posted on 2014-08-13, 00:00authored byDae Soo Jung, Tae Hoon Hwang, Ji Hoon Lee, Hye Young Koo, Rana A. Shakoor, Ramazan Kahraman, Yong Nam Jo, Min-Sik Park, Jang Wook Choi
Utilizing the unparalleled theoretical
capacity of sulfur reaching
1675 mAh/g, lithium–sulfur (Li–S) batteries have been
counted as promising enablers of future lithium ion battery (LIB)
applications requiring high energy densities. Nevertheless, most sulfur
electrodes suffer from insufficient cycle lives originating from dissolution
of lithium polysulfides. As a fundamental solution to this chronic
shortcoming, herein, we introduce a hierarchical porous carbon structure
in which meso- and macropores are surrounded by outer micropores.
Sulfur was infiltrated mainly into the inner meso- and macropores,
while the outer micropores remained empty, thus serving as a “barricade”
against outward dissolution of long-chain lithium polysulfides. On
the basis of this systematic design, the sulfur electrode delivered
1412 mAh/gsulfur with excellent capacity retention of 77%
after 500 cycles. Also, a control study suggests that even when sulfur
is loaded into the outer micropores, the robust cycling performance
is preserved by engaging small sulfur crystal structures (S2–4). Furthermore, the hierarchical porous carbon was produced in ultrahigh
speed by scalable spray pyrolysis. Each porous carbon particle was
synthesized through 5 s of carrier gas flow in a reaction tube.