Micronuclear battery based on a coalescent energy transducer.

Micronuclear batteries harness energy from the radioactive decay of radioisotopes to generate electricity on a small scale, typically in the nanowatt or microwatt range1,2. Contrary to chemical batteries, the longevity of a micronuclear battery is tied to the half-life of the used radioisotope, enabling operational lifetimes that can span several decades3. Furthermore, the radioactive decay remains unaffected by environmental factors such as temperature, pressure and magnetic fields, making the micronuclear battery an enduring and reliable power source in scenarios in which conventional batteries prove impractical or challenging to replace4. Common radioisotopes of americium (241Am and 243Am) are α-decay emitters with half-lives longer than hundreds of years. Severe self-adsorption in traditional architectures of micronuclear batteries impedes high-efficiency α-decay energy conversion, making the development of α-radioisotope micronuclear batteries challenging5,6. Here we propose a micronuclear battery architecture that includes a coalescent energy transducer by incorporating 243Am into a luminescent lanthanide coordination polymer. This couples radioisotopes with energy transducers at the molecular level, resulting in an 8,000-fold enhancement in energy conversion efficiency from α decay energy to sustained autoluminescence compared with that of conventional architectures. When implemented in conjunction with a photovoltaic cell that translates autoluminescence into electricity, a new type of radiophotovoltaic micronuclear battery with a total power conversion efficiency of 0.889% and a power per activity of 139 microwatts per curie (µW Ci-1) is obtained.

Tunable liquid-solid hybrid thermal metamaterials with a topology transition.

Thermal metamaterials provide rich control of heat transport which is becoming the foundation of cutting-edge applications ranging from chip cooling to biomedical. However, due to the fundamental laws of physics, the manipulation of heat is much more constrained in conventional thermal metamaterials where effective heat conduction with Onsager reciprocity dominates. Here, through the inclusion of thermal convection and breaking the Onsager reciprocity, we unveil a regime in thermal metamaterials and transformation thermotics that goes beyond effective heat conduction. By designing a liquid-solid hybrid thermal metamaterial, we demonstrate a continuous switch from thermal cloaking to thermal concentration in one device with external tuning. Underlying such a switch is a topology transition in the virtual space of the thermotic transformation which is achieved by tuning the liquid flow via external control. These findings illustrate the extraordinary heat transport in complex multicomponent thermal metamaterials and pave the way toward an unprecedented regime of heat manipulation.

Revealing Fast Negative Capacitance in PbZr0.2Ti0.8O3 Thin Film with Acicular Ferroelastic Domains.

Negative capacitance effects with fast response times hold great potential for reducing the power consumption in high-frequency nanoelectronics. Nevertheless, the negative capacitance effect faces considerable complexity arising from the dynamic interplay among electrostatic, nucleation energies, and domain evolution. This intricate balance poses a formidable challenge to achieving fast negative capacitance. Herein, we have achieved a fast negative capacitance time of ∼16.23 ns in PbZr0.2Ti0.8O3 (PZT) thin film, and our investigation confirms the presence of acicular ferroelastic domains within the PZT thin film. Under reversal electric fields, these acicular ferroelastic domains undergo a unique flipping process, transitioning through domain expansion and contraction. This distinct domain flipping manner accelerates the nucleation and growth of ferroelectric domains, thereby facilitating the observed fast negative capacitance. The realization of fast negative capacitance holds substantial promise for reducing operational time and power consumption, offering prospects for the design of nanoelectronics with significantly lower power requirements.

Revealing the Mechano-Electrochemical Coupling Behavior and Discharge Mechanism of Fluorinated Carbon Cathodes toward High-Power Lithium Primary Batteries.

Unclear reaction mechanisms and unsatisfactory power performance hinder the further development of advanced lithium/fluorinated carbon (Li/CFx ) batteries. Herein, the mechano-electrochemical coupling behavior of a CFx cathode is investigated by in situ monitoring strain/stress using digital image correlation (DIC) techniques, electrochemical methods, and theoretical equations. The DIC monitoring results present the distribution and dynamic evolution of the plane strain and indicate strong dependence toward the material structure and discharge rate. The average plane principal strain of fully discharged 2D fluorinated graphene nanosheets (FGNSs) at 0.5 C is 0.50%, which is only 38.5% that of conventional bulk-structure CFx . Furthermore, the superior structural stability of the FGNSs is demonstrated by the microstructure and component characterization before and after discharge. The plane stress evolution is calculated based on theoretical equations, and the contributions of electrochemical and mechanical factors are examined and discussed. Subsequently, a structure-dependent three-region discharge mechanism for CFx electrodes is proposed from a mechanical perspective. Additionally, the surface deformation of Li/FGNSs pouch cells formed during the discharge process is monitored using in situ DIC. This study reveals the discharge mechanism of Li/CFx batteries and facilitates the design of advanced CFx materials.

