Abstract: Provided is a high entropy composite oxide of formula ([M1]pMnqFexCryNiz)3O4 having a spinel crystal, wherein the [M1], p, q, x, y and z are as defined in the specification. A method for producing the high entropy composite oxide, and anode materials including the same are further provided. With the entropy stabilization effect and plenty of oxygen vacancies, the anode materials including the high entropy composite oxide show the advantage of high Li+ transport rate, high electric capacity, redox durability, and good cycling stability, thereby having a bright prospect for application.

Abstract: Provided is a high-entropy composite glycerate represented by NiCrFeCoMn(C3H5O4)n and an electrocatalyst thereof, wherein n is a positive integer from 1 to 3, and wherein each of the Ni, Cr, Fe, Co and Mn includes an atom percent of 5 to 35 based on the total amount of the Ni, Cr, Fe, Co and Mn. Each of the metals is homogenously distributed within the high-entropy composite glycerate, and the high-entropy composite glycerate can reduce an overpotential for oxygen evolution reaction by the synergistic effect resulting from the structure formed by the quinary-metal glycerate. The high-entropy composite glycerate is suitable for catalyzing oxygen evolution reaction, and therefore has a prospect for application. Methods for preparing the high-entropy composite glycerate are also provided.

Abstract: Provided is a high-entropy composite glycerate represented by NiCrFeCoMn(C3H5O4)n and an electrocatalyst thereof, wherein n is a positive integer from 1 to 3, and wherein each of the Ni, Cr, Fe, Co and Mn includes an atom percent of 5 to 35 based on the total amount of the Ni, Cr, Fe, Co and Mn. Each of the metals is homogenously distributed within the high-entropy composite glycerate, and the high-entropy composite glycerate can reduce an overpotential for oxygen evolution reaction by the synergistic effect resulting from the structure formed by the quinary-metal glycerate. The high-entropy composite glycerate is suitable for catalyzing oxygen evolution reaction, and therefore has a prospect for application. Methods for preparing the high-entropy composite glycerate are also provided.

Abstract: Provided is a high entropy composite oxide of formula ([M1]pMnqFexCryNiz)3O4 having a spinel crystal, wherein the [M1], p, q, x, y and z are as defined in the specification. A method for producing the high entropy composite oxide, and anode materials including the same are further provided. With the entropy stabilization effect and plenty of oxygen vacancies, the anode materials including the high entropy composite oxide show the advantage of high Li+ transport rate, high electric capacity, redox durability, and good cycling stability, thereby having a bright prospect for application.

Abstract: A method to manufacture a carbon fiber electrode comprises synthesizing polyamic acid (PAA) as a polyimide (PI) precursor from pryomellitic dian hydride (PMDA) and oxydianiline (ODA) as monomers and triethylamine (TEA) as a catalyst, adding dimethylformamide (DMF) to the polyamic acid (PAA) solution to prepare a spinning solution and subjecting the spinning solution to electrostatic spinning at a high voltage to obtain a PAA nanofiber paper, converting the PAA nanofiber paper into a polyimide (PI) nanofiber paper by heating, and converting the polyimide (PI) nanofiber paper into a carbon nanofiber (CNF) paper by heating under an Ar atmosphere. Also, the method to manufacture a polyimide carbon nanofiber electrode and/or a carbon nanotube composite electrode may utilize carbon nanofibers having diameters that are lessened by optimizing electrostatic spinning in order to improve spinnability.

Abstract: A method to manufacture a carbon fiber electrode comprises synthesizing polyamic acid (PAA) as a polyimide (PI) precursor from pryomellitic dian hydride (PMDA) and oxydianiline (ODA) as monomers and triethylamine (TEA) as a catalyst, adding dimethylformamide (DMF) to the polyamic acid (PAA) solution to prepare a spinning solution and subjecting the spinning solution to electrostatic spinning at a high voltage to obtain a PAA nanofiber paper, converting the PAA nanofiber paper into a polyimide (PI) nanofiber paper by heating, and converting the polyimide (PI) nanofiber paper into a carbon nanofiber (CNF) paper by heating under an Ar atmosphere. Also, the method to manufacture a polyimide carbon nanofiber electrode and/or a carbon nanotube composite electrode may utilize carbon nanofibers having diameters that are lessened by optimizing electrostatic spinning in order to improve spinnability.