TY - JOUR
T1 - Engineering of the Crystalline Lattice of Hard Carbon Anodes Toward Practical Potassium-Ion Batteries
AU - Zhong, Lei
AU - Zhang, Wenli
AU - Sun, Shirong
AU - Zhao, Lei
AU - Jian, Wenbin
AU - He, Xing
AU - Xing, Zhenyu
AU - Shi, Zixiong
AU - Chen, Yanan
AU - Alshareef, Husam N.
AU - Qiu, Xueqing
N1 - Funding Information:
The authors acknowledge the financial support from the National Natural Science Foundation of China (No. 22108044, 22208061), the National Key Research and Development Plan (No. 2018YFB1501503), the Research and Development Program in Key Fields of Guangdong Province (No. 2020B1111380002), the Basic Research and Applicable Basic Research in Guangzhou City (202201010290), and the financial support from the Guangdong Provincial Key Laboratory of Plant Resources Biorefinery (No. 2021GDKLPRB07).
Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2023/2/16
Y1 - 2023/2/16
N2 - Hard carbons have attracted increased interest as an alternative of graphite for the anodes of potassium-ion batteries (PIBs). However, the practical applications of hard carbon anodes are hampered by their low capacities, high potential platforms, and large potential hysteresis. Hard carbons coupled with graphitic nanodomains can achieve stable potassium-ion storage behaviors with low potential platforms and low potential hysteresis. Herein, the crystalline lattice in hard carbon anodes is tuned by incorporating graphene oxide in renewable lignin precursors. The modified hard carbon (i.e., QLGC) anodes show graphitized nanodomains in the carbon matrix with an expanded interlayer spacing (0.42 nm) in the amorphous regions, which results in a stable potassium-ion (de)intercalation behavior. Thus, the QLGC anodes exhibit a high capacity of 164 mAh g−1 with low potential hysteresis in the low potential platform region. Moreover, the QLGC anode delivered a highly stabilized capacity of 283 mAh g−1 at 50 mA g−1, a high-rate capability, and stable cycling performance. Furthermore, the charge storage mechanisms of QLGC anode are elucidated by electro-kinetic analysis and ex/in situ physicochemical characterizations. This study opens a new avenue for designing hard carbon anodes with engineered crystalline lattices toward practical PIBs.
AB - Hard carbons have attracted increased interest as an alternative of graphite for the anodes of potassium-ion batteries (PIBs). However, the practical applications of hard carbon anodes are hampered by their low capacities, high potential platforms, and large potential hysteresis. Hard carbons coupled with graphitic nanodomains can achieve stable potassium-ion storage behaviors with low potential platforms and low potential hysteresis. Herein, the crystalline lattice in hard carbon anodes is tuned by incorporating graphene oxide in renewable lignin precursors. The modified hard carbon (i.e., QLGC) anodes show graphitized nanodomains in the carbon matrix with an expanded interlayer spacing (0.42 nm) in the amorphous regions, which results in a stable potassium-ion (de)intercalation behavior. Thus, the QLGC anodes exhibit a high capacity of 164 mAh g−1 with low potential hysteresis in the low potential platform region. Moreover, the QLGC anode delivered a highly stabilized capacity of 283 mAh g−1 at 50 mA g−1, a high-rate capability, and stable cycling performance. Furthermore, the charge storage mechanisms of QLGC anode are elucidated by electro-kinetic analysis and ex/in situ physicochemical characterizations. This study opens a new avenue for designing hard carbon anodes with engineered crystalline lattices toward practical PIBs.
KW - graphitic nanodomains
KW - hard carbon
KW - lignin
KW - potassium-ion batteries
KW - potential platforms
UR - http://www.scopus.com/inward/record.url?scp=85144041129&partnerID=8YFLogxK
U2 - 10.1002/adfm.202211872
DO - 10.1002/adfm.202211872
M3 - Article
AN - SCOPUS:85144041129
SN - 1616-301X
VL - 33
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 8
M1 - 2211872
ER -