Efficient solar-to-fuels production from a hybrid microbial-water-splitting catalyst system

被引:323
作者
Torella, Joseph P. [1 ]
Gagliardi, Christopher J. [2 ]
Chen, Janice S. [1 ]
Bediako, D. Kwabena [2 ]
Colon, Brendan [1 ]
Way, Jeffery C. [3 ]
Silver, Pamela A. [1 ]
Nocera, Daniel G. [2 ]
机构
[1] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[2] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[3] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
基金
美国国家科学基金会;
关键词
bioelectrochemistry; isopropanol; biofuel; renewable energy; Ralstonia; OXYGEN-EVOLVING CATALYST; ELECTROCHEMICAL REDUCTION; BIOFUEL PRODUCTION; IN-SITU; ALCALIGENES-EUTROPHUS; SYNTHETIC BIOLOGY; CARBON-DIOXIDE; CO2; REDUCTION; GROWTH; PHOSPHATE;
D O I
10.1073/pnas.1424872112
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
Photovoltaic cells have considerable potential to satisfy future renewable-energy needs, but efficient and scalable methods of storing the intermittent electricity they produce are required for the large-scale implementation of solar energy. Current solar-to-fuels storage cycles based on water splitting produce hydrogen and oxygen, which are attractive fuels in principle but confront practical limitations from the current energy infrastructure that is based on liquid fuels. In this work, we report the development of a scalable, integrated bioelectrochemical system in which the bacterium Ralstonia eutropha is used to efficiently convert CO2, along with H-2 and O-2 produced from water splitting, into biomass and fusel alcohols. Water-splitting catalysis was performed using catalysts that are made of earth-abundant metals and enable low overpotential water splitting. In this integrated setup, equivalent solar-to-biomass yields of up to 3.2% of the thermodynamic maximum exceed that of most terrestrial plants. Moreover, engineering of R. eutropha enabled production of the fusel alcohol isopropanol at up to 216 mg/L, the highest bioelectrochemical fuel yield yet reported by >300%. This work demonstrates that catalysts of biotic and abiotic origin can be interfaced to achieve challenging chemical energy-to-fuels transformations.
引用
收藏
页码:2337 / 2342
页数:6
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