Building a lunar human base is one of the important goals of human lunar exploration.This paper proposes a method for the production of oxygen by combining photothermal synergistic water decomposition with high-temper...Building a lunar human base is one of the important goals of human lunar exploration.This paper proposes a method for the production of oxygen by combining photothermal synergistic water decomposition with high-temperature carbon dioxide electrolysis,utilizing the full solar spectrum.The optimal oxygen production rates under different solid oxide electrolysis cell inlet temperatures T_(e),ultraviolet(UV)separation wavelengths λ_(2),infrared(IR)separation wavelengths,and photovoltaic cell materials were explored.The results indicate that the inlet temperature of the solid oxide electrolysis cell should be as high as possible so that more carbon dioxide can be converted into carbon monoxide and oxygen.Furthermore,when the ultraviolet separation wavelength is approximately 385 nm,the proportion of solar energy allocated to the photoreaction and electrolysis cell is optimal,and the oxygen production rate is highest at 2.754×10^(-4) mol/s.Moreover,the infrared separation wavelength should be increased as much as possible within the allowable range to increase the amount of solar radiation allocated to the electrolysis cell to improve the rate of oxygen generation.In addition,copper indium gallium selenide(CIGS)has a relatively large separation wavelength,which can result in a high oxygen production rate of 3.560×10^(-4) mol/s.The proposed integrated oxygen production method can provide a feasible solution for supplying oxygen to a lunar human base.展开更多
Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-inten...Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-intensive process of separat-ing mixed reduction products and the economic viability of the carbon sources (reactants) used. To tackle these challenges simultaneously, solid-state electrolyte (SSE) reactors are emerging as a promising solution. In this review, we focus on the feasibility of applying SSE for tandem electrochemical CO_(2) capture and conversion. The configurations and fundamental principles of SSE reactors are first discussed, followed by an introduction to its applications in these two specific areas, along with case studies on the implementation of tandem electrolysis. In comparison to conventional H-type cell, flow cell and membrane electrode assembly cell reactors, SSE reactors incorporate gas diffusion electrodes and utilize a solid electro-lyte layer positioned between an anion exchange membrane (AEM) and a cation exchange membrane (CEM). A key inno-vation of this design is the sandwiched SSE layer, which enhances efficient ion transport and facilitates continuous product extraction through a stream of deionized water or humidified nitrogen, effectively separating ion conduction from product collection. During electrolysis, driven by an electric field and concentration gradient, electrochemically generated ions (e.g., HCOO- and CH3COO-) migrate through the AEM into the SSE layer, while protons produced from water oxidation at the anode traverse the CEM into the central chamber to maintain charge balance. Targeted products like HCOOH can form in the middle layer through ionic recombination and are efficiently carried away by the flowing medium through the porous SSE layer, in the absence of electrolyte salt impurities. As CO_(2)RR can generate a series of liquid products, advancements in catalyst discovery over the past several years have facilitated the industrial application of SSE for more efficient chemicals production. Also noteworthy, the cathode reduction reaction can readily consume protons from water, creating a highly al-kaline local environment. SSE reactors are thereby employed to capture acidic CO_(2), forming CO_(3)^(2-) from various gas sources including flue gases. Driven by the electric field, the formed CO_(3)^(2-) can traverse through the AEM and react with protons originating from the anode, thereby regenerating CO_(2). This CO_(2) can then be collected and utilized as a low-cost feedstock for downstream CO_(2) electrolysis. Based on this principle, several cell configurations have been proposed to enhance CO_(2) capture from diverse gas sources. Through the collaboration of two SSE units, tandem electrochemical CO_(2) capture and con-version has been successfully implemented. Finally, we offer insights into the future development of SSE reactors for prac-tical applications aimed at achieving carbon neutrality. We recommend that greater attention be focused on specific aspects, including the fundamental physicochemical properties of the SSE layer, the electrochemical engineering perspective related to ion and species fluxes and selectivity, and the systematic pairing of consecutive CO_(2) capture and conversion units. These efforts aim to further enhance the practical application of SSE reactors within the broader electrochemistry community.展开更多
基金supported by the National Natural Science Foundation of China(52106276 and 52130601).
