Identification and implementation of clean, sustainable, and affordable energy sources is of paramount importance for both environmental and human health concerns in the future. Sustainable hydrogen-based economies require that hydrogen production from protic media, such as H2O or mineral acids (HX), be coupled to solar power. Closed catalytic cycles for solar-to-hydrogen energy conversion from protic media must meet two technological hurdles: 1) proton reduction to generate dihydrogen, and 2) anion oxidation. A closed cycle for generating H2 from HX requires both proton reduction to form H2 as well as halide oxidation to generate X2. Thus far, molecular catalysts for authentic HX splitting have not been developed. Proof-of-concept systems, which employ chemical traps to promote X2 formation have been developed, however, these systems are not amenable to use in energy storage. This proposal aims to develop inexpensive catalysts based on earth- abundant, first-row transition metals for photochemical HX splitting. If successful, the proposed research would constitute a closed solar-to-hydrogen conversion scheme, in which mineral acids (HX) are converted to H2 and X2 using solar power. The resultant hydrogen could be used as fuel, either by sequestration as a liquid fuel by hydrogenation of small molecule substrates such as CO2 or by being used directly in hydrogen fuel cells. To accomplish the goal of developing a solar-to-hydrogen scheme, low-valent transition metal complexes, capable of proton reduction will first be developed. Simultaneously, investigations of metal dihalide complexes will allow critical requirements for halide oxidation to be defined. To enable the challenging, but necessary, X2 photoelimination, ligands wil be designed to provide access to highly oxidizing excited states. Studies of each of the fundamental steps of HX splitting - proton reduction and halide oxidation - will elucidate fundamental parameters required for each of the constituent half reactions. Informed by the requisite ligand features for each of the fundamental steps of HX splitting, transition metal catalysts will be designed to enable authentic HX splitting photocatalysis to be achieved.

Public Health Relevance

Identification and implementation of clean, sustainable, and affordable energy sources is of paramount importance for both environmental and human health concerns in the future. In 2005 it was estimated that particulate air pollution, whose major source in urban environments is automobile exhaust, is to blame for 500,000 deaths each year. Herein, I propose the development of novel transition metal catalysts for HX splitting, which would enable use of non-polluting hydrogen-based fuels and sever the connection between energy and petroleum-based fuels.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM103211-03
Application #
8536144
Study Section
Special Emphasis Panel (ZRG1-F04-D (20))
Program Officer
Lees, Robert G
Project Start
2012-08-06
Project End
2014-08-05
Budget Start
2013-08-06
Budget End
2014-08-05
Support Year
3
Fiscal Year
2013
Total Cost
$52,190
Indirect Cost
Name
Harvard University
Department
Type
DUNS #
082359691
City
Cambridge
State
MA
Country
United States
Zip Code
02138
Powers, David C; Hwang, Seung Jun; Zheng, Shao-Liang et al. (2014) Halide-bridged binuclear HX-splitting catalysts. Inorg Chem 53:9122-8
Powers, David C; Anderson, Bryce L; Hwang, Seung Jun et al. (2014) Photocrystallographic observation of halide-bridged intermediates in halogen photoeliminations. J Am Chem Soc 136:15346-55
Powers, David C; Chambers, Matthew B; Teets, Thomas S et al. (2013) Halogen Photoelimination from Dirhodium Phosphazane Complexes via Chloride-Bridged Intermediates. Chem Sci 4: