Abstract: A positive electrode active material includes a core containing Li1+xMn1yAyP1?zRzO4, a first coating layer covering the core and containing a crystalline pyrophosphate MaP2O7 and a crystalline oxide M?bOc, and a second coating layer covering the first coating layer.

Abstract: An organic-inorganic hybrid porous material. The organic-inorganic hybrid porous material contains a doping element A are provided. In some embodiments, the element A is one or more selected from: Li, Na, K, Rb, Cs, Sr, Zn, Mg, Ca, or any combination thereof. An external specific surface area of the organic-inorganic hybrid porous material is 1 to 100 m2/g. A ratio of the external specific surface area to a total specific surface area of the organic-inorganic hybrid porous material is 0.7 to 0.9.

Abstract: A positive electrode active material is granular and comprises a compound represented by formula 1: (NaxAy)a?bM1[M2(CN)6]?, wherein A is selected from at least one of alkali metal elements and has an ionic radius greater than that of sodium, M1 and M2 are each independently selected from at least one of transition metal elements, 0<y?0.2, 0<x+y?2, 0???1, a+b=2, 0.85?a?0.98, (represents a vacancy, and b represents the number of vacancies; and when the positive electrode active material is dissolved, at a temperature of 20° C., into an aqueous solution having a concentration of 5 g/100 g water, a pH value of the aqueous solution is in a range of 7.6 to 8.5. The positive electrode active material has good cycling and rate performance, and a high specific capacity.

Abstract: The present application provides a positive electrode active material which may be in a particulate form and comprise a compound represented by Formula 1: NaxAyM1[M2(CN)6]?·zH2O??Formula 1 wherein, A is selected from at least one of an alkali metal element and an alkaline earth metal element, and the ionic radius of A is greater than the ionic radius of sodium; M1 and M2 are each independently selected from at least one of a transition metal element, 0<y?0.2, 0<x+y?2, 0<??1, and 0?z?10; and the particles of the positive electrode active material may have a gradient layer in which the content of the A element decreases from the particle surface to the particle interior.

Abstract: A continuous reaction system for preparing a ferromanganese oxalate precursor may comprise a first dissolution reactor, a second dissolution reactor, a first reactor, a second reactor, a material storage tank, and an ultrasonic reactor; the first dissolution reactor may be configured to accommodate a metal salt solution required for preparing the ferromanganese oxalate precursor, and the second dissolution reactor may be configured to accommodate a precipitant solution required for preparing the ferromanganese oxalate precursor; the first reactor may include a first feed port and a first overflow port, and the first feed port of the first reactor may be interconnected to a first discharge port of the first dissolution reactor and a second discharge port of the second dissolution reactor respectively through two pipelines.

Abstract: A lithium manganese iron phosphate positive electrode active material, preparation method, a positive electrode plate, a secondary battery and an electrical apparatus are disclosed. The method comprises: mixing and grinding an iron source, a solid base and optionally a source of doping element M After grinding, impurities are removed to obtain a nanoscale iron-containing oxide; mixing the obtained nanoscale iron-containing oxide with a solvent, a lithium source, a manganese source, a phosphorus source, optionally a source of doping element N, optionally a source of doping element Q and optionally a source of doping element R in a predetermined ratio and then grinding. After grinding, granulating to obtain a powder; and sintering the powder to obtain the lithium manganese iron phosphate positive electrode active material. A lithium manganese iron phosphate positive electrode active material having both good electrochemical performance and high tap density can be obtained.

Abstract: A hard carbon. A total quantity of adsorbed nitrogen under a relative pressure P/P0 of nitrogen between 10?8 and 0.035 is V1 cm3 (STP)/g and a total quantity of adsorbed nitrogen under a relative pressure P/Po of nitrogen between 0.035 and 1 is V2 cm3 (STP)/g in a nitrogen adsorption isotherm determined at a temperature of 77 K for the hard carbon. The hard carbon satisfies: V2/V1?0.20 and 20?V1?150, where P represents an actual pressure of nitrogen, and P0 represents a saturated vapor pressure of nitrogen at a temperature of 77 K.

Abstract: The present application provides a method for preparing a perovskite film, and a related perovskite film, solar cell and solar cell device thereof. The preparation method may include the steps of (1) providing a target material comprising the following elements: lead, a halogen, and one or more alkali metals; (2) sputtering using the target material in step (1), where a process gas is a noble gas, optionally, argon, so as to obtain a film; (3) subjecting the film obtained in step (2) to a chemical bath treatment, wherein the chemical bath is a solution of AX, A is selected from one or more of formamidine or methylamine, and X is a halogen; and (4) sputtering on the film obtained in step (3) using a tin metal, where a process gas comprises a noble gas, optionally, a mixture of argon and a halogen gas, so as to obtain the perovskite film.

Abstract: A perovskite solar battery, including a transparent conductive glass substrate, a hole transport layer, a perovskite light-absorbing layer, an electron transport layer, and an electrode are described. The hole transport layer is a nickel oxide hole transport layer. Simple-substance nickel exists on a contact surface of the hole transport layer in contact with the perovskite light-absorbing layer. On the contact surface of the hole transport layer in contact with the perovskite light-absorbing layer, a ratio between simple-substance nickel and trivalent nickel is 85:15 to 99:1, optionally 90:10 to 99:1, and further optionally 95:5 to 99:1. This application further provides a method for preparing a perovskite solar battery.

