Molecular Design of a Metal-Nitrosyl Ferroelectric with Reversible Photoisomerization.

The development of photo-responsive ferroelectrics whose polarization may be remotely controlled by optical means is of fundamental importance for basic research and technological applications. Herein, we report the design and synthesis of a new metal-nitrosyl ferroelectric crystal (DMA)(PIP)[Fe(CN)5(NO)] (1) (DMA = dimethylammonium, PIP = piperidinium) with potential phototunable polarization via a dual-organic-cation molecular design strategy. Compared to the parent non-ferroelectric (MA)2[Fe(CN)5(NO)] (MA = methylammonium) material with a phase transition at 207 K, the introduction of larger dual organic cations both lowers the crystal symmetry affording robust ferroelectricity and increases the energy barrier of molecular motions, endowing 1 with a large polarization of up to 7.6 µC cm-2 and a high Curie temperature (Tc) of 316 K. Infrared spectroscopy shows that the reversible photoisomerization of the nitrosyl ligand is accomplished by light irradiation. Specifically, the ground state with the N-bound nitrosyl ligand conformation can be reversibly switched to both the metastable state I (MSI) with isonitrosyl conformation and the metastable state II (MSII) with side-on nitrosyl conformation. Quantum chemistry calculations suggest that the photoisomerization significantly changes the dipole moment of the [Fe(CN)5(NO)]2- anion, thus leading to three ferroelectric states with different values of macroscopic polarization. Such optical accessibility and controllability of different ferroelectric states via photoinduced nitrosyl linkage isomerization open up a new and attractive route to optically controllable macroscopic polarization.

Mechanistic Insight into the Promotion of the Low-Temperature NH3-Selective Catalytic Reduction Activity over MnxCe1-xOy Catalysts: A Combined Experimental and Density Functional Theory Study.

CeO2 has attracted much attention in the field of selective catalytic reduction of NO with NH3 (NH3-SCR). However, poor low-temperature activity and a narrow operation window restrict the industrial application of Ce-based oxide catalysts. Herein, the low-temperature NH3-SCR activity of Ce-based oxide catalysts was dramatically improved by Mn doping, and the mechanism was elucidated at the atomic level by experimental measurements and density functional theory calculations. We found that the addition of Mn significantly promoted the formation of surface oxygen vacancies. The oxygen vacancies easily captured O2 in air and formed active oxygen species (superoxide and peroxide) on the surface. The surface active oxygen species efficiently oxidized NO into NO2 and then facilitated the "fast SCR" reaction. This study provides atomic-level insights into the promotion of the NH3-SCR activity over Mn-Ce composite oxides and is beneficial for the development of low-temperature Ce-based catalysts.

Tailoring of a visible-light-absorbing biaxial ferroelectric towards broadband self-driven photodetection.

In terms of strong light-polarization coupling, ferroelectric materials with bulk photovoltaic effects afford a promising avenue for optoelectronic devices. However, due to severe polarization deterioration caused by leakage current of photoexcited carriers, most of ferroelectrics are merely capable of absorbing 8-20% of visible-light spectra. Ferroelectrics with the narrow bandgap (<2.0 eV) are still scarce, hindering their practical applications. Here, we present a lead-iodide hybrid biaxial ferroelectric, (isopentylammonium)2(ethylammonium)2Pb3I10, which shows large spontaneous polarization (~5.2 µC/cm2) and a narrow direct bandgap (~1.80 eV). Particularly, the symmetry breaking of 4/mmmFmm2 species results in its biaxial attributes, which has four equivalent polar directions. Accordingly, exceptional in-plane photovoltaic effects are exploited along the crystallographic [001] and [010] axes directions inside the crystallographic bc-plane. The coupling between ferroelectricity and photovoltaic effects endows great possibility toward self-driven photodetection. This study sheds light on future optoelectronic device applications.

Ultrafast solid-liquid intercalation enabled by targeted microwave energy delivery.

