Immobilization of Perylenetetracarboxylic Dianhydride on Al2O3 for Efficiently Photocatalytic Sulfide Oxidation.

Perylenetetracarboxylic dianhydride (PTCDA) derivatives have received significant attention as molecule photocatalysts. However, the poor recyclability of molecule-type photocatalysts hinders their widespread applications. Herein, immobilization of PTCDA on Al2O3 was achieved by simply physical mixing, which not only dramatically improved their recyclability, but also surprisingly improved the reactivity. A mechanism study suggested that the photo-exited state (PTCDA*) of PTCDA could promote the oxidation of thioanisole to generate PTCDA•-, which sequentially reduces oxygen to furnish superoxide radicals to achieve the catalytic cycle. Herein, the immobilization support Al2O3 was able to facilitate the strong adsorption of thioanisole, thereby boosting the photocatalytic activity. This work provides a new insight that the immobilization of organic molecular photocatalysts on those supports with proper adsorption sites could furnish highly efficient, stable, and recyclable molecular-based heterogeneous photocatalysts.

Photosynthesis of C-1-Deuterated Aldehydes via Chlorine Radical-Mediated Selective Deuteration of the Formyl C-H Bond.

C-1-deuterated aldehydes are essential building blocks in the synthesis of deuterated chemicals and pharmaceuticals. This has led chemists to devise mild methodologies for their efficient production. Ideally, hydrogen-deuterium exchange (HDE) is the most effective approach. However, the traditional HDE for creating C-1-deuterated aldehydes often requires a complex system involving multiple catalysts and/or ligands. In this study, we present a mild photocatalytic HDE of the formyl C-H bond with D2O. This process is facilitated by chlorine radicals that are generated in situ from low-cost FeCl3. This strategy demonstrated a broad reaction scope and high functional group tolerance, affording good yields and ≤99% D incorporation. To bridge the gap between research and industrial applications, we designed a new flow photoreactor equipped with a high-intensity light-emitting diode bucket, enabling the synthesis of C-1-deuterated aldehydes on a scale of 85 g. Finally, we successfully produced several important deuterated aldehydes that are integral to the synthesis of deuterated pharmaceuticals.

Stabilizing Few-Atom Platinum Clusters by Zinc Single-Atom-Glue for Efficient Anti-Markovnikov Alkene Hydrosilylation.

Few-atom metal clusters (FAMCs) exhibit superior performance in catalyzing complex molecular transformations due to their special spatial environments and electronic states, compared to single-atom catalysts (SACs). However, achieving the efficient and accurate synthesis of FAMCs while avoiding the formation of other species, such as nanoparticles and SACs, still remains challenges. Herein, we report a two-step strategy for synthesis of few-atom platinum (Pt) clusters by predeposition of zinc single-atom-glue (Zn1) on MgO nanosheets (Ptn-Zn1/MgO), where FAMCs can be obtained over a wide range of Pt contents (0.09 to 1.45 wt%). Zn atoms can act as Lewis acidic sites to allow electron transfer between Zn and Pt through bridging O atoms, which play a crucial role in the formation and stabilization of few-atom Pt clusters. Ptn-Zn1/MgO exhibited a high selectivity of 93% for anti-Markovnikov alkene hydrosilylation. Moreover, an excellent activity with a turnover frequency of up to 1.6 ×104 h-1 can be achieved, exceeding most of the reported Pt SACs. Further theoretical studies revealed that the Pt atoms in Ptn-Zn1/MgO possess moderate steric hindrance, which enables high selectivity and activity for hydrosilylation. This work presents some guidelines for utilizing atomic-scale species to increase the synthesis efficiency and precision of FAMCs.

Photochemical C(sp3)-H Activation for Diversity-Oriented Synthesis of 3-Functionalized Oxindoles.

Heteroatom-adjacent C(sp3) radical cyclization of N-arylacrylamides provides a straightforward pathway to synthesize valuable 3-functionalized oxindoles. Traditional cyclization reactions normally require harsh conditions or transition-metal catalysts. Here, we developed a metal-free, diversity-oriented synthesis of 3-functionalized oxindoles via photochemically induced selective cleavage of C(sp3)-H bonds. A variety of 3-substituted oxindoles with functionalities such as ethers, polyhalogens, benzyl, and formyl groups can be obtained by a rational design. This strategy is characterized by its simple operation and mild conditions, aligning well with the developmental requirements for sustainable chemistry. The gram-scale continuous-flow synthesis and efficient construction of bioactive molecules highlight its practical utility.