Ultra-thin and Mechanically Stable LiCoO2-Electrolyte Interphase Enabled by Mg2+ Involved Electrolyte.

LiCoO2 (LCO) cathode materials have attracted significant attention for its potential to provide higher energy density in current Lithium-ion batteries (LIBs). However, the structure and performance degradation are exacerbated by increasing voltage due to the catastrophic reaction between the applied electrolyte and delithiated LCO. The present study focuses on the construction of physically and chemically robust Mg-integrated cathode-electrolyte interface (MCEI) to address this issue, by incorporating Magnesium bis(trifluoromethanesulfonyl)imide (Mg[TFSI]2) as an electrolyte additive. During formation cycles, the strong MCEI is formed and maintained its 2 nm thickness throughout long-term cycling. Notably, Mg is detected not only in the robust MCEI, but also imbedded in the surface of the LCO lattice. As a result, the parasitic interfacial side reactions, surface phase reconstruction, particle cracking, Co dissolution and shuttling are considerably suppressed, resulting in long-term cycling stability of LCO up to 4.5 V. Therefore, benefit from the double protection of the strong MCEI, the Li||LCO coin cell and the Ah-level Graphite||LCO pouch cell exhibit high capacity retention by using Mg-electrolyte, which are 88.13% after 200 cycles and 90.4% after 300 cycles, respectively. This work provides a novel approach for the rational design of traditional electrolyte additives.

Harnessing the Synergistic Interplay between Atomic-Scale Vacancies and Ligand Effect to Optimize the Oxygen Reduction Activity and Tolerance Performance.

Defect engineering is an effective strategy for regulating the electrocatalysis of nanomaterials, yet it is seldom considered for modulating Pt-based electrocatalysts for the oxygen reduction reaction (ORR). In this study, we designed Ni-doped vacancy-rich Pt nanoparticles anchored on nitrogen-doped graphene (Vac-NiPt NPs/NG) with a low Pt loading of 3.5 wt . % and a Ni/Pt ratio of 0.038 : 1. Physical characterizations confirmed the presence of abundant atomic-scale vacancies in the Pt NPs induces long-range lattice distortions, and the Ni dopant generates a ligand effect resulting in electronic transfer from Ni to Pt. Experimental results and theoretical calculations indicated that atomic-scale vacancies mainly contributed the tolerance performances towards CO and CH3OH, the ligand effect derived from a tiny of Ni dopant accelerated the transformation from *O to *OH species, thereby improved the ORR activity without compromising the tolerance capabilities. Benefiting from the synergistic interplay between atomic-scale vacancies and ligand effect, as-prepared Vac-NiPt NPs/NG exhibited improved ORR activity, sufficient tolerance capabilities, and excellent durability. This study offers a new avenue for modulating the electrocatalytic activity of metal-based nanomaterials.

Probing Particle-Carbon/Binder Degradation Behavior in Fatigued Layered Cathode Materials through Machine Learning Aided Diffraction Tomography.

Understanding how reaction heterogeneity impacts cathode materials during Li-ion battery (LIB) electrochemical cycling is pivotal for unraveling their electrochemical performance. Yet, experimentally verifying these reactions has proven to be a challenge. To address this, we employed scanning µ-XRD computed tomography to scrutinize Ni-rich layered LiNi0.6Co0.2Mn0.2O2 (NCM622) and Li-rich layered Li[Li0.2Ni0.2Mn0.6]O2 (LLNMO). By harnessing machine learning (ML) techniques, we scrutinized an extensive dataset of µ-XRD patterns, about 100,000 patterns per slice, to unveil the spatial distribution of crystalline structure and microstrain. Our experimental findings unequivocally reveal the distinct behavior of these materials. NCM622 exhibits structural degradation and lattice strain intricately linked to the size of secondary particles. Smaller particles and the surface of larger particles in contact with the carbon/binder matrix experience intensified structural fatigue after long-term cycling. Conversely, both the surface and bulk of LLNMO particles endure severe strain-induced structural degradation during high-voltage cycling, resulting in significant voltage decay and capacity fade. This work holds the potential to fine-tune the microstructure of advanced layered materials and manipulate composite electrode construction in order to enhance the performance of LIBs and beyond.

The Total Ionizing Dose Effects on Perovskite CsPbBr3 Semiconductor Detector.

