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GaInP2 has shown promise as the wide bandgap top junction in tandem absorber photoelectrochemical (PEC) water splitting devices. Among previously reported dual-junction PEC devices with a GaInP2 top cell, those with the highest performance incorporate an AlInP2 window layer (WL) to reduce surface recombination and a thin GaInP2 capping layer (CL) to protect the WL from corrosion in electrolytes. However, the stability of these III–V systems is limited, and durability continues to be a major challenge broadly in the field of PEC water splitting. This work provides a systematic investigation into the durability of GaInP2 systems, examining the impacts of the window layer and capping layer among single junction pn-GaInP2 photocathodes coated with an MoS2 catalytic and protective layer. The photocathode with both a CL and WL demonstrates the highest PEC performance and longest lifetime, producing a significant current for >125 h. In situ optical imaging and post-test characterization illustrate the progression of macroscopic degradation and chemical state. The surface architecture combining an MoS2 catalyst, CL, and WL can be translated to dual-junction PEC devices with GaInP2 or other III–V top junctions to enable more efficient and stable PEC systems.

While photoelectrochemical (PEC) solar-to-hydrogen efficiencies have greatly improved over the past few decades, advances in PEC durability have lagged behind. Corrosion of semiconductor photoabsorbers in the aqueous conditions needed for water splitting is a major challenge that limits device stability. In addition, a precious-metal catalyst is often required to efficiently promote water splitting. Herein, we demonstrate unassisted water splitting using a nonprecious metal molybdenum disulfide nanomaterial catalytic protection layer paired with a GaInAsP/GaAs tandem device. This device was able to achieve stable unassisted water splitting for nearly 12 h, while a sibling sample with a PtRu catalyst was only stable for 2 h, highlighting the advantage of the nonprecious metal catalyst. In situ optical imaging illustrates the progression of macroscopic degradation that causes device failure. In addition, this work compares unassisted water splitting devices across the field in terms of the efficiency and stability, illustrating the need for improved stability.

Electrochemical transformation of potent greenhouse gases such as CO2 and CH4 to produce useful carbon-based products is a highly desirable sustainability goal. However, selectivity challenges remain in aqueous electrochemical processes as selective CO2 reduction to desired products is difficult and electrochemical CH4 oxidation often proceeds at very low rates. The formation of C–C coupled products in these fields is particularly desirable as this provides a path for the production of high-value fuels and chemicals. We have developed a cyclic electrochemical strategy which can produce acetylene, a C–C coupled product, from such carbon sources and water, with favorable current density and selectivity. This strategy is exemplified with a lithium-mediated cycle: an active Li0 surface is electrochemically generated from LiOH, the newly formed Li0 reacts with a carbon source to form Li2C2, and Li2C2 is hydrolyzed to form acetylene and regenerate LiOH. We demonstrate this process primarily using CO2 gas, achieving a current efficiency of 15% to acetylene (which represents 82% of the maximum based on stoichiometric production of oxygenated byproducts, e.g. LiCO3 and/or Li2O), as verified by gas chromatography and Fourier transform infrared radiation studies. We also explore CH4, CO, and C as alternative precursors in the acetylene synthesis. Notably, the use of graphitic carbon at higher temperatures resulted in over 55% current efficiency to acetylene, with opportunity for further optimization. Importantly, this cycling method avoids the formation of common side products observed during aqueous electrochemical CO2 and CH4 redox reactions, such as H2, CO, HCO2−, or CO2. Theoretical considerations elucidate the feasibility and general applicability of this cycle and the process steps have been characterized with specific electrochemical and materials chemistry techniques. The continued development of this strategy may lead to a viable route for the sustainable production o

Silicon has shown promise for use as a small band gap (1.1 eV) absorber material in photoelectrochemical (PEC) water splitting. However, the limited stability of silicon in acidic electrolyte requires the use of protection strategies coupled with catalysts. Herein, spin coating is used as a versatile method to directly coat silicon photoanodes with an IrOₓ oxygen evolution reaction (OER) catalyst, reducing the processing complexity compared to conventional fabrication schemes. Biphasic strontium chloride/iridium oxide (SrCl₂:IrOₓ) catalysts are also developed, and both catalysts form photoactive junctions with silicon and demonstrate highphotoanode activity. The iridium oxide photoanode displays a photocurrent onset at 1.06 V vs reversible hydrogen electrode (RHE), while the SrCl₂:IrOₓ photoanode onsets earlier at 0.96 V vs RHE. The differing potentials are consistent with the observed photovoltages of 0.43 and 0.53 V for the IrOₓ and SrCl₂:IrOₓ, respectively. By measuring the oxidation of a reversible redox couple, Fe(CN)₆ ³¯⁄⁴¯, we compare the charge carrier extraction of the devices and show that the addition of SrCl₂ to the IrOx catalyst improves the silicon−electrolyte interface compared to pure IrOₓ. However, the durability of the strontium-containing photoanode remains a challenge, with its photocurrent density decreasing by 90% over 4 h. The IrOₓ photoanode, on the other hand, maintained a stable photocurrent density over this timescale. Characterization of the as-prepared and post-tested material structure via Auger electron spectroscopy identifies catalyst film cracking and delamination as the primary failure modes. We propose that improvements to catalyst adhesion should further the viability of spin coating as a technique for photoanode preparation.

