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We report GHz longitudinal as well as shear acoustic phonon photoexcitation and photodetection using femtosecond laser pulses in a spin-crossover molecular crystal. From our experimental observation of time domain Brillouin scattering triggered by the photoexcitation of acoustic waves across the low-spin (LS) to high-spin (HS) thermal crossover, we reveal a link between the molecular spin state and photoexcitation of coherent GHz acoustic phonons. In particular, we experimentally evidence a non-thermal pathway for the laser excitation of GHz phonons. We also provide experimental insights into the optical and mechanical parameters evolving across the LS/HS spin crossover temperature range. [ABSTRACT FROM AUTHOR]

The complex optical index refraction of an iron (II) spin-crossover coordination polymer is measured in the Terahertz frequency range by Terahertz time-domain spectroscopy (THz-TDS). By scanning the temperature from 288 to 333 K, we have recorded the evolution of the THz spectrum within the low spin - high spin thermal hysteresis loop. We were able to simultaneously infer the refractive index and absorption variations. The low spin-high spin transition has a marked spectral signature in the millimeter wavelength. In the 0.1–0.6 THz frequency range, the variation of real and imaginary part of the index of refraction is 6% and 20%, respectively. A marked absorption is observed above 500 GHz. The THz-TDS provides a clear direct fingerprint of this class of materials, which are interestingly potential candidates for optical data storage and processing devices. [ABSTRACT FROM AUTHOR]

In the New Order era, forest management and utilization in East Kalimantan does not assure the sustainability of wood production. Forest has tended to be depleted and degraded instead, characterized by lack of special kinds of wood and change in forest structure due to uncontrolled deforestration. In this sense, natural forest could be beneficially managed if expected value in the long term equal to current value. This is the importance of local government capital share in the forest management. Apart of that, forest management in the previous period has contributed to the creation of labor market and income generation for the worker. However, there seems to be factual that forest industry was unable to produce tricle down effect for the people lived surround the forest. This paper tries to evaluate the policy and practice of forest management during New Order and Reform era, particularly in line with the effort of promoting social welfare in East Kalimantan. Keywords: Pengelolaan hutan lestari, Kalimantan Timur.

A correction for the article "Ultrafast non-thermal laser excitation of gigahertz longitudinal and shear acoustic waves in spin-crossover molecular crystals [Fe(PM-AzA)2(NCS)2]" that was published in the previous issue is presented.

We report GHz longitudinal as well as shear acoustic phonon photoexcitation and photodetection using femtosecond laser pulses in a spin-crossover molecular crystal. From our experimental observation of time domain Brillouin scattering triggered by the photoexcitation of acoustic waves across the low-spin (LS) to high-spin (HS) thermal crossover, we reveal a link between the molecular spin state and photoexcitation of coherent GHz acoustic phonons. In particular, we experimentally evidence a non-thermal pathway for the laser excitation of GHz phonons. We also provide experimental insights into the optical and mechanical parameters evolving across the LS/HS spin crossover temperature range. [ABSTRACT FROM AUTHOR]

Symmetry-breaking is pivotal for controlling ferroelectric, ferroelastic and/or ferromagnetic functions of materials, which enables applications in sensors, memory devices, transducers or actuators. Commonly, ferroic phases emerge from descending symmetry-breaking, as the laws of thermodynamics dictate that the ordered low entropy phases form at low temperature, which limits practical applications of many materials at room temperature. Rare examples of ascending symmetry-breakings have been observed, but the driving force remains often unclear. Here, we report on a ferroelastic symmetry-breaking occurring at high temperature in a spin-crossover material, studied by magnetic, DSC and X-ray diffraction measurements. Our DFT calculations and our model, based on the Landau theory of phase transitions, explain how the cooperative thermal switching of the molecular spin state drives a ferroelastic symmetry breaking at high temperature, through a coupled Jahn-Teller distortion. Ferroelastic materials have rich properties, with important applications in memory, multifunctional and novel controllable devices. The electronic bistability in soft functional materials represents an important source of entropy gain, capable of overcoming the cost of symmetry-breaking entropy, which opens up new perspectives for stabilizing high-temperature and low-symmetry ferroic functions of advanced materials.

