Electronic Absorption Research Articles

Optimizing toughness in high entropy alloys using a genetic algorithm: A combined computational and experimental approach

A genetic algorithm (GA) was developed to search for high entropy alloys (HEAs) with good combinations of mechanical properties. The algorithm was designed find single-phase face-centered cubic (FCC) HEAs, already known for their ductility, with high Hall-Petch constants (K) and high critical resolved shear stresses (τY). The objective was to develop a methodology that allows the design of HEAs in a multi-objective environment, focusing on alloys that exhibit enhanced ductility and strength, achieved through an increase in its yield point without significant loss of its ultimate deformation via adjustments of K and τY values, resulting in an alloy with high toughness. The most promising alloy suggested by the genetic algorithm was an unconventional composition (Co32.73Cu15.11Fe0.72Hf0.72Mn35.97Mo3.96Ni10.43Sn0.36), with eight different elements in non-equiatomic ratios with maximized K and τY values. This alloy was then experimentally produced and characterized by scanning electron microscopy (SEM), synchrotron x-ray diffraction (XRD), transmission electron microscopy (TEM) and microhardness, with the objective of validating the predictions made by the GA. An advantage of the proposed method is the possibility of more systematically identifying and exploring new compositions in the complex composition space characteristic of these multicomponent alloys, as it directs its search towards domains that can be used to solve challenging problems involving multi-objective optimization. However, the thermodynamic parameters used for single-phase FCC prediction, namely the valence electron concentration (VEC) and the dimensionless thermodynamic parameter φ, exhibited limitations. These limitations were further explored in the present study, as evidenced by the fact that the microstructure of the selected alloy was not single-phase, which hindered the study of the mechanical properties, predicted exclusively for monophasic FCC alloys. Therefore, this work highlights the necessity for the development of novel thermodynamic equations for phase prediction, or even the integration of the genetic algorithm with other methodologies, such as CALPHAD calculations, to achieve enhanced results.

A microwave discharge in high-velocity flows initiated by a half-wave antenna

A microwave discharge in high-velocity (150—250 m/s) air flows induced on a half-wave vibrator is studied. A cw magnetron microwave generator with a frequency of 2.45 GHz and an output power of up to 5 kW was used for initiation of the microwave discharge. The high-speed video imaging was used for studying the discharge structure, determining the diameter and length of the plasma channel as a function of flow velocity and pressure. Electron concentration and temperature, along with characteristic gas temperature, were determined based on the optical spectra. The possibility of using this microwave discharge for ignition of hydrocarbon–air mixtures in combustion chambers of ramjet engines is proved experimentally.

Tailoring ZrWNb-Based Refractory High Entropy Alloys: A Multidirectional Characterization Through Elemental, Physical, Thermodynamic, and Nuclear Radiation Attenuation Properties

This study explores the development and characterization of 18 novel ZrWNb[(X)(Y)] (where XY are Hf, Ta, Mo, V, Ti) refractory high entropy alloys (RHEAs) designed to enhance mechanical robustness, thermodynamic stability, and radiation shielding effectiveness. Through a rigorous analysis, we evaluated the elastic modulus, entropy, and enthalpy of mixing, atomic size difference, valence electron concentration, and the omega parameter to understand the alloys’ phase behavior and structural integrity. Our findings revealed a broad range of elastic modulus values, indicating diverse mechanical adaptability suitable for high-stress applications. The thermodynamic assessment highlighted several RHEAs with favorable phase stability, particularly ZrWNbTaHf and ZrWNbTiTaHf, which are poised for high-performance usage due to their balanced mixing entropy and enthalpy. This study also benchmarks the RHEAs against conventional alloys, with sample R1 exhibiting the lowest fast neutron effective removal cross section, underscoring its superior neutron shielding capabilities. Additionally, R1 demonstrated exceptional photon attenuation, as evidenced by its competitive half-value layer performance across an extensive energy spectrum. Collectively, these results position R1 as a standout candidate, offering a significant advancement in materials science for applications demanding stringent radiation shielding, such as in nuclear reactor environments and space exploration.

A Poly(2,7-anthrylene) with peri-Fused Porphyrin Edges.

