Dual-mode tunable absorber based on quasi-bound states in the continuum.

In this Letter, we propose a novel, to the best of our knowledge, dual-mode tunable absorber that utilizes quasi-bound states in the continuum (q-BIC) based on the periodically arranged silicon cylinders tetramer. By introducing asymmetry perturbation through manipulating the diameters of diagonal cylinders in the all-dielectric structure, the symmetry-protected BIC (SP-BIC) transforms into q-BIC, leading to the emergence of one transmission and one reflection Fano-like resonant mode. The relationship between the quality factor of each mode and the asymmetry parameter α is analyzed, revealing an exponential dependence with an exponent of -1.75, i.e., Q ∝ α-1.75. To explain the underlying physics, multipole decomposition analysis and Aleksandra's theory are applied. Subsequently, a monolayer graphene is introduced to the all-dielectric structure to demonstrate the application of the dual-mode tunable absorber. When the critical coupling condition is satisfied, each mode can achieve the theoretical maximum absorption, demonstrating the distinctive capability of our proposed absorber for tuning and efficient light absorption. This research provides valuable insights into light-matter interactions and opens up possibilities for optical modulation and the development of graphene-based devices.

Building up a view and understanding of the multifunctional activity of black phosphorous nanosheet modified with the metal atom.

Constructing metal-semiconductor interfaces by loading metal atoms onto two-dimensional material to build atomically dispersed single-atom catalysts (SACs) has emerged as a new frontier for improving atom utilization and designing multifunctional electrocatalysts. Nowadays, studies on black phosphorus nanosheets in electrocatalysis have received much attention and the successful preparation of metal nanoparticle/black phosphorus (BP) hybrid electrocatalysts indicates BP nanosheets can serve as a potential support platform for SACs. Herein, by using large-scale ab initio calculations, we explored a large composition space of SACs with transition metal atoms supported on BP monolayer (M-BP) and built a comprehensive picture of activity trend, stability, and electronic origin towards oxygen reduction and evolution reaction (ORR and OER) and hydrogen evolution reaction (HER). The results show that the catalytic activity can be widely tuned by reasonable regulation of metal atoms. Ni-, Pd-, and Pt-BP could effectively balance the binding strength of the target intermediates, thus achieving efficient bifunctional activity for OER and ORR. Favorable bifunctional catalytic performance for OER and HER can be realized on Rh-BP. Especially, Pt-BP exhibits promising trifunctional activity towards OER, ORR, and HER. Multiple-level corrections among overpotential, Gibbs free energy, orbital population, and d-band center reveal that the trend and origin of catalytic activity are intrinsically determined by the d-band center of metal sites. The thermodynamic and dynamic stability simulations demonstrate that the active metal centers are firmly anchored on BP substrate with intact M-P bonds. These findings provide a theoretical basis for the rational design of BP-based SACs toward promising multifunctional activity.

Effects of organic substrates on sulfate-reducing microcosms treating acid mine drainage: Performance dynamics and microbial community comparison.

Bioremediation techniques utilizing sulfate-reducing bacteria (SRB) for acid mine drainage (AMD) treatment have attracted growing attention in recent years, yet substrate bioavailability for SRB is a key factor influencing treatment effectiveness and long-term stability. This study investigated the effects of external organic substrates, including four complex organic wastes (i.e., sugarcane bagasse, straw compost, shrimp shell (SS), and crab shell (CS)) and a small-molecule organic acid (i.e., propionate), on AMD removal performance and associated microbial communities during the 30-day operation of sulfate-reducing microcosms. The results showed that the pH values increased in all five microcosms, while CS exhibited the highest neutralization ability and a maximum alkalinity generation of 1507 mg/L (as CaCO3). Sulfate reduction was more effective in SS and CS microcosms, with sulfate removal efficiencies of 95.6% and 86.0%, respectively. All sulfate-reducing microcosms could remove heavy metals to different degrees, with the highest removal rate of >99.0% observed for aluminum. The removal efficiency of manganese, the most recalcitrant metal, was the highest (96%) in the CS microcosm. Correspondingly, SRB was more abundant in the CS and SS microcosms as revealed by sequencing analysis, while Desulfotomaculum was the dominant SRB in the CS microcosm, accounting for 10.8% of total effective bacterial sequences. Higher abundances of functional genes involved in fermentation and sulfur cycle were identified in CS and SS microcosms. This study suggests that complex organic wastes such as CS and SS could create and maintain preferable micro-environments for active growth and metabolism of functional microorganisms, thus offering a cost-efficient, stable, and environmental-friendly solution for AMD treatment and management.