Perovskite materials have surged to the forefront of materials science, captivating researchers worldwide with their distinctive crystal lattice arrangement and remarkable optical, electric and dielectric attributes. The current study focuses on the development of a novel zero-dimensional (0D) Ge(II)-based hybrid perovskite, formulated as NH 3 (CH 2 ) 2 NH 3 GeF 6 , and synthesized through a gradual evaporation process conducted at room temperature. The crystal structure is characterized by an arrangement of organic cations and isolated octahedral [GeF 6 ] 2- groups. This configuration is stabilized by relatively weak intermolecular bonds. A comprehensive analysis of the material's thermal properties using differential scanning calorimetry (DSC) revealed a distinct phase transition occurring at approximately 323 K, which was further confirmed through electrical measurements. The studied compound provided a broad absorption range across the visible spectrum and an optical band gap of 3.30 eV, indicating its potential for semiconducting applications in optoelectronic devices. Photoluminescence PL analysis displays a blueish broad-band emission with a high color rendering index CRI value of 91, when excited at 325 nm. This emission primarily originates from the self-trapped excitons (STEs) recombination in the inorganic [GeF 6 ] 2- . Herein, the temperature-dependent behavior of grain conductivity exhibited an Arrhenius-type pattern, with an activation energy ( E a ) of 0.46 eV, confirming the semiconductor nature of the investigated compound. In addition, a deep investigation of the alternating current conductivity, analyzed using Jonscher's law, demonstrates that the conduction mechanism is effectively described by the correlated barrier hopping (CBH) model. The dielectric performances show a significant dielectric constant (ε' ∼ 10 3 ). Thus, all these interesting physical properties of this hybrid perovskite have paved the way for advancements in various technological applications, particularly in the field of electronic capacitors., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

The Cu-glutathione (GSH) redox system, essential in biology, is designed here as a supramacromolecular assembly in which the tetrahedral 18e Cu(I) center loses a thiol ligand upon adsorption onto ZIF-8, as shown by EXAFS and DFT calculation, to generate a very robust 16e planar trigonal single-atom Cu(I) catalyst. Synergy between Cu(I) and ZIF-8, revealed by catalytic experiments and DFT calculation, affords CO 2 conversion into high-value-added chemicals with a wide scope of substrates by reaction with terminal alkynes or propargyl amines in excellent yields under mild conditions and reuse at least 10 times without significant decrease in catalytic efficiency., (© 2024 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

Due to their remarkable properties, including remarkable porosity and extensive surface area, metal-organic frameworks (MOFs) are being investigated for various applications. Herein, we report the first Co(II)-based mixed ligand MOF, formulated Co 4 (HTrz) 2 (d-cam) 2.5 (μ-OH) 3 . Its 3D structure framework is composed of helical chains {[Co 4 (μ 3 -HTrz) 4 ] 8+ } n connected by d-camphorate ligand building blocks and featured as an extended structure in an AB-AB fashion. The investigated compound displays a wide absorption range across the visible spectrum, characterized by an optical gap energy of 3.7 eV, indicating its semiconducting nature and efficient sunlight absorption capabilities across various wavelengths. The electrochemical performance demonstrated an excellent reversibility, cyclability, structural stability, as well as a specific capacity of up to 100 cycles at a scan rate of 0.1 mV·s -1 and a current density of 50 mA·g -1 . Thus, it showcases its ability to retain the capacity over numerous charge-discharge cycles. Additionally, the investigated sample displayed an impressive rate capability during the Li-ion charge/discharge process. Therefore, the material's remarkable electrochemical properties can be ascribed to the synergistic effects of its large specific surface area of 348.294 m 2 ·g -1 and well-defined pore size distribution of 20.448 Å, making it a promising candidate for high-performance Li-ion batteries.

A novel semiconducting Ni(II)-based hybrid material with the formula (C 7 H 12 N 2 ) NiCl 4 , which exhibits interesting optical and electrical properties, is reported. The crystal structure was investigated using SCXRD, whereas physical properties were studied by means of thermal analysis, Ft-Infrared, optical, and electrical measurements. Its crystal packing is formed through organic rings surrounded by inorganic [NiCl 4 ] 2- tetrahedral and stacked along the a -crystallographic axis. This arrangement is stabilized by a dense network of intermolecular hydrogen bonds. The investigated compound displayed a wide absorption range across the visible spectrum, characterized by an optical gap energy of 2.64 eV, indicating its semiconducting nature and efficient sunlight absorption capabilities across various wavelengths. Such features are of utmost importance in achieving a high energy conversion efficiency in solar cell applications. Further analyses of the thermal behavior using differential scanning calorimetry revealed a single-phase transition occurring at around 413 K, which was further confirmed through electrical measurements. A deep investigation of the electric and dielectric performances demonstrated a significant dielectric constant (ε' ∼ 10 4 ) at low frequencies and low dielectric loss at high frequencies. Thus, it highlights its exceptional dielectric potential, particularly in applications related to electronic capacitors., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