Anthracene has served as an important building block of conjugated polymers with the connecting positions playing a crucial role for the electronic structures. Herein, anthracene units have been coupled through their 2,7-carbons to develop an unprecedented, conjugated polymer, namely, poly(2,7-anthrylene) featuring additional peri-fused porphyrin edges. The synthesis starts from a 2,7-dibromo-9-nickel(II) porphyrinyl-anthracene as the pivotal precursor. Polymerization is achieved by an AA-type Yamamoto coupling, followed by a polymer-analogous oxidative cyclodehydrogenation to obtain a peri-fusion between porphyrin and anthracene moieties. Although further cyclodehydrogenation between the repeating units cannot be achieved in solution, the thermal treatment of the precursor polymer derived from 2,7-dibromo-9-porphyrinyl-anthracene on a metal surface realizes the full cyclodehydrogenation. The difference between solution and on-surface reactivity can be rationalized by the larger dihedral angle between repeat units in solution, which is reduced under the pronounced interaction with the metal surface. The peri-fusion in the title polymer gives rise to a narrow electronic band gap optical absorptions extending far into the near-infrared region. Oligomeric models are synthesized as well to support the analyses of the electronic and photophysical properties.

Synthesis, characterization, and color performance of bis-azo and bis-pyrazole derivatives for dyeing of polyester

In this study, a novel series of bis-azo dyes 3–10 were synthesized via a two-step process. Initially, benzene-1,4-bis(diazonium) chloride was reacted with several active methylene compounds, such as ethyl acetoacetate, acetyl acetone, ethyl cyanoacetate, and malononitrile. yielding the corresponding bis-azo dyes 3–6. Subsequently, these dyes were cyclized through condensation with phenylhydrazine, resulting in the formation of bis-pyrazole derivatives 7–10. Comprehensive spectroscopic characterization, employing techniques like infrared (IR), nuclear magnetic resonance (NMR), and ultraviolet-visible (UV–Vis) spectroscopy, along with elemental analysis, elucidated the structural features, and electronic transitions of the synthesized dyes. The electronic absorption properties were investigated experimentally and computationally, revealing bathochromic and hypsochromic shifts influenced by substituents and tautomeric forms. The dyes showcased excellent dyeing performance on polyester fabrics, exhibiting notable color strength, perspiration fastness, light fastness, and wash fastness. Theoretical investigations of the electronic properties were conducted utilizing Density Functional Theory (DFT) methodology, employing the B3LYP functional with the 6–31G(d,p) basis set, enabling a comprehensive understanding of the structure-performance relationships governing the dyeing behavior of these dyes on polyester.

Harnessing multifunctional antimony doped Tin (IV) sulfide nanosheets for chlorpyrifos degradation and hydrogen evolution

Multifunctional photocatalysts are vital for advancing environmental sustainability and clean energy. The hydrothermal method helped in optimized antimony (Sb) doping in the Tin (IV) sulfide (SnS2) lattice, increasing surface area with nanosheet assortment, as confirmed by Scanning Electron Microscopy and BET (Brunauer, Emmett and Teller) analysis. Moreover, the Fermi level shift towards conduction band within the semiconductor, increasing free electron concentration which enhanced conductivity and altered electronic properties. Photocatalysts were evaluated for Chlorpyrifos pesticide degradation, with studies conducted on photocatalytic parameters such as catalyst dosage, pesticide concentration, and pH to ascertain optimal degradation conditions. The 6 wt% Sb-doped SnS2 (6Sb:SnS2) demonstrated highest degradation efficiency within 60 min and degradation obeyed a pseudo first-order kinetic model with a rate constant of 0.0349 min−1. The degradation pathway of Chlorpyrifos and its transformation products was elucidated through High-Performance Liquid Chromatography-tandem mass spectroscopy. In addition, Sb doping empowers the surface traps and hydrophilicity of photocatalysts towards successful interaction between photogenerated electrons/holes with adsorbed oxidizable/reducible species. Moreover, 6Sb:SnS2 exhibited superior hydrogen evolution of 214.39 µmolg−1h−1, along with improved stability. Significantly, 6Sb:SnS2 attained Apparent Quantum Yield (AQY400 nm) of 39.49 % attributed to the doping induced band structure modification of SnS2 to match the hydrogen ion reduction potential.

