Education

PhD, University of Wisconsin-Madison (2018)
MS, National Taiwan University (2009)
BS, National Taiwan Normal University (2007)   

Professional Experience

Honors and Awards

Research Interest

1. Application of molecular metal complexes for homogeneous catalysis
2. Development of innovativeelectrocatalytic strategiesfor energy conversion
3. Utilization of photochemistryforvalue-added chemicals andrenewable fuels producing

Publications

1. Yang, Q.; Wang, Y.-H.; Qiao, Y.; Gau, M.; Carroll, P. J.; Walsh, P. J.; Schelter, E. J. Examination of Speciation and the Role of Alcohols on the Photocatalytic Cerium-Chloride System for the Activation of C–H Bonds (manuscript submitted).
2. Wang, Y.-H.; Mondal, B.; Stahl, S. S. Molecular Cobalt Catalysts for O₂ Reduction to H₂O₂: Benchmarking Catalyst Performance via Rate-Overpotential Correlations (manuscript under revision).
3. Wang, Y.-H.; Schneider, G. P.; Goldsmith, Z. K.; Mondal, B.; Hammes-Schiffer, S.; Stahl, S. S. "Brønsted Acid Scaling Relationships Enable Control Over Product Selectivity from O₂ Reduction with a Mononuclear Cobalt Porphyrin Catalyst" ACS Cent. Sci. 2019, 5, 1024-1034 (DOI: 10.1021/acscentsci.9b00194).
4. Wang, Y.-H.; Goldsmith, Z. K.; Schneider, P. E.; Anson, C. W.; Gerken, J. B.; Ghosh, S.; Hammes-Schiffer, S.; Stahl, S. S. Kinetic and Mechanistic Characterization of Low-Overpotential, H₂O₂-Selective Reduction of O₂ Catalyzed by N₂O₂-Ligated Cobalt Complexes. J. Am. Chem. Soc. 2018, 140, 10890–10899 (DOI: 10.1021/jacs.8b06394).
5. Wang, Y.-H.; Pegis, M. L.; Mayer, J. M.; Stahl, S. S. Molecular Cobalt Catalysts for O₂ Reduction: Low-Overpotential Production of H₂O₂ and Comparison with Iron-Based Catalysts. J. Am. Chem. Soc. 2017, 139, 16458–16461 (DOI: 10.1021/jacs.7b09089).
6. Yang, F. Z.; Wang, Y.-H.; Chang, M. C.; Yu, K. H.; Huang, S. L.; Liu, Y. H.; Wang, Y.; Liu, S. T.; Chen. J. T.Kinetic and Mechanistic Studies of Geometrical Isomerism in Neutral Square-Planar Methylpalladium Complexes Bearing Unsymmetrical Bidentate Ligands of α-Aminoaldimines. Inorg. Chem, 2009, 48, 7639–7644 (DOI: 10.1021/ic900296y).