In chemical reactions, the breaking and formation of chemical bonds usually need external energy to overcome the activation barriers. Conventional energy delivery transfers energy from heating sources via various media, hence losing efficiency and inducing side reactions. In contrast, microwave (MW) heating is known to be highly energy efficient through dipole interaction with polar media, but how exactly it transmits energy to initiate chemical reactions has been unknown. Here, we report a rigorous determination of energy delivery mechanisms underlying MW-enabled rapid hydrothermal synthesis, by monitoring the structure and temperature of all the involved components as solid-liquid intercalation reaction occurs using in situ synchrotron techniques. We reveal a hitherto unknown direct energy transmission between MW irradiation source and the targeted reactants, leading to greatly reduced energy waste, and so the ultrafast kinetics at low temperature. These findings open up new horizons for designing material synthesis reactions of high efficiency and precision.

Soft Perovskite-Type Antiferroelectric with Giant Electrocaloric Strength near Room Temperature.

Antiferroelectric materials, characterized by an antiparallel array of adjacent dipoles, are holding a bright future for solid-state refrigeration based on their electrocaloric (EC) effects. Despite great advances of inorganic oxides and some organic soft polymers, their EC effects are achieved under quite high electric fields that result in too low EC strengths for practical application. Currently, it is a challenge to exploit soft antiferroelectric with strong EC strengths. Here, by the mixed-cation alloying, we present a new perovskite-type soft antiferroelectric, (isopentylammonium)2CsPb2Br7 (1), which incorporates both an organic spacing cation and an inorganic perovskitizer Cs+ moiety. Remarkably, the synergic cooperativity between the reorientation of the organic spacer and atomic displacement of Cs+ cation triggers its multiple ferroelectric-antiferroelectric-paraelectric phase transitions at 321 and 350 K. Their natural polarization vs electric field hysteresis loops are characterized to confirm ferroelectric and antiferroelectric orders of 1, respectively. It is emphasized that, under a low electric field of 13 kV/cm, the antipolar dipole realignment in 1 endows a giant near-room-temperature EC strength (ΔTEC/ΔE) of 15.4 K m MV-1 at antiferroelectric phase. This merit is on par with the record-high value of BaTiO3 (∼16 K m/MV) but far beyond the state-of-the-art soft polymers. The underlying EC mechanism for 1 is ascribed to the extremely low critical field to switch dipoles, involving the reorientation of the organic spacer and the shift of the Cs+ cation. Besides, notable EC entropy change (∼4.1 J K-1 kg-1) and temperature change (∼2 K) reveal potentials of 1 for solid-state refrigeration. As far as we know, this discovery of near-room-temperature EC strengths is unprecedented in the hybrid perovskite family, which sheds light on the exploration of new soft antiferroelectrics toward high-efficiency refrigeration devices.

3D-to-2D Dimensional Reduction for Exploiting a Multilayered Perovskite Ferroelectric toward Polarized-Light Detection in the Solar-Blind Ultraviolet Region.

Polarized-light detection in solar-blind ultraviolet region is indispensable for optoelectronic applications, whereas new 2D candidates targeted at solar-blind UV range remain extremely scarce. 2D hybrid perovskite ferroelectrics that combine polarization and semiconducting properties are of increasing interest. Here, using the 3D-to-2D dimensional reduction of CH3 NH3 PbCl3 , we designed a multilayered hybrid perovskite ferroelectric, (CH3 CH2 NH3 )2 (CH3 NH3 )2 Pb3 Cl10 , which shows spontaneous polarization and a high Curie temperature (390 K) comparable with that of BaTiO3 (393 K). The wide band gap (ca. 3.35 eV) and anisotropic absorbance stemming from its intrinsic 2D motif, greatly favor its polarization-sensitive activity in UV region. The device displays excellent polarization-sensitive behavior under 266 nm, along with a large dichroic ratio (ca. 1.38) and high on/off current ratio (ca. 2.3×103 ).

Giant and Broadband Multiphoton Absorption Nonlinearities of a 2D Organometallic Perovskite Ferroelectric.