Spin-crossover particles of [Fe(Htrz) 2 trz](BF 4 ) with sizes of some hundred nanometers are studied by in situ electron microscopy. Despite their high radiation sensitivity, it was possible to analyze the particles by imaging and diffraction so that a detailed analysis of crystallographic defects in individual particles became possible. The presence of one or several tilt boundaries, where the tilt axis is the direction of the polymer chains, is detected in each particle. An in situ exposure of the particles to temperature variations or short laser pulses to induce the spin crossover shows that the defect structure only changes after a high number of transformations between the low-spin and high-spin phases. The observations are explained by the anisotropy of the atomic architecture within the crystals, which facilitates defects between weakly linked crystallographic planes.

An unusual expansion dynamics of individual spin crossover nanoparticles is studied by ultrafast transmission electron microscopy. After exposure to nanosecond laser pulses, the particles exhibit considerable length oscillations during and after their expansion. The vibration period of 50-100 ns is of the same order of magnitude as the time that the particles need for a transition from the low-spin to the high-spin state. The observations are explained in Monte Carlo calculations using a model where elastic and thermal coupling between the molecules within a crystalline spin crossover particle govern the phase transition between the two spin states. The experimentally observed length oscillations are in agreement with the calculations, and it is shown that the system undergoes repeated transitions between the two spin states until relaxation in the high-spin state occurs due to energy dissipation. Spin crossover particles are therefore a unique system where a resonant transition between two phases occurs in a phase transformation of first order., (© 2023 The Authors. Small published by Wiley-VCH GmbH.)

In this paper, we report the chemical strategy followed to obtain, in a direct way, nanoparticles of the Rb x Mn[Fe(CN) 6 ] ( x +2)/3 · n H 2 O (RbMnFe) Prussian blue analogue with the aim of keeping the switching ability of this compound at the nanoscale. The switching properties come from a reversible electron transfer between the iron and manganese ions and depends on the rubidium content in the structure that has to be higher than 0.6. Despite the multifunctionality of this family of compounds and its interest in various applications, no systematic studies were performed to obtain well-defined nanoparticles. This paper relates to such an investigation. To draw relationship between size reduction, composition, and switching properties, a special attention was brought to the determination of the composition through elemental analysis and structure refinement of powder X-ray diffraction patterns together with infrared spectroscopy and elemental analysis. Several chemical parameters were explored to control both the size reduction and the composition following a direct synthetic approach. The results show that the smaller the particles, the lower the rubidium content. This observation might prevent the observation of switching properties on very small particles. Despite this antagonist effect, we achieved switchable particles of around 200 nm without any use of surfactant. Moreover, the size reduction is associated with the observation of the electron transfer down to 52% of rubidium in the nanoparticles against 64% in microparticles. This work is of particular interest in processing such nanoparticles into devices.

Spin crossover (SCO) is a promising switching phenomenon when implemented in electronic devices as molecules, thin films or nanoparticles. Among the properties modulated along this phenomenon, optically induced mechanical changes are of tremendous importance as they can work as fast light-induced mechanical switches or allow to investigate and control microstructural strains and fatigability. The development of characterization techniques probing nanoscopic behavior with high spatio-temporal resolution allows to trigger and visualize such mechanical changes of individual nanoscopic objects. Here, ultrafast transmission electron microscopy (UTEM) is used to precisely probe the length changes of individual switchable nanoparticles induced thermally by nanosecond laser pulses. This allows revealing of the mechanisms of spin switching, leading to the macroscopic expansion of SCO materials. This study is conducted on individual pure SCO nanoparticles and SCO nanoparticles encapsulating gold nanorods that serve for plasmonic heating under laser pulses. Length changes are compared with time-resolved optical measurements performed on an assembly of these particles., (© 2021 Wiley-VCH GmbH.)

