2010
DOI: 10.1021/cr1002326
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Solar Water Splitting Cells

Abstract: earned a B.S. degree in chemistry from the University of Dayton in 2001 and as an undergraduate worked on conductive polymer syntheses at the Air Force Research Laboratory at Wright Patterson Air Force Base. He completed an M.S. degree in 2004 and Ph.D. degree in 2008 at Portland State University and joined the Lewis group at Caltech in 2008. He is currently an NSF-ACCF postdoctoral fellow (2009) and has been studying the electrical characteristics of inorganic semiconductors in contact with conductive polymer… Show more

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Cited by 8,617 publications
(7,346 citation statements)
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References 266 publications
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“…A common activity metric in the field of solar fuels is the voltage to obtain j disk =10 mA cm0pt-22.84526ptdisk2.84526pt because it matches a 10 % efficient solar cell 62, 63, 64. The LiMn 2 O 4 –carbon composite electrode provided 10 mA cm0pt-22.84526ptdisk2.84526pt at 0.520(2) V overpotential (1.749(2) V versus RHE) at pH 14, which is similar to or better than other first‐row transition metal nanoparticles such as MnO (0.51(4) V), Mn 2 O 3 (0.53(4) V), MnO 2 (0.50(3) V), Co 3 O 4 (0.50(1) V), and NiFe 2 O 4 (0.51(1) V), but higher than that of Mn 3 O 4 (0.43(2) V) 62.…”
Section: Resultsmentioning
confidence: 99%
“…A common activity metric in the field of solar fuels is the voltage to obtain j disk =10 mA cm0pt-22.84526ptdisk2.84526pt because it matches a 10 % efficient solar cell 62, 63, 64. The LiMn 2 O 4 –carbon composite electrode provided 10 mA cm0pt-22.84526ptdisk2.84526pt at 0.520(2) V overpotential (1.749(2) V versus RHE) at pH 14, which is similar to or better than other first‐row transition metal nanoparticles such as MnO (0.51(4) V), Mn 2 O 3 (0.53(4) V), MnO 2 (0.50(3) V), Co 3 O 4 (0.50(1) V), and NiFe 2 O 4 (0.51(1) V), but higher than that of Mn 3 O 4 (0.43(2) V) 62.…”
Section: Resultsmentioning
confidence: 99%
“…To address this challenge, many promising strategies such as photocatalytic or photoelectrochemical or electrocatalytic water splitting have been extensively explored 2, 3, 4, 5, 6. Water electrolysis such as water‐alkali electrolyzers or chlor‐alkali electrolyzers currently adopted in industrial processes is more suitable for centralized hydrogen production because the input energy is electricity which can be easily concentrated and be converted from abundant but dispersive energy sources such as wind energy, tide energy, and solar energy 7, 8, 9.…”
Section: Introductionmentioning
confidence: 99%
“…The evolution of hydrogen through electrocatalytic splitting water is one of the important strategies for hydrogen production 2. Although the Pt‐based materials have been proven to be the most efficient electrocatalysts for hydrogen evolution reaction (HER), the high cost, limited supply, and poor durability hinder their global‐scale application 3, 4. Therefore, much effort has been dedicated to develop robust nonnoble‐metal HER catalysts,5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22 such as cobalt‐, nickel‐, iron‐, tungsten‐, and molybdenum‐based materials.…”
mentioning
confidence: 99%