rapid photoreduction reaction of nitrate. The initial pH and the nitrate concentration considerably affect the product distribution and nitrate conversion. Based on a preliminary simulation study, we speculated that the photoinduced reaction may effectively proceed in oceans, lakes and rivers because of ever-increasing nitrate and organic emissions. This research is helpful to understand nitrogen cycle mechanism and develop water environmental control technologies.