Multiphoton absorption (MPA) has been utilized for important technological applications. High-order multiphoton harvesting (e.g., five-photon absorption, 5PA) exhibits unique properties that could benefit biophotonics. Within this field, perovskite oxide ferroelectrics (e.g., BaTiO3 ) enable low-order optical nonlinearities of 2PA/3PA processes. However, it is challenging to obtain efficient, high-order 5PA effects. Herein, for the first time, giant and broadband MPA properties are presented in the 2D hybrid perovskite ferroelectric (IA)2 (MA)2 Pb3 Br10 (1; IA = isoamylammonium and MA = methylammonium), where multiphoton-excited optical nonlinearities related to different MPA mechanisms over a broadband range of 550-2400 nm are observed. Strikingly, its 5PA absorption cross-section (σ5 ) reaches up to 1.2 × 10-132 cm10 s4 photon-4 (at 2400 nm), almost 10 orders larger than some state-of-the-art organic molecules and a record-high value among all known ferroelectrics. This unprecedented 5PA effect results from the quantum-confined motif of inorganic trilayer sheets (wells) and organic cations (barriers) in 1. Moreover, its large ferroelectric polarization of 5 µC cm-2 could promote modulation of MPA effects under external electric fields. As far as it is known, this is the first report on giant, broadband high-order MPA properties in ferroelectrics, which provides potential, novel electric-ordered materials for next-generation biophotonic applications.

Multilayered 2D Cesium-Based Hybrid Perovskite with Strong Polarization Sensitivity: Dimensional Reduction of CsPbBr3.

3D perovskite CsPbBr3 has recently taken a blooming position for optoelectronic applications. However, due to the lack of natural anisotropy of optical attributes, it is a great challenge to fulfil polarization-sensitive photodetection. Here, for the first time, we exploited dimensionality reduction of CsPbBr3 to tailor a 2D-multilayered hybrid perovskite, (TRA)2 CsPb2 Br7 (1, in which TRA is (carboxy)cyclohexylmethylammonium), serving as a potential polarized-light detecting candidate. Its unique quantum-confined 2D structure results in intrinsic anisotropy of electrical conductivity, optical absorbance, and polarization-dependent responses. Particularly, it exhibits remarkable dichroism with the photocurrent ratio (Ipc /Ipa ) of ≈2.1, being much higher than that of the isotropic CsPbBr3 crystal and reported CH3 NH3 PbI3 nanowire (≈1.3), which reveals its great potentials for polarization-sensitive photodetection. Further, crystal-based detectors of 1 show fascinating responses to the polarized light, including high detectivity (>1010 Jones), fast responding time (≈300 µs), and sizeable on/off current ratios (>104 ). To our best knowledge, this is the first study on 2D Cs-based hybrid perovskite exhibiting strong polarization-sensitivity. The work highlights an effective pathway to explore new polarization sensitive candidates for hybrid perovskites and promotes their future electronic applications.

Dimensional Reduction of Cs2 AgBiBr6 : A 2D Hybrid Double Perovskite with Strong Polarization Sensitivity.

By dimensional reduction of the 3D motif of Cs2 AgBiBr6 , a lead-free 2D hybrid double perovskite, (i-PA)2 CsAgBiBr7 (1, i-PA=isopentylammonium), was successfully designed. It adopts a quantum-confined bilayered structure with alternating organic and inorganic sheets. Strikingly, the unique 2D architecture endows it highly anisotropic nature of physical properties, including electric conductivity and optical absorption (the ratio αb /αc =1.9 at 405 nm). Such anisotropy attributes result in the strong polarization-sensitive responses with large dichroic ratios up to 1.35, being comparable to some 2D inorganic materials. This is the first study on the hybrid double perovskites with strong polarization sensitivity. A crystal device of 1 also exhibits rapid response speed (ca. 200 µs) and excellent stabilities. The family of 2D hybrid double perovskites are promising optoelectronic candidates, and this work paves a new pathway for exploring new green polarization-sensitive materials.

Two Heteromorphic Crystals of Antimony-Based Hybrids Showing Tunable Optical Band Gaps and Distinct Photoelectric Responses.

