All-Inorganic Perovskite NiTiO3/Cs3Sb2I9 Heterostructure for Photocatalytic CO2 Reduction to CH4 with High Selectivity.

Developing efficient and stable halide perovskite-based photocatalysts for highly selectivity reduction CO2 to valuable fuels remains a significant challenge due to their intrinsic instability. Herein, a novel heterostructure featuring 2D Cs3Sb2I9 nanosheets on a 3D flower-like mesoporous NiTiO3 framework using a top-down stepwise membrane fabrication technique is constructed. The unique bilayer heterostructure formed on the 3D mesoporous framework endowed NiTiO3/Cs3Sb2I9 with sufficient and close interface contact, minimizing charge transport distance, and effectively promoting the charge transfer at the interface, thus improving the reaction efficiency of the catalyst surface. As revealed by characterization and calculation, the coupling of Cs3Sb2I9 with NiTiO3 facilitates the hydrogenation process during catalytic, directing reaction intermediates toward highly selective CH4 production. Furthermore, the van der Waals forces inherent in the 3D/2D heterostructure with face-to-face contact provide superior stability, ensuring the efficient realization of photocatalytic CO2 reduction to CH4. Consequently, the optimized 3D/2D NiTiO3/Cs3Sb2I9 heterostructure demonstrates an impressive CH4 yield of 43.4 µmol g-1 h-1 with a selectivity of up to 88.6%, surpassing most reported perovskite-based photocatalysts to date. This investigation contributes to overcoming the challenges of commercializing perovskite-based photocatalysts and paves the way for the development of sustainable and efficient CO2 conversion technologies.

Metal Valence State Modulation Strategy to Design Core@shell Hollow Carbon Microspheres@MoSe2/MoOx Multicomponent Composites for Anti-Corrosion and Microwave Absorption.

The exploitation of multicomponent composites (MCCs) has become the main pathway for obtaining advanced microwave absorption materials (MAMs). Herein, a metal valence state modulation strategy is proposed to tune the electromagnetic (EM) parameters and improve microwave absorption performances. Core@shell hollow carbon microspheres@MoSe2 and hollow carbon microspheres@MoSe2/MoOx MCCs with various mixed-valence states content are well-designed and produced by a simple hydrothermal reaction or/and heat treatment process. The results reveal that the thermal treatment of hollow carbon microspheres@MoSe2 in Ar and Ar/H2 leads to the in situ formation of MoOx and multivalence state, respectively, and the enhanced content of Mo4+ in the designed MCCs greatly boosts their impedance matching characteristics, polarization, and conduction loss capacities, which lead to their evidently improved EM wave absorption properties. Amongst, the as-prepared hollow carbon microspheres@MoSe2/MoOx MCCs achieve an effective absorption bandwidth of 5.80 GHz under a matching thickness of 1.97 mm and minimum reflection loss of -21.49 dB. Therefore, this work offers a simple and universal method to fabricate core@shell hollow carbon microspheres@MoSe2/MoOx MCCs, and a novel and feasible metal valence state modulation strategy is proposed to develop high-efficiency MAMs.

Two-dimensional ZrC2 as a novel anode material with high capacity for sodium ion battery.

Rational design of high-performance anode materials is of paramount importance for developing rechargeable lithium ion batteries (LIBs) and sodium ion batteries (SIBs). In this work, a ZrC2 monolayer is predicted by performing the particle swarm optimization (PSO) algorithm. The high energetic, dynamic, and thermal stabilities of the ZrC2 monolayer are confirmed by cohesive energy, phonon dispersion, and molecular dynamics simulations, respectively. Unexpectedly, we find that the theoretical specific capacity for Na on the ZrC2 monolayer reaches as high as 932 mA h g-1, which is even higher than that of Li. Meanwhile, the diffusion energy barrier of Na on the ZrC2 monolayer is only 0.02 eV, ensuring the ultrafast charge/discharge rate. Additionally, the calculated open-circuit voltage (OCV) suggests that the change of Na intercalation voltage is steady. Therefore, our results consistently demonstrate that the ZrC2 monolayer can be an ideal anode material for SIBs.

Synthesis and enhanced microwave absorption properties: a strongly hydrogenated TiO2 nanomaterial.

