Solar thermochemical splitting of water to generate hydrogen

被引:85
|
作者
Rao, C. N. R. [1 ]
Dey, Sunita [1 ]
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res, Chem & Phys Mat Unit, Council Sci & Ind Res Ctr Excellence, Sheikh Saqr Lab,Int Ctr Mat Sci, Bangalore 560064, Karnataka, India
关键词
thermochemical H2O splitting; metal oxides; perovskites; thermochemical CO2 splitting; LANTHANUM MANGANITE PEROVSKITES; OXYGEN-EXCHANGE MATERIALS; CA/SR A-SITE; FUEL PRODUCTION; B-SITE; THERMODYNAMIC CHARACTERIZATION; ELECTRICAL-CONDUCTIVITY; CHEMICAL DIFFUSION; SYNGAS PRODUCTION; SOLID-SOLUTIONS;
D O I
10.1073/pnas.1700104114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Solar photochemical means of splitting water (artificial photosynthesis) to generate hydrogen is emerging as a viable process. The solar thermochemical route also promises to be an attractive means of achieving this objective. In this paper we present different types of thermochemical cycles that one can use for the purpose. These include the low-temperature multistep process as well as the high-temperature two-step process. It is noteworthy that the multistep process based on the Mn(II)/Mn(III) oxide system can be carried out at 700 degrees C or 750 degrees C. The two-step process has been achieved at 1,300 degrees C/900 degrees C by using yttrium-based rare earth manganites. It seems possible to render this high-temperature process as an isothermal process. Thermodynamics and kinetics of H2O splitting are largely controlled by the inherent redox properties of the materials. Interestingly, under the conditions of H2O splitting in the high-temperature process CO2 can also be decomposed to CO, providing a feasible method for generating the industrially important syngas (CO+ H-2). Although carbonate formation can be addressed as a hurdle during CO2 splitting, the problem can be avoided by a suitable choice of experimental conditions. The choice of the solar reactor holds the key for the commercialization of thermochemical fuel production.
引用
收藏
页码:13385 / 13393
页数:9
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