Ultrathin multi-band coherent perfect absorber in graphene with high-contrast gratings.

High-contrast gratings (HCGs) can be designed as a resonator with high-quality factor and surface-normal emission, which are excellent characters for designing optical devices. In this work, we combine HCGs with plasmonic graphene structure to achieve an ultrathin five-band coherent perfect absorber (CPA). The presented CPA can achieve multi- and narrow-band absorption with high intensity under a relatively large incident angle. The good agreement between theoretical analysis and numerical simulated results demonstrates that our proposed HCGs-based structure is feasible to realize CPA. Besides, by dynamically adjusting the Fermi energy of graphene, we realize the active tunability of resonance frequency and absorption intensity simultaneously. Benefitting from the combination of HCGs and the one-atom thickness of graphene, the proposed device possesses an extremely thin feature. Our work proposes a novel method to manipulate coherent perfect absorption and is helpful to design tunable multi-band and ultrathin absorbers.

Ultrasensitive tunable terahertz sensor based on five-band perfect absorber with Dirac semimetal.

For non-invasive detection, terahertz (THz) sensing shows more promising performance compared to visible and infrared regions. But so far, figure of merit (FOM) of THz sensor has been exceeding low due to weak radiation and absorption loss. Here, we propose an easily implemented THz sensor based on bulk Dirac semimetal (BDS). The presented structure not only achieves narrowband absorption and dynamic tunability at five perfect absorption bands, but also exhibits excellent sensing performance with a FOM of 813. These fascinating properties can be explained by the combination of the classical magnetic resonance induced by the anti-parallel current, the electric resonance of adjacent unit cells resulting from the air slots at both ends of the absorber, and Mie resonance supported by coating, respectively. Our work can provide a new avenue for the design of multi-band photodetectors and sensors in the future.

Bidirectional and dynamically tunable THz absorber with Dirac semimetal.

Traditional absorbers are usually sandwich structures in which a metallic ground plane is employed to prevent the transmission. Such absorbers suffer from a major drawback that incident light can only irradiate from the front of the absorbers. In this paper, a novel absorber with bulk Dirac semimetal (BDS)-AlCuFe quasicrystals is proposed to realize bidirectional and dynamically tunable terahertz (THz) perfect absorption. The proposed structure consists of two layers of AlCuFe plates with rectangular apertures and a dielectric spacer. By adjusting transverse distance between the top and bottom rectangular apertures, perfect absorption could be realized under TM polarization. Simulation results show that perfect absorption can be obtained whether light irradiates from the front or back of the system, indicating a performance of bidirectional absorption. In addition, benefiting from the variable Fermi level of AlCuFe, the resonance frequency can be dynamically tuned in the THz range. Our work will stimulate more investigations on BDS-based bidirectional absorbers and optical modulators.

Dirac semimetals based tunable narrowband absorber at terahertz frequencies.

In this paper, a bulk Dirac semimetals (BDSs) based tunable narrowband absorber at terahertz frequencies is proposed and it has the attractive property of being polarization-independent at normal incidence because of its 90° rotational symmetry. Numerical results show that the absorption bandwidth is about 1.469e-2 THz and the total quality factor Q, defined as Q = f0/Δf, reaches about 94.6, which can be attributed to the low power loss of the guided mode resonance in the dielectric layer. The simulation results are analyzed with coupled mode theory. Interestingly, on the premise of maintaining the absorbance at a level greater than 0.95, the absorption frequency can be tuned from 1.381 to 1.395 THz by varying the Fermi energy of BDSs from 50 to 80 meV. Our results may also provide potential applications in optical filter and bio-chemical sensing.

Tunable plasmon-induced absorption in an integrated graphene nanoribbon side-coupled waveguide.

By designing a novel graphene plasmonic band-pass filter with two gold ribbons, we have numerically and analytically investigated the transmission properties of plasmon-induced absorption (PIA) in a compact graphene nanoribbon side-coupled waveguide. The formation and evolution of the PIA window are dependent on the superposition of super resonances and the near-field coupling intensity between the designed two resonators. Interestingly, the induced absorption window not only can be engineered longitudinally in intensity, but also dynamically tuned horizontally in the resonant wavelength by changing the Fermi energy of the graphene layers. Optical time delay near 1.0 ps can be realized in the PIA window, which exhibits excellent slow light features. Double PIA resonance is also discussed. This result may have potential applications in graphene plasmonic switching and buffering.

