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: Disclosed are a lithium metal composite electrode material for a lithium metal battery, a preparation method for the same, and an electrode, battery, battery module, battery pack and apparatus comprising the same. The lithium metal composite electrode material comprises: lithium metal particles and a lithium-containing conductive layer serving as a supporting framework, the supporting framework being filled with the lithium metal particles; wherein the lithium-containing conductive layer comprises an inorganic lithium compound and a lithium alloy.

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: This application provides an electrolytic solution and a lithium metal battery containing the electrolytic solution. The electrolytic solution includes a lithium salt, an organic solvent, and an additive. The additive includes a sultam compound represented by Structural Formula I. R is selected from substituted or unsubstituted C1 to C10 hydrocarbyls, where a substituent is selected from a phenyl, C1 to C6 alkyls, or C1 to C6 alkenyls. X is a sulfur atom or a phosphorus atom. R1 and R2 each are independently selected from an oxygen atom, a fluorine atom, a chlorine atom, a bromine atom, and substituted or unsubstituted C1 to C10 hydrocarbyls. Both R1 and R2 are not oxygen atoms concurrently.

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: Embodiments of the present disclosure relate to a method, an electronic device, and a computer program product for system feature management. The method for system feature management provided by the embodiments of the present disclosure includes loading a feature item set including multiple feature items, where the multiple feature items respectively correspond to multiple microservices, the feature items each include at least an availability indicator and a status indicator, the availability indicator indicates whether the feature item is available, and the status indicator indicates whether the feature item is enabled while the feature item is available; and disabling a first feature item in the feature item set in response to an availability indicator of the first feature item indicating that the first feature item is unavailable. In this way, software can be made to better adapt to more platforms.

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 perovskite solar cell includes a transparent electrode, an electron transport layer, a perovskite layer, a hole transport layer, and a second electrode in sequence. The perovskite layer includes a main perovskite layer and a two-dimensional perovskite coating layer covering both surface and periphery of the main perovskite layer. The two-dimensional perovskite coating layer includes a first overlay layer disposed between the main perovskite layer and the electron transport layer, a second overlay layer disposed between the main perovskite layer and the hole transport layer, and a third overlay layer covering the periphery of the main perovskite layer.

Abstract: This application provides a polymer current collector, a preparation method thereof, and a secondary battery, battery module, battery pack, and apparatus associated therewith. The polymer current collector provided in this application includes polymer film layers, where the polymer film layers include a first polymer film layer and a second polymer film layer, a resistivity of the first polymer film layer is denoted as ?1, a resistivity of the second polymer film layer is denoted as ?2, and the current collector satisfies ?1>?2. The polymer current collector in this application can induce to deposit of lithium metal from a low conductivity side to a high conductivity side, avoiding risks of depositing lithium ions on the surface of the current collector and thereby increasing cycle life of lithium metal batteries.

Abstract: This application provides a perovskite solar cell structurally including a transparent electrode, an electron transport layer, a perovskite layer, a hole transport layer and a second electrode in sequence, where the perovskite layer may include a main perovskite layer and a one-dimensional perovskite coating layer covering surface and periphery of the main perovskite layer, where the one-dimensional perovskite coating layer may include: a first overlay layer disposed between the main perovskite layer and the electron transport layer; and a second overlay layer disposed between the main perovskite layer and the hole transport layer.

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: Embodiments of the present disclosure relate to a method, an electronic device, and a computer program product for request controlling. The method includes determining, in response to receiving a request for computing resources, a first control window including a plurality of control time slots, the request being received in a receive time slot of the plurality of control time slots. The method further includes determining a quantity of available computing resources within the first control window according to a position of the receive time slot in the plurality of control time slots. The method further includes processing the request within the first control window if the quantity of available computing resources does not exceed a threshold. The method can improve the capability of controlling requests for computing resources, and reduce congestion caused by a large number of requests exceeding the load of computing resources.

Abstract: A fullerene derivative having a C60 fullerene group and a group of a compound of formula (1), a compound of formula (2), and/or a compound of formula (3) attached thereto, where the structural formulas of the compounds of formula (1), formula (2), and formula (3) are as follows: where R1, R2, R3, R4, R5, R6, R7, R8, R9, n1, n2, n3, m1, m2, and m3 are as defined in the specification.

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 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.