Interfacial Loss Research Articles

Interfacial Proton Precompensation: Suppressing Deprotonation-Driven Lattice Collapse for Enhanced Efficiency and Stability in Perovskite Solar Cells.

The chemical property of the buried interface plays a crucial role in improving the performance and stability of perovskite solar cells (PSCs). The SnO2/perovskite interface prepared from SnO2 alkaline hydrogel with high proton affinity triggers directional migration and irreversible reactions of protons, exacerbating the disintegration of perovskite crystal. In this study, we proposed proton precompensation strategy to suppress the deprotonation effect of the buried interface and improve the durability of the devices. By modulating the chemical environment and surface energy state of the buried interface, the domain-limiting and spontaneous compensation of protons in formamidinium (FA+) under Coulomb force were achieved, thereby stabilizing the perovskite crystal structure. The stability of target perovskite films under UV illumination and heating at 85 °C was significantly enhanced. As a result, the devices can retain around 90% of their initial power conversion efficiency (PCE) after 1000 h of continuous irradiation at the maximum power point (MPP). Moreover, due to the reduction of defect content at the buried interface and the improvement of conductivity and carrier mobility by the precompensation treatment, the interfacial energy loss and non-radiative recombination were substantially diminished. The target PSC devices exhibited much higher PCE of 25.55% than the control devices (23.03%).

Interfacial Proton Precompensation: Suppressing Deprotonation‐Driven Lattice Collapse for Enhanced Efficiency and Stability in Perovskite Solar Cells

The chemical property of the buried interface plays a crucial role in improving the performance and stability of perovskite solar cells (PSCs). The SnO2/perovskite interface prepared from SnO2 alkaline hydrogel with high proton affinity triggers directional migration and irreversible reactions of protons, exacerbating the disintegration of perovskite crystal. In this study, we proposed proton precompensation strategy to suppress the deprotonation effect of the buried interface and improve the durability of the devices. By modulating the chemical environment and surface energy state of the buried interface, the domain‐limiting and spontaneous compensation of protons in formamidinium (FA+) under Coulomb force were achieved, thereby stabilizing the perovskite crystal structure. The stability of target perovskite films under UV illumination and heating at 85 °C was significantly enhanced. As a result, the devices can retain around 90% of their initial power conversion efficiency (PCE) after 1000 h of continuous irradiation at the maximum power point (MPP). Moreover, due to the reduction of defect content at the buried interface and the improvement of conductivity and carrier mobility by the precompensation treatment, the interfacial energy loss and non‐radiative recombination were substantially diminished. The target PSC devices exhibited much higher PCE of 25.55% than the control devices (23.03%).

Boosting Carrier Transport in Quasi-2D/3D Perovskite Heterojunction for High-Performance Perovskite/Organic Tandems.

Wide-bandgap (WBG) perovskites are continuously in the limelight owing to their applicability in tandem solar cells. The main bottlenecks of WBG perovskites are interfacial non-radiative recombination and carrier transport loss caused by interfacial defects and large energy-level offsets, which induce additional energy losses when WBG perovskites are stacked with organic solar cells in series because of unbalanced carrier recombination in interconnecting layer (ICL). To solve these issues, 1,3-propanediammonium iodide (PDADI) is incorporated to form Dion-Jacobson -phase quasi-2D perovskites with mixed high-n-values in WBG perovskites. PDADI simultaneously repairs the shallow/deep defects and establishes a Type-II energy-level alignment between quasi-2D/3D and 3D perovskites for rapid carrier extraction. More importantly, the short-chain diammonium cation in quasi-2D perovskite with high n-values results in a short Pb-I inorganic layer spacing, which enhances the interlayer electronic coupling and weakens the quantum-well confinement effect that restricts carrier transport. The suppressed transport loss increases the electron concentration in the ICL for balanced carrier recombination. The 0.0628 and 1.004 cm2 perovskite/organic tandems achieve remarkable efficiencies of 25.92% and 24.63%, respectively. The quasi-2D capping layer can inhibit ion migration, allowing perovskite/organic tandems to show excellent operational stability (T85 >1000h).

