skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: >10% solar-to-hydrogen efficiency unassisted water splitting on ALD-protected silicon heterojunction solar cells
Solar water splitting using photoelectrochemical cells (PEC's) is a promising pathway toward clean and sustainable storage of renewable energy. Practical realization of solar-driven synthesis of hydrogen and oxygen integrating light absorption and electrolysis of water has been challenging because of (1) the limited stability of good photovoltaic materials under the required electrochemical conditions, and (2) photovoltaic efficiency losses due to light absorption by catalysts, the electrolyte, and generated bubbles, or reflection at their various interfaces. Herein, we evaluate a novel integrated solar water splitting architecture using efficient silicon heterojunction photovoltaic cells that avoids such losses and exhibits a solar-to-hydrogen (STH) efficiency in excess of 10%. Series-connected silicon Heterojunction with Intrinsic Thin layer (HIT) cells generate sufficient photovoltage for unassisted water splitting, with one of the cells acting as the photocathode. Platinum is deposited on the back (dark) junction of this HIT cell as the catalyst for the hydrogen evolution reaction (HER). The photocathode is protected from corrosion by a TiO 2 layer deposited by atomic layer deposition (ALD) interposed between the HIT cell and the Pt, enabling stable operation for >120 hours. Combined with oxygen evolution reaction (OER) catalysts deposited on a porous metal dark anode, these PEC's achieve stable water splitting with a record high STH efficiency for an integrated silicon photosynthesis device.  more » « less
Award ID(s):
1805084
PAR ID:
10107115
Author(s) / Creator(s):
; ; ; ; ; ; ; ;
Date Published:
Journal Name:
Sustainable Energy & Fuels
Volume:
3
Issue:
6
ISSN:
2398-4902
Page Range / eLocation ID:
1490 to 1500
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    In this manuscript we study the impact of edge losses in silicon heterojunction solar cells. The edge of the cells may play a larger role due to the large diffusion length of the carriers and the presence of a high conductive layer in this type of architecture. We fabricate silicon heterojunction solar cells with different areas and masking schemes to evaluate the impact of the edge on the open-circuit voltage. We measured lower open-circuit voltages on cells which have larger ratio of cell perimeter-to-area but have similar lifetimes and similar implied characteristics. The solar cell with 6 cm^2 shows open-circuit voltage 7 mV lower than the cell with 150.3 cm^2 . Electroluminescence and photoluminescence imaging are used to evaluate the diffusion of carriers at the edges of the cells. We show the out diffusion of carriers at the edges of the cell which demonstrates the cell is affected by the surroundings 
    more » « less
  2. Energy harvesting from solar and water has created ripples in materials energy research for the last several decades, complemented by the rise of Hydrogen as a clean fuel. Among these, water electrolysis leading to generation of oxygen and hydrogen, has been one of the most promising routes towards sustainable alternative energy generation and storage, with applications ranging from metal-​air batteries, fuel cells, to solar-​to-​fuel energy conversion systems. In fact, solar water splitting is one of the most promising method to produce Hydrogen without depleting fossil-​fuel based natural resources. However, the efficiency and practical feasibility of water electrolysis is limited by the anodic oxygen evolution reaction (OER)​, which is a kinetically sluggish, electron-​intensive uphill reaction. A slow OER process also slows the other half- cell reaction, i.e. the hydrogen evolution reaction (HER) at the cathode. Hence, designing efficient catalysts for OER process from earth-​abundant resources has been one of the primary concerns for advancing solar water splitting. In the Nath group we have focused on transition metal chalcogenides as efficient OER electrocatalysts. We have proposed the idea that these chalcogenides, specifically, selenides and tellurides will show much better OER catalytic activity due to increasing covalency around the catalytically active transition metal site, compared to the oxides caused by decreasing electronegativity of the anion, which in turn leads to variation of chem. potential around the transition metal center, [e.g. lowering the Ni 2+ -​-​> Ni 3+ oxidn. potential in Ni-​based catalysts where Ni 3+ is the actually catalytically active species]​. Based on such hypothesis, we have synthesized a plethora of transition metal selenides including those based on Ni, Ni-​Fe, Co, and Ni-​Co, which show high catalytic efficiency characterized by low onset potential and overpotential at 10 mA​/cm 2 [Ni 3 Se 2 - 200 - 290 mV; Co 7 Se 8 - 260 mV; FeNi 2 Se 4 -​NrGO - 170 mV (NrGO - N-​doped reduced graphene oxide)​; NiFe 2 Se 4 - 210 mV; CoNi 2 Se 4 - 190 mV; Ni 3 Te 2 - 180 mV]​. 
