Desalination Fuel Cells with High Thermodynamic Energy Efficiency

被引:18
作者
Abu Khalla, Shada [1 ,2 ]
Atlas, Imri [2 ,3 ]
Litster, Shawn [4 ]
Suss, Matthew E. [1 ,2 ,5 ]
机构
[1] Technion Israel Inst Technol, Nancy & Stephen Grand Technion Energy Program, IL-3200003 Haifa, Israel
[2] Technion Israel Inst Technol, Fac Mech Engn, IL-3200003 Haifa, Israel
[3] Technion Israel Inst Technol, Russell Berrie Nanotechnol Inst, IL-3200003 Haifa, Israel
[4] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
[5] Technion Israel Inst Technol, Wolfson Dept Chem Engn, IL-3200003 Haifa, Israel
关键词
water desalination; energy conversion; hydrogen fuel cell; electrode catalyst; thermodynamic energy efficiency; desalination fuel cell; WATER DESALINATION; EXCHANGE MEMBRANE; MICROBIAL DESALINATION; TEMPERATURE-RANGE; POWER-GENERATION; ELECTRODIALYSIS; CHALLENGES; CHLORIDE; BATTERY; ELECTROCATALYSTS;
D O I
10.1021/acs.est.1c07288
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Sustainably-produced hydrogen is currently intensively investigated as an energy carrier to replace fossil fuels. We here characterize an emerging electrochemical cell termed a desalination fuel cell (DFC) that can continuously generate electricity and desalinate water while using hydrogen and oxygen gases as inputs. We investigated two operational modes, a near-neutral pH operation with H-2, O-2, and feedwater inputs (H-2 vertical bar O-2), and a pH-gradient mode with H-2, O-2, feedwater, acid, and base inputs (H-2 + B vertical bar O-2 + A). We show that our cell can desalinate water with 30 g/L of salt content to near-zero salt concentration, while generating an enormous amount of electricity of up to 8.6 kW h per m(3) of treated water when operated in the pH-gradient mode and up to about 1 kW h per m(3) for the near-neutral mode. We quantify the thermodynamic energy efficiency of our device in both operational modes, showing that significantly higher efficiency is achievable in the pH-gradient mode, with up to 95.6%. Further, we present results elucidating the key bottlenecks in the DFC process, showing that the cell current and voltage are limited in the near-neutral pH operation due to a lack of H+ to serve as a reactant, and further reinforce the deleterious effect of halide poisoning on the cathode Pt catalyst and cell open circuit voltage. Such findings demonstrate that new fuel cell catalyst materials, tailored for environments associated with water treatment, can unlock yetimproved performance.
引用
收藏
页码:1413 / 1422
页数:10
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