Optimization of Electromagnetic-Wave Reflectivity Performance of Electromagnetic Shielding Yarn Prepared by Evaporation-Induced Sintering of Ga60.5In25Sn13Zn1.5 Alloy with Nanosilicates.

Electromagnetic interference (EMI) shielding textiles have received widespread attention, and liquid metal (LM) shows superiority in flexible and deformable electronics. Here, we introduce a novel method using nanosilicates to help sinter LM through capillary evaporation, resulting in strong adhesion to substrates. By adjustment of the amount of nanosilicates, flexible EMI shielding yarns are created using dip-coating and curing processes. The sintered LM tightly adhered to the undulating and uneven surfaces of polyurethane (PU) yarns. The as-fabricated ION/LM@PU ("ION" is abbreviation of "ionogel") has strong EMI shielding and low EM-wave reflection due to the high electrical conductivity of the LM layer and good impedance matching of P(AAm-co-AA) ionogel. The addition of an ionogel enhances EM-wave absorption and strengthens interfacial polarization, making it an effective green EMI shielding yarn for reducing secondary reflection pollution. ION/LM@PU exhibited high total electromagnetic interference shielding effectiveness (EMI SET) (∼56 dB), low reflected power coefficient (R) (∼0.153), high impedance matching (|Zin/Z0| ≈ 0.660), high tensile strength (∼23.75 MPa), and high elastic recovery (∼0.92 at 10th stretch-release cycle). The EMI shielding mechanism of ION/LM@PU ± 60° is composed of reflective loss and absorption loss (including multireflective loss, conduction loss, dipole polarization loss, and interfacial polarization loss).

Stereo-Hindrance Induced Conformal Self-Assembled Monolayer for High Efficiency Inverted Perovskite Solar Cells.

Self-assembled monolayers (SAMs) are employed as hole-selective contacts in inverted perovskite solar cells (PSCs) and have achieved record power conversion efficiency (PCE) over 26%. However, the tendency of extensively employed SAM [2-(3,6-Dimethoxy-9H-carbazol-9-yl)ethyl]phosphonic acid to aggregate leads to its uneven coverage to the transparent conducting oxide substrate, which subsequently compromises the photovoltaic performance. Herein, a novel tert-butyl functionalized phosphonic acid carbazole SAM is developed, i.e., (4-(3,6-di-tert-butyl-9H-carbazol-9-yl)butyl)phosphonic acid (tBu-4PACz), and introduced to a mixed SAM system as the hole-extraction layer in inverted PSCs. The stereo-hindrance of the bulky tert-butyl group prevents undesired aggregation and leads to better conformality, which facilitates more efficient hole-extraction and suppresses interfacial recombination losses. The tBu-4PACz SAM-based inverted PSC has achieved record level PCE of 26.25% (26.21%, certificated) with outstanding fill factors over 86%. Moreover, the mixed SAM based inverted PSC devices maintained over 94.7% of their initial efficiency after 500h continuous maximum power-point tracking under simulation 1-sun irradiation.

In situ formation SiC nanowires on loofah sponge-derived porous carbon for efficient electromagnetic wave absorption

A lightweight, heterogeneous, three-dimensional network-structured composite has been meticulously developed with the specific goal of optimizing impedance matching and elevating electromagnetic wave absorption properties. SiC nanowires-carbon composites were synthesized through a novel process involving combined carbothermal reduction and chemical vapor deposition, utilizing loofah sponge as the foundational material. Accessible and cost-effective organosilane waste was applied as the silicon source. The resulting composites manifest exceptional electromagnetic wave absorption performance with a minimum reflection loss of − 46.34 dB and a wide effective bandwidth of 3.84 GHz at a thin thickness of 1.9 mm. Superior electromagnetic wave absorption is attributed to synergistic interplay of multiple interfacial polarizations, dipole polarization, conductive losses, and multiple reflections and scattering. This work presents an innovative pathway toward fabricating highly efficient electromagnetic wave-absorbing materials while effectively repurposing recycled waste.

