posted on 2017-01-12, 00:00authored byByung
Gon Kim, Changshin Jo, Jaeho Shin, Yeongdong Mun, Jinwoo Lee, Jang Wook Choi
Despite
the extraordinary gravimetric energy densities, lithium-oxygen
(Li-O2) batteries are still facing a technological challenge;
limited round trip efficiency leading to insufficient cycle life.
Recently, carbonaceous electrode materials were found to be one of
the primary origins of the limited cycle life, as they produce irreversible
side products during discharge. A few investigations based on noncarbonaceous
materials have demonstrated largely suppressed accumulation of irreversible
side products, but such studies have focused mainly on the materials
themselves rather than delicate morphology control. As such, here,
we report the synthesis of mesoporous titanium nitride (m-TiN) with
a 2D hexagonal structure and large pores (>30 nm), which was templated
by a block copolymer with tunable chain lengths, and introduce it
as a stable air-cathode backbone. Due to the well-aligned pore structure
and decent electric conductivity of TiN, the battery reaction was
quite reversible, resulting in robust cycling performance for over
100 cycles under a potential cutoff condition. Furthermore, by protecting
the Li metal with a poreless polyurethane separator and engaging a
lithium iodide redox mediator, the original capacity was retained
for 280 cycles under a consistent capacity condition (430 mAh g–1). This study reveals that when the appropriate structure
and material choice of the air-cathode are coupled with an advanced
separator and an effective solution-phase redox mediator, the cycle
lives of Li-O2 batteries can be enhanced dramatically.