Atomically isolated Sb(CN)3 on sp2-c-COFs with balanced hydrophilic and oleophilic sites for photocatalytic C-H activation.

Activation of carbon-hydrogen (C-H) bonds is of utmost importance for the synthesis of vital molecules. Toward achieving efficient photocatalytic C-H activation, our investigation revealed that incorporating hydrophilic C≡N-Sb(CN)3 sites into hydrophobic sp2 carbon-conjugated covalent organic frameworks (sp2-c-COFs) had a dual effect: It simultaneously enhanced charge separation and improved generation of polar reactive oxygen species. Detailed spectroscopy measurements and simulations showed that C≡N-Sb(CN)3 primarily functioned as water capture sites, which were not directly involved in photocatalysis. However, the potent interaction between water molecules and the Sb(CN)3-modified framework notably enhanced charge dynamics in hydrophobic sp2-c-COFs. The reactive species ·O2- and ·OH (ad) subsequently combined with benzyl radical, leading to the formation of benzaldehyde, benzyl alcohol, and lastly benzyl benzoate. Notably, the Sb(CN)3-modified sp2-c-COFs exhibited a 54-fold improvement in reaction rate as compared to pristine sp2-c-COFs, which achieved a remarkable 68% conversion rate for toluene and an 80% selectivity for benzyl benzoate.

Selective Photoelectrochemical Oxidation of Glycerol to Glyceric Acid on (002) Facets Exposed WO3 Nanosheets.

Glycerol is a byproduct of biodiesel production. Selective photoelectrochemical oxidation of glycerol to high value-added chemicals offers an economical and sustainable approach to transform renewable feedstock as well as store green energy at the same time. In this work, we synthesized monoclinic WO3 nanosheets with exposed (002) facets, which could selectively oxidize glycerol to glyceric acid (GLYA) with a photocurrent density of 1.7 mA cm-2 , a 73 % GLYA selectivity and a 39 % GLYA Faradaic efficiency at 0.9 V vs. reversible hydrogen electrode (RHE) under AM 1.5G illumination (100 mW cm-2 ). Compared to (200) facets exposed WO3 , a combination of experiments and theoretical calculations indicates that the superior performance of selective glycerol oxidation mainly originates from the better charge separation and prolonged carrier lifetime resulted from the plenty of surface trapping states, lower energy barrier of the glycerol-to-GLYA reaction pathway, more abundant active sites and stronger oxidative ability of photogenerated holes on the (002) facets exposed WO3 . Our findings show great potential to significantly contribute to the sustainable and environmentally friendly chemical processes via designing high performance photoelectrochemical cell via facet engineering for renewable feedstock transformation.

Photoinduced Phosphination of Arenes Enabled by an Electron Donor-Acceptor Complex Using Thianthrenium Salts.

Herein, we describe a metal-free approach for the cross-coupling of arenes or styryl-thianthrenium salts (TTs) with diarylphosphines via an electron donor-acceptor (EDA) complex. Various tertiary phosphines were obtained with high site selectivity and good functional group tolerance. This method enables straightforward construction of C-P bonds via C-H activation of arenes and allows the late-stage functionalization of natural products or pharmaceutical molecules. Mechanistic studies support the approach involving a photoinduced EDA complex.

Atomic high-spin cobalt(II) center for highly selective electrochemical CO reduction to CH3OH.

In this work, via engineering the conformation of cobalt active center in cobalt phthalocyanine molecular catalyst, the catalytic efficiency of electrochemical carbon monoxide reduction to methanol can be dramatically tuned. Based on a collection of experimental investigations and density functional theory calculations, it reveals that the electron rearrangement of the Co 3d orbitals of cobalt phthalocyanine from the low-spin state (S = 1/2) to the high-spin state (S = 3/2), induced by molecular conformation change, is responsible for the greatly enhanced CO reduction reaction performance. Operando attenuated total reflectance surface-enhanced infrared absorption spectroscopy measurements disclose accelerated hydrogenation of CORR intermediates, and kinetic isotope effect validates expedited proton-feeding rate over cobalt phthalocyanine with high-spin state. Further natural population analysis and density functional theory calculations demonstrate that the high spin Co2+ can enhance the electron backdonation via the dxz/dyz-2π* bond and weaken the C-O bonding in *CO, promoting hydrogenation of CORR intermediates.

Charge Density Modulation of Pyrene-Related Small Molecules by Nitrogen Heteroatoms Precisely Regulates Photocatalytic Generation of Hydrogen.

