Although
graphite has been used as anodes of lithium-ion batteries
(LiBs) for 30 years, its unsatisfactory energy density makes it insufficient
toward some new electronic products such as unmanned aerial vehicles.
Herein, in situ synthesis of nano-GeP confined in nitrogen-doped carbon
(GeP@NC) fibers was designed and performed via coaxial electrospinning
followed by a phosphating process. This way ensured the paper-like
GeP@NC-x electrode with high conductivity, high flexibility,
and lightweight properties, which simultaneously solved the key scientific
problems of difficulty in structural design and severe volume expansion
of GeP. The inner diameter and wall thickness of the nanofibers can
be effectively controlled by adjusting the size of electrospinning
needles. It was suggested that the fibers not only effectively inhibited
the growth of GeP, resulting in the synthesis of nano-GeP with size
less than 50 nm, but also alleviated the volume expansion/agglomeration
and improved the diffusion kinetics of Li+ in nano-GeP
during cycling. The Li+ diffusion coefficient can be improved
by reducing the inner diameter and wall thickness of the fibers. As
a model system, the paper-like electrode (GeP@NC-2) with a fiber diameter
of 280 nm and a wall thickness of 110 nm exhibited the best electrochemical
performance. When applied as anodes in LiBs, it displayed a reversible
capacity of 612 mAh g–1 at the 600th cycle at 1
A g–1, while GeP@NC-0 with a solid structure only
delivered 239 mAh g–1. Furthermore, the GeP@NC-2
also exhibited good long-term cycling stability at 5 A g–1, and the capacity displayed a slight difference of 221.2 and 209.0
mAh g–1 in a voltage range of 0∼3 V and 0∼1.5
V, respectively. The well-defined synthetic approach combined with
unique nanostructural design provided a meaningful reference for the
rational design and development of next-generation flexible and high-performance
LiB anodes.