Molecular systems can exhibit multi-stimuli switching of their properties, with spin crossover materials having unique magnetic transition triggered by temperature and light, among others. Light-induced room temperature operation is however elusive, as optical changes between metastable spin states require cryogenic temperatures. Furthermore, electrical detection is hampered by the intrinsic low conductivity properties of these materials. We show here how a graphene underlayer reveals the light-induced heating that triggers a spin transition, paving the way for using these molecules for room temperature optoelectronic applications.

Switchable materials are increasingly considered for implementation in devices or multifunctional composites leading to a strong need in terms of reliable synthetic productions of well-defined objects. Here, an innovative and robust template-free continuous process was developed to synthesize nanoparticles of a switchable coordination polymer, including the use of supercritical CO 2 , aiming at both quenching the particle growth and drying the powder. This all-in-one process offers a 12-fold size reduction in a few minutes while maintaining the switching properties of the selected spin crossover coordination polymer., (© 2020 Wiley-VCH GmbH.)

The current craze for research around the spin crossover phenomenon can be justified to some extent by the mechanical properties due to the decrease of volume associated with the transition of the metal ion from the HS state to the LS state. As demonstrated here, the molecular complex [Fe(PM-pBrA) 2 (NCS) 2 ] exhibits, on the contrary, an increase of the unit-cell volume from HS to LS. This counter-intuitive and unprecedented behavior that concerns both the thermal and the photoexcited spin conversions is revealed by a combination of single-crystal and powder X-ray diffraction complemented by magnetic measurements. Interestingly, this abnormal volume change appears concomitant with the wide rotation of a phenyl ring which induces a drastic modification, though reversible, of the structural packing within the crystal. In addition, the light-induced HS state obtained through the Light-Induced Excited Spin-State Trapping shows a remarkably high relaxation temperature, namely T(LIESST), of 109 K, one of the highest so far reported. The above set of quite unusual characteristics opens up new fields of possibilities within the development of spin crossover materials., (© 2020 Wiley-VCH GmbH.)

An accurate high-pressure X-ray diffraction investigation, at various temperatures, on a powder of a spin-crossover (SCO) complex has allowed the rare deconvolution of the structural features of the high-spin and low-spin phases. As a result, the pressure dependence of the structural parameters of the high-spin and low-spin phases can be discussed independently in the pressure domain where both phases co-exist within the powder. Consequently, crucial unprecedented information is given, such as the variation of bulk moduli with temperature, similar here in amplitude for both spin phases, the temperature-dependence of the pressure-induced SCO abruptness, the temperature dependence of the pressure at which SCO occurs, and arguments for a possible piezo-hysteresis. Performed on the molecular complex [Fe(PM-PeA) 2 (NCSe) 2 ] (PM-PeA=N-(2'-pyridylmethylene)-4-(phenylethynyl) aniline), this study reveals a pressure-induced SCO at 0.16 GPa and demonstrates that, when increasing temperature, the pressure of transition increases linearly, the abruptness of the pressure-induced SCO strongly increases, and the bulk moduli decrease., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A new surfactant-free, flow-focusing droplet microfluidic approach was developed as an important alternative to existing synthesis techniques for the preparation of spin crossover nanoparticles. It enables great control of the mixing of the reactants, and produces crystals of [Fe(pyrazine)(Pt(CN)4)] with an unexpected 20-fold downsizing compared to classical bulk synthesis.

Spin-crossover (SCO) triazole-based coordination polymers can be synthesized by micelle techniques, which almost always lead to rod-shaped nanoparticles. In order to notably reach new morphologies, we explore here the potentiality of the spray-drying (SD) method to get SCO materials. Three SCO coordination polymers and a mononuclear complex are investigated. In all cases, the SD method obtains particles definitely showing SCO. The features of the latter are yet always different from those of the referenced materials, in the sense that SCO is more gradual and incomplete, in adequacy with the poor crystallinity of the powders obtained by SD. In the case of coordination polymers, the particles are preferentially spherical. Indications of possible polymorphism and/or new materials induced by the use of the SD method are evidenced. In the case of the mononuclear complex, the SD method has allowed reproducing, in a quick and easy way, the well-known bulk compound. This exploratory work demonstrates the relevance of the concept and opens the way to a systematic scrutiny of all the experimental parameters to tune the size, morphology, and properties of the SD-synthesized SCO particles.