Abstract: Provided are a perovskite betavoltaic-photovoltaic battery. The battery includes a first electrode, a first charge transport layer, a perovskite layer, a second charge transport layer, and a second electrode in sequence. The first electrode is a transparent electrode. The first charge transport layer is an electron transport layer and the second charge transport layer is a hole transport layer, or, the first charge transport layer is a hole transport layer and the second charge transport layer is an electron transport layer. The perovskite layer is doped with a fluorescent substance. At least one of the first electrode, the first charge transport layer, the second charge transport layer, or the second electrode is radioactive. When the first electrode and/or the second electrode is radioactive, the first electrode and/or the second electrode is an irradiated electrode formed by compounding a radioactive source and a conductor material.

Abstract: A positive electrode active material includes LiaAxMn1-yByP1-zCzO4-nDn. A includes one or more selected from group IA, group IIA, group IIIA, group IIB, group VB, and group VIB. B includes one or more selected from group IA, group IIA, group IIIA, group IVA, group VA, group IIB, group IVB, group VB, group VIB, and group VIII. C includes one or more selected from group IIIA, group IVA, group VA and group VIA. D includes one or more selected from group VIA and group VIIA. a is selected from 0.85 to 1.15. x is selected from 0 to 0.1. y is selected from 0.001 to 0.999. z is selected from 0 to 0.5. n is selected from 0 to 0.5.

Abstract: A perovskite solar battery, including a transparent conductive glass substrate, a hole transport layer, a perovskite light-absorbing layer, an electron transport layer, and an electrode are described. The hole transport layer is a nickel oxide hole transport layer. Simple-substance nickel exists on a contact surface of the hole transport layer in contact with the perovskite light-absorbing layer. On the contact surface of the hole transport layer in contact with the perovskite light-absorbing layer, a ratio between simple-substance nickel and trivalent nickel is 85:15 to 99:1, optionally 90:10 to 99:1, and further optionally 95:5 to 99:1. This application further provides a method for preparing a perovskite solar battery.

Abstract: A perovskite radiovoltaic-photovoltaic battery having a first electrode, a first charge transport layer, a perovskite layer, a second charge transport layer, and a second electrode in sequence, wherein the first electrode is a transparent electrode, the first charge transport layer is an electron transport layer and the second charge transport layer is a hole transport layer, or the first charge transport layer is a hole transport layer and the second charge transport layer is an electron transport layer, and the second electrode is a radiating electrode formed by compounding an electrical conductor material with a radioactive source.

Abstract: A perovskite solar cell includes following components provided successively from bottom to top: a transparent conductive glass substrate, a first transport layer, a perovskite layer, a second transport layer, a conductive electrode, and a back plate glass. The perovskite solar cell further includes an encapsulating adhesive. The transparent conductive glass substrate, the back plate glass, and the encapsulating adhesive form an enclosed space. The enclosed space contains a mixture of an inert gas and a methylamine gas, where a volume ratio of the inert gas to the methylamine gas is in a range from 9:1 to 5:5.

Abstract: A perovskite solar cell includes following components provided successively from bottom to top: a transparent conductive glass substrate, a first transport layer, a perovskite layer, a second transport layer, a conductive electrode, and a back plate glass. The perovskite solar cell further includes an encapsulating adhesive. The transparent conductive glass substrate, the back plate glass, and the encapsulating adhesive form an enclosed space. The enclosed space contains a mixture of an inert gas and a methylamine gas, where a volume ratio of the inert gas to the methylamine gas is in a range from 9:1 to 5:5.

Abstract: Embodiments of this application provide a perovskite solar cell, a preparation method thereof, and an electric device. The perovskite solar cell includes: a back plate; a transparent substrate, where a sealed cavity is formed between the transparent substrate and the back plate; and a perovskite solar cell device, where the perovskite solar cell device is located in the sealed cavity; where the sealed cavity contains ammonia gas having a volume fraction of 10%-100% and residual inert gas. The 10%-100% ammonia gas can improve chemical stability of a perovskite material, thus improving thermal stability of the perovskite solar cell device, and further improving efficiency and service life of the perovskite solar cell.

Abstract: A perovskite radiovoltaic-photovoltaic battery having a first electrode, a first charge transport layer, a perovskite layer, a second charge transport layer, and a second electrode in sequence, wherein the first electrode is a transparent electrode, the first charge transport layer is an electron transport layer and the second charge transport layer is a hole transport layer, or the first charge transport layer is a hole transport layer and the second charge transport layer is an electron transport layer, and the second electrode is a radiating electrode formed by compounding an electrical conductor material with a radioactive source.

Abstract: An A/M/X crystalline material, a photovoltaic device, and preparation methods thereof are provided. The photovoltaic device includes a photoactive crystalline material layer. The photoactive crystalline material layer includes a penetrating crystal, where the penetrating crystal is a crystal penetrating through the photoactive crystalline material layer, and a percentage p of a quantity of penetrating crystals in a total quantity of crystals of the photoactive crystalline material layer is ?80%. The photoactive crystalline material layer includes a backlight side and a backlight crystal, where the backlight crystal is a crystal exposed to the backlight side and has a backlight crystal face exposed to the backlight side. At least one region of the backlight side has an average flatness index Ravg being ?75.

Abstract: The present application provides a separator, a secondary battery, a battery module, a battery pack, and a power consumption apparatus. The separator may include a porous base film and a bonding layer coated on one or both faces of the porous base film. The bonding layer may be composed of ethylene carbonate and an optional nucleating agent.

Abstract: An organic-inorganic hybrid porous material. The organic-inorganic hybrid porous material contains a doping element A are provided. In some emodiments, the element A is one or more selected from: Li, Na, K, Rb, Cs, Sr, Zn, Mg, Ca, or any combination thereof. An external specific surface area of the organic-inorganic hybrid porous material is 1 to 100 m2/g. A ratio of the external specific surface area to a total specific surface area of the organic-inorganic hybrid porous material is 0.7 to 0.9.