Two-dimensional Carbon Material Research Articles

Electronic, thermoelectric and electrical transport properties of single layer γ-graphyne

Recently, graphyne has emerged as the sole two-dimensional carbon material exhibiting both sp and sp2 hybridization. It’s remarkable attributes have ignited considerable interest, particularly in the realm of optoelectronics, driven by its narrow band gap, signifying its vast potential in this field. In this paper we investigated electronic, thermoelectric and electrical transport properties of single layer γ-graphyne systematically and comparatively by using density functional theory (DFT). Our findings reveal that γ-graphyne displays pronounced absorption peaks within both the infrared (IR) and visible regions (VR), indicating its robust optical characteristics. Additionally, γ-graphyne showcases exceptional thermoelectric performance. The insights gained from this study elucidate the properties of γ-graphyne and suggest its applicability across various domains, including optical sensing and thermoelectric energy conversion devices.

Graphsene as a novel porous two-dimensional carbon material for enhanced oxygen reduction electrocatalysis

Graphene allotropes with varied carbon configurations have attracted significant attention for their unique properties and chemical activities. This study introduces a novel two-dimensional carbon-based material, termed Graphsene (GrS), through theoretical study. Comprising tetra-, penta-, and dodeca-carbon rings, GrS’s cohesive energy calculations demonstrate its superior structural stability over existing graphene allotropes, including graphyne and graphdiyne families. Phonon dispersion analysis confirms GrS’s dynamic stability and its relatively low thermal conductivity. All calculated GrS elastic constants meet the Born criteria, ensuring mechanical stability. Ab-initio molecular dynamic simulations show GrS maintains its structure at 300 K. HSE06 calculations reveal a narrow electronic bandgap of 20 meV, with the electronic band structure featuring a highly anisotropic Dirac-like cone due to its intrinsic structural anisotropy along armchair and zigzag directions. Notably, GrS is predicted to offer exceptional catalytic performance for the oxygen reduction reaction, favoring the four-electron reduction pathway with high selectivity under both acidic and alkaline conditions. This discovery opens promising avenues for developing metal-free catalyst materials in clean energy production.

Scanning Tunneling Spectroscopy Investigation of Au-bis-acetylide Networks on Au(111): The Influence of Metal-Organic Hybridization.

Graphdiyne (GDY) is an appealing two-dimensional carbon material, but the on-surface synthesis of a single layer remains challenging. Demetalation of well-crystalline metal acetylide networks, though in its infancy, provides a new avenue to on-surface synthesized GDY substructures. In spite of the synthetic efforts and theoretical concerns, there are few reports steeped in elaborate characterization of the electronic influence of metalation. In this context, we focused on the surface supported Au-bis-acetylide network, which underwent demetalation after further annealing to form hydrogen-substituted GDY. We made a comprehensive study on the geometric structure and electronic structure and the corresponding demetalized structure on Au(111) through STM, noncontact atomic force microscopy (nc-AFM), scanning tunneling spectroscopy (STS), and density functional theory (DFT) simulations. The bandgap of the Au-bis-acetylide network on Au(111) is measured to be 2.7 eV, while the bandgap of a fully demetalized Au-bis-acetylide network is estimated to be about 4.1 eV. Our findings reveal that the intercalated Au adatoms are positioned closer to the metal surface compared with the organic skeletons, facilitating electronic hybridization between the surface state and unoccupied frontier molecular orbitals of organic components. This leads to an extended conjugation through Au-bis-acetylene bonds, resulting in a reduced bandgap.

Graphene-Enhanced CuW Composites for High-Voltage Circuit Breaker Electrical Contacts

To address the issue of over-standard short-circuit currents in a power system, it is imperative to enhance the comprehensive performance of the electrical contacts, which serve as the lynchpin of circuit breakers, so as to improve the breaking capacity of high-voltage circuit breakers. Graphene, as the most prominent two-dimensional carbon material in recent years, has garnered widespread applications across various fields. In this study, graphene-enhanced CuW composites for high-voltage circuit breaker electrical contacts were prepared innovatively using integrated vacuum infiltration technology. The innovative graphene-enhanced CuW composites significantly improved the mechanical, electrical, and ablation resistance properties, and have been successfully applied in the 252 kV/63 kA high-voltage SF6 circuit breakers, achieving 20 times effective consecutive full-capacity short-circuit current breaking. It provides a new route for the development and application of high-performance CuW electrical contacts. Looking ahead, it is planned to extend their application to higher voltage grade high-voltage circuit breakers.