Fabrication and electromagnetic wave absorption modulation of high-performance (TaNbTiV)₂AlC MAX phase

Electromagnetic (EM) wave technology is widely used in both military and civilian applications, increasing interest in EM wave absorption materials for information security and environmental protection. This study examines the synthesis and EM wave absorption properties of M-site compositional complex MAX phase (TaNbTiV)2AlC. Using Ta, Nb, Ti, V, Al, and graphite powders, pure (TaNbTiV)2AlC was synthesized at 1400 °C. SEM and EDS confirmed homogeneous elemental distribution and morphology, while TEM and SAED analyses revealed the atomic structure. EM wave absorption was tested using (TaNbTiV)2AlC/paraffin wax composites with varying (TaNbTiV)2AlC content in the 2–18 GHz range. The main attenuation mechanisms identified were interfacial polarization, dielectric loss, and conductive loss. Optimal absorption was achieved at 30 vol% (TaNbTiV)2AlC, with a reflection loss of −43.83 dB and an effective absorption bandwidth of 3.49 GHz. The study demonstrates that the control of establishing a “near-conductive network” of fillers could be advantageous in achieving optimal electromagnetic wave absorption performance using fillers possessing high electrical conductivity, such as MAX phase materials.

Suppressing high voltage chemo-mechanical degradation in single crystal nickel-rich cathodes for high-performance all-solid-state lithium batteries

Sulfide-based all-solid-state lithium batteries (SASSLBs) suffer from electrochemo.mechanical damage to Ni-rich oxide-based cathode active materials (CAMs), primarilycaused by severe volume changes, results in significant stress and strain cuase micro-cracks, and interfacial contact loss at potentials > 4.3 V(vs. Li/Li+). Quantifying micro-cracks and voids in cathode active materials (CAMs) can reveal the degradation mechanisms of Ni-rich oxide-based cathodes during electrochemical cycling. Nonetheless, the origin of electrochemical-mechanical damage remains unclear. Herein, We have developed a multifunctional PEG-based soft buffer layer (SBL) on the surface of carbon black (CB). This layer functions as a percolation network in the single crystal LiNi0.83Co0.07Mn0.1O2 and Li6PS5Cl composite cathode layer, ensuring superior ionic conductivity, reducing void formation and particle cracking, and promoting uniform utilization of the cathode active material in all-solid-state lithium batteries (ASSLBs). STEM-HAADF combined with nanoscale X-ray holo-tomography and plasma-focused ion beam scanning electron microscopy confirmed that the PEG-based SBL mitigated strain induced by reaction heterogeneity in the cathode. This strain produces lattice stretches, distortions, and the formation of curved transition metal oxide layers near the surface, contributing to structural degradation at elevated voltages. Consequently, ASSLBs with a LiNi0.83Co0.07Mn0.1O2 cathode containing LCCB-10 (CB/PEG mass ratio: 100/10) demonstrate a high areal capacity (2.53 mAh g–1/0.32 mA g–1) and remarkable rate capability (0.58 mAh g–1 at 1.4 mA g–1), with 88% capacity retention over 1000 cycles.

Introducing defects and crystalline/amorphous heterostructures on mesoporous TiO2 to realize broadband microwave absorption

Titanium dioxide (TiO2), once considered a promising material for microwave absorption, still faces significant challenges in achieving broadband absorption performance. To address this issue, herein, a simple approach is reported for successfully introducing defects and crystalline/amorphous heterostructures onto mesoporous TiO2 (Meso-am-TiO2-x). This study demonstrates the superior microwave absorbing properties of Meso-am-TiO2-x, particularly in the low-frequency range. A reflection loss of up to -25.7 dB is achieved with a thickness of 4.6 mm, and the effective absorption bandwidth (EAB) value extends to 4.32 GHz. The experimental results indicate that the synergistic effects of the high specific surface area of mesoporous TiO2, defects-induced conduction loss, defect-induced dipole polarization loss, and interfacial polarization loss between the crystalline and amorphous heterostructures enhance the microwave absorption properties of Meso-am-TiO2-x. This study provides insights toward developing innovative low-frequency broadband TiO2 absorbers.