Different built-in electric fields for transmission-mode GaAs photocathodes through doping engineering: Design and modeling

In order to enhance the emission performance of transmission-mode GaAs photocathodes used in optoelectronic field, different exponential doping structures are designed for the GaAs emission layer to generate different types of built-in electric fields. These built-in electric fields include the constant, increasing and decreasing types, which can help photoelectron transport toward the emission surface. By solving the one-dimensional continuity equation using the finite difference method, the electron concentration distribution and quantum efficiency of the three types of exponential doping GaAs photocathodes are derived. Meanwhile, the light absorption distributions in the emission layer are simulated by the finite difference time domain method. By comparing the optical absorption distribution and the electron concentration distribution, it is concluded that, among the three types of exponential doping structures, the exponential doping structure generating the increasing built-in electric field has the most sufficient long-wave light absorption capacity and the strongest photoelectron transport ability, thereby achieving the highest quantum efficiency. This theoretical work can help understand the mechanism of improving the photoemission performance of GaAs photocathodes through doping engineering.

Boosting charge separation and active sites exposure by hollow S-scheme MoSe2/Fe2O3 heterojunction for enhanced photocatalytic peroxymonosulfate activation towards ciprofloxacin removal

Regulating the properties of heterogeneous catalyst for efficient peroxymonosulfate (PMS) activation to pollutants degradation remains a challenge in photo-assisted Fenton-like reaction (PF) system. In this study, the novel S-scheme MoSe2/Fe2O3 (H-FMS) heterojunction with hollow nanostructure was successfully developed as visible-light-driven PMS activator for removal of ciprofloxacin (CIP). The prepared H-FMS catalyst in PMS/H-FMS/light system exhibits outstanding photocatalytic performance for CIP degradation, achieving 95.92 % removal of 5 mg/L CIP in 30 min with 0.5 mM PMS. The construction of S-scheme heterojunction provides photoinduced carriers with longer lifetime and higher redox abilities, thus sufficient photogenerated carriers are supplied to directly activate PMS. Simultaneously, the hollow nanostructure possessing multiple light reflection and scattering behaviors further facilitates the utilization of visible light. More importantly, high concentration of photoinduced electrons with high reduction ability in MoSe2 is conducive to continuous exposure of Mo4+ active sites for PMS activation through cycling between transition metal valence states. Overall, effectively separated electron-hole pairs and continuously exposed transition metal active sites both contribute to efficient activation of PMS as well as multi-path generation of ROS, leading to significant improvement in CIP degradation. The results of quenching experiment, electron spin resonance (ESR) technology, liquid chromatography-mass spectrometry (LC-MS) and density functional theory (DFT) calculation confirm that both free radicals (SO4∙-, •OH and O2∙-) and non radicals (1O2 and h+) attack the active sites of CIP possessing high Fukui index, thus contributing to CIP degradation. This work would provide a novel insight for future development and application of photocatalytic PMS activation catalysts in water remediation.

Periodic Bonding Behaviors of Actinide Atoms (An = Th-Cm) with Negatively Curved Nanographene.

The nanographene with negative curvature has been extensively studied due to its interesting properties and potential applications. In the present work, we have performed all-electron scalar relativistic density functional theory (DFT) calculations to understand the periodic interaction mechanisms of actinide atoms (An = Th, Cm) with the TB8C nanographene. The encapsulated complexes (An@TB8C) were formed due to the octagonal vacancy in the TB8C nanographene. TB8C shows fairly high affinity toward An atoms, especially for Th and Pa. AIMD simulations further confirmed the effective trapping of An atom with TB8C. The partial covalent characters of An-C bonds in An@TB8C were revealed through various bond analysis methods. The 6d electrons of An play an important role in the participation of chemical bonds. The delocalization index (DI) is proposed as a useful descriptor in the study of bond strength involving the actinides. Electronic absorption spectra were simulated for further identification in the experiments. The current work has expanded the potential molecular properties and applications of nanographene.

Optimizing strength-ductility synergy of the solid-solution Ti50–ZrVNbCr MEAs via coordinately adjusting VEC and lattice constant

In this study, a series of Ti50–ZrVNbCr alloys were designed under with the constant atomic radius mismatch. It was suggested that valence electron concentration (VEC) and lattice constant, which evolve oppositely in the series of the Ti50–ZrVNbCr alloys, jointly influence the mechanical properties. Based on modeling, the evolution of ductility and yield strength of the designed alloys was predicted. Ductility was predicted to be superior in the VEC range from 4.22 to 4.25, with the lattice constant correspondently ranging from 3.340 Å to 3.334 Å. The optimization of strength-ductility synergy was discussed in terms of coordinately adjusting VEC and lattice constant. The experimental results were quite consistent with the prediction results, showing that the alloy with the VEC value of 4.25 and the lattice constant of 3.334 Å, which consisted of 50 at.%Ti, 28.1 at.%Zr, 9.4 at.%V, 9.4 at.%Nb, and 3.1 at.%Cr, possessed the best ductility and superior strength-ductility synergy.