Fallen autumn leaves – The source of highly porous carbon for Zn-ion hybrid supercapacitors

Over the years, many sophisticated synthetic two-dimensional (2D) carbon materials have become increasingly popular for supercapacitors, e.g. zinc-ion hybrid supercapacitors (ZHSC) due to their ordered structure and high energy density. Additionally, ZHSC is a very demanding device, where finding efficient materials is challenging and the energy storage mechanism remains unclear. Biomass-derived carbon materials exhibit many drawbacks due to their impurities and defective structure, low stability and poor capacitance. In this study, a ZHSC was assembled via carbonization and activation of leaves collected from city streets and utilized as a cathode material. The AC650_Zn-foil presented a high specific capacitance of 95 F·g−1 and a high energy density of 86 W·h·kg−1 at 210 W·kg−1. Furthermore, a superior power density of 40,960 W·kg−1 at 33 W·h·g−1 was presented compared to other investigated materials. In addition, we identified the processes that occurred in the following device, which demonstrated a mechanism that determines the migration of Zn ions, as well as the chemical reactions involved in Zn ions.

Exploring the impact of stress on the electronic structure and optical properties of graphdiyne nanoribbons for advanced optoelectronic applications

Graphdiyne (GDY), a two-dimensional carbon material with sp- and sp2-hybridization, is recognized for its unique electronic properties and well-dispersed porosity. Its versatility has led to its use in a variety of applications. The precise control of this material's properties is paramount for its effective utilization in nano-optical devices. One effective method of regulation, which circumvents the need for additional disturbances, involves the application of external stress. This technique provides a direct means of eliciting changes in the electronic characteristics of the material. For instance, when subjected to uniaxial stress, electron transfer occurs at the triple bond. This results in an armchair-edged graphdiyne nanoribbon (A(3)-GDYNR) with a planar width of 2.07 nm, which exhibits a subtle plasmon effect at 500 nm. Conversely, a zigzag-edged graphdiyne nanoribbon (Z(3)-GDYNR) with a planar width of 2.86 nm demonstrates a pronounced plasmon effect within the 250–1200 nm range. This finding suggests that the zigzag nanoribbon surpasses the armchair nanoribbon in terms of its plasmon effect. First principles calculations and ab initio molecular dynamics further confirmed that under applied stress Z(3)-GDYNR exhibits less deformation than A(3)-GDYNR, indicating superior stability. This work provides the necessary theoretical basis for understanding graphene nanoribbons (GDYNRs).

High thermally conductive polyimide film designed with heterostructural Cring-C3N4 filler and multilayer strategy

With the emerging of advanced flexible electronic, the PI film with excellent thermally conductive, flexible, lightweight, electrically insulating qualities is in high demand as a potential substrate and encapsulation material. Conventional thermally conductive fillers such as ceramic, metal and carbon material with high hardness, high density or electrical conductivity are unsuitable to prepare the advanced PI film. Furthermore, the confined loading of thermally conductive filler in PI matrix limited by its film-forming property is another obstacle to optimizing the thermal conductivity of PI film. In this work, the development of novel filler (carbon nitride in-plane grafted by two-dimensional carbon material, Cring-C3N4) with intrinsic thermal conductivity and a design of three-layer structure for the introduction of high filler loading have dramatically improved the thermal conductivity of PI film. Benefitting by the planar heterostructure construction of g-C3N4 and Cring, the existence of Cring increases the phonon transfer rate in g-C3N4, and the presence of g-C3N4 prevents the electron movement in the facet of Cring-C3N4 endowing its excellent electrical insulation property. The design of three-layer structure in which the first and third layers served as mechanical support layers with a fixed filler content (20 wt%). The second layer has the higher filler content to enhance the quantity of thermally conductive filler in PI film. Resultantly, the maximum out-of-plane thermal conductivity of the PI/Cring-C3N4 composite film is 1.35 Wm−1K−1, which is 10 times higher than the pure PI film. In addition, the PI/Cring-C3N4 composite film exhibit excellent photothermal conversion ability in which the saturation temperature of PI/Cring-C3N4 can reach 283.6 °C under 0.75 W/cm2 laser radiation being 6 times higher than that of the corresponding PI film. After the incorporation of Cring-C3N4, the PI composite film still has excellent thermal stability, low CTE, electrical insulation and mechanical properties. This work provides a novel idea for the preparation of advanced high thermal conductivity PI film.