Quantifying Heterogeneous Interface Effect of Fe3O4(111)/C for Enhanced Low-Frequency Electromagnetic Wave Absorption

How to tailor electromagnetic parameters of multi-component materials is the fundamental issues for low-frequency electromagnetic wave absorbers (EMA). However, there remains a challenge to accurately elucidate the impact of respective components at heterogeneous interfaces on the EMAs, not to mentioning the further quantitative contribution of the interfacial effect to the electromagnetic loss. In this paper, we for the first time separated the Fe3O4(111)/C heterogeneous interface of Fe3O4@C via a controllable interfacial separation strategy, meanwhile ensuring the consistent microstructure and the ratio of each component, as well as the unchanged macroscopic structure of the particles. Once all potential influences on electromagnetic parameters have been independently studied, the unique difference in heterogeneous interfaces enabled us to quantitatively evaluate the effect of them on electromagnetic parameters. Both experimental and density functional theory (DFT) calculation results consistently demonstrate that the Fe3O4(111)/C heterointerface increases carrier concentration and conductivity, thereby enhancing the imaginary part of the dielectric constant. Very distinguished from traditional interfacial polarisation mechanism presented in previous publications, this study introduces a novel interfacial loss mechanism primarily characterized by conductivity loss, which is rigorously investigated in a quantitative way. This discovery offers a novel approach for designing controllable heterogeneous interfaces and manipulating electromagnetic parameters in multicomponent EMAs.

AgNWs self-assembly along coaxially electrospun SEBS-PVP core-sheath fibers for stretchable conductive membranes with low interfacial losses

In this paper, core-sheath fibers with poly(styrene-ethylene/butylene-styrene) triblock copolymer (SEBS) as the core layer and polyvinylpyrrolidone (PVP) of different molecular weights as the sheath layer were prepared by coaxial electrospinning. Amphiphilic triblock copolymers were added to the SEBS core layer, and the fusion of incompatible SEBS-PVP at the core-sheath interface was further promoted by appropriate solvent post-treatment. Polydopamine (PDA) was in situ polymerized on the surface of SEBS-PVP fibers, so that silver nanowires (AgNWs) with high aspect ratios were conformally self-assembled along the fibers to form good interfacial bonding, so that the SEBS-PVP/AgNW composite membrane has high conductivity and exhibits good interfacial transfer effect in cyclic stretching under large strain. Based on core-sheath nanofibers and self-assembly, the excellent interfacial transfer gives SEBS-PVP/AgNW low viscoelastic loss, integrated large tensile strain sensing and stable Joule heating effect, which is conducive to the development and application of multifunctional stretchable electronics.

Interface kinetic manipulation enabling efficient and reliable Mg3Sb2 thermoelectrics

Development of efficient and reliable thermoelectric generators is vital for the sustainable utilization of energy, yet interfacial losses and failures between the thermoelectric materials and the electrodes pose a significant obstacle. Existing approaches typically rely on thermodynamic equilibrium to obtain effective interfacial barrier layers, which underestimates the critical factors of interfacial reaction and diffusion kinetics. Here, we develop a desirable barrier layer by leveraging the distinct chemical reaction activities and diffusion behaviors during sintering and operation. Titanium foil is identified as a suitable barrier layer for Mg3Sb2-based thermoelectric materials due to the creation of a highly reactive ternary MgTiSb metastable phase during sintering, which then transforms to stable binary Ti-Sb alloys during operation. Additionally, titanium foil is advantageous due to its dense structure, affordability, and ease of manufacturing. The interfacial contact resistivity reaches below 5 μΩ·cm2, resulting in a Mg3Sb2-based module efficiency of up to 11% at a temperature difference of 440 K, which exceeds that of most state-of-the-art medium-temperature thermoelectric modules. Furthermore, the robust Ti foil/Mg3(Sb,Bi)2 joints endow Mg3Sb2-based single-legs as well as modules with negligible degradation over long-term thermal cycles, thereby paving the way for efficient and sustainable waste heat recovery applications.