    more » « less
  3. The intrinsic and doped amorphous silicon layers in silicon heterojunction solar cells parasitically absorb light in the short wavelength region of the solar spectrum, lowering the generation current available to the device. Herein, a promising alternative to the hole‐selective amorphous silicon contact layers using only wide bandgap, transparent oxide materials is presented. Using thermal atomic layer deposition, a 1 nm hydrogenated aluminum oxide layer is deposited followed by a 4 nm molybdenum oxide layer on n‐type crystalline silicon. This contact stack provides an effective carrier lifetime of 1.14 ms. It is shown that the molybdenum oxide layer is successfully deposited with a high work function, which facilitates efficient hole extraction and repels majority carriers from the c‐Si surface. Then the implied open‐circuit voltage, saturation current density, and contact resistivity are recorded as a function of contact annealing temperature and show that they are relatively stable up to 200 °C. 
    more » « less
  4. The rapid rise in single-junction perovskite solar cell (PSC) efficiencies, tunable bandgap and low-cost solution processability make PSCs an attractive candidate for tandems with Si bottom cells. However, the challenge is to fabricate a high-performance semitransparent perovskite top cell in combination with an appropriate silicon bottom cell with high response to long wavelength photons that are filtered through the perovskite top cell. Currently, semitransparent perovskite cells show much lower performance compared to their opaque counterparts while high-performance silicon bottom cells, such as heterojunction with intrinsic thin layer (HIT) and interdigitated back contact (IBC), maybe too expensive to meet the cost and efficiency targets for commercial viability. Here, we demonstrate a 26.7% perovskite-Si four terminal (4T) tandem cell comprising a highly efficient 17.8% CsFAMAPbIBr semitransparent, 1.63-eV bandgap perovskite top cell and a ≥ 22% efficiency n-type Si bottom cell fabricated with a conventional boron diffused emitter on the front and carrier selective n+ poly-Si/SiOx passivated contact on the rear. This is among the highest efficiency perovskite/Si 4T tandems published to-date and represents the first demonstration of the use of the high temperature-resistant single side n-TOPCon Si cell in a 4T configuration. 
    more » « less
  5. Photocatalytic water splitting is a wireless method for solar-to-hydrogen conversion. To date, however, the efficiency of photocatalytic water splitting is still very low. Here, we have investigated the design, synthesis, and characterization of quadruple-band InGaN nanowire arrays, which consist of In 0.35 Ga 0.65 N, In 0.27 Ga 0.73 N, In 0.20 Ga 0.80 N, and GaN segments, with energy bandgaps of ∼2.1 eV, 2.4 eV, 2.6 eV, and 3.4 eV, respectively. Such multi-band InGaN nanowire arrays are integrated directly on a nonplanar wafer for enhanced light absorption. Moreover, a doping gradient is introduced along the lateral dimension of the nanowires, which forms a built-in electric field and promotes efficient charge carrier separation and extraction for water redox reactions. We have demonstrated that the quadruple-band InGaN nanowire photocatalyst can exhibit a solar-to-hydrogen efficiency of ∼5.2% with relatively stable operation. This work demonstrates a novel strategy using multi-band semiconductor nanostructures for artificial photosynthesis and solar fuel conversion with significantly improved performance. 
    more » « less