Nanoengineering of Porous 2D Structures with Tunable Fluid Transport Behavior for Exceptional H2O2 Electrosynthesis.

Precision nanoengineering of porous two-dimensional structures has emerged as a promising avenue for finely tuning catalytic reactions. However, understanding the pore-structure-dependent catalytic performance remains challenging, given the lack of comprehensive guidelines, appropriate material models, and precise synthesis strategies. Here, we propose the optimization of two-dimensional carbon materials through the utilization of mesopores with 5-10 nm diameter to facilitate fluid acceleration, guided by finite element simulations. As proof of concept, the optimized mesoporous carbon nanosheet sample exhibited exceptional electrocatalytic performance, demonstrating high selectivity (>95%) and a notable diffusion-limiting disk current density of -3.1 mA cm-2 for H2O2 production. Impressively, the electrolysis process in the flow cell achieved a production rate of 14.39 mol gcatalyst-1 h-1 to yield a medical-grade disinfectant-worthy H2O2 solution. Our pore engineering research focuses on modulating oxygen reduction reaction activity and selectivity by affecting local fluid transport behavior, providing insights into the mesoscale catalytic mechanism.

Metal-organic framework-derived two-dimensional in-plane Janus catalysts promoting oxygen electroreduction to hydrogen peroxide.

We use MOFs material as precursor to synthesize carbon based two-dimensional (2D) materials loaded with In2 S3 -In2 O3 (In-S-O) nanoparticles. The In-S-O nanoparticles have exhibited Janus architecture composed of two compounds with different crystal structures that are combined in-plane on 2D carbon material surface. The excellent properties of this in-plane Janus material include 2D nanoarchitecture and its Janus properties formed by combining two different crystal structures. It has exhibited excellent electrochemical performances due to its abundant electrochemical active sites and large specific surface area. According to experiments, the electron transfer number of the material for two-electron oxygen reduction is about 2.4, and the hydrogen peroxide yield is 32 mg/h cm2 . In the further test of liquid flow electrolytic cell, the yield can reach up to 172 mg/h cm2 .

1D hollow tubular/2D nanosheet hybrid dimensional porous carbon prepared by one-step carbonization using natural minerals as templates for supercapacitors.

The reasonable construction of one-dimensional (1D)/two-dimensional (2D) hybrid dimensional porous carbon materials with complementary advantages and disadvantages is an important approach to addressing the structural and performance deficiencies of single carbon materials, while also significantly improving the electrochemical performance of super-capacitors. In this study, 1D hollow tubular/2D nanosheet hybrid dimensional porous carbon was synthesized through one-step carbonization using 1D fibrous brucite and 2D layered magnesium carbonate hydroxide as templates. By adjusting the feed ratio of 1D fibrous and 2D layered templates, the morphology, pore structure and specific surface area (SSA) of the prepared 1D hollow tubular/2D nanosheet hybrid dimensional porous carbon were controlled. The prepared hybrid dimensional porous carbons were characterized using scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and nitrogen adsorption-desorption. And their electrochemical performance was also studied by cyclic voltammograms (CV), galvanostatic charge/discharge (GCD) and electrochemical impedance spectroscopy (EIS). The results show that the use of templates with different dimensions significantly influences the morphology, pore structure, SSA and electrochemical performance of the synthesized hybrid dimensional porous carbon. The hybrid dimensional porous carbon (3F) exhibits a high specific capacitance and excellent cycling stability. 3F demonstrates the specific capacitance of 245.3 F g-1 at 1 A g-1. Furthermore, the capacity retention rate remains as high as 93.4% after 8000 cycles at 10 A g-1. This work reveals that hybrid dimensional porous carbon composed of 1D hollow carbon tubes and 2D carbon nanosheets has great potential for use in supercapacitor electrode materials.