Due to its improved physical and chemical performances, a strongly hydrogenated TiO2 was designed and produced successfully by using a sealing-transfer reduction method at a relatively low temperature (425 °C). The microstructures, electromagnetic and microwave absorbing properties were investigated in detail. Experimental results revealed that: (1) the minimum reflection loss (RL) value of the hydrogenated TiO2 up to -53.8 dB (99.999 99% of EM wave attenuation) was reached at 11.2 GHz, and the RL values below -20 dB (99%) were obtained in a frequency range of 7.3-16.8 GHz. (2) Compared to pristine TiO2 and black TiO2 in other reports, the present hydrogenated TiO2 exhibited greatly improved microwave absorption performance. Moreover, the mechanism was also discussed. It was demonstrated that the excellent microwave absorption performance of the black TiO2 arose from the strong dielectric loss, excellent impedance matching and attention loss due to associated relaxation and interfacial polarization. It is expected that the hydrogenated TiO2 exhibits great potential applications in the area of high performance microwave absorbing materials. In addition, it is believed that the black TiO2 @ magnetic metals composites will display an excellent microwave absorbing property.

Photonic microwave waveforms generation based on time-domain processing.

A new photonic approach of microwave waveform generator based on time-domain synthesis is proposed and experimentally demonstrated, in which two single-drive Mach-Zehnder modulators biased at quadrature point are severed as optical pulse carvers and various microwave waveforms can be generated by carving and overlapping optical field envelopes. The theoretical analysis and simulation are developed. In experiment, a square waveform with 50% duty cycle, triangular waveform with full duty cycle, and sawtooth (or reversed-sawtooth) waveform with 50% duty cycle are generated. Furthermore, a frequency doubling sawtooth (or reversed-sawtooth) waveform with full duty cycle is also obtained.

Lignin-Derived Lightweight Carbon Aerogels for Tunable Epsilon-Negative Response.

Electromagnetic (EM) metamaterials have garnered considerable attention due to their capacity to achieve negative parameters, significantly influencing the integration of natural materials with artificially structural media. The emergence of carbon aerogels (CAs) offers an opportunity to create lightweight EM metamaterials, notable for their promising EM shielding or absorption effects. This paper introduces an efficient, low-cost method for fabricating CAs without requiring stringent drying conditions. By finely tuning the ZnCl2/lignin ratio, the porosity is controlled in CAs. This control leads to an epsilon-negative response in the radio-frequency region, driven by the intrinsic plasmonic state of the 3D carbon network, as opposed to traditional periodic building blocks. This approach yields a tunable and weakly epsilon-negative response, reaching an order of magnitude of -103 under MHz frequencies. Equivalent circuit analysis highlights the inductive characteristics of CAs, correlating their significant dielectric loss at low frequencies. Additionally, EM simulations are performed to evaluate the distribution of the electric field vector in epsilon-negative CAs, showcasing their potential for effective EM shielding. The lignin-derived, lightweight CAs with their tunable epsilon-negative response hold promise for pioneering new directions in EM metamaterials and broadening their application in diverse extreme conditions.

Mixed-Dimensional Assembly Strategy to Construct Reduced Graphene Oxide/Carbon Foams Heterostructures for Microwave Absorption, Anti-Corrosion and Thermal Insulation.

Considering the serious electromagnetic wave (EMW) pollution problems and complex application condition, there is a pressing need to amalgamate multiple functionalities within a single substance. However, the effective integration of diverse functions into designed EMW absorption materials still faces the huge challenges. Herein, reduced graphene oxide/carbon foams (RGO/CFs) with two-dimensional/three-dimensional (2D/3D) van der Waals (vdWs) heterostructures were meticulously engineered and synthesized utilizing an efficient methodology involving freeze-drying, immersing absorption, secondary freeze-drying, followed by carbonization treatment. Thanks to their excellent linkage effect of amplified dielectric loss and optimized impedance matching, the designed 2D/3D RGO/CFs vdWs heterostructures demonstrated commendable EMW absorption performances, achieving a broad absorption bandwidth of 6.2 GHz and a reflection loss of - 50.58 dB with the low matching thicknesses. Furthermore, the obtained 2D/3D RGO/CFs vdWs heterostructures also displayed the significant radar stealth properties, good corrosion resistance performances as well as outstanding thermal insulation capabilities, displaying the great potential in complex and variable environments. Accordingly, this work not only demonstrated a straightforward method for fabricating 2D/3D vdWs heterostructures, but also outlined a powerful mixed-dimensional assembly strategy for engineering multifunctional foams for electromagnetic protection, aerospace and other complex conditions.