Organic semiconductor materials hold promising applications in photocatalytic hydrogen evolution due to their high modifiability and wide range of light absorption capability. In this study, we present an effective strategy for promoting the separation of photoexcited electrons from organic conjugated centers to active sites by modifying different nitrogen-containing groups on pyrene molecules. Building on this foundation, the well-designed catalyst Py-m-2N has demonstrated good performance by achieving a photocatalytic hydrogen evolution rate of 48.86 mmol g-1 h-1, even in the absence of the precious metal platinum cocatalyst. This achievement places the pyrene-based photocatalyst ahead of the majority of its organic counterparts. Our comprehensive characterization and density functional theory calculations reveal that the nitrogen atom not only serves as an active site for hydrogen production but also plays a pivotal role in efficiently accumulating bulk-phase electrons. This electron enrichment process enhances the transport of photoexcited electrons from the light-absorbing pyrene units to the active nitrogen sites. This work provides inspiration for the future design of effective nitrogen-atom-modified organic semiconductor photocatalysts at the molecular level.

Single-Atom-Based Oxygen Reduction Reaction Catalysts for Proton Exchange Membrane Fuel Cells: Progress and Perspective.

Single-atom catalysts (SACs) are regarded as promising non-noble-metal alternatives for the oxygen reduction reaction (ORR) in proton exchange membrane fuel cells due to their high atom utilization efficiency and excellent catalytic properties. However, the insufficient long-term stability issues of SACs under the working conditions seriously hinder their practical application. In this perspective, the recent progress of SACs with optimized ORR catalytic activity is first reviewed. Then, the possible degradation mechanisms of SACs in the ORR process and effective strategies for improving their ORR durability are summarized. Finally, some challenges and opportunities are proposed to develop stable single-atom-based ORR electrocatalysts in the future.

Molecular Heptazine-Triazine Junction over Carbon Nitride Frameworks for Artificial Photosynthesis of Hydrogen Peroxide.

Revealing the photocatalytic mechanism between various junctions and catalytic activities has become a hotspot in photocatalytic systems. Herein, an internal molecular heptazine/triazine (H/T) junction in crystalline carbon nitride (HTCN) is constructed and devoted to selective two-electron oxygen reduction reaction (2e- ORR) for efficient hydrogen peroxide (H2 O2 ) production. In-situ X-ray diffraction spectra under various temperatures authenticate the successful formation of molecular H/T junction in HTCN during the calcining process rather than physically mixing. The increased surface photovoltage and transient photovoltage signals, and the decreased exciton binding energy undoubtably elucidate that an obvious increasement of carrier density and diffusion capability of photogenerated electrons are realized over HTCN. Additionally, the analyses of in situ photoirradiated Kelvin probe force microscopy and femto-second transient absorption spectra reveal the successful construction of the strong internal built-in-electric field and the existence of the majority of long-lived shallow trapped electrons associated with molecular H/T junction over HTCN, respectively. Benefiting from these, the photocatalytic results exhibit an incredible improvement (96.5-fold) for H2 O2 production. This novel work provides a comprehensive understanding of the long-lived reactive charges in molecular H/T junctions for strengthening the driving-force for photocatalytic H2 O2 production, which opens potential applications for enhancing PCN-based photocatalytic redox reactions.

Room-Temperature Chemoselective Hydrogenation of Nitroarene Over Atomic Metal-Nonmetal Catalytic Pair.

Constructing atomic catalytic pair emerges as an attractive strategy to achieve better catalytic performance. Herein, an atomic Ir1 ─P1 /NPG catalyst with asymmetric Ir─N2 P1 sites that delivers superb activity and selectivity for hydrogenation of various functionalized nitrostyrene is reported. In the hydrogenation reaction of 3-nitrostyrene, Ir1 ─P1 /NPG (NPG refers to N, P-codoped graphene) shows a turnover frequency of 1197 h-1 , while the reaction cannot occur over Ir1 /NG (NG refers to N-doped graphene). Compared to Ir1 /NG, the charge density of the Ir site in Ir1 ─P1 /NPG is greatly elevated, which is conducive to H2 dissociation. Moreover, as revealed by density functional theory calculations and poisoning experiments, the P site in Ir1 ─P1 /NPG is found able to bind nitrostyrene, while the neighboring Ir site provides H to reduce the nitro group in chemoselective hydrogenation of nitrostyrene. This work offers a successful example of establishing atomic catalytic pair for driving important chemical reactions, paving the way for the development of more advanced catalysts to further improve the catalytic performance.

Atomically precise vacancy-assembled quantum antidots.