4-6 carbophene: A two-dimensional carbon material with Dirac cone and superior activity for electrochemical oxygen reduction reactions

The positive exploration of efficient and cost-effective electrocatalysts for the oxygen reduction reaction (ORR) is crucial for the sustainable development of energy conversion and storage technologies. Recently, a new type of two-dimensional (2D) carbon crystals, called 4-6 carbophene, has been successfully synthesized. It consists of a four-carbon ring and a six-carbon ring. In this work, we have discovered that 4-6 carbophene is a two-dimensional Dirac cone material through density-functional theory (DFT) calculations. Therefore, we further investigated the oxygen reduction reaction on 4-6 carbophene to understand its catalytic properties. The results demonstrate that on 4-6 carbophene, the ORR prefers a direct four-electron pathway. Under acidic conditions, the ORR overpotential of 4-6 carbophene is as low as 0.59 V, which is comparable to some metal benchmark catalysts, demonstrating that 4-6 carbophene is a metal-free ORR candidate catalyst. In addition, the richly charged carbon atoms on 4-6 carbophene exhibit remarkable charge transfer when binding to the adsorbed intermediates. This results in a strong binding strength. Thus, 4-6 carbophene has favorable ORR catalytic activity. This work not only provides promising low-cost catalysts in pure carbon materials for ORR, promoting the development of metal-free ORR catalysts, but also enhances the understanding of Dirac cone two-dimensional materials for applications in catalysis.

Type-II CoMoO4/Graphdiyne heterojunction promotes visible-light-driven photocatalytic hydrogen production activity

Photocatalytic hydrogen production technology has great challenges in designing and synthesizing stable photocatalyst and inhibiting high recombination rate of carriers. In this paper, CoMoO4/GDY type-II heterojunctions were successfully constructed by coupling a new two-dimensional layered carbon material graphdiyne (GDY) with molybdate (CoMoO4), and the positive effect of GDY on photocatalytic hydrogen production system was studied. The introduction of GDY provides a large number of reaction sites for the reaction. Moreover, due to the strong light absorption and excellent electrical conductivity of GDY, the photoelectrochemical properties of molybdate (CoMoO4) are enhanced. The construction of type-II heterojunctions effectively promotes the spatial separation of photogenerated electrons and holes. The electron transfer mechanism of the photocatalyst was verified based on DFT and in-situ irradiation X-ray photoelectron spectroscopy. The experimental results show that the photocatalytic performance of CoMoO4/GDY photocatalyst is the best (121 μmol), which is 2 times and 45 times that of CoMoO4 and GDY, respectively. This study provides a unique idea for the application of GDY in the field of photocatalysis.

A facile and large-scale route to prepare nitrogen/oxygen (N/O) co-doped two-dimensional carbon nanomesh with excellent microwave absorption properties

Two-dimensional porous carbon materials have been considered good candidates for developing lightweight microwave absorbers because of their low density and tunable dielectric constant. However, large-scale synthesis, with precise control of the microstructure, by a simple method, remains is still a great challenging. Herein, a two-dimensional N/O co-doped carbon nanomesh (NOCN) was prepared via large-scale route by simple carbonization of analogue polyurea (PU) nanosheet consisted of p-phenyldiisocyanate and urea, and the graphitization degree, porous structure, sheet size and the heteroatom doping content could be easily adjusted by controlling carbonization temperature. Thus, the electromagnetic parameter and the corresponding microwave absorption can be regulated. When the carbonization temperature was 900 °C (NOCN-900), the obtained sample exhibited the best microwave absorption performance, and the reflection loss (RL) value was −54.2 dB with an effective absorption bandwidth (EAB) of 7.44 GHz at a thickness of 2.3 under fill loading of only 5 wt%. The facile and large-scale synthesis route combined with excellent performance makes NOCN-900 to be a great promising candidate for practical application.

Tunable plasmonic hybrid photonic device based on squared graphene and black phosphorus metamaterials

The yearning to utilize and control the captivating property of two-dimensional carbon materials has attracted plenty of attention in biosensing and optoelectronics. In this paper, we proposed a novel graphene-black phosphorus (BP) hybrid photonic device to exhibit strong absorption of 97.0 % at 12.23 μm in the x-direction and it is 93.3 % at 13.42 μm in the y-direction. Due to the surface plasmon resonance of graphene and distinctive anisotropic effective electron masses of black phosphorus along the armchair and zigzag axes, the electromagnetic coupling achieves an enhanced performance than individual graphene or BP layer. Additionally, by adjusting the Fermi energy of graphene, the doping level of BP, and the geometric parameters, the resonant absorption peaks can be tuned independently in both TE and TM polarization. The advantages of our proposed plasmonic hybrid photonic device include high anisotropic resonance, flexible tunability, great stability, and a simple design. These make it promising for applications in photodetectors, polarizers, and imaging systems.