Understanding the Behaviors of Plasmon-Induced Hot Carriers and Their Applications in Photocatalysis.

Photocatalysis driven by plasmon-induced hot carriers has been gaining increasing attention. Recent studies have demonstrated that plasmon-induced hot carriers can directly participate in photocatalytic reactions, leading to great enhancement in solar energy conversion efficiency, by improving the catalytic activity or changing selectivity. Nevertheless, the utilization efficiency of hot carriers remains unsatisfactory. Therefore, how to correctly understand the generation and transfer process of hot carriers, as well as accurately differentiate between the possible mechanisms, have become a key point of attention. In this review, we overview the fundamental processes and mechanisms underlying hot carrier generation and transport, followed by highlighting the importance of hot carrier monitoring methods and related photocatalytic reactions. Furthermore, possible strategies for the further characterization of plasmon-induced hot carriers and boosting their utilization efficiency have been proposed. We hope that a comprehensive understanding of the fundamental behaviors of hot carriers can aid in designing more efficient photocatalysts for plasmon-induced photocatalytic reactions.

Flower-like NiO to flower-like NiO/Ni@C microspheres: An effective strategy to comprehensively improve the loss capabilities.

It was well recognized that the penetrated electromagnetic (EM) wave could be dissipated by means of magnetic loss, polarization loss and conduction loss. In order to improve their loss capacities and take full advantage of flower-like geometrical morphology, in this study, we proposed a simple route for the production of flower-like core@shell structure NiO/Ni@C microspheres through the carbon thermal reaction using NiO microflowers as precursor. The obtained results revealed that our proposed strategy successfully synthesized the core@shell structure magnetic carbon-based multicomponent nanocomposites without destroying the geometrical morphology of precursor. By regulating the annealing temperature, the as-prepared NiO/Ni@C microspheres with different contents of Ni and degrees of graphitization could be selectively synthesized, which effectively boosted their magnetic loss, polarization loss and conduction loss capabilities. Therefore, the elaborately designed NiO/Ni@C microspheres displayed the superior microwave absorption performances including strong absorption capability, broad absorption bandwidth and thin matching thicknesses compared to the NiO precursor. In summary, our findings not only provided a simple route to design and synthesize flower-like core@shell structure magnetic carbon-based nanocomposites as novel microwave absorbers, but also presented an effective strategy to comprehensively improve their loss capacities.

Metaphosphate-Bridged Interface Boosts High-Performance Lithium Storage.

Carbon materials with well-dispersed SnOx particles exhibit excellent lithium-storage performance. However, the volume change of SnOx and the weak interaction between SnOx and carbon induce an unsteady SnOx-C interface during the lithiation/delithiation process. This phenomenon results in enhanced charge transfer resistance and reduced electrical contact of active materials, which leads to low reversibility of tin oxidation, restricted capacity, sluggish kinetics, structural deterioration, and rapid capacity decay. Herein, tin oxide/carbon composites with a metaphosphate-bridged interface are synthesized to construct a robust interfacial contact between tin oxides and carbon. The metaphosphate group functions as a bridge between SnOx and carbon and results in excellent electrochemical stability during the charge/discharge process, which is favorable for electrode structural integrity. The formation of the metaphosphate-bridged interface provides a steady transport channel for e-/Li+ and thus improves the reversibility of the conversion reaction. The enhanced charge transfer and interaction can also boost the charge transfer between SnOx and carbon, which leads to higher SnOx utilization. Thus, the prepared P-SnOx/C anode exhibits enhanced lithium-storage performance in terms of specific capacity, cycling stability, and rate performance.

Constructing MoSe2/MoS2 and MoS2/MoSe2 inner and outer-interchangeable flower-like heterojunctions: A combined strategy of interface polarization and morphology configuration to optimize microwave absorption performance.

Interfacial polarization and geometrical morphology play a significant role in the attenuation of electromagnetic (EM) wave. Herein, the two-dimensional (2D)/2D heterojunction with flower-like geometrical morphology is proposed and produced, which may simultaneously provide a large contact area for achieving strong interfacial polarization and activates more sites for the possible multiple EM wave reflection and scattering. By adopting a simple two-step hydrothermal method, MoSe2/MoS2and MoS2/MoSe2 inner and outer-interchangeable heterojunctions consisting of 2D MoSe2 and MoS2 nanosheets with flower-like geometrical morphology were successfully synthesized. The results revealed that the hydrothermal temperatures significantly impacted the flower-like geometrical morphology and MoS2 content. By optimizing the microstructures, the designed MoSe2/MoS2 and MoS2/MoSe2 heterojunctions presented enhanced comprehensive EM wave absorption properties (EMWAPs), possessing strong absorption capability, wide absorption bandwidth and thin matching thicknesses. Generally, this work demonstrates that the optimized EMWAPs of designed heterojunctions mainly originate from the special interfaces and morphology configuration, which also paves a new way for the designing and synthesis of transition metal dichalcogenides-based heterojunction as a novel and desirable candidate for high-performance microwave absorbers.

