Assistant Professor, Inorganic chemistry
office: EIS 210
- Assistant Professor, San Diego State University, 2016-present
- Postdoctoral Fellow, National Renewable Energy Lab, 2013-2016
- Postdoctoral Research Associate, Princeton University, 2011-2013
- PhD, Tulane University, 2006-2011
The growing need for clean and renewable energy has motivated the development of deployable systems to harvest and store earth's abundant solar energy resources. One promising approach is to collect and store solar energy within chemical bonds by forming fuels such as hydrogen and alcohols (solar fuels). This approach is similar to that of the natural photosynthestic process and thus has been dubbed "artificial photosynthesis." An example of this process is by utilizing the semiconductor as both the light absorber as well as the catalyst to split water into H2 and O2. The ultimate goal of these efforts is to develop a standalone photoelectrochemical cell in which water reduction and oxidation reactions occur efficiently under photo induced bias (ideally 1 sun), precluding the introduction of external electricity. In order to achieve this goal, the integration of stable light absorbing materials and effective catalysts to enhance the interfacial kinetics and fundamental mechanistic understanding of this coupled water splitting system still necessitate further explorations. In my lab, the majority of research focuses on two areas of solar energy conversion described below.
Development of Light Absorber-Catalyst Artificial Photosynthesis Assembles
Semiconductor electrodes that have been modified by molecular catalysts have been investigated extensively with various polymeric backbone attachments. However, few studies have been focused on the direct attachment of molecular catalysts onto semiconductor surfaces. By carefully adjusting the energetics between semiconductor and molecular catalyst interface, the efficiency of energy extraction from the photogenerated electron-hole pairs can be optimized. Adding an active catalyst unit to the surface of semiconductor is a feasible strategy to both improve the stability and maintain catalytic activity of a photoelectrochemical device. In a previous study we showed that by using an atomic layer deposited TiO2 layer as well as an earth abundant molecular catalyst we were able to protect the GaInP2 surface.
In the natural photosynthetic process, chemical energy is generated by light conversion followed by proton and electron transfer events (or proton coupled electron process). This process typically begins with light being absorbed by a harvesting pigment. The energy generated by light absorption is then transferred through different chromophores via energy cascade and eventually reaches a reaction center. At the reaction center, the light energy is converted to chemical energy through a multi-electron, multi proton transfer reactions. The basis of artificial photosynthesis is to mimic the photosynthetic process using semiconductors and molecular catalyst assemblies. Through an improved understanding of the coupled electron and energy transfer process in design assemblies could provide significant information for the future design and implementation of industrial scale artificial photosynthesis systems.
Understanding the Electron and Energy Transfer Mechanism in Light Harvesting Systems
Graduate students who work in my lab will receive an interdisciplinary training in inorganic chemistry (i.e. organometallic ligand and catalyst development, solid state chemistry), physical chemistry (i.e. nanosecond charge transfer and surface chemistry) and material science (i.e. surface characterization and material chemistry). State-of-the-art analytical techniques such as NMR spectroscopy, IR, fluorimetry, and ICP-MS will be used to shine light on the reaction mechanism. SEM, TEM and XPS will help us to monitor the morphology change for the material interface. In addition, the interactive nature of our research would provide us various collaborative opportunities between departments, schools and national labs, resulting in excellent learning opportunities for the graduate students. We always welcome graduate students and postdocs who are talented, determined and responsible to join our lab and together we will work towards finding alternative solutions to solve our energy crisis and environmental issues.
- "rGO supported PdNi-CeO2 nanocomposite as an efficient catalyst for hydrogen evolution from the hydrolysis of NH3BH3,"
Y.H. Zhang, Z.Y. Zhou., S.Q. Wang, N.B. Williams, Y. Cheng, S.Z. Luo, and J. Gu,
Int. J. Hydro. Energy (in press) (2018). (doi:10.1016/j.ijhydene.2018.08.053.)
- "Fine Tuning Electronic Structure of Catalysts through Atomic Engineering for Enhanced Hydrogen Evolution,"
Y.C. Huang, J. Hu, H. X. Xu, W. Bian, J. X. Ge, D. J. Zang, D. J. Cheng, Y. K. Lv, C. Zhang, J. Gu, Y.G. Wei,
Adv. Energy. Mater. (in press) (2018). (doi:10.1002/aenm.201800789.)