A universal strategy for producing 2D functional carbon-rich materials from 2D porous organic polymers for dual-carbon lithium-ion capacitors

Two-dimensional (2D) carbon materials have attracted enormous attention, but the complicated synthesis methods, inhomogeneous structure and uncontrollable properties still limit their use. Here we report a universal protocol for fabricating a series of heteroatom-doped 2D porous polymers, including pyrrole and indole as nitrogen-dopant sources, and 3,4-ethoxylene dioxy thiophene as a sulfur-dopant source by a simple chemical crosslinking reaction. This bottom-up strategy allows for the large-scale synthesis of functionalized ultrathin carbon nanosheets with a high heteroatom doping content and abundant porosity. Consequently, the obtained N-doped carbon-rich nanosheets (NCNs) sample has a specific capacity of 573.4 mAh g−1 at 5 A g−1 as an anode for lithium-ion capacitors (LICs), and the optimized sample has a specific capacitance of 100.0 F g−1 at 5 A g−1 when used as a cathode for a LIC. A dual-carbon LIC device was also developed that had an energy density of 168.4 Wh kg−1 at 400 W kg−1, while maintaining outstanding cycling stability with a retention rate of 86.3% after 10 000 cycles. This approach has the potential to establish a way for the precise synthesis of substantial amounts of 2D functionalized carbon nanosheets with the desired structure and properties.

Cotton yarns decorated with hydrothermally reduced graphene oxide for flexible supercapacitors

Cotton fibers, a natural cellulose, have played a critical role in the development of wearable energy storage, owning to their wearability, integrability, eco-benignity, and cost effectiveness. Graphene, a two-dimensional carbon material, possesses excellent electrochemical properties that can be incorporated into cotton yarns to enhance their performance. However, the conventional chemical reduction processes use corrosive chemical reducing agents that limit their wide application. In the current study, a reduced graphene oxide (rGO)/cotton (RC) yarn supercapacitor was fabricated employing a facile and green hydrothermal approach without the use of any chemical reductants. The reduction efficiency of external GO nanoparticles and the morphology change of internal cotton fiber under different hydrothermal treatments are investigated to explore their effects on the energy storage performance of the resultant RC electrodes and supercapacitors. The RC yarn electrode can reach a capacitance of 13.31 mF cm−1 at of 0.1 mA cm−1. The assembled asymmetric supercapacitor exhibited a high specific capacitance of 2.99 mF cm−1 (9.54 mF cm−2, and 381.43 mF cm−3) at 0.02 mA cm−1 (0.06 mA cm−2 and 2.55 mA cm−3) with a high energy density of 0.42 μWh cm−1 (1.32 μWh cm−2 and 0.05 mWh cm−3) at a power density of 10 μW cm−1 (31.84 μW cm−2 and 1.27 mW cm−3). This work develops a green versatile strategy for fabricating RC supercapacitors, which may provide a new avenue for wearable energy storage devices.

Graphite-Catalyzed Electro-Oxidation of Hydrazine Derivatives Using Sodium Chloride under Green and Sustainable Chemistry

The development of efficient and environmentally friendly catalysts for the electro-oxidation of hydrazine derivatives is of great importance in various industrial applications. In this study, we report the utilization of graphite-based catalysts for the electro-oxidation of hydrazine derivatives, using sodium chloride as a green and sustainable chemical approach. Graphite, a two-dimensional carbon material with exceptional properties, offers numerous advantages as a catalyst, including its high surface area, excellent electrical conductivity, and chemical stability. These characteristics make graphite an ideal candidate for promoting electrochemical reactions. Sodium chloride (NaCl), a readily available and cost-effective salt, serves as a green alternative to traditional oxidants used in hydrazine oxidation processes. By replacing conventional oxidizing agents with NaCl, we aim to reduce the environmental impact associated with the production and disposal of hazardous chemicals. This process enables the transformation of the HN-NH bond within hydrazines, leading to the formation of azo compounds (N = N). Azo compounds are important organic molecules with diverse applications in organic synthesis. This novel approach has successfully showcased the efficacy of utilizing various azo compounds in 13 different examples, yielding excellent or moderate to good results. The method capitalizes on electricity as the final oxidizing agent, providing an environmentally friendly oxidation strategy. Its high efficiency and gentle reaction conditions make this technique valuable for synthesizing azo derivatives, even when working with hydrazines containing diverse functional groups, resulting in yields ranging from moderate to excellent. Through systematic experiments, we evaluated the catalytic performance of graphite-based catalysts in the electro-oxidation of hydrazine derivatives. The catalysts demonstrated remarkable catalytic activity due to their efficient conversion of hydrazine derivatives into desired products. Moreover, the system exhibited good stability and recyclability, suggesting its suitability for practical applications.