Patterning antidots, which are regions of potential hills that repel electrons, into well-defined antidot lattices creates fascinating artificial periodic structures, leading to anomalous transport properties and exotic quantum phenomena in two-dimensional systems. Although nanolithography has brought conventional antidots from the semiclassical regime to the quantum regime, achieving precise control over the size of each antidot and its spatial period at the atomic scale has remained challenging. However, attaining such control opens the door to a new paradigm, enabling the creation of quantum antidots with discrete quantum hole states, which, in turn, offer a fertile platform to explore novel quantum phenomena and hot electron dynamics in previously inaccessible regimes. Here we report an atomically precise bottom-up fabrication of a series of atomic-scale quantum antidots through a thermal-induced assembly of a chalcogenide single vacancy in PtTe2. Such quantum antidots consist of highly ordered single-vacancy lattices, spaced by a single Te atom, reaching the ultimate downscaling limit of antidot lattices. Increasing the number of single vacancies in quantum antidots strengthens the cumulative repulsive potential and consequently enhances the collective interference of multiple-pocket scattered quasiparticles inside quantum antidots, creating multilevel quantum hole states with a tunable gap from the telecom to far-infrared regime. Moreover, precisely engineered quantum hole states of quantum antidots are geometry protected and thus survive on oxygen substitutional doping. Therefore, single-vacancy-assembled quantum antidots exhibit unprecedented robustness and property tunability, positioning them as highly promising candidates for advancing quantum information and photocatalysis technologies.

Exploring, Identifying, and Removing the Efficiency-Limiting Factor of Mixed-Dimensional 2D/3D Perovskite Solar Cells.

ConspectusThree-dimensional (3D) halide perovskite (HP) solar cells have been thriving as promising postsilicon photovoltaic systems. However, despite the decency of efficiency, they suffer from poor stability. Partial dimensionality reduction from 3D to 2D was found to significantly meliorate the instability, thus mixed-dimensional 2D/3D HP solar cells have been expected to combine favorable durability and high efficiency. Nevertheless, their power conversion efficiency (PCE) does not live up to the expectation, hardly exceeding 19%, in sharp contrast with the ∼26% benchmark for pure 3D HP solar cells. The low PCE primarily arises from the restricted charge transport of the mixed-phasic 2D/3D HP layer. Understanding its photophysical dynamics, including its nanoscopic phase distribution and interphase carrier transfer kinetics, is essential for fathoming the underlying restriction mechanism. This Account outlines the three historical photophysical models of the mixed-phasic 2D/3D HP layer (denoted as models I, II, and III hereafter). Model I opines (i) a gradual dimensionality transition in the axial direction and (ii) a type II band alignment between 2D and 3D HP phases, hence favorably driving global carrier separation. Model II takes the view that (i) 2D HP fragments are interspersed in the 3D HP matrix with a macroscopic concentration variation in the axial direction and (ii) 2D and 3D HP phases instead form a type I band alignment. Photoexcitations would rapidly transfer from wide-band-gap 2D HPs to narrow-band-gap 3D HPs, which then serve as the charge transport network. Model II is currently the most widely accepted. We are one of the earliest groups to unveil the ultrafast interphase energy-transfer process. Recently, we further amended the photophysical model to consider also (i) an interspersing pattern of phase distribution but (ii) the 2D/3D HP heterojunction to be a p-n heterojunction with built-in potential. Anomalously, the built-in potential of the 2D/3D HP heterojunction increases upon photoexcitation. Therefore, local 3D/2D/3D misalignments would severely impede charge transport due to carrier blocking or trapping. Contrary to models I and II which hold 2D HP fragments as the culprit, model III rather suspects the 2D/3D HP interface for blunting the charge transport. This insight also rationalizes the distinct photovoltaic performances of the mixed-dimensional 2D/3D configuration and the 2D-on-3D bilayer configuration. To extinguish the detrimental 2D/3D HP interface, our group also developed an approach to alloy the multiphasic 2D/3D HP assembly into phase-pure intermediates. The accompanying challenges that are coming are also discussed.

Optical Logic Gates Excited by a Gauss Vortex Interference Beam Based on Spatial Self-Phase Modulation in 2D MoS2.