Electrochemical processes for ammonia synthesis could potentially replace the high temperature and pressure conditions of the Haber‐Bosch process, with voltage offering a pathway to distributed fertilizer production that leverages the rapidly decreasing cost of renewable electricity. However, nitrogen is an unreactive molecule and the hydrogen evolution reaction presents a major selectivity challenge. An electrode of electrodeposited lithium in tetrahydrofuran solvent overcomes both problems by providing a surface that easily reacts with nitrogen and by limiting the access of protons with a nonaqueous electrolyte. Under these conditions, we measure relatively high faradaic efficiencies (ca. 10 %) and rates (0.1 mA cm−2) toward NH3. We observe the development of a solid electrolyte interface layer as well as the accumulation of lithium and lithium‐containing species. Detailed DFT studies suggest lithium nitride and hydride to be catalytically active phases given their thermodynamic and kinetic stability relative to metallic lithium under reaction conditions and the fast diffusion of nitrogen in lithium.

Electrochemical transformation of potent greenhouse gases such as CO2 and CH4 to produce useful carbon-based products is a highly desirable sustainability goal. However, selectivity challenges remain in aqueous electrochemical processes as selective CO2 reduction to desired products is difficult and electrochemical CH4 oxidation often proceeds at very low rates. The formation of C-C coupled products in these fields is particularly desirable as this provides a path for the production of high-value fuels and chemicals. We have developed a cyclic electrochemical strategy which can produce acetylene, a C-C coupled product, from such carbon sources and water, with favorable current density and selectivity. This strategy is exemplified with a lithium-mediated cycle: an active Li0 surface is electrochemically generated from LiOH, the newly formed Li0 reacts with a carbon source to form Li2C2, and Li2C2 is hydrolyzed to form acetylene and regenerate LiOH. We demonstrate this process primarily using CO2 gas, achieving a current efficiency of 15% to acetylene (which represents 82% of the maximum based on stoichiometric production of oxygenated byproducts, e.g.LiCO3 and/or Li2O), as verified by gas chromatography and Fourier transform infrared radiation studies. We also explore CH4, CO, and C as alternative precursors in the acetylene synthesis. Notably, the use of graphitic carbon at higher temperatures resulted in over 55% current efficiency to acetylene, with opportunity for further optimization. Importantly, this cycling method avoids the formation of common side products observed during aqueous electrochemical CO2 and CH4 redox reactions, such as H2, CO, HCO2−, or CO2. Theoretical considerations elucidate the feasibility and general applicability of thi

Photoelectrochemical water splitting is a promising route for sustainable hydrogen production. Herein, we demonstrate a photoelectrode motif that enables a nanostructured large-surface area electrocatalyst without requiring a nanostructured semiconductor surface with the goal of promoting electrocatalysis while minimizing surface recombination. We compare the photoelectrochemical H2 evolution activity of two silicon photocathode nanostructuring strategies: (1) direct nanostructuring of the silicon surface and (2) incorporation of nanostructured zinc oxide to increase the electrocatalyst surface area on planar silicon. We observed that silicon photocathodes that utilized nanostructured ZnO supports outperformed nanostructured silicon electrodes by ∼50 mV at open circuit under 1 sun illumination and demonstrated comparable electrocatalytic activity.

Electrocatalytic N-2 reduction to ammonia has recently attracted a great deal of interest as a possible renewable energy-driven alternative to the Haber-Bosch process. However, the detection of NH3 after attempting electrocatalytic reduction of N-2 can be hampered by low NH3 yields, ambient NH3 contamination, and the need for multistep chemical separation of NH3 from the electrolyte. Herein, we report a frequency-selective pulse nuclear magnetic resonance (NMR) method and quantify the efficacy of this method to measure the concentration of NH3 (present in the assay as NH4+) in an electrolyte after electrocatalysis. This NMR method was demonstrated to be effective in a variety of nondeuterated, nonaqueous and aqueous electrolytes, and did not require the separation of NH3 from the electrolyte. NH3 sensitivity down to 1 mu M was readily achieved with isotopic and chemical specificity. Compatible electrolytes and solvents included ethanol, tetrahydrofuran, dimethyl sulfoxide, acetonitrile, propylene carbonate, diethyl either, hexanes, and water. The efficacy of the commonly employed Berthelot method was also quantified and compared to the NMR method in a range of nonaqueous and aqueous electrolytes, including ethanol, THF, propylene carbonate, and water.