Enhancing the Mechanical Properties and Aging Resistance of 3D-Printed Polyurethane through Polydopamine and Graphene Coating.

Three-dimensional (3D) printing is a versatile manufacturing method widely used in various industries due to its design flexibility, rapid production, and mechanical strength. Polyurethane (PU) is a biopolymer frequently employed in 3D printing applications, but its susceptibility to UV degradation limits its durability. To address this issue, various additives, including graphene, have been explored to enhance PU properties. Graphene, a two-dimensional carbon material, possesses remarkable mechanical and electrical properties, but challenges arise in its dispersion within the polymer matrix. Surface modification techniques, like polydopamine (PDA) coating, have been introduced to improve graphene's compatibility with polymers. This study presents a method of 3D printing PU scaffolds coated with PDA and graphene for enhanced UV stability. The scaffolds were characterized through X-ray diffraction, Fourier-transform infrared spectroscopy, mechanical testing, scanning electron microscopy, and UV durability tests. Results showed successful PDA coating, graphene deposition, and improved mechanical properties. The PDA-graphene-modified scaffolds exhibited greater UV resistance over time, attributed to synergistic effects between PDA and graphene. These findings highlight the potential of combining PDA and graphene to enhance the stability and mechanical performance of 3D-printed PU scaffolds.

Proton penetration mechanism and selective hydrogen isotope separation through two-dimensional biphenylene.

Hydrogen isotope separation is of prime significance in various scientific and industrial applications. Nevertheless, the existing technologies are often expensive and energy demanding. Two-dimensional carbon materials are regarded as promising candidates for cost-effective separation of different hydrogen isotopes. Herein, based on theoretical calculations, we have systematically investigated the proton penetration mechanism and the associated isotope separation behavior through two-dimensional biphenylene, a novel graphene allotrope. The unique non-uniform rings with different sizes in the biphenylene layer resemble the topological defects of graphene, serving as proton transmission channels. We found that a proton can readily pass through biphenylene with a low energy barrier in some specific patterns. Furthermore, large kinetic isotope effect ratios for proton-deuteron (13.58) and proton-triton (53.10) were observed in an aqueous environment. We thus conclude that biphenylene would be a potential carbon material used for hydrogen isotope separation. This subtle exploitation of the natural structural specificity of biphenylene provides new insight into the search for materials for hydrogen isotope separation.

Progress on Single-Atom Photocatalysts for H2 Generation: Material Design, Catalytic Mechanism, and Perspectives.

Solar energy utilization is of great significance to current challenges of the energy crisis and environmental pollution, which benefit the development of the global community to achieve carbon neutrality goals. Hydrogen energy is also treated as a good candidate for future energy supply since its combustion not only supplies high-density energy but also shows no pollution gas. In particular, photocatalytic water splitting has attracted increasing research as a promising method for H2 production. Recently, single-atom (SA) photocatalysts have been proposed as a potential solution to improve catalytic efficiency and lower the costs of photocatalytic water splitting for H2 generation. Owing to the maximized atom utilization rate, abundant surface active sites, and tunable coordination environment, SA photocatalysts have achieved significant progress. This reviewreviews developments of advanced SA photocatalysts for H2 generation regarding the different support materials. The recent progress of titanium dioxide, metal-organic frameworks, two-dimensionalcarbon materials, and red phosphorus supported SA photocatalysts are carefully discussed. In particular,the material designs, reaction mechanisms, modulation strategies, and perspectives are highlighted for realizing improved solar-to-energy efficiency and H2 generation rate. This work will supply significant references for future design and synthesis of advanced SA photocatalysts.