Honors & Awards

  • Dreyfus Postdoctoral Fellowship for Environmental Chemistry, The Camille and Henry Dreyfus Foundation
  • Division of Inorganic Chemistry Young Investigator Award, The American Chemical Society

Professional Education

  • Doctor of Philosophy, Texas A&M University College Station (2016)

Stanford Advisors

All Publications

  • Synthetic Routes for a 2D Semiconductive Copper Hexahydroxybenzene Metal-Organic Framework JOURNAL OF THE AMERICAN CHEMICAL SOCIETY Park, J., Hinckley, A. C., Huang, Z., Feng, D., Yakoyenko, A. A., Lee, M., Chen, S., Zou, X., Bao, Z. 2018; 140 (44): 14533–37


    Conductive metal-organic frameworks (c-MOFs) have shown outstanding performance in energy storage and electrocatalysis. Varying the bridging metal species and the coordinating atom are versatile approaches to tune their intrinsic electronic properties in c-MOFs. Herein we report the first synthesis of the oxygen analog of M3(C6X6)2 (X = NH, S) family using Cu(II) and hexahydroxybenzene (HHB), namely Cu-HHB [Cu3(C6O6)2], through a kinetically controlled approach with a competing coordination reagent. We also successfully demonstrate an economical synthetic approach using tetrahydroxyquinone as the starting material. Cu-HHB was found to have a partially eclipsed packing between adjacent 2D layers and a bandgap of approximately 1 eV. The addition of Cu-HHB to the family of synthetically realized M3(C6X6)2 c-MOFs will enable greater understanding of the influence of the organic linkers and metals, and further broadens the range of applications for these materials.

    View details for DOI 10.1021/jacs.8b06666

    View details for Web of Science ID 000449887800002

    View details for PubMedID 30176142

  • Stabilization of Hexaaminobenzene in a 2D Conductive Metal-Organic Framework for High Power Sodium Storage JOURNAL OF THE AMERICAN CHEMICAL SOCIETY Park, J., Lee, M., Feng, D., Huang, Z., Hinckley, A. C., Yakoyenko, A., Zou, X., Cui, Y., Bao, Z. 2018; 140 (32): 10315–23


    Redox-active organic materials have gained growing attention as electrodes of rechargeable batteries. However, their key limitations are the low electronic conductivity and limited chemical and structural stability under redox conditions. Herein, we report a new cobalt-based 2D conductive metal-organic framework (MOF), Co-HAB, having stable, accessible, dense active sites for high-power energy storage device through conjugative coordination between a redox-active linker, hexaaminobenzene (HAB), and a Co(II) center. Given the exceptional capability of Co-HAB for stabilizing reactive HAB, a reversible three-electron redox reaction per HAB was successfully demonstrated for the first time, thereby presenting a promising new electrode material for sodium-ion storage. Specifically, through synthetic tunability of Co-HAB, the bulk electrical conductivity of 1.57 S cm-1 was achieved, enabling an extremely high rate capability, delivering 214 mAh g-1 within 7 min or 152 mAh g-1 in 45 s. Meanwhile, an almost linear increase of the areal capacity upon increasing active mass loading up to 9.6 mg cm-2 was obtained, demonstrating 2.6 mAh cm-2 with a trace amount of conducting agent.

    View details for DOI 10.1021/jacs.8b06020

    View details for Web of Science ID 000442183700037

    View details for PubMedID 30041519

  • Ionically Conductive Self-Healing Binder for Low Cost Si Microparticles Anodes in Li-Ion Batteries ADVANCED ENERGY MATERIALS Munaoka, T., Yan, X., Lopez, J., To, J. F., Park, J., Tok, J., Cui, Y., Bao, Z. 2018; 8 (14)
  • 3D Long-Range Triplet Migration in a Water-Stable Metal-Organic Framework for Upconversion-Based Ultralow-Power in Vivo Imaging JOURNAL OF THE AMERICAN CHEMICAL SOCIETY Park, J., Xu, M., Li, F., Zhou, H. 2018; 140 (16): 5493–99


    Triplet-triplet annihilation upconversion (TTA-UC) has gained increasing attention because it allows for harvesting of low-energy photons in the solar spectrum with high efficiency in relevant applications including solar cells and bioimaging. However, the utilization of conventional TTA-UC systems for low-power bioapplications is significantly hampered by their general incompatibility and low efficiency in aqueous media. Herein we report a metal-organic framework (MOF) as a biocompatible nanoplatform for TTA-UC to realize low-power in vivo imaging. Our MOF consists of a porphyrinic sensitizer in an anthracene-based Zr-MOF as a TTA-UC platform. In particular, closely aligned chromophores in the MOF facilitate a long-range 3D triplet diffusion of 1.6 μm allowing efficient energy migration in water. The tunable ratio between sensitizer and annihilator by our synthetic method also allows an optimization of the system for maximized TTA-UC efficiency in water at a very low excitation power density. Consequently, the low-power imaging of lymph node in a live mouse was successfully demonstrated with an excellent signal-to-noise ratio (SNR > 30 at 5 mW cm-2).

    View details for DOI 10.1021/jacs.8b01613

    View details for Web of Science ID 000431095100025

    View details for PubMedID 29634258

  • Robust and conductive two-dimensional metal-organic frameworks with exceptionally high volumetric and areal capacitance NATURE ENERGY Feng, D., Lei, T., Lukatskaya, M. R., Park, J., Huang, Z., Lee, M., Shaw, L., Chen, S., Yakovenko, A. A., Kulkarni, A., Xiao, J., Fredrickson, K., Tok, J. B., Zou, X., Cui, Y., Bao, Z. 2018; 3 (1): 30–36
  • Tailoring properties of metal-organic frameworks Park, J., Feng, D., Bao, Z., Zhou, H. AMER CHEMICAL SOC. 2017
  • Tunable electronic properties in a 2D metal-organic framework platform Park, J., Feng, D., Bao, Z. AMER CHEMICAL SOC. 2017