A generalizable strategy for constructing ultralight three-dimensional hierarchical network heterostructure as high-efficient microwave absorber.

Using previous models and theories to construct and develop high-efficient microwave absorbers (MAs) should be a strategic and effective ways to optimize the electromagnetic wave attenuation. Herein, the ultralow density and flexible graphene oxide foam (GOF) and reduced graphene oxide foam (RGOF)/MoS2 nanosheets were designed and fabricated by the method of chemical vapor deposition and hydrothermal reaction. The obtained GOF and RGOF/MoS2 samples exhibited very excellent microwave absorption properties while their densities were merely 0.0082 and 0.0084 g•cm-3, respectively. More importantly, benefiting from the excellent synergistic effect between RGOF and MoS2, the designed RGOF/MoS2 well inherited the combined advantages of GOF and MoS2 in terms of strong absorption abilities, broad absorption bandwidth and thin matching thicknesses. The values of minimum reflection loss and effective frequency bandwidth for RGOF/MoS2 sample could reach up to -62.92 dB with the matching thickness of 2.27 mm and 4.48 GHz with the matching thickness of 2.12 mm, which were very desirable for high-performance MAs. Moreover, the obtained results indicated that the microwave absorption properties of RGOF/MoS2 sample could be further optimized by regulating the MoS2 content. Therefore, a new and effective strategy was proposed to develop high efficiency MAs with ultra-lightweight, wide-band, thin thickness and strong absorption capabilities.

Morphology optimization strategy of flower-like CoNi2S4/Co9S8@MoS2 core@shell nanocomposites to achieve extraordinary microwave absorption performances.

Morphology optimization is an effective strategy to take full advantage of interface polarization for the improvement of electromagnetic wave attenuation capability. Herein, a general route was proposed to produce the flower-like core@shell structured MoS2-based nanocomposites through a simple hydrothermal process. Through the in-situ hydrothermal reaction between the Mo and S sources on the surface of CoNi nanoparticles, flower-like core@shell structured CoNi2S4/Co9S8@MoS2 nanocomposites could be successfully synthesized. By regulating the hydrothermal temperature, the flower-like geometrical morphology of samples could be effectively optimized, and the as-prepared sample (S2) synthesized at 200 °C displayed very excellent flower-like morphology compared to the samples (S1 and S3) obtained at 180 and 220 °C. Owing to the excellent interface polarization effect, the as-prepared S2 presented the evidently superior comprehensive microwave absorption properties in terms of strong aborption capability, wide absorption bandwidth and thin matching thicknesses compared to those of S1 and S3. The as-prepared core@shell structured CoNi2S4/Co9S8@MoS2 sample with very excellent flower-like morphology simultaneously displayed the minimal reflection loss of -50.61 dB with the matching thickness of 2.98 mm, and the effective absorption bandwidth of 8.40 GHz with the matching thickness of 2.36 mm. Therefore, we provided a general route for the production of flower-like core@shell structured MoS2-based nanocomposites, which could make the best of interface polarization to develop high-efficiency microwave absorbers.

Magnetic modulation of core@shell MoS2-based flower-like multicomponent nanocomposites to improve microwave attenuation.