Carbon nanolayer-mounted single metal sites enable dipole polarization loss under electromagnetic field.

Surface modulation strategies have spurred great interest with regard to regulating the morphology, dispersion and flexible processability of materials. Unsurprisingly, customized modulation of surfaces is primed to offer a route to control their electronic functions. To regulate electromagnetic wave (EMW) absorption applications by surface engineering is an unmet challenge. Thanks to pyrolyzing surface-anchored metal-porphyrin, here we report on the surface modulation of four-nitrogen atoms-confined single metal site on a nitrogen-doped carbon layer (sM(N4)@NC, M = Ni, Co, Cu, Ni/Cu) (sM=single metal; NC= nitrogen-doped carbon layer) that registers electromagnetic wave absorption. Surface-anchored metal-porphyrins are afforded by attaching them onto the polypyrrole surface via a prototypical click reaction. Further, sM(N4)@NC is experimentally found to elicit an identical dipole polarization loss mechanism, overcoming the handicaps of conductivity loss, defects, and interfacial polarization loss among the current EMW absorber models. Importantly, sM(N4)@NC is found toexhibit an effective absorption bandwidth of 6.44 and reflection loss of -51.7 dB, preceding state-of-the-art carbon-based EMW absorbers. This study introduces a surface modulation strategy to design EMW absorbers based on single metal sites that enable fine-tunable and controlled absorption mechanism with atomistic precision.

Surface modification of fibres with silane for enhancing the durability of FRP composites as reinforcement for seawater sea sand concrete (SWSSC): A review

This review discusses the necessity of surface modification to effectively use fibre-reinforced polymers (FRPs) as reinforcements for seawater and sea sand concrete (SWSSC). FRPs can be a viable reinforcement material for SWSSC as an alternative to the traditional carbon steel reinforcement that will suffer unacceptably high rates of corrosion due to the very high chloride content of the SWSSC environment. FRPs exhibit mechanical properties similar to steels but suffer insignificant degradation/corrosion due to chloride. However, the fibres in certain FRPs (such as basalt FRPs and glass FRPs) suffer degradation due to attack by the alkaline environment of concrete, causing degradation in fibre-matrix interfacial strength and loss of FRPs’s overall mechanical strength and durability. Therefore, fibres used in such FRPs require suitable surface modification to ameliorate their degradation, enabling their practical use as reinforcements of SWSSC. While carbon fibre-reinforced polymers (CFRPs) demonstrate superior resistance to alkali-induced degradation, their widespread use in large-scale civil engineering is hindered by high costs. In this review, more economic alternatives, i.e., basalt fibre-reinforced polymers (BFRPs) and glass fibre-reinforced polymers (GFRPs) are critically reviewed. To enhance the durability of FRPs and mitigate alkali-induced degradation of the basalt/glass fibres, suitable surface modifications are necessary to safeguard the mechanical properties of FRPs. Underpinned by a comprehensive discussion on the necessity of surface modification of fibres for the use of FRPs in SWSSC environment, this review focuses on the potential of advanced approaches for surface modifications of the fibres, i.e., coatings of silanes, and silanes impregnated with graphene nanoplatelets (GNPs), graphene oxide (GO) and its functionalised derivatives or metal oxides (such as SiO2, ZrO2, Al2O3, TiO2 and CeO2). This review critically discusses the opportunities for suitable surface modification of basalt and glass fibres for enabling the durable use of FRPs as reinforcements for sweater sea sand concrete.

Design and Simulation for Minimizing Non-Radiative Recombination Losses in CsGeI2Br Perovskite Solar Cells.