Synthesis and Characterization of Solvated Lanthanide(II) Bis(triisopropylsilyl)phosphide Complexes.

Lanthanide (Ln) silylamide chemistry is well-developed, but the corresponding silylphosphide chemistry is immature; there are only ten structurally characterized examples of Ln(II) bis(trimethylsilyl)phosphide complexes to date and no reported derivatives with bulkier R-groups. Here, we report the synthesis of the first f-block bis(triisopropylsilyl)phosphide complexes, [Ln{P(SiiPr3)2}2(THF)x] (1-Ln; Ln = Sm, Eu, x = 3; Ln = Yb, x = 2), by the respective salt metathesis reactions of parent [LnI2(THF)2] with 2 equiv of [Na{P(SiiPr3)2}]n in toluene. Complexes 1-Ln were characterized by a combination of NMR, EPR, ATR-IR, electronic absorption and emission spectroscopies, elemental analysis, SQUID magnetometry, and single crystal X-ray diffraction. These data contrast with those obtained for related Ln(II) bis(trimethylsilyl)phosphide complexes due to the bulkier ligands in 1-Ln and also with Ln(II) bis(triisopropylsilyl)amide complexes due to a combination of longer Ln-P vs. Ln-N bonds and the softer nature of P- vs. N-donor ligands.

Crystallographic and Optical Spectroscopic Study of Metal–Organic 2D Polymeric Crystals of Silver(I)– and Zinc(II)–Squarates

Metal–organic framework materials, as innovative functional materials for nonlinear optical technologies, feature linear and nonlinear optical responses, such as a laser damage threshold, outstanding mechanical properties, thermal stability, and optical transparency. Their non-centrosymmetric crystal structure induces a higher-order nonlinear optical response, which guarantees technological applications. ZnII– and AgI–squarate complexes are attractive templates for these purposes due to their good crystal growth, optical transparency, high thermal stability, etc. However, the space group type of the catena-((μ2-squarato)-tetra-aqua-zinc(II)) complex ([Zn(C4O4)(H2O)4]) is debatable, (1) showing centro- and non-centrosymmetric monoclinic C2/c and Cc phases. The same is valid for the catena-((μ3-squarato)-(μ2-aqua)-silver(I)) complex (Ag2C4O4), (2) exhibiting, so far, only a C2/c phase. This study is the first to report new crystallographic data on (1) and (2) re-determined at different temperatures (293(2) and 300(2)K) and the non-centrosymmetric Cc phase of (2), having different numbers of molecules per unit cell compared with the C2/c phase. There are high-resolution crystallographic measurements of single crystals, experimental electronic absorption, and vibrational spectroscopic data, together with ultra-high-resolution mass spectrometric ones. The experimental results are supported for theoretical optical and nonlinear optical properties obtained via high-accuracy static computational methods and molecular dynamics, using density functional theory as well as chemometrics.

Computational prediction of Thermo-Elastic and charge carriers transport properties of Ba2MnReO6, Ba2NiReO6, and Sr2MnReO6 double Perovskite compounds

The present work involves a computational investigation of the elastic, thermal, and thermoelectric characteristics of Ba2MnReO6, Ba2NiReO6, and Sr2MnReO6 from the Double Perovskite family. The study verified the mechanical stability of the three compounds and investigated Young’s modulus, Poisson, bulk, and shear modulusin various stress orientations. We were also able to compute longitudinal, transverse, and average sound velocities (Vl, Vt, and Vm, in m/s), and the findings revealed that Sr2MnReO6 had a greater longitudinal velocity than the other two compounds. Thermodynamic characteristics revealed that Ba2MnReO6, Ba2NiReO6, and Sr2MnReO6exhibit low lattice thermal conductivity (Kl) at medium temperatures, strong heat absorption, and a moderate coefficient of thermal expansion.The analysis of the electron and hole charge carriers’ transport characteristics revealed that, when doped with an electron concentration close to 1020 cm−3, the two materials, Ba2MnReO6 and Sr2MnReO6, may have an excellent figure of merit surpassing 0.6 at temperatures over 600 K.