Nanocomposites with a three-dimensional (3D) flower-like geometrical morphology were considered as excellent microwave absorbers (MAs) because of the numerous effective sites for the multiple reflections of electromagnetic (EM) wave. Herein, for optimizing the EM matching characteristic and taking full advantage of interface polarization, a strategy of magnetic modulation was proposed to further improve the EM wave absorption performances (EMWAPs) of MoS2-based nanocomposites. We adopted a simple hydrothermal route and a combined method of hydrothermal treatment/hydrogen reduction to synthesize core@shell CoFe2O4@MoS2 and CoFe@MoO2/MoS2 flower-like nanocomposites, respectively. The obtained results indicated that the hydrogen reduction effectively improved their magnetic properties and magnetic loss capabilities, and their 3D flower-like geometrical morphologies were well maintained during the hydrogen reduction process. The obtained core@shell CoFe@MoO2/MoS2 flower-like nanocomposites presented the extraordinary comprehensive EMWAPs including the optimal reflection loss value of -54.83 dB with the matching thicknesses (dm) value of 2.05 mm and effective absorption bandwidth value of 6.40 GHz with the dm value of 2.59 mm, which were evidently superior to the properties of CoFe2O4@MoS2. Therefore, the findings provided an effective pathway to further improve EMWAPs of MoS2-based core@shell nanocomposites and the as-prepared core@shell CoFe@MoO2/MoS2 flower-like nanocomposites could be utilized as the novel high-efficient MAs.

1T-MoS2 Coordinated Bimetal Atoms as Active Centers to Facilitate Hydrogen Generation.

Anchoring single metal atoms has been demonstrated as an effective strategy to boost the catalytic performance of non-noble metal 1T-MoS2 towards hydrogen evolution reaction (HER). However, the dual active sites on 1T-MoS2 still remain a great challenge. Here, first-principles calculations were performed to systematically investigate the electrocatalytic HER activity of single and dual transition metal (TM) atoms bound to the 1T-MoS2 monolayer (TM@1T-MoS2). The resulted Ti@1T-MoS2 exhibits excellent structural stability, near-thermoneutral adsorption of H* and ultralow reaction barrier (0.15 eV). It is a promising single metal atom catalyst for HER, outperformed the reported Co, Ni and Pd anchoring species. Surprisingly, by further introducing Pd atoms coordinated with S atoms or S vacancies on the Ti@1T-MoS2 surface, the resulted catalyst not only maintains the high HER activity of Ti sites, but also achieves new dual active moiety due to the appropriate H* adsorption free energy on Pd sites. This work is of great significance for realizing dual active centers on 1T-MoS2 nanosheets and offers new thought for developing high-performance electrocatalysts for HER.

Solving the Trifunctional Activity Challenge of Catalysts in Unitized Regenerative Fuel Cells via 1T-MoS2-Coordinated Single Pd Atoms.

Developing high-efficiency and low-cost multifunctional electrocatalysts is the core of unitized regenerative fuel cells (URFC), yet it remains a great challenge. Here, by performing first-principles calculations, we report the atomic-level electrocatalytic activity mechanism of 3d, 4d, and 5d monoatomic transition metals (TM) bound to the 1T-MoS2 monolayer for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Their structural stabilities are evaluated via the formation energy, elastic constant, and molecular dynamics simulations. Compared with the Co-N4-C single atom catalyst (SAC), the resulting Pd@1T-MoS2 SAC exhibits better bifunctional catalytic activity, with OER overpotential as low as 0.43 V and an ORR overpotential of 0.40 V. The dual volcano plot demonstrates that the bifunctional OER and ORR activities of Pd@1T-MoS2 originate from the neither strong nor weak OH* adsorption and the suitable d-band center (-1.83 eV) of the Pd active center. In conjunction with the intrinsic activity of the 1T-MoS2 monolayer for hydrogen evolution reaction, the Pd@1T-MoS2 SAC is a competitive and promising trifunctional electrocatalyst for sustainable energy conversion and storage systems.

Parity anomaly of lattice Maxwell fermions in two spatial dimensions.

Unconventional lattice fermions with high degeneracies that are not Weyl or Dirac fermions have attracted increased attention in recent years. In this paper, we consider pseudospin-1 Maxwell fermions and the (2 + 1)-dimensional parity anomaly, which are not constrained by the fermion doubling theorem. We derive the Hall conductivity of a single Maxwell fermion and explain how each Maxwell fermion has a quantized Hall conductance of e 2/h. Parity is spontaneously broken in the effective theory of lattice Maxwell fermions interacting with an (auxiliary) U(1) gauge field, leading to an effective anomaly-induced Chern-Simons theory. An interesting observation about the parity anomaly is that the lattice Maxwell fermions are not constrained by the fermion doubling theorem, so a single Maxwell fermion can exist in a lattice. In addition, our work considers the quantum anomaly in odd-dimensional spinor space.

Outstanding comprehensive performance versus facile synthesis: Constructing core and shell-interchangeable nanocomposites as microwave absorber.