CsGeI2Br-based perovskites, with their favorable band gap and high absorption coefficient, are promising candidates for the development of efficient lead-free perovskite solar cells (PSCs). However, bulk and interfacial carrier non-radiative recombination losses hinder the further improvement of power conversion efficiency and stability in PSCs. To overcome this challenge, the photovoltaic potential of the device is unlocked by optimizing the optical and electronic parameters through rigorous numerical simulation, which include tuning perovskite thickness, bulk defect density, and series and shunt resistance. Additionally, to make the simulation data as realistic as possible, recombination processes, such as Auger recombination, must be considered. In this simulation, when the Auger capture coefficient is increased to 10-29 cm6 s-1, the efficiency drops from 31.62% (without taking Auger recombination into account) to 29.10%. Since Auger recombination is unavoidable in experiments, carrier losses due to Auger recombination should be included in the analysis of the efficiency limit to avoid significantly overestimating the simulated device performance. Therefore, this paper provides valuable insights for designing realistic and efficient lead-free PSCs.

CNTs/lamellar VSe2/Fe3O4 self-assembled a variety of unique three-dimensional multilayer interface structures and microwave absorption properties

Fabrication of microwave absorption (MA) materials of matched small thickness, low density, broad effective absorption bandwidth (EAB), as well as high absorption performance remains a technical challenge to be solved today. In this paper, three-dimensional (3D) VSe2/CNTs/Fe3O4 ternary composites with a variety of self-assembled structures were fabricated by a two-step hydrothermal and one-step carbothermal reduction method. Via varying the content of Fe3O4 in the composites, different 3D multilayer interfacial structures, such as star fruit-, bitter melon-, goldfish-, starfish-, peony- and chrysanthemum-shaped structures were self-assembled, and excellent MA absorption characteristics were obtained. The best reflection loss (RLmin) was −50.96 dB at 1.8 mm thickness. The maximum EAB was 4.93 GHz at 2.0 mm thickness. Carbon nanotubes mainly contributed to conduction and polarization losses. In situ generated VSe2 nanosheets and Fe3O4 nanoparticles promoted the assembly of multilevel interfacial structures, thus contributing to interfacial polarization loss and dipole polarization loss. Fe3O4 also created magnetic losses. This study lays the foundation for fabricating highly efficient MA materials in special self-assembled heterostructures with ternary synergistic effects at the nanoscale.

Architectural Design of a Multichannel Porous Carbon Fiber for Efficient Electromagnetic Microwave Absorption.

An ingenious microstructure of electromagnetic microwave absorption materials is crucial to achieve strong absorption and a broad bandwidth. Herein, one-dimensional (1D) carbon fibers with implantation of zero-dimensional (0D) ZIF-8-derived carbon frameworks and construction of a three-dimensional (3D) microcosmic multichannel porous structure are fabricated by electro-blown spinning, solvent-thermal reaction, and high-temperature pyrolysis techniques. The 1D carbon fiber skeleton with a multichannel structure provides a direct axial conductive pathway for charge transport, which plays an important role in dielectric loss. The 0D surface carbon frameworks offer plenty of heterogeneous interfaces to trigger intensive interfacial polarization loss and act as dihedral angles for microwave scattering. The 3D microcosmic multichannel pores can not only generate multiple reflections as much as possible to dissipate electromagnetic microwave energy but also supply huge interior cavities to improve impedance matching. Thanks to the synergistic effect of a strong electrically conductive pathway for enhancing the conductive loss, a plenteous heterogeneous interface for triggering intensive interfacial polarization loss, microcosmic multichannel pores for generating multiple reflections and improving impedance matching, and N and O atom doping for inducing dipole polarization, the optimal sample with an ingenious microstructure delivers an excellent absorption performance of a minimum reflection loss of -35.5 dB at a thickness of 5.0 mm and an effective absorption bandwidth of 6.72 GHz (10.96-17.68 GHz) at a thickness of 2.0 mm. Such a well-designed multichannel porous carbon fiber may pave the way for the exploitation of high-performance microwave absorbing materials.

Bulk and Interfacial Behavior of Potato Protein-Based Microgels.