The electrochemical synthesis of ammonia from nitrogen under mild conditions and using renewable electricity is in principle an attractive alternative1-4 to the demanding, energy-intense Haber-Bosch process, which dominates industrial ammonia production. However, the electrochemical alternative faces considerable scientific and technical challenges5,6 and most experimental studies reported thus far achieve only low selectivities and conversions. In fact, the amount of ammonia produced is usually so small that it is difficult to firmly attribute it to electrochemical nitrogen fixation7-9 and exclude contamination due to ammonia that is either present in air, human breath or ion-conducting membranes9, or generated from labile nitrogen-containing compounds (for example, nitrates, amines, nitrites and nitrogen oxides) that are typically present in the nitrogen gas stream10, in the atmosphere or even the catalyst itself. Although these many and varied sources of potential experimental artefacts are beginning to be recognized and dealt with11,12, concerted efforts to develop effective electrochemical nitrogen reduction processes would benefit from benchmarking protocols for the reaction and from a standardized set of control experiments to identify and then eliminate or quantify contamination sources. Here we put forward such a rigorous procedure that, by making essential use of 15N2, allows us to reliably detect and quantify the electroreduction of N2 to NH3. We demonstrate experimentally the significance of various sources of contamination and show how to remove labile nitrogen-containing compounds present in the N2 gas and how to perform quantitative isotope measurements with cycling of 15N2 gas to reduce both contamination and the cost of isotope measurements. Following this protocol, we obtain negative results when using the m

Graphene may be an almost ideal protection layer for semiconductor photoelectrodes. It can be grown in nearly pinhole-free large area layers and has been shown to inhibit the oxidn. of metals in air as well as in aq. electrochem. environments. In this study, the chem., electrochem., and photoelectrochem. behavior of graphene-coated n-type Si(111) photoanodes was compared to that of H-terminated and Me terminated n-type Si(111) photoanodes in contact with aq. K_3[Fe(CN)_6]/K_4[Fe(CN)_6] as well as in contact with a series of oneelectron redox couples in non-aq. electrolytes. The n-Si/Graphene electrodes exhibited stable short-circuit photocurrent densities of over 10 mA cm^(-2) for over 1000 s of operation in aq. electrolyte, whereas n-Si-H and n- Si-Me electrodes yielded nearly complete decay of the c.d. within approx. 30 s and 120 s, resp. The values of the open-circuit photovoltages and the flat-band potentials of the Si were a function of both the Fermi level of the graphene and the electrochem. potential of the electrolyte soln., indicating that the n-Si/Graphene interface did not form a buried junction with the soln. contact. The use of addnl. layers of graphene further improved stability while leading to a junction that was increasingly pinned by the Si/graphene interface. Finally, the chem. stability of graphene in acidic and basic environments relevant to solar water splitting was demonstrated and the possibility for non-covalent hydrogen evolution catalyst attachment via pi-pi interactions between graphene and pyrene moieties appended to known mol. hydrogen evolution catalysts was explored.

Graphene may be an almost ideal protection layer for semiconductor photoelectrodes. It can be grown in nearly pinhole-free large area layers and has been shown to inhibit the oxidn. of metals in air as well as in aq. electrochem. environments. In this study, the electrochem. behavior of graphene-coated n-type Si(111) photoanodes was compared to that of H-terminated n-type Si(111) photoanodes in contact with aq. K_3[Fe(CN)_6]/K_4[Fe(CN)_6] as well as in contact with a series of one-electron redox couples in non-aq. electrolytes. The n-Si/Graphene electrodes exhibited stable short-circuit photocurrent densities of over 10 mA cm^(-2) for over 1000 s of operation in aq. electrolytes, whereas n-Si-H electrodes yielded nearly complete decay of the c.d. within approx. 30 s. The values of the open-circuit photovoltages and the flat-band potentials of the Si were a function of both the Fermi level of the graphene and the electrochem. potential of the electrolyte soln., indicating that the n-Si/Graphene interface did not form a buried junction with the soln. contact. The use of addnl. layers of graphene further improved stability while leading to a junction that was increasingly pinned by the Si/graphene interface.