Perovskite CsPbBr3 semiconductors exhibit unusually high defect tolerance leading to outstanding and unique optoelectronic properties, demonstrating strong potential for γ-radiation and X-ray detection at room temperature. However, the total dose effects of the perovskite CsPbBr3 must be considered when working in a long-term radiation environment. In this work, the Schottky type of perovskite CsPbBr3 detector was fabricated. Their electrical characteristics and γ-ray response were investigated before and after 60Co γ ray irradiation with 100 and 200 krad (Si) doses. The γ-ray response of the Schottky-type planar CsPbBr3 detector degrades significantly with the increase in total dose. At the total dose of 200 krad(Si), the spectral resolving ability to γ-ray response of the CsPbBr3 detector has disappeared. However, with annealing at room temperature for one week, the device's performance was partially recovered. Therefore, these results indicate that the total dose effects strongly influence the detector performance of the perovskite CsPbBr3 semiconductor. Notably, it is concluded that the radiation-induced defects are not permanent, which could be mitigated even at room temperature. We believe this work could guide the development of perovskite detectors, especially under harsh radiation conditions.

Anomalous Blue Shift of Exciton Luminescence in Diamond.

Generally speaking, for a semiconductor, the temperature dependence of excitonic emission corresponds to that of its band gap. However, an anomalous behavior is exhibited by the excitonic luminescence of diamond where as the temperature increases (from 10 to 300 K), its indirect exciton luminescence peak displays a spectral-distinguishable blue shift, whereas the indirect band-gap absorption shows a weak red shift. According to experimental high-resolution deep-ultraviolet spectra and theoretical analysis, the weak red shift of its indirect band gap is ascribed to its large Debye temperature (ΘD ≈ 2220 K), which makes the lattice constant change comparatively little in a large temperature range, so the change of its band gap is relatively small; in this case, as the temperature rises, the thermal population of valence-band holes that moves to a high-energy state far away from the Fermi surface contributes to the macroscopic blue shift of its excitonic emission.

Surface Wettability for Skin-Interfaced Sensors and Devices.

The practical applications of skin-interfaced sensors and devices in daily life hinge on the rational design of surface wettability to maintain device integrity and achieve improved sensing performance under complex hydrated conditions. Various bio-inspired strategies have been implemented to engineer desired surface wettability for varying hydrated conditions. Although the bodily fluids can negatively affect the device performance, they also provide a rich reservoir of health-relevant information and sustained energy for next-generation stretchable self-powered devices. As a result, the design and manipulation of the surface wettability are critical to effectively control the liquid behavior on the device surface for enhanced performance. The sensors and devices with engineered surface wettability can collect and analyze health biomarkers while being minimally affected by bodily fluids or ambient humid environments. The energy harvesters also benefit from surface wettability design to achieve enhanced performance for powering on-body electronics. In this review, we first summarize the commonly used approaches to tune the surface wettability for target applications toward stretchable self-powered devices. By considering the existing challenges, we also discuss the opportunities as a small fraction of potential future developments, which can lead to a new class of skin-interfaced devices for use in digital health and personalized medicine.

Cryogenic Scintillation Performance of Cs4PbI6 Perovskite Single Crystals.

All-inorganic Cs4PbI6 single crystals (SCs) is emerging scintillators for radiation detection. In this study, we report on the X-ray scintillation properties of Cs4PbI6 SCs at the temperature range of 50-290 K. The temperature-dependent radioluminescence (RL) spectrum and decay time were investigated. It was found that the RL spectra show very pronounced temperature-dependent changes in the overall shape. The RL intensity increases with a decrease in the temperature under X-ray excitation. The emission bands at 318, 360, and 554 nm are attributed to the near-band-edge emission in Cs4PbI6 SCs, the 3P1 → 1S0 transition of the Pb2+ ion, and the emission of δ-CsPbI3 aggregates dispersed in the Cs4PbI6 SC matrix, respectively. With decreasing temperature, the fast and slow decay times tend to slow down and are estimated to be 46.0 ns (33.22%) and 820 ns (66.78%) at 50 K, which are far superior to that of the common cryogenic scintillator. These cryogenic scintillation characteristics of Cs4PbI6 SCs demonstrate its potential for cryogenic detection.

Cryogenic Scintillation Properties of Lead-Free Cs3Cu2I5 Single Crystals.