- "Hollow NiCo Layered Double Hydroxide Supported Pd Catalysts for Superior Hydrogen Evolution Activity for Hydrolysis of Ammonia Borane,"
Y.H. Zhou, S.Q. Wang, Z.Y. Zhang, Y. Cheng, J. Gu,
Chem. Cat. Chem. 10, 3206-3213 (2018). (doi:10.1002/cctc.201800459.)
- "Microbial Photoelectrosynthesis for Self-Sustaining Hydrogen Generation,"
Lu Lu, Nicholas B. Williams, John A. Turner, Pin-Ching Maness, Jing Gu, and Zhiyong Jason Ren,,
Environmental Science & Technology 51, 13494-13501 (2017). (doi:10.1021/acs.est.7b03644.)
- "Self-optimizing, highly surface-active layered metal dichalcogenide catalysts for hydrogen evolution,"
Yuanyue Liu, Jingjie Wu, Ken P. Hackenberg, Jing Zhang, Y. Morris Wang, Yingchao Yang, Kunttal Keyshar, Jing Gu, Tadashi Ogitsu, Robert Vajtai, Jun Lou, Pulickel M. Ajayan, Brandon C. Wood, and Boris I. Yakobson,,
Nature Energy 2 (2017). (doi:10.1038/nenergy.2017.127.)
- "Design of Metastable Tin Titanium Nitride Semiconductor Alloys,"
Andre Bikowski, Sebastian Siol, Jing Gu, Aaron Holder, John S. Mangum, Brian Gorman, William Tumas, Stephan Lany, and Andriy Zakutayev,,
Chemistry of Materials 29, 6511-6517 (2017). (doi:10.1021/acs.chemmater.7b02122.)
- "Fe2PO5-Encapsulated Reverse Energetic ZnO/Fe2O3 Heterojunction Nanowire for Enhanced Photoelectrochemical Oxidation of Water,"
Dong-Dong Qin, Cai-Hua He, Yang Li, Antonio C. Trammel, Jing Gu, Jing Chen, Yong Yan, Duo-Liang Shan, Qiu-Hong Wang, Jing-Jing Quan, Chun-Lan Tao, and Xiao-Quan Lu,,
Chemsuschem 10, 2796-2804 (2017). (doi:10.1002/cssc.201700501.)
- "Multiple exciton generation for photoelectrochemical hydrogen evolution reactions with quantum yields exceeding 100%,"
Yong Yan, Ryan W. Crisp, Jing Gu, Boris D. Chernomordik, Gregory F. Pach, Ashley R. Marshall, John A. Turner, and Matthew C. Beard,,
Nature Energy 2 (2017). (doi:10.1038/nenergy.2017.52.)
- "Assembly of g-C3N4-based type II and Z-scheme heterojunction anodes with improved charge separation for photoelectrojunction water oxidation,"
Cai-He Wang, Dong-Dong Qin, Duo-Liang Shan, Jing Gu, Yong Yan, Jing Chen, Qiu-Hong Wang, Cai-Hua He, Yang Li, Jing-Jing Quan, and Xiao-Quan Lu,,
Physical Chemistry Chemical Physics 19, 4507-4515 (2017). (doi:10.1039/c6cp08066a.)
- "A graded catalytic-protective layer for an efficient and stable water-splitting photocathode,"
Jing Gu, Jeffery A. Aguiar, Suzanne Ferrere, K. Xerxes Steirer, Yong Yan, Chuanxiao Xiao, James L. Young, Mowafak Al-Jassim, Nathan R. Neale, and John A. Turner,,
Nature Energy 2, 16192 (2017). (doi:10.1038/nenergy.2016.192.)
- "PH3-Treated TiO2 Nanorods with Dual-Doping Effect for Photoelectrochemical Oxidation of Water,"
Dong-Dong Qin, Xue-Huai Wang, Yang Li, Jing Gu, Xing-Ming Ning, Jing Chen, Xiao-Quan Lu, and Chun-Lan Tao,,
Journal of Physical Chemistry C 120, 22195-22201 (2016). (doi:10.1021/acs.jpcc.6b06903.)