Tunable graphene-based plasmonic multispectral and narrowband perfect metamaterial absorbers at the mid-infrared region.

We numerically investigate the optical performance of a periodically patterned H-shaped graphene array by the finite-difference time-domain (FDTD) in the mid-infrared region. The simulated results reveal that absorption spectra of the proposed structure consist of two dramatic narrowband perfect absorption peaks located at 6.3 µm (Mode 1) and 8.6 µm (Mode 2) with high absorption coefficients of 99.65% and 99.80%, respectively. Two impressive absorption bandwidths that are the full width at half-maximum (FWHM) of the resonant frequency of 90 nm and 188 nm are obtained. The dipole resonance mode is supported by graphene ribbon at a wavelength of 6.3 µm. While the other absorption, attributed to the hybridized mode, is a new resonance that is different from the dipole resonance. The spectral position of the absorption peaks can be dynamically tuned by controlling the refractive index of the dielectric and the Fermi energy of graphene. Furthermore, we can obtain multispectral absorption peaks by applying multilayer graphene arrays. These design approaches enable us to control the number of absorption spectra and such absorbers will benefit the easy-to-fabricate nanophotonic devices for optical filtering, thermal detectors, and electromagnetic wave energy storage.

Experimental observation of exceptional bound states in a classical circuit network.

Exceptional bound (EB) states represent a unique new class of robust bound states protected by the defectiveness of non-Hermitian exceptional points. Conceptually distinct from the more well-known topological states and non-Hermitian skin states, they were recently discovered as a novel source of negative entanglement entropy in the quantum entanglement context. Yet, EB states have been physically elusive, being originally interpreted as negative probability eigenstates of the propagator of non-Hermitian Fermi gases. In this work, we show that EB states are in fact far more ubiquitous, also arising robustly in broad classes of systems whether classical or quantum. This hinges crucially on a newly-discovered spectral flow that rigorously justifies the EB nature of small candidate lattice systems. As a highlight, we present their first experimental realization through an electrical circuit, where they manifest as prominent stable resonant voltage profiles. Our work brings a hitherto elusive but fundamentally distinctive quantum phenomenon into the realm of classical metamaterials, and provides a novel pathway for the engineering of robust modes in otherwise sensitive systems..

Understanding the Activity and Design Principle of Dual-Atom Catalysts Supported on C2N for Oxygen Reduction and Evolution Reactions: From Homonuclear to Heteronuclear.

Using large-scale ab initio calculations and taking the two-dimensional C2N monolayer as a substrate, we sampled a large combinatorial space of C2N-supported homonuclear and heteronuclear dual-atom catalysts and built a detailed view of catalytic activity and stability toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The results indicate that regulating combinations of metal pairs could widely tune the catalytic performance. Pd2-, Pt2-, and PdPt-C2N could effectively balance the adsorption strength of intermediates and achieve optimal bifunctional activity. The favorable catalytic performance could also be realized on GaPd-C2N for the ORR and PdRh-C2N for the OER, surpassing corresponding homonuclear counterparts. The thermodynamic and electrochemical stability simulations reveal that these metal pairs can be stably anchored onto the C2N matrix. Multiple-level descriptors, including Gibbs free energy, d-band center, and bonding/antibonding orbital population, are established to track the activity trend and reveal the origin of activity, indicating that catalytic activity is intrinsically governed by the d-band center of metal pairs.

Stimulation of atrazine degradation by activated carbon and cathodic effect in soil microbial fuel cell.

Soil microbial fuel cells (MFCs) have been increasingly studied in recent years and have attracted significant attention as an environmentally sustainable bioelectrochemical technology. However, the poor conductivity of the soil matrix and the neglect of the cathodic function have limited its application. In this study, quartz sand and activated carbon were subjected to investigation on their influence on atrazine degradation. Atrazine was introduced in different layers (cathode, upper layer) to explore the cathodic effect on atrazine removal. The results revealed that activated carbon could reduce the internal resistance (693 Ω) and generate the highest power density (25.51 mW/m2) of the soil MFCs, and thus increase the removal efficiency (97.92%) of atrazine. The dynamic degradation profiles of atrazine were different for different adding layers. The cathode electrode acted as an electron donor could increase the distance of the effective influence of the soil MFCs' cathode from the middle to the cathode layer. The cathode (region) and the region close to the cathode could degrade atrazine with the atrazine removal efficiencies ranging from 60.67% to 92.79%, and the degradation ability of the cathode was stronger than that of other layers. The degradation effect followed the order: cathode > upper > lower > middle). Geobacter, Desulfobulbus, and Desulfuromonas belonging to the δ-Proteobacteria class were identified as the dominant electroactive microorganisms in the anode layer, while their relative abundances are quite low in the upper and cathode layers. Pseudomonas is an atrazine-degrading bacterium, but its relative abundance was only 0.13-0.51%. Thus, bioelectrochemistry rather than microbial degradation was the primary driving force.