This study aims to understand the bulk and interfacial performance of potato protein microgels. Potato protein (PoP) was used to produce microgels of submicrometer diameter via a top-down approach of thermal cross-linking followed by high-shear homogenization of the bulk gel. Bulk "parent" gels were formed at protein concentrations [PoP] = 5-18 wt %, which subsequently varied in their bulk shear elastic modulus (G') by several orders of magnitude (1-100 kPa), G' increasing with increasing [PoP]. The PoP microgels (PoPM) formed from these parent gels had diameters varying between 100 and 300 nm (size increasing with increasing G' and [PoP]), as observed via dynamic light scattering and atomic force microscopy (AFM) of PoPM adsorbed onto silicon. Interfacial rheology (interfacial shear storage and loss moduli, Gi' and Gi″) and interfacial tension (γ) of adsorbed films of PoP (i.e., nonheated PoP) and PoPM (both at tetradecane-water interfaces) were also studied, as well as the bulk rheology of the PoPM dispersions. The results showed that PoPM dispersions (at 50 vol %) had significantly higher bulk viscosity and shear thinning properties compared to the nonmicrogelled PoP at the same overall [PoP], but the bulk rheological behavior was in sharp contrast to the interfacial rheological performance, where Gi' and Gi″ of PoP were higher than for any of the PoPM. This suggests that the deformability and size of the microgels were key in determining the interfacial rheology of the PoPM. These findings may be attributed to the limited capacity for "unfolding" and lateral interactions of the larger PoPM at the interface, which are presumed to be stiffer due to their production from the strongest PoP gels. Our study further confirmed that heating and cooling the adsorbed films of PoPM after their adsorption showed little change, highlighting that hydrogen bonding was limited between the microgel particles.

Synthesis of hierarchical carbon Nanofibers-CoNi/C composites for enhanced microwave absorption efficiency

Developing lightweight, highly absorption and broadband microwave absorbents to combat severe electromagnetic radiation pollution poses a significant challenge. In this study, we designed a novel chain-like CNFs-CoNi/C nanocomposite by in-situ growth of bimetallic MOFs on the CNFs followed by calcination. The resulting CoNi/C composite with hollow structure was uniformly distributed along the 1D CNFs. The unique porous structure and heterogeneous interface derived from MOFs facilitated efficient scattering and multiple reflections of microwaves. By harnessing interfacial polarization loss, dipole polarization loss, and conduction loss mechanisms synergistically, the chain-shaped porous multi-stage CNFs-CoNi/C composite exhibited exceptional microwave absorption performance at a filling ratio of 10 %. It achieves a maximum reflection loss of −70 dB and an absorption bandwidth (EAB) for RL ≤ -10 exceeding 4.82 GHz with a corresponding thickness as low as 1.25 mm. This study introduced a lightweight and highly absorptive material that offers valuable insights into developing high-performance electromagnetic wave absorbing materials through organic composite comprising MOF and carbon materials.

High-efficiency and thermally stable FACsPbI3 perovskite photovoltaics.

α-FA1-xCsxPbI3 is a promising absorber material for efficient and stable perovskite solar cells (PSCs)1,2. However, the most efficient α-FA1-xCsxPbI3 PSCs require the inclusion of methylammonium chloride (MACl) additive3,4, which generates volatile organic residues (i.e., MA) that limit device stability at elevated temperatures5. To date, the highest certified power-conversion efficiency (PCE) of α-FA1-xCsxPbI3 PSCs without MACl was only ~24% (ref.6,7), and has yet to exhibit any stability advantages. Here, we identify interfacial contact loss caused by the Cs+ accumulation for the conventional α-FA1-xCsxPbI3 PSCs, which deteriorates the device performance and stability. Through in-situ GIWAXS analysis and DFT calculations, we demonstrate an intermediate phase-assisted crystallization pathway enabled by acetate surface coordination to fabricate high-quality α-FA1-xCsxPbI3 film, without using MA-additive. We herein report a certified stabilized power output (SPO) efficiency of 25.94% and a reverse-scanning PCE of 26.64% for α-FA1-xCsxPbI3 PSCs, exhibiting negligible contact losses and enhanced operational stability. The devices retain >95% of their initial PCEs after over 2,000 hours operating at maximum power point under 1 sun, 85 °C, and 60% relative humidity (ISOS-L-3).