Perovskite scintillators have become increasingly popular in recent years because of their simple production and high sensitivity to X-ray. Due to large Stokes shifts, high light yield, eco-friendly fabrication, and good stability, the lead-free Cu-based perovskites have gained much attention. In this paper, we prepared the Cs3Cu2I5 single crystals (SCs) by the solution-processed method. At room temperature, we measured the emission band at 440 nm with an average decay time of 595 ns under X-ray excitation. Under 137Cs γ-ray excitation, we determined that the light yield of Cs3Cu2I5 SCs was 23 000 photons/MeV. Notably, under alpha particle excitation by 241Am, the light yield of Cs3Cu2I5 SCs is approximately 3.2 times higher than that of the commercial scintillator LYSO(Ce). In addition, we systematically investigated the cryogenic scintillation properties of Cs3Cu2I5 SCs at the temperature range of 60-300 K. With decreasing temperature, the intensity of the emission band at 440 nm significantly increases, and an additional emission band at 336 nm emerges below 100 K. Meanwhile, the temperature-dependent decay times were determined. The fast and slow decay time of Cs3Cu2I5 SCs are estimated to be 221 and 1193 ns, respectively, at 60 K. Our findings highlight the great potential for Cs3Cu2I5 SCs to be a cryogenic scintillator.

Moisture-resistant MXene-sodium alginate sponges with sustained superhydrophobicity for monitoring human activities.

Wearable mechanical sensors are easily influenced by moisture resulting in inaccuracy for monitoring human health and body motions. Though the superhydrophobic barrier has been extensively explored as passive water repel strategy on the sensor surface, the dense superhydrophobic surface not only limits the sensor working under large deformations but also inevitable degradation in high humidity or saturation water vapor environments. This work reports a superhydrophobic MXene-sodium alginate sponge (SMSS) pressure sensor with a low voltage Joule heating effect to provide sustain moisture-insensitive property for both sensing performance and superhydrophobicity by heating-driven water molecules away. Because of the positive temperature coefficient under pressure applied, the Joule heating can provides a stable temperature to the moisture-insensitivity property during the whole dynamic pressure cycled. Therefore, the pressure sensor with a simple spray-coating superhydrophobic coating on the outer layer demonstrates key capabilities even in extreme use scenarios with high humidity or water vapor and also provides stable and reliable bio-signal monitoring.

Durable Flexible Polymer-Encapsulated Cs4PbI6 Thin Film for High Sensitivity X-ray Detection.

Because of the extraordinary properties including high atomic numbers and large µτ products, metal halide perovskites have been widely employed and used for radiation detecting. Cs4PbI6 material has a high X-ray attenuation coefficient and excellent electrical properties that have a good potential in X-ray detection applications. Here, we have designed a flexible polymer-encapsulated Au/Cs4PbI6/Au X-ray detector with outstanding sensitivity of 256.20 µC Gy-1 cm-2 irradiated by 30 keV X-ray at 10 V bias, long-time stability, and durable flexibility without obvious degradation after bending for 600 cycles. These features demonstrate that this polymer-encapsulated durable flexible and sensitive X-ray detector could open a new possibility for next-generation radiation applications in dosimeter, imaging technologies.

Spatiotemporal Release of Reactive Oxygen Species and NO for Overcoming Biofilm Heterogeneity.

The heterogeneity in biofilms is a major challenge in biofilm therapies due to different susceptibility of bacteria and extracellular polymeric substances (EPS) to antibacterial agents. Here, we describe a therapeutic strategy that overcame biofilm heterogeneity, where antibacterial agent (NO) and EPS dispersant (reactive oxygen species (ROS)-inducing Fe3+ ) were separately loaded in the yolk and shell compartment of a yolk-shell nanoplatform. Compared with traditional combinational chemotherapies which suffer from inconsistent pharmacokinetics profiles, this strategy drew on the pharmacokinetic complementarity of ROS and NO, where ROS with a short diffusion distance and a high redox potential corrupted the EPS, facilitating NO, which has a long diffusion distance and a broad antimicrobial spectrum, to penetrate the biofilm and eliminate the resident bacteria. Additionally, the construction of a three-dimensional spherical biofilm model is novel and clinically relevant.

Theory-Guided Regulation of FeN4 Spin State by Neighboring Cu Atoms for Enhanced Oxygen Reduction Electrocatalysis in Flexible Metal-Air Batteries.

