We report two ternary phase diagrams that show the synthesis conditions to prepare protein@ZIF biocomposites with different phases, including BSA@ZIF-C and insulin@ZIF-C. For each biocomposite, we measured distinct encapsulation efficiency and release profile properties.

With suitable water dissociation (WD) catalysts, bipolar membranes (BPMs) can efficiently dissociate water into H+ and OH– at the junction between anion- and cation-exchange layers (AEL and CEL, respectively). First, however, water must be transported through the AEL or CEL and thus against the outward flow of hydrated H+ and OH–. This is a challenge intrinsic to the BPM architecture and limits operation to current densities typically less than ∼0.5 A·cm–2. Here we explore how water transport affects durability and performance in reference alkaline and acidic membrane electrolyzers, and we use the insight gained to design BPMs with improved water transport. We demonstrate a thin-CEL BPM (2-μm Nafion CEL|​∼200 nm TiO2|∼200 nm NiO + ionomer|​50 μm Sustainion AEL) which maintains a pH difference of ∼14 units between the anode and cathode for current densities of up to 3.4 A·cm–2 with a total water electrolysis voltage of ∼4 V and an estimated WD overpotential of ∼1.5 V. Such high-current-density operation is crucial for key emerging BPM applications, including in water and carbon-dioxide electrolyzers and in (regenerative) fuel cells.

Anion‐exchange‐membrane water electrolyzers (AEMWEs) in principle operate without soluble electrolyte using earth‐abundant catalysts and cell materials and thus lower the cost of green H2. Current systems lack competitive performance and the durability needed for commercialization. One critical issue is a poor understanding of catalyst‐specific degradation processes in the electrolyzer. While non‐platinum‐group‐metal (non‐PGM) oxygen‐evolution catalysts show excellent performance and durability in strongly alkaline electrolyte, this has not transferred directly to pure‐water AEMWEs. Here, AEMWEs with five non‐PGM anode catalysts are built and the catalysts’ structural stability and interactions with the alkaline ionomer are characterized during electrolyzer operation and post‐mortem. The results show catalyst electrical conductivity is one key to obtaining high‐performing systems and that many non‐PGM catalysts restructure during operation. Dynamic Fe sites correlate with enhanced degradation rates, as does the addition of soluble Fe impurities. In contrast, electronically conductive Co3O4 nanoparticles (without Fe in the crystal structure) yield AEMWEs from simple, standard preparation methods, with performance and stability comparable to IrO2. These results reveal the fundamental dynamic catalytic processes resulting in AEMWE device failure under relevant conditions, demonstrate a viable non‐PGM catalyst for AEMWE operation, and illustrate underlying design rules for engineering anode catalyst/ionomer layers with higher performance and durability.

The diverse optical, magnetic, and electronic behaviors of most colloidal semiconductor nanocrystals emerge from materials with limited structural and elemental compositions. Conductive metal−organic frameworks (MOFs) possess rich compositions with complex architectures but remain unexplored as nanocrystals, hindering their incorporation into scalable devices. Here, we report the controllable synthesis of conductive MOF nanoparticles based on Fe(1,2,3-triazolate) 2 . Sizes can be tuned to as small as 5.5 nm, ensuring indefinite colloidal stability. These solutionprocessable MOFs can be analyzed by solution-state spectroscopy and electrochemistry and cast into conductive thin films with excellent uniformity. This unprecedented analysis of MOF materials reveals a strong size dependence in optical and electronic behaviors sensitive to the intrinsic porosity and guest−host interactions of MOFs. These results provide a radical departure from typical MOF characterization, enabling insights into physical properties otherwise impossible with bulk analogues while offering a roadmap for the future of MOF nanoparticle synthesis and device fabrication.

Metrics & MoreArticle Recommendations CONSPECTUS: Catalyzing the oxygen evolution reaction (OER) is important for key energy-storage technologies, particularly water electrolysis and photoelectrolysis for hydrogen fuel production. Under neutral-to-alkaline conditions, first-row transitionmetal oxides/(oxy)hydroxides are the fastest-known OER catalysts and have been the subject of intense study for the past decade. Critical to their high performance is the intentional or accidental addition of Fe to Ni/Co oxides that convert to layered (oxy)hydroxide structures during the OER. Unraveling the role that Fe plays in the catalysis and the molecular identity of the true "active site" has proved challenging, however, due to the dynamics of the host structure and absorbed Fe sites as well as the diversity of local structures in these disordered active phases.In this Account, we highlight our work to understand the role of Fe in Ni/Co (oxy)hydroxide OER catalysts. We first discuss how we characterize the intrinsic activity of the first-row transition-metal (oxy)hydroxide catalysts as thin films by accounting for the contributions of the catalyst-layer thickness (mass loading) and electrical conductivity as well as the underlying substrate's chemical interactions with the catalyst and the presence of Fe species in the electrolyte. We show how Fe-doped Ni/Co (oxy)hydroxides restructure during catalysis, absorb/desorb Fe, and in some cases degrade or regenerate their activity during electrochemical testing. We highlight the relevant techniques and procedures that allowed us to better understand the role of Fe in activating other first-row transition metals for OER. We find several modes of Fe incorporation in Ni/Co (oxy)hydroxides and show how those modes correlate with activity and durability. We also discuss how this understanding informs the incorporation of earthabundant transition-metal OER catalysts in anion-exchange-membrane water electrolyzers (AEMWE) that provide a locally basic anode environment but run on pure water and have advantages over the more-developed proton-exchange-membrane water electrolyzers (PEMWE) that use platinum-group-metal (PGM) catalysts. We outline the key issues of introducing Fe-doped Ni/Co (oxy)hydroxide catalysts at the anode of the AEMWE, such as the oxidative processes triggered by Fe species traveling through the polymer membrane, pH-gradient effects on the catalyst stability, and possibly limited catalyst utilization in the compressed stack configuration. We also suggest possible mitigation strategies for these issues. Finally, we summarize remaining challenges including the long-term stability of Fe-doped Ni/Co (oxy)hydroxides under OER conditions and the lack of accurate models of the dynamic active surface that hinder our understanding of, and thus ability to design, these catalysts.