Organic-inorganic hybrid perovskites, most markedly CH3NH3PbI3, have attracted extensive interest because of their potential use in optoelectronic and photovoltaic applications. Nevertheless, the toxicity of lead restricts their further application. Here, we successfully synthesized two lead-free heteromorphic hybrids, (C7H18N2O)3Sb4I18·H2O (1) and (C7H18N2O)Sb2I8·H2O (2, C7H18N2O2+ is N-aminopropylmorpholinium), both of which belong to the zero-dimensional tetranuclear perovskite-like structure. However, the inorganic [Sb4I18] cluster of 1 adopts a tetragonal topology, while 2 features the distorted [Sb4I16] motif; this disparity leads to a significant distinction between their electronic structures as well as an optical band gap ( Eg). Their absorption cutoffs are measured to be 708 nm (for 1, Eg = 1.71 eV) and 578 nm (for 2, Eg = 2.11 eV), respectively. In particular, 1 exhibits a stronger photoelectric response in a wider optical region compared to that of 2, and the "on/off" ratio of conductivity of 1 is estimated to ∼300 under sunlight illumination. Density functional theory calculation discloses that different inorganic motifs make greater contributions to their electronic structure and photoelectric response. It is believed that the heteromorphic method allows a potential pathway for construction of new lead-free hybrid materials as light absorbers for photoelectric application.

In situ quantification of interphasial chemistry in Li-ion battery.

The solid-electrolyte interphase (SEI) is probably the least understood component in Li-ion batteries. Considerable effort has been put into understanding its formation and electrochemistry under realistic battery conditions, but mechanistic insights have mostly been inferred indirectly. Here we show the formation of the SEI between a graphite anode and a carbonate electrolyte through combined atomic-scale microscopy and in situ and operando techniques. In particular, we weigh the graphitic anode during its initial lithiation process with an electrochemical quartz crystal microbalance, which unequivocally identifies lithium fluoride and lithium alkylcarbonates as the main chemical components at different potentials. In situ gas analysis confirms the preferential reduction of cyclic over acyclic carbonate molecules, making its reduction product the major component in the SEI. We find that SEI formation starts at graphite edge sites with dimerization of solvated Li+ intercalation between graphite layers. We also show that this lithium salt, at least in its nascent form, can be re-oxidized, despite the general belief that an SEI is electrochemically inert and its formation irreversible.

A heterobimetallic single-source precursor enabled layered oxide cathode for sodium-ion batteries.

A single-source precursor NaCo(acac)3 (acac = acetylacetone) for layered oxide cathodes of sodium-ion batteries (SIBs) is reported here. It features a 1D chain structure, and is prepared in nearly quantitative yield employing commercially available reagents. The complex is stable in open air and tends to dissolve in various strongly polar solvents, including H2O and methanol. The phase-pure layered oxide cathode material P2-NaxCoO2 for SIBs is obtained through calcining the complex, and exhibits an excellent rate capability, even superior to the recently reported P2-NaxCoO2 microspheres. More analogue complexes could be obtained through cationic replacement for the synthesis of other high-performance layered metal oxides for SIBs.

A versatile single molecular precursor for the synthesis of layered oxide cathode materials for Li-ion batteries.

A carbonyl-bridged single molecular precursor LiTM(acac)3 [transition metal (TM) = cobalt/manganese/nickel (Co/Mn/Ni), acac = acetylacetone], featuring a one-dimensional chain structure, was designed and applied to achieve the layered oxide cathode materials: LiTMO2 (TM = Ni/Mn/Co, NMC). As examples, layered oxides, primary LiCoO2, binary LiNi0.8Co0.2O2 and ternary LiNi0.5Mn0.3Co0.2O2 were successfully prepared to be used as cathode materials. When they are applied to lithium-ion batteries (LIBs), all exhibit good electrochemical performance because of their unique morphology and great uniformity of element distribution. This versatile precursor is predicted to accommodate many other metal cations, such as aluminum (Al3+), iron (Fe2+), and sodium (Na+), because of the flexibility of organic ligand, which not only facilitates the doping-modification of the NMC system, but also enables synthesis of Na-ion layered oxides. This opens a new direction of research for the synthesis of high-performance layered oxide cathode materials for LIBs.