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Efficient pH-gradient-enabled microscale bipolar interfaces in direct borohydride fuel cells
被引:73
|作者:
Wang, Zhongyang
[1
,2
]
Parrondo, Javier
[1
,2
]
He, Cheng
[1
,2
]
Sankarasubramanian, Shrihari
[1
,2
]
Ramani, Vijay
[1
,2
]
机构:
[1] Washington Univ, Ctr Solar Energy & Energy Storage, St Louis, MO 63130 USA
[2] Washington Univ, Dept Energy Environm & Chem Engn, McKelvey Sch Engn, St Louis, MO USA
关键词:
SODIUM-BOROHYDRIDE;
OXIDATION REACTION;
ELECTROCHEMICAL OXIDATION;
HYDROGEN EVOLUTION;
EXCHANGE MEMBRANES;
CATALYST SUPPORT;
OXYGEN REDUCTION;
ANODIC-OXIDATION;
PERFORMANCE;
AU;
D O I:
10.1038/s41560-019-0330-5
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
The disparate pH requirements for borohydride oxidation and peroxide reduction in direct borohydride fuel cells (DBFCs) currently hinder their performance and efficiency. Here we develop a pH-gradient-enabled microscale bipolar interface (PMBI) that facilitates sharply different local pH environments at the anode and cathode of a DBFC. Using a recessed planar electrode in conjunction with transmission electron microscopy, we show that the PMBI maintained a sharp local pH gradient (0.82 pH units nm(-1) on average) at the electrocatalytic reaction site. The PMBI configuration enabled enhanced performance in a DBFC compared with either all-anion-or all-cation-exchange configurations (330 mA cm(-2) at 1.5 V and a peak power density of 630 mW cm(-2) at 1.0 V, respectively). The high power densities obtained at voltages well above 1.0 V-achieved by virtue of the effective separation of anolyte and catholyte locally at the electrocatalytically active sites by the PMBI-provide a pathway to reduce fuel cell stack size for autonomous propulsion applications.
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页码:281 / 289
页数:9
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