文摘Building a lunar human base is one of the important goals of human lunar exploration.This paper proposes a method for the production of oxygen by combining photothermal synergistic water decomposition with high-temperature carbon dioxide electrolysis,utilizing the full solar spectrum.The optimal oxygen production rates under different solid oxide electrolysis cell inlet temperatures T_(e),ultraviolet(UV)separation wavelengths λ_(2),infrared(IR)separation wavelengths,and photovoltaic cell materials were explored.The results indicate that the inlet temperature of the solid oxide electrolysis cell should be as high as possible so that more carbon dioxide can be converted into carbon monoxide and oxygen.Furthermore,when the ultraviolet separation wavelength is approximately 385 nm,the proportion of solar energy allocated to the photoreaction and electrolysis cell is optimal,and the oxygen production rate is highest at 2.754×10^(-4) mol/s.Moreover,the infrared separation wavelength should be increased as much as possible within the allowable range to increase the amount of solar radiation allocated to the electrolysis cell to improve the rate of oxygen generation.In addition,copper indium gallium selenide(CIGS)has a relatively large separation wavelength,which can result in a high oxygen production rate of 3.560×10^(-4) mol/s.The proposed integrated oxygen production method can provide a feasible solution for supplying oxygen to a lunar human base.
文摘Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-intensive process of separat-ing mixed reduction products and the economic viability of the carbon sources (reactants) used. To tackle these challenges simultaneously, solid-state electrolyte (SSE) reactors are emerging as a promising solution. In this review, we focus on the feasibility of applying SSE for tandem electrochemical CO_(2) capture and conversion. The configurations and fundamental principles of SSE reactors are first discussed, followed by an introduction to its applications in these two specific areas, along with case studies on the implementation of tandem electrolysis. In comparison to conventional H-type cell, flow cell and membrane electrode assembly cell reactors, SSE reactors incorporate gas diffusion electrodes and utilize a solid electro-lyte layer positioned between an anion exchange membrane (AEM) and a cation exchange membrane (CEM). A key inno-vation of this design is the sandwiched SSE layer, which enhances efficient ion transport and facilitates continuous product extraction through a stream of deionized water or humidified nitrogen, effectively separating ion conduction from product collection. During electrolysis, driven by an electric field and concentration gradient, electrochemically generated ions (e.g., HCOO- and CH3COO-) migrate through the AEM into the SSE layer, while protons produced from water oxidation at the anode traverse the CEM into the central chamber to maintain charge balance. Targeted products like HCOOH can form in the middle layer through ionic recombination and are efficiently carried away by the flowing medium through the porous SSE layer, in the absence of electrolyte salt impurities. As CO_(2)RR can generate a series of liquid products, advancements in catalyst discovery over the past several years have facilitated the industrial application of SSE for more efficient chemicals production. Also noteworthy, the cathode reduction reaction can readily consume protons from water, creating a highly al-kaline local environment. SSE reactors are thereby employed to capture acidic CO_(2), forming CO_(3)^(2-) from various gas sources including flue gases. Driven by the electric field, the formed CO_(3)^(2-) can traverse through the AEM and react with protons originating from the anode, thereby regenerating CO_(2). This CO_(2) can then be collected and utilized as a low-cost feedstock for downstream CO_(2) electrolysis. Based on this principle, several cell configurations have been proposed to enhance CO_(2) capture from diverse gas sources. Through the collaboration of two SSE units, tandem electrochemical CO_(2) capture and con-version has been successfully implemented. Finally, we offer insights into the future development of SSE reactors for prac-tical applications aimed at achieving carbon neutrality. We recommend that greater attention be focused on specific aspects, including the fundamental physicochemical properties of the SSE layer, the electrochemical engineering perspective related to ion and species fluxes and selectivity, and the systematic pairing of consecutive CO_(2) capture and conversion units. These efforts aim to further enhance the practical application of SSE reactors within the broader electrochemistry community.
