Abstract: A preparation method of perovskite film based on semicarbazide hydrochloride (SEM-HCl) additive and a preparation method of photovoltaic device are provided, a perovskite optimized crystallization strategy is provided, a tin-based perovskite thin film is prepared based on a solution method, and a purpose of regulating and controlling perovskite crystallization is achieved by means of a cross-linking effect of special groups in SEM-HCl and perovskite components. Defects of crystals of the prepared perovskite film are reduced, the non-radiative recombination in a transmission process of carriers is suppressed, and a photoelectric conversion efficiency and a photovoltaic device stability are remarkably improved.

Abstract: A backside emitter solar cell structure having a heterojunction, and a method and a device for producing the same. A backside intrinsic layer is first formed on the back side of the substrate, then a frontside intrinsic layer and a frontside doping layer are formed on the front side of the substrate, and finally a backside doping layer is formed on the back side of the substrate.

Abstract: A lithium metal composite oxide powder, which comprises primary particles and secondary particles that are aggregates of the primary particles, and has an ?-NaFeO2 type crystal structure, wherein a half width (A) of a diffraction peak in a range of 2?=18.7±1° in a powder X-ray diffraction measurement for the lithium metal composite oxide powder using CuK? ray is 0.135° or more and 0.165° or less, and a c-axis lattice constant of the ?-NaFeO2 type crystal structure is 14.178 ? or more and 14.235 ? or less.

Abstract: Provided is a lithium secondary battery having a higher capacity and a longer life. The lithium secondary battery includes: a positive electrode including a material capable of intercalation and deintercalation of a lithium ion; a lithium ion-conductive electrolyte including a salen-based metal complex; and a negative electrode including a material capable of occlusion and release of a lithium metal or a lithium ion. The salen-based metal complex is selected from (R,R)-(?)-N,N?-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminotitanium chloride (TiSl), VSl, CrSl, MnSl, FeSl, CoSl, and RuSl.

Abstract: Provided are a negative electrode active material including a three-dimensional composite. The three-dimensional composite includes secondary particles containing a silicon carbide-based (SiCx, 0<x?1) nanosheet having a bent portion and amorphous carbon. Also provided are a method of producing the same, and a negative electrode and a lithium secondary battery including the negative electrode active material.

Abstract: Provided are an oxide including a compound represented by Formula 1, a method of pre paring the same, a solid electrolyte including the oxide, and an electrochemical device including the oxide: LiaTa2?yAyP1?xMxO8?zXz??Formula 1 wherein, in Formula 1, M is an element having an oxidation number of +3, A is an element having an oxidation number of +4, +5, or +6, or a combination thereof, when A is an element having an oxidation number of +4, a is 1+y+2x?z, when A is an element having an oxidation number of +5, a is 1+2x?z, when A is an element having an oxidation number of +6, a is 1?y+2x?z, X is a halogen atom or a pseudohalogen, and 0?y<0.6, 0?x<1, and 0?z<1, with the proviso that x, y and z are not 0 at the same time.

Abstract: An additive for a lithium secondary battery includes a compound represented by Formula 1 below, where R1 to R4 are as defined in the disclosure. An electrolyte for a lithium secondary battery includes: a lithium salt; a non-aqueous organic solvent; and the additive. A lithium secondary battery includes: a cathode; an anode; and the electrolyte.

Abstract: A battery includes a wound electrode assembly. The wound electrode assembly has a flat shape. The wound electrode assembly includes a first separator, a positive electrode plate, a second separator, and a negative electrode plate. The first separator, the positive electrode plate, the second separator, and the negative electrode plate are stacked in this order and then wound spirally. In a cross section perpendicular to a winding axis of the wound electrode assembly, the first separator has a first winding start edge inside an innermost circumference of the wound electrode assembly; the second separator has a second winding start edge inside the innermost circumference of the wound electrode assembly; the first winding start edge faces the second winding start edge with the winding axis interposed therebetween; and the first winding start edge is located apart from the second winding start edge.

Abstract: An electrochemically active material comprising a surface is provided, wherein the surface comprises an oligomer. A method of functionalising the surface with the oligomer is also provided.

Abstract: In a secondary batter, dead spaces between a wound electrode body and the inner peripheral surfaces of a rectangular battery case are made small. The secondary battery includes a wound electrode body in which a positive electrode sheet, a negative electrode sheet, and a separator interposed between the positive electrode sheet and the negative electrode sheet are superimposed and wound around a winding axis, and a rectangular battery case that houses the wound electrode body. The wound electrode body has a first flat surface, a second flat surface, a third flat surface, and a fourth flat surface positioned on the outer peripheral surfaces around the winding axis. The first flat surface and the second flat surface face each other with the winding axis interposed therebetween. The third flat surface and the fourth flat surface face each other with the winding axis interposed therebetween.

Abstract: The present application provides a perovskite solar cell, including conductive glass, a hole transport layer, a perovskite layer, an electron transport layer and a back electrode, where a passivation layer may be disposed between the hole transport layer and the perovskite layer, and the passivation layer may include an amide and/or a cation thereof, where the amide may include a compound of formula (1) and/or formula (2): where R1 and R2 are each independently selected from hydrogen, —R, —NR2, —NHR, —NH2, —OH, —OR, —NHCOR, —OCOR, and —CH2COOH, where R represents a straight or branched chain alkyl group having 1-10 carbon atoms, m is an integer of 0 to 10; and n is an integer of 1 to 10; and where Ar is selected from a C5-C10 aryl or heteroaryl group.