Dual-gate AlGaN channel HEMTs: advancements in E-mode performance with N-shaped graded composite barriers

Abstract This work evaluates the performance of dual gate AlGaN channel HEMTs on SiC substrate. The study analyzes two HEMT structures that differ only in barrier design, one design consists of fixed composite barriers (FCB-HEMT) i.e. there is fixed Aluminum composition x = 0.48 in the first Al x Ga1−x N barrier and x = 0.42 in the second Al x Ga1−xN barrier while the other design comprises N-shaped graded composite barriers (NGCB-HEMT) i.e. the Aluminum content varies gradually from 0.4 to 0.48 in the first AlGaN barrier and from 0.34 to 0.42 in the second AlGaN barrier. The paper concentrates on energy band diagrams, electron concentration profile, electric field distribution, drain and transfer characteristics, and the effects of high temperature on drain characteristics and mobility of the NGCB-HEMT. It has been reported that at zero gate bias, the FCB-HEMT has a drain current density of 0.137 A mm−1 while it decreases to 0.0058 A mm−1 in the case of NGCB-HEMT, thus presenting a novel approach towards enhancement-mode AlGaN HEMTs. Hence, grading can be optimized in the composite barriers to achieve enhancement mode operation of AlGaN channel HEMTs. Furthermore, the study reveals that the critical electric field of FCB-HEMT is 6.9975 M V cm−1, while that of NGCB-HEMT is 5.3124 M V cm−1, demonstrating their usefulness in electronic devices that operate at high voltages and harsh temperatures. Moreover, at higher temperatures, the phenomenon of optical phonon scattering leads to decreased mobilities, which in turn causes low drain currents relative to the drain voltage.

High-temperature transport properties of a two-dimensional weakly doped parabolic semiconductor

A version of the Mexican-hat Hamiltonian is used to study high-temperature transport properties of a two-dimensional weakly doped semiconductor with electron-hole symmetric bands. For a finite doping level and a temperature-dependent band gap, we find a closed analytical form of the temperature-dependent chemical potential. The effective concentrations of charge carriers participating in transport coefficients are analyzed in the space spanned by the total electron concentration and temperature. It is shown that these concentrations are the sum of a residual contribution and two thermally activated contributions, with a complicated dependence on temperature. The analytical expression for the Hall coefficient RHis also found. It is argued that it is a non-monotonic function of the doping level with the maximum at the doping nmax that is a linear function of temperature at high enough temperatures. The analysis of the real part of the interband conductivity shows that it is inversely proportional to incoming photon energy at low temperatures and that it is nearly constant over a wide energy range at high temperatures. This results are expected to be of significant importance in understanding transport and optical properties of weakly doped two-dimensional semiconductors with nearly symmetric parabolic bands.&#xD.

Ultrasensitive self-powered broadband ultraviolet photodetectors based on n-(Ga0.9Sn0.1)2O3/n-TiO2 heterojunction

Ga2O3-based self-powered ultraviolet (UV) photodetectors (PDs) have recently attracted much interest, but they need to be fabricated via complex and expensive vacuum equipments, and the photoresponse performances are not quite good. To solve these problems, we have developed high-property (Ga0.9Sn0.1)2O3/TiO2 heterojunction UV PDs by a low-cost, effective, and facile sol-gel way. Sn4+ possesses higher valence in comparison with Ga3+, and Sn-O bonding energy is weaker than Ga-O bonding energy, which are both in favor of increasing electron concentrations of n-type Ga2O3, resulting in improved photocurrent. TiO2 can form type-II band alignment when it contacts with (Ga0.9Sn0.1)2O3, which is beneficial for separating and transporting photo-generated carriers of the heterojunction PDs. Consequently, a high responsivity of 57.86 mA/W, large detectivity of 9.33×1011 Jones, and quick response rate with a rise/decay time of 0.05/0.66 s at a light wavelength of 230 nm and 0 V bias are achieved in the Au/(Ga0.9Sn0.1)2O3/TiO2/FTO heterojunction PDs. More encouragingly, because the (Ga0.9Sn0.1)2O3 and TiO2 possess strong absorption characteristics for UVC, and UVB and UVA light, respectively, the heterojunction self-powered PDs present superior broadband detection capacity across ultraviolet A to ultraviolet C spectrum.