Iron, nitrogen-codoped carbon (Fe-N-C) nanocomposites have emerged as viable electrocatalysts for the oxygen reduction reaction (ORR) due to the formation of FeNx Cy coordination moieties. In this study, results from first-principles calculations show a nearly linear correlation of the energy barriers of key reaction steps with the Fe magnetic moment. Experimentally, when single Cu sites are incorporated into Fe-N-C aerogels (denoted as NCAG/Fe-Cu), the Fe centers exhibit a reduced magnetic moment and markedly enhanced ORR activity within a wide pH range of 0-14. With the NCAG/Fe-Cu nanocomposites used as the cathode catalyst in a neutral/quasi-solid aluminum-air and alkaline/quasi-solid zinc-air battery, both achieve a remarkable performance with an ultrahigh open-circuit voltage of 2.00 and 1.51 V, large power density of 130 and 186 mW cm-2 , and good mechanical flexibility, all markedly better than those with commercial Pt/C or Pt/C-RuO2 catalysts at the cathode.

Hollow nanosphere arrays with a high-index contrast for enhanced scintillating light output from ß-Ga2O3 crystals.

ß-Ga2O3 is a new type of fast scintillator with potential applications in medical imaging and nuclear radiation detection with high count-rate situations. Because of the severe total internal reflection with its high refractive index, the light extraction efficiency of ß-Ga2O3 crystals is rather low, which would limit the performance of detection systems. In this paper, we use hollow nanosphere arrays with a high-index contrast to enhance the light extraction efficiency of ß-Ga2O3 crystals. We can increase the transmission diffraction efficiency and reduce the reflection diffraction efficiency through controlling the refractive index and the thickness of the shell of the hollow nanospheres, which can lead to a significant increase in the light extraction efficiency. The relationships between the light extraction efficiency and the refractive index and thickness of the shell of the hollow nanospheres are investigated by both numerical simulations and experiments. It is found that when the refractive index of the shell of the hollow nanospheres is higher than that of ß-Ga2O3, the light extraction efficiency is mainly determined by the diffraction efficiency of light transmitted from the surface with the hollow nanosphere arrays. When the refractive index of the shell is less than that of ß-Ga2O3, the light extraction efficiency is determined by the ratio of the diffraction efficiency of the light transmitted from the surface with the hollow nanosphere arrays to the diffraction efficiency of the light that can escape from the lateral surface.

Highly sensitive X-ray detector based on a ß-Ga2O3:Fe single crystal.

ß-Ga2O3 semiconductor crystal is of wide band gap and high radiation resistance, which shows great potential for applications such as medical imaging, radiation detections, and nuclear physical experiments. However, developing ß-Ga2O3-based X-ray radiation detectors with high sensitivity, fast response speed, and excellent stability remains a challenge. Here we demonstrate a high-performance X-ray detector based on a Fe doped ß-Ga2O3 (ß-Ga2O3:Fe) crystal grown by the float-zone growth method, which consists of two vertical Ti/Au electrodes and a ß-Ga2O3:Fe crystal with high resistivity. The resistivity of the ß-Ga2O3:Fe crystal exceeds 1012 Ω cm owed to the compensation of the Fe ions and the free electrons. The detector shows short response time (0.2 s), high sensitivity (75.3 µC Gyair -1 cm-2), and high signal-to-noise ratio (100), indicating great potential for X-ray radiation detection.

Improved light output from thick ß-Ga2O3 scintillation crystals via graded-refractive-index photonic crystals.

ß-Ga2O3 is a promising candidate as a fast scintillation crystal for radiation detection in fast X-ray imaging and high-energy physics experiments. However, total internal reflection severely limits its light output. Conventional photonic crystals can improve the light output, but such improvement decreases dramatically with increased scintillator thickness due to the strong backward reflection by the photonic crystals. Here, graded-refractive-index photonic crystals composed of nanocone arrays are designed and fabricated on the surfaces of ß-Ga2O3 crystals with various thicknesses. Compared to the conventional photonic crystals, there is still an obvious light output improvement by using the graded-refractive-index photonic crystals when the thickness of the crystals is increased by three times. The effect of thickness on the improved light output is investigated with numerical simulations and experiments. Overall, the graded-refractive-index photonic crystals are beneficial to the improvement of light output from thick scintillators.

Light output enhancement of scintillators by using mixed-scale microstructures.

Scintillators play an important role in the field of nuclear radiation detection. However, the light output of the scintillators is often limited by total internal reflection due to the high refractive indices of the scintillators. Furthermore, the light emission from scintillators typically has an approximately Lambertian profile, which is detrimental to the collection of the light. In this paper, we demonstrate a promising method to achieve enhancement of the light output from scintillators through use of mixed-scale microstructures that are composed of a photonic crystal slab and a microlens array. Simulations and experimental results both show significant improvements in the scintillator light output. The X-ray imaging characteristics of scintillators are improved by the application of the mixed-scale microstructures. The results presented here suggest that the application of the proposed mixed-scale microstructures to scintillators will be beneficial in the nuclear radiation detection field.