Physico-Chemical Structure and Gasification Performance of Co-Pyrolytic Char Produced by the Pyrolysis of Polyvinyl Chloride Blends with Two Rank Coals.

Co-pyrolysis of waste plastics and coal has been considered to be an environmentally friendly and scalable waste treatment technology. This study investigated the influence of polyvinyl chloride (PVC) on the physico-chemical structure and gasification performance of co-pyrolytic char with lignite (PZ) and bituminous (SM) coal. The structure characteristics were explored by applying an X-ray diffractometer and a specific surface area analyzer. The quantitative analysis on the influence of PVC on pore characteristics and carbon microcrystal structure was conducted by the fractal theory and deconvolution method. The gasification performance was explored using a thermogravimetric analyzer. When the PZ blending ratio was larger than 50%, the specific surface area of PVCPZ chars enlarged significantly due to the increment of mesopores. Nevertheless, the effect of SM on the pore structure was not pronounced, and the specific surface area of PVCSM chars was as small as PVC char. A higher PZ blending ratio benefited the formation of mesopores with an aperture smaller than 10 nm for PVCPZ chars, whereas SM had little influence on pore diameter distributions of PVCSM chars attributed to the remarkable coating effects. The values of fractal dimension of co-pyrolytic char were larger than PVC char, revealing that the adjunction of coal increased the pore surface coarseness and improved the complicacy of the pore structure. Quantitative analysis on XRD spectra indicated that the disorder extent of the carbon structure was improved because of coal addition, and the influence of lignite on the disorder degree of the carbon structure was more significant. The gasification reaction of co-pyrolytic char showed significant synergistic effects, resulting in the improvement of gasification performance.

Electrochemical impedance spectroscopy applied to microbial fuel cells: A review.

Electrochemical impedance spectroscopy (EIS) is an efficient and non-destructive test for analyzing the bioelectrochemical processes of microbial fuel cells (MFCs). The key factors limiting the output performance of an MFC can be identified by quantifying the contribution of its various internal parts to the total impedance. However, little attention has been paid to the measurement conditions and diagrammatic processes of the EIS for MFC. This review, starting with the analysis of admittance of bioelectrode, introduces conditions for the EIS measurement and summarizes the representative equivalent circuit plots for MFC. Despite the impedance from electron transfer and diffusion process, the effect of unnoticeable capacitance obtained from the Nyquist plot on MFCs performance is evaluated. Furthermore, given that distribution of relaxation times (DRT) is an emerging method for deconvoluting EIS data in the field of fuel cell, the application of DRT-analysis to MFC is reviewed here to get insight into bioelectrode reactions and monitor the biofilm formation. Generally, EIS measurement is expected to optimize the construction and compositions of MFCs to overcome the low power generation.

Biodegradation performance and diversity of enriched bacterial consortia capable of degrading high-molecular-weight polycyclic aromatic hydrocarbons.

Polycyclic aromatic hydrocarbons (PAHs) are key organic pollutants in the environment that pose threats to the ecosystem and human health. The degradation of high molecular weight (HMW) PAHs by enriched bacterial consortia has been previously studied, while the involved metabolisms and microbial communities are still unclear and warrant further investigations. In this study, five bacterial consortia capable of utilizing different PAHs (naphthalene, anthracene, and pyrene) as the sole carbon and energy sources were enriched from PAH-contaminated soil samples. Among the five consortia, consortium TC exhibited the highest pyrene degradation efficiency (91%) after 19 d of incubation. The degradation efficiency was further enhanced up to 99% by supplementing yeast extract. Besides, consortium TC showed tolerances to high concentrations of pyrene (up to 1000 mg/L) and different heavy metal stresses (including Zn2+, Cd2+, and Pb2+). The dominant genus in consortium TC, GS, and PL showing relatively higher degradation efficiency for anthracene and pyrene was Pseudomonas, whereas consortium PG and GD were predominated by genus Achromobacter and class Enterobacteriaceae, respectively. Consortium TC, as a highly efficient HMW PAH-degrading consortium, could be applied for synergistic biodegradation of HMW PAHs and in situ bioremediation of the sites contaminated with both PAHs and heavy metals.