Structural Aspects, Binding Interactions, Biological Activity of Co(II)‐ and Ni(II)‐N′‐(2‐fluorobenzoyl)benzo[d]thiazole‐2‐carbohydrazide Chelatess

ABSTRACTN′‐(2‐Fluorobenzoyl)benzo[d]thiazole‐2‐carbohydrazide (OFBBTCH, HL) and its chelates with Co(II) and Ni(II) have been synthesized and characterized by elemental analysis, liquid chromatography‐mass spectrometry (LC–MS), Fourier transform infrared spectroscopy (FT‐IR), ultra‐violet visible (UV–vis), nuclear magnetic resonance (NMR) spectroscopy, thermogravimetric analysis (TGA), and powder X‐ray diffraction. The conductance measurements reveal that the chelates are non‐electrolytic, and the spectral analysis indicates octahedral geometry of the chelates. The kinetic and thermodynamic parameters were obtained by Coats–Redfern relations, which shows positive Gibbs's free energy and negative entropy for both chelates. The equilibrium studies carried out by pH‐metry revealed the dissociation constant (pKa) of OFBBTCH as 8.13 and the formation of 1:1 and 1:2 Co(II)‐L and Ni(II)‐L complexes in solution. The CT‐DNA binding studies carried out by electron absorption, fluorescence quenching, steady state emissions and viscosity studies revealed hyperchromism and groove binding for HL and chelates. The Kb values calculated from electron absorption studies are 2.4 × 106, 4 × 106, and 9 × 106 M−1, from the fluorescence quenching studies Ksv values are 0.1722, 0.278, and 0.748 M−1, and Kapp values are 5.9 × 104, 1.3 × 105, and 2.9 × 105 M−1 for HL, Co(II)‐OFBBTCH and Ni(II)‐OFBBTCH, respectively. Bovine serum albumin (BSA) and human serum albumin (HSA) binding interactions were carried out by electron absorption and fluorescence quenching studies. The light switching properties of the chelates, the hydrolytic and oxidative cleavage of CT‐DNA, and the antioxidant properties were evaluated. Anti‐microbial studies carried out by pour plate method showed high activity for Ni(II)‐OFBBTCH chelate. Cytotoxicity of the compounds was performed for HeLa and MCF cell lines by MTT assay. Molecular docking studies revealed the docking of HL and Co(II)‐HL at the minor groove, and Ni(II)‐HL was docked at the major groove with hydrogen bonding.

CURRENT OSCILLATIONS IN IMPURITY SEMICONDUCTORS WITH BOTH SIGNS OF CURRENT CARRIERS IN THE PRESENCE OF AN EXTERNAL ELECTRIC FIELD, A TEMPERATURE GRADIENT AND A WEAK MAGNETIC FIELD (μ_± H<<C)

It is theoretically shown for the first time that in an external electric and weak magnetic fields, when there is a temperature gradient, an impurity semiconductor radiates energy from itself with a certain frequency. The values of the frequency of current oscillations and the limit of change of the external electric field are found. It is shown that the resistance in the medium has only ohmic character. It is stated that in the above semiconductor, when the concentration of electrons and holes are determined from the obtained expression in theory, the injection of contacts plays a major role for the appearance of the indicated current oscillation in the circuit.

Two-frequency pulsed laser irradiation to stimulate the development of coniferous trees

The possibility of using radiation from a two-frequency pulsed copper vapor laser with wavelengths of 510.6 nm and 578.2 nm with an exposure of 30 to 120 s to stimulate the development of coniferous trees (spruce, pine, larch) with a single seed irradiation is shown. The stimulation effect manifests itself at various early stages of development, such as the awakening of seeds in the aquatic environment in the first hours of the experiment (according to electron absorption spectroscopy data), seed germination, and seedling growth under stressful cultivation conditions. Possible causes of light exposure to plant seeds are discussed.

Mesoporous C-doped C3N5 as a superior photocatalyst for CO2 reduction

Use of naturally abundant solar light for CO2 reduction is a green pathway to reduce carbon footprint. C3N5 is a promising visible-light photocatalyst with enhanced local electron concentration and more active NN sites compared to g-C3N4. We herein report development of mesoporous C-doped C3N5 through a simple copolymerisation of 3-amino-1,2,4-triazole with trimesic acid via hard-templating method, which demonstrated enhanced light absorption ability and delocalised π-electron density (as evident from density functional theory calculation), resulting in efficient charge transfer to the active surface sites of the photocatalyst. The optimised C-doped mesoporous C3N5 exhibited a superior photocatalytic CO2 reduction activity with the CO evolution of 116.6 µmol·g−1, which is 4-fold and 12-fold times higher than that of C3N5 and g-C3N4 respectively. The enhanced photocatalytic CO2 conversion efficiency can be attributed to the synergetic effects of π-electron modulation by C-doping and enhanced surface-active sites brought by mesoporosity.