Vortex beams with optical orbital angular momentum have broad prospects in future high-speed and large-capacity optical communication. In this investigation of materials science, we found that low-dimensional materials have feasibility and reliability in the development of optical logic gates in all-optical signal processing and computing technology. We found that spatial self-phase modulation patterns through the MoS2 dispersions can be modulated by the initial intensity, phase, and topological charge of a Gauss vortex superposition interference beam. We utilized these three degrees of freedom as the input signals of the optical logic gate, and the intensity of a selected checkpoint on spatial self-phase modulation patterns as the output signal. By setting appropriate thresholds as logic codes 0 and 1, two sets of novel optical logic gates, including AND, OR, and NOT gates, were implemented. These optical logic gates are expected to have great potential in optical logic operations, all-optical networks, and all-optical signal processing.

Encapsulating Semiconductor Quantum Dots in Supramolecular Cages Enables Ultrafast Guest-Host Electron and Vibrational Energy Transfer.

In the field of supramolecular chemistry, host-guest systems have been extensively explored to encapsulate a wide range of substrates, owing to emerging functionalities in nanoconfined space that cannot be achieved in dilute solutions. However, host-guest chemistry is still limited to encapsulation of small guests. Herein, we construct a water-soluble metallo-supramolecular hexagonal prism with a large hydrophobic cavity by anchoring multiple polyethylene glycol chains onto the building blocks. Then, assembled prisms are able to encapsulate quantum dots (QDs) with diameters of less than 5.0 nm. Furthermore, we find that the supramolecular cage around each QD strongly modifies the photophysics of the QD by universally increasing the rates of QD relaxation processes via ultrafast electron and vibrational energy transfer. Taken together, these efforts expand the scope of substrates in host-guest systems and provide a new approach to tune the optical properties of QDs.

Metal-Free Electrochemically Reductive Deuteration of C═N Bonds with D2O toward Deuterated Amines.

Environmentally friendly and highly efficient synthesis of α-deuterated amines is achieved via a concise electrochemical process using D2O as deuterium source without any external reductants or catalysts. Various imines are compatible, affording the desired products in high yields and D-incorporation. Gram-scale synthesis and flow-cell electrochemistry technology are used to synthesize deuterated pharmaceutical amines and their intermediates. Mechanistic studies reveal a plausible process, including the formation of carbanion species followed by deuterium atom transfer.

Semi-heterogeneous photo-Cu-dual-catalytic cross-coupling reactions using polymeric carbon nitrides.

A merger of copper catalysis and semiconductor photocatalysis using polymeric carbon nitride (PCN) for multi-type cross-coupling reactions was developed. This dual-catalytic system enables mild C-H arylation, chalcogenation, and C-N cross-coupling reactions under visible light irradiation with a broad substrate scope. Good-to-excellent yields were obtained with appreciable site selectivity and functional group tolerance. Metal-free and low-cost PCN photocatalyst can easily be recovered and reused several times.

Multicarbons generation factory: CuO/Ni single atoms tandem catalyst for boosting the productivity of CO2 electrocatalysis.

Tandem electrocatalysis is an emerging concept for effective electrochemical CO2 reduction reaction (CO2RR) towards multicarbons (C2+). This decouples the multiple steps of CO2-to-C2+ into two steps of CO2-to-CO and CO-to-C2+ catalyzed by individual catalysts, to improve the Faradic efficiency (FE). However, due to the mass-transport limitation of CO from the generation site to the long-distance consumption site, such a strategy still remains challenge for high-rate production of C2+ products. Herein, we designed CuO/Ni single atoms tandem catalyst, which made the catalytic sites of Ni and Cu for independently catalyzing CO2-to-CO and CO-to-C2+ compactly neighbored, enabling the in-situ generation and rapid consumption of CO. The CuO/Ni SAs tandem catalyst achieved a particularly high partial current density of C2+ products (1220.8 mA/cm2), while still maintained outstanding C2+ products FE (81.4%) and excellent selectivities towards ethylene (FE 54.1%) and ethanol (FE 28.8%), enabling the profitable production of multicarbons by CO2RR.

Non-equilibrium Nanoassemblies Constructed by Confined Coordination on a Polymer Chain.

Biological systems employ non-equilibrium self-assembly to create ordered nanoarchitectures with sophisticated functions. However, it is challenging to construct artificial non-equilibrium nanoassemblies due to lack of control over assembly dynamics and kinetics. Herein, we design a series of linear polymers with different side groups for further coordination-driven self-assembly based on shape-complementarity. Such a design introduces a main-chain confinement which effectively slows down the assembly process of side groups, thus allowing us to monitor the real-time evolution of lychee-like nanostructures. The function related to the non-equilibrium nature is further explored by performing photothermal conversion study. The ability to observe and capture non-equilibrium states in this supramolecular system will enhance our understanding of the thermodynamic and kinetic features as well as functions of living systems.