It is still a great challenge to develop high-performance microwave absorption materials (MAMs). Herein, we first proved the excellent synergistic effect of Fe3O4/MoS2 heterostructure based on the theoretical calculations. To effectively utilize the synergistic effect and morphology, core and shell-interchangeable Fe3O4@MoS2 and MoS2@Fe3O4 nanocomposites (NCs) were elaborately constructed. By controlling the hydrothermal temperature, different MoS2 morphologies and contents of Fe3O4@MoS2 NCs were produced, which simultaneously displayed the optimal reflection loss (RL) values (~-50 dB), broad absorption bandwidth (⩾5.0GHz) and high chemical stabilities. With the synthesis temperature increasing from 170 °C to 200 °C, their outstanding microwave absorption (MA) capabilities moved towards the high frequency region and thin matching thickness. Impressively, the Fe3O4@MoS2 obtained at 200 °C presented a minimum RL value of -50.75 dB with the thickness of 2.90 mm and an absorption bandwidth of 5.0 GHz with the thickness of 1.71 mm, and the excellent MA capabilities (RL values <-30 dB) with the low matching thicknesses (<2 mm) could be observed in the frequency range of X and Ku bands. Moreover, compared to the reverse structure MoS2@Fe3O4, the core@shell structure Fe3O4@MoS2 exhibited evidently superior MA comprehensive properties in terms of low optimal RL value, broad absorption bandwidth and high chemical stability, which could be ascribed to the improved impedance matching and microwave attenuation characteristics. Generally, the proposed flower-like core@shell structure Fe3O4@MoS2 NCs presented very extraordinary MA comprehensive properties, which were very attractive candidates for high-performance MAMs.

Water-assisted and controllable synthesis of core/shell/shell structured carbon-based nanohybrids, and their magnetic and microwave absorption properties.

By controlling the pyrolysis temperature, core/shell/shell structured Fe/Fe5C2/carbon nanotube bundles (Fe/Fe5C2/CNTBs), Fe/Fe3C/helical carbon nanotubes (Fe/Fe3C/HCNTs) and Fe/Fe3C/chain-like carbon nanospheres (Fe/Fe3C/CCNSs) with high encapsulation efficiency could be selectively synthesized in large-scale by water-assisted chemical vapor deposition method. Water vapor was proved to play an important role in the growth process. Because of α-Fe nanoparticles tightly wrapped by two layers, the obtained core/shell/shell structured nanohybrids showed high stabilities and good magnetic properties. The minimum reflection loss values of the as-prepared nanohybrids reached approximately -15.0, -46.3 and -37.1 dB, respectively. The excellent microwave absorption properties of the as-prepared core/shell/shell structured nanohybrids were considered to the quarter-wavelength matching model. Moreover, the possible enhanced microwave absorption mechanism of the as-prepared Fe/Fe3C/HCNTs and Fe/Fe3C/CCNSs were discussed in details. Therefore, we proposed a simple, inexpensive and environment-benign strategy for the synthesis of core/shell/shell structured carbon-based nanohybrids, exhibiting a promising prospect as high performance microwave absorbing materials.

Preparation of porous Fe2O3 nanorods-reduced graphene oxide nanohybrids and their excellent microwave absorption properties.

In this paper, α-Fe2O3 nanoparticles (NPs)-reduced graphene oxide (RGO), α-FeOOH nanorods (NRs)-RGO and porous α-Fe2O3 NRs-RGO could be selectively synthesized by hydrothermal method. The investigations indicated that the obtained α-Fe2O3 NPs, α-FeOOH NRs and porous α-Fe2O3 NRs were either attached on the surface of RGO sheets or coated uniformly by the RGO sheets. And the as-prepared nanohybrids exhibited excellent microwave absorption performance, which was proved to be ascribed to the quarter-wavelength matching model. The optimum reflection loss (RL) values for α-Fe2O3 NPs-RGO, α-FeOOH NRs-RGO and porous α-Fe2O3 NRs-RGO were ca. -32.3, -37.4 and -71.4 dB, respectively. Moreover, compared to the obtained α-Fe2O3 NPs-RGO and α-FeOOH NRs-RGO, the as-prepared porous α-Fe2O3 NRs-RGO nanohybrids exhibited enhanced microwave absorption properties because of their special structure and synergetic effect. The possible enhanced microwave absorption mechanisms were discussed in details. Our results confirmed that the geometrical morphology had a great influence on their microwave absorption properties, which provided a promising approach to exploit high performance microwave absorbing materials.