Graphenal Polymers for Energy Storage Linjie Zhi*, Long Hao National Center for Nanoscience and Technology, China Zhongguancun Beiyitiao No. 11, Beijing, 100190, P. R. China Zhilj@nanoctr.cn Abstract Nowadays, rapidly developing global economy has triggered serious environmental problems and excessive consumption of fossil fuels. Consequently, exploiting sustainable clean energy as well as efficient energy conversion and storage technologies is urgently required. Lithium ion batteries and supercapacitors are two important types of energy storage devices, which have high energy density and high power density respectively. Normally, the performance of both Lithium ion batteries and supercapacitors are mainly decided by their electrode materials. Carbon materials especially graphenerelated materials have been the star materials in the past few years for their abundant sources, flexible structures, and controllable functionalities. [1] However, when we zoom in the structures of these materials, it’s easy to recognize that these so-called “graphene-related” materials in energy storage applications have totally different structure characters from “graphene” itself. They contain both graphene units and chemical functions, and are generally formed by the aromatic C-C coupling or the chemical tailoring of graphene structures. These structures are the chemical combination of grapheme units and functional polymeric fragments, which we define them as “graphenal polymers” These graphenal polymers have great advantages in energy storage devices. For example, in lithium ion batteries and supercapacitors, the conductivity is very important to their rate capacities, which can be solved by the “graphenal” part; while the active materials (e.g. SnO2, Sn, SnS, Si, etc in lithium ion batteries) need to be well attached with the conductive networks of the electrode or the electrochemical active surface (in supercapacitors), which can be solved by the “polymer” part. Based on these graphenal polymers, we have investigated experimentally a serious of materials for enhancing their properties in lithium ion batteries [2] and supercapacitors.[3] In general, two strageties can be selected to fabricate graphenal polymers. One is the “top-down” method using graphite or graphene as starting materials, while the other is the “bottom-up” method starting from small molecules via such as CVD procedure.[4] Recently, we also recognized we could build graphenal polymers step by step, from small molecules to 2D porous organic networks (PONs), then to graphenal polymers, with which we can controllably maintain the functional groups and enhance the conductivity at the same time to enhance their electrochemical performances.[5] In short, graphenal polymer is one class of new materials highly attractive for energy conversion and energy storage applications. References [1] L. Hao, X. Li, L. Zhi, Advanced Materials 2013, 25, 3899; B. Luo, S. Liu, L. Zhi, Small 2012, 8, 630. [2] B. Luo, Y. Fang, B. Wang, J. S. Zhou, H. H. Song, L. J. Zhi, Energy & Environmental Science 2012, 5, 5226; B. Luo, B. Wang, X. Li, Y. Jia, M. Liang, L. Zhi, Adv Mater 2012, 24, 3538; B. Luo, B. Wang, M. Liang, J. Ning, X. Li, L. Zhi, Adv Mater 2012, 24, 1405; B. Wang, B. Luo, X. Li, L. Zhi, Materials Today 2012, 15, 544; J. Li, Z. Z. Yang, H. X. Qiu, Y. G. Dai, Q. B. Zheng, G. P. Zheng, J. H. Yang, Journal of Materials Chemistry A 2013, 1, 11451; B. Wang, X. Li, B. Luo, Y. Jia, L. Zhi, Nanoscale 2013, 5, 1470; B. Wang, X. Li, B. Luo, J. Yang, X. Wang, Q. Song, S. Chen, L. Zhi, Small 2013, 9, 2399; B. Wang, X. Li, X. Zhang, B. Luo, M. Jin, M. Liang, S. A. Dayeh, S. T. Picraux, L. Zhi, ACS Nano 2013, 7, 1437. [3] Y. Fang, B. Luo, Y. Jia, X. Li, B. Wang, Q. Song, F. Kang, L. Zhi, Adv Mater 2012, 24, 6348; J. Yan, Z. J. Fan, W. Sun, G. Q. Ning, T. Wei, Q. Zhang, R. F. Zhang, L. J. Zhi, F. Wei, Advanced Functional Materials 2012, 22, 2632. [4] B. Wang, X. Li, X. Zhang, B. Luo, Y. Zhang, L. Zhi, Adv Mater 2013, 25, 3560; B. Wang, X. Li, T. Qiu, B. Luo, J. Ning, J. Li, X. Zhang, M. Liang, L. Zhi, Nano Lett 2013, 13, 5578; X. Li, L. Zhi, Nanoscale 2013, 5, 8864. [5] L. Hao, B. Luo, X. L. Li, M. H. Jin, Y. Fang, Z. H. Tang, Y. Y. Jia, M. H. Liang, A. Thomas, J. H. Yang, L. J. Zhi, Energy & Environmental Science 2012, 5, 9747.