Accumulation of high-molecular-weight polycyclic aromatic hydrocarbon impacted the performance and microbial ecology of bioretention systems.

Bioretention has been considered as an effective management practice for urban stormwater in the removal of pollutants including polycyclic aromatic hydrocarbons (PAHs). However, the accumulation of high-molecular-weight (HMW) PAHs in bioretention systems and their potential impact on the pollutants removal performance and microbial ecology are still not fully understood. In this study, comparisons of treatment effectiveness, enzyme activity and microbial community in bioretention systems with different types of media amendments were carried out at different spiking levels of pyrene (PYR). The results showed that the removal efficiencies of chemical oxygen demand (COD) and total nitrogen in the bioretention systems were negatively impacted by the PYR levels. The relative activities of soil dehydrogenase and urease were increasingly inhibited by the elevated PYR level, indicating the declining microbial activity regarding organic matter decomposition. The spiking of PYR negatively affected microbial diversity, and distinct time- and influent-dependent changes in microbial communities were observed. The relative abundance of PAH-degrading microorganisms increased in PYR-spiked systems, while the abundance of nitrifiers decreased. The addition of media amendments was beneficial for the enrichment of microorganisms that are more resistant to PYR-related stress, therefore elevating the COD concentration removal rate by ∼50%. This study gives new insight into the multifaceted impacts of HMW PAH accumulation on microbial fingerprinting and enzyme activities, which may provide guidance on better stormwater management practices via bioretention in terms of improved system longevity and performance.

Correction to: Two Switchable Plasmonically Induced Transparency Effects in a System with Distinct Graphene Resonators.

An amendment to this paper has been published and can be accessed via the original article.

Two Switchable Plasmonically Induced Transparency Effects in a System with Distinct Graphene Resonators.

General plasmonic systems to realize plasmonically induced transparency (PIT) effect only exist one single PIT mainly because they only allow one single coupling pathway. In this study, we propose a distinct graphene resonator-based system, which is composed of graphene nanoribbons (GNRs) coupled with dielectric grating-loaded graphene layer resonators, to achieve two switchable PIT effects. By designing crossed directions of the resonators, the proposed system exists two different PIT effects characterized by different resonant positions and linewidths. These two PIT effects result from two separate and polarization-selective coupling pathways, allowing us to switch the PIT from one to the other by simply changing the polarization direction. Parametric studies are carried to demonstrate the coupling effects whereas the two-particle model is applied to explain the physical mechanism, finding excellent agreements between the numerical and theoretical results. Our proposal can be used to design switchable PIT-based plasmonic devices, such as tunable dual-band sensors and perfect absorbers.

Physico-chemical properties and gasification reactivity of co-pyrolysis char from different rank of coal blended with lignocellulosic biomass: Effects of the cellulose.

In this paper, the influence of cellulose on the physicochemical properties and the gasification reactivity of co-pyrolysis char was investigated. A specific surface area analyzer and an X-ray diffraction system were used to characterize the pore structure and the micro-crystalline structure of char. Fractal theory and deconvolution method were applied to quantitatively investigate the influence of cellulose on the structure of co-pyrolysis char. The results indicate that the improvements in the pore structure due to the presence of cellulose are more pronounced in the case of anthracite char with respect to bituminous char. Cellulose promotes the ordering of micro-scale structure and the uniformity of both anthracite and bituminous char, while the negative synergetic effect was observed during gasification of co-pyrolysis char. The exponential relationships between fractal dimension and specific surface area were determined, along with the relations between the gasification reactivity index and the microcrystalline structure parameter.

Study on product distributions and char morphology during rapid co-pyrolysis of platanus wood and lignite in a drop tube fixed-bed reactor.

The rapid co-pyrolytic behavior of platanus wood and Pingzhuang lignite was explored in a drop tube fixed-bed reactor under nitrogen atmosphere. Synergistic effects were evaluated using the deviations between experimental and predicted values of product yields and gas components. Surface morphology of residual chars were also investigated applying the scanning electron microscopy technique (SEM). This study found that the experimental values of gas volume yields were greater than the predicted, and the maximum gas volume yield exhibited with 50% biomass blending ratio at 1000°C. Positive or negative synergistic effects happened in gas components at different blending ratios and temperatures. The SEM results indicated that the differences of char surface morphology were evident. The fractal dimensions of residual chars increased with increasing biomass blending ratio, which may improve their gasification or combustion reactivity. The change in product yields and gas components was attributed to the secondary reactions and tar cracking.