Abstract: A solid electrolyte material comprising Li, T, X and A wherein T is at least one of P, As, Si, Ge, Al, and B; X is BH4; A is S, Se, or N. The solid electrolyte material may include glass ceramic and/or mixed crystalline phases, and exhibits high ionic conductivity and compatibility with high voltage cathodes and lithium metal anodes.

Abstract: Provided is apparatus for introducing a quasi-solid electrolyte into one or a plurality of lithium battery cells, the apparatus comprising: (a) a cell-holding device to hold one or a plurality of lithium battery cells and is in a working relation to a liquid electrolyte-filling device that injects a liquid electrolyte into the battery cells, wherein the liquid electrolyte comprises a lithium salt dissolved in a first liquid solvent having a first lithium salt concentration from 0.001 M to 3.0 M (mole/L); and (b) a solvent vapor-removing device in a working relation to the cell-holding device, wherein the vapor-removing device comprises a pumping device to move solvent vapors away from the battery cells so that the electrolyte has a final lithium salt concentration higher than the first concentration and higher than 2.0 M. Also provided is a method of operating the apparatus.

Abstract: The non-aqueous electrolyte secondary battery disclosed herein includes the laminated electrode body having cell units in each of which a first electrode, a first separator, a second electrode, and a second separator are stacked. The first electrode has a first active material layer, and the second electrode has a second active material layer. A facing area which faces the second active material layer is formed in a central portion of the first active material layer. The first separator and the first electrode are bonded to each other by a first adhesive, and the first adhesive is not disposed in the facing area and is disposed in an area other than the facing area. The first separator and the second separator are not bonded to the second active material layer, and are joined to each other outside the second electrode.

Abstract: The present invention relates to the field of anode materials of lithium batteries, and in particular, relates to a silicon/carbon composite material with a highly compact structure. The silicon/carbon composite material with the highly compact structure includes silicon particles and a carbon coating layer, and further includes a highly compact carbon matrix, wherein the silicon particles are distributed inside the highly compact carbon matrix evenly and dispersively and forms an inner core; and the silicon/carbon composite with the highly compact structure is compact inside without voids or has few closed voids inside. The present invention provides the silicon/carbon composite material with the highly compact structure with a reduced volumetric expansion effect and an improved cycle performance, a method for preparing the same, and a use thereof.

Abstract: A method for formation of cylindrical and prismatic can cells may include providing a battery, where the battery includes one or more cells, with each cell including at least one silicon-dominant anode, a cathode, and a separator. The battery also includes a metal can that contains the one or more cells such that during formation a pressure between 50 kPa and 1 MPa is applied to the one or more cells. The battery may include strain absorbing materials arranged between the one or more cells and interior walls of the can. The strain absorbing materials may include foam. The strain absorbing materials may include a solid electrolyte layer. The strain absorbing materials may include PMMA, PVDF, or a combination thereof. The pressure during a formation process may be due to a thickness of the strain absorbing materials being thicker than an expansion of the one or more cells.

Abstract: The present disclosure is related to structures for and methods for producing thermoelectric devices. The thermoelectric devices include multiple stages of thermoelements. Each stage includes alternating n-type and p-type thermoelements. The stages are sandwiched between upper and lower sets of metal links fabricated on a pair of substrate layers. The metal links electrically connect pairs of n-type and p-type thermoelements from each stage. There may be additional sets of metal links between the multiple stages. The individual thermoelements may be sized to handle differing amounts of electric current to optimize performance based on their location within the multistage device.

Abstract: A solar power generation system for providing a predetermined operating power level and predetermined operating voltage level requirement is provided. The system includes at least one solar-array panel. Each of the solar-array panels includes a multiplicity of PV solar sub cells. A preconfigured number of the PV solar sub cells are electrically connected in series to form a serial-unit or each forming an individual serial unit having just one PV solar sub cell. A preconfigured number of the serial units are electrically connected in series to form a string of serial-units. The PV solar sub cells are also connected in parallel to neighboring sub cells to form a crisscross matrix array that facilitates bypassing malfunctioning serial units, thereby improving the performance of the system. A PV solar sub cell is at least 50% smaller in area than a regular PV solar cell.

Abstract: Disclosed is a copolymer as PAES-g-PEG or PAEK-g-PEG as an arylene-based polymer having ion conductivity and mechanical strength and having a functional group as a substituent at a chain-end of PEG, wherein the functional group includes one selected from a group consisting of a hydroxyl group (—OH), methacrylate (-MA), a double hydroxyl group (-2OH), a nitrile group (—CN) and an ionic liquid group (-PYRTFSI). Further, disclosed is a solid electrolyte membrane for a secondary battery including the copolymer and thus having improved ion conductivity, lithium ion transport ability, and excellent mechanical strength.

Abstract: A non-aqueous electrolyte solution for a lithium secondary battery and a lithium secondary battery including the same are disclosed herein. In some embodiments, a non-aqueous electrolyte solution for a lithium secondary battery, includes an additive having metal ion adsorbability and capable of forming a stable ion conductive film on the surface of an electrode. In some embodiments, a lithium secondary battery including the same has an improved an abnormal voltage drop phenomenon.