SinoGreenTech Academic Portal
Open AccessDOI: 10.1007/s40843-025-3769-2Original Research

Suppression of Schottky Effect with Highly Corrosion-Resistant Coating on Porous Transport Layers for Interface Optimization in Proton Exchange Membrane Electrolyzers

School of Chemical Engineering and Technology, Sun Yat-sen University

Read Executive PreviewQuick FAQ
Suppression of Schottky Effect with Highly Corrosion-Resistant Coating on Porous Transport Layers for Interface Optimization in Proton Exchange Membrane Electrolyzers
Graphical Abstract / Figure
Published In
SCIENCE CHINA Materials
Published:January 15, 2026Edition:Vol. 69, Issue 6 • pp. 100-112Citation:Yun Liu et al. (2026), SCIENCE CHINA Materials
Impact Factor3.5 (Q2 Scopus)
Source Journal中国科学: 材料
Strategic Intelligence Pillar
Water Electrolysis for Green Hydrogen: Low-Iridium PEM & High-Pressure Alkaline Systems
Explore Topic Pillar

Key Takeaways & Executive Findings

  • • • The MoIrOx-coated Ti felt PTL achieves a current density of 3.27 A cm−2 at 2 V, a 59.5% improvement over uncoated Ti felts, directly enhancing hydrogen production rate and cell efficiency. • • The coating suppresses the Schottky barrier and pinch-off effect by forming a conductive interlayer that isolates TiOx from the ionomer, reducing charge transfer resistance and enabling stable operation with ultra-low catalyst loadings. • • The MoIrOx coating is applied via scalable spray deposition and thermal treatment, offering a cost-effective route to mitigate corrosion-induced performance degradation in acidic PEMWE environments. • • The work demonstrates a 59.5% increase in current density, which translates to significant energy savings and reduced capital costs for large-scale green hydrogen production, while minimizing reliance on precious metals.

Abstract

Proton exchange membrane water electrolyzers (PEMWEs) are pivotal for sustainable hydrogen production, yet the corrosion-induced TiOx on porous transport layers (PTLs) introduces Schottky contact barriers and pinch-off effects, severely impeding charge transfer and efficiency. Here, a cost-effective MoIrOx coating via spray deposition and thermal treatment on Ti felts is proposed. The coating forms a conductive interlayer that establishes a Schottky barrier staircase, reducing the effective electron transfer barrier and isolating TiOx from the ionomer to mitigate the pinch-off effect. The optimal PTL achieves a current density of 3.27 A cm−2 at 2 V, surpassing uncoated Ti felts by 59.5%. The MoIrOx interlayer suppresses localized electron accumulation at the interface, enabling stable operation with ultra-low catalyst loadings by preventing direct ionomer-TiOx contact. This work demonstrates a scalable strategy to enhance PEMWE efficiency and durability while minimizing precious metal reliance, offering critical insights into interface engineering for electrolyzers.

1. Introduction

The commercialization of proton exchange membrane water electrolyzers (PEMWEs) is hindered by the corrosion of titanium-based porous transport layers (PTLs) under harsh acidic and high-potential conditions. The resulting TiOx passivation layer introduces Schottky contact barriers at the PTL/catalyst interface, impeding electron transfer and causing the pinch-off effect—a nanoscale phenomenon where energy band bending at the semiconductor-electrolyte-catalyst junction increases charge transfer resistance. These interfacial losses degrade cell efficiency and durability, limiting the economic viability of green hydrogen production.

Existing mitigation strategies, such as applying noble metal coatings (e.g., Pt or Ir), are effective but cost-prohibitive for large-scale deployment. This work introduces a cost-effective MoIrOx coating applied via spray deposition and thermal treatment on Ti felts. The coating forms a conductive interlayer that establishes a Schottky barrier staircase, reducing the effective electron transfer barrier and isolating TiOx from the ionomer to mitigate the pinch-off effect. This approach directly addresses the interfacial bottleneck, achieving a 59.5% improvement in current density at 2 V while minimizing precious metal loading, offering a scalable pathway to enhance PEMWE performance and durability.

SinoTechIntel Interactive Document Reader
Page 1–5 of Preview
100%
Download Full PDF

Loading authentic research manuscript (Pages 1–5)...

Cite This Research Paper
Yun Liu, Bingqian Pang, Sihan Mao, Wenjuan Shi, Tianjiao Wang, Peng Rao, Jing Li, Min Wang, Yuliang Yuan, Xiaodong Shi, Xinlong Tian, Zhenye Kang (2026). Suppression of Schottky Effect with Highly Corrosion-Resistant Coating on Porous Transport Layers for Interface Optimization in Proton Exchange Membrane Electrolyzers. SCIENCE CHINA Materials. https://doi.org/10.1007/s40843-025-3769-2
SinoGreenTech Academic & Legal Disclaimer

Research & Educational Purpose Only: The translations, structured abstracts, analytical annotations, and data reports provided by SinoGreenTechare intended exclusively for academic research, internal corporate R&D, and educational benchmarking. They do not constitute formal engineering, chemical safety, legal, or professional advice.

Copyright & Intellectual Property Notice: Original copyright of the underlying source articles and experimental data remains with the respective authors, institutions, and original publishing journals. SinoGreenTech claims intellectual property only over its proprietary translations, analytical syntheses, and AEO structured enhancements in accordance with international fair use and academic citation principles.

Frequently Asked Questions

What is the specific improvement in current density achieved by the MoIrOx-coated PTL compared to uncoated Ti felt, and what is the underlying mechanism?

The MoIrOx-coated PTL achieves a current density of 3.27 A cm−2 at 2 V, which is 59.5% higher than uncoated Ti felts. This improvement is attributed to the suppression of the Schottky barrier and pinch-off effect. The MoIrOx coating forms a conductive interlayer that creates a Schottky barrier staircase, reducing the effective electron transfer barrier. Additionally, it isolates TiOx from the ionomer, preventing the pinch-off effect that causes energy band bending and increased charge transfer resistance.

How does the MoIrOx coating mitigate the pinch-off effect, and what is the role of the interlayer in preventing direct ionomer-TiOx contact?

The pinch-off effect arises from extensive contact between TiOx (a wide-bandgap n-type semiconductor) and the ionomer, leading to significant energy band bending and increased charge transfer barriers. The MoIrOx coating acts as a conductive interlayer that physically separates TiOx from the ionomer, preventing direct contact. This isolation reduces the nanoscale interaction that causes pinch-off, thereby lowering the charge transfer barrier and improving interfacial conductivity.

What is the scalability of the spray deposition and thermal treatment method for industrial production of coated PTLs?

Spray deposition and thermal treatment are well-established, scalable techniques used in industrial coating processes. The method allows for uniform coating on large-area Ti felts, and the materials (Mo and Ir) can be applied in thin layers to minimize precious metal usage. The demonstrated performance improvement (59.5% increase in current density) suggests that this approach can be economically viable for large-scale PEMWE manufacturing, though further optimization of coating thickness and uniformity is needed for full-scale production.

What is the long-term stability of the MoIrOx-coated PTL under PEMWE operating conditions, and how does it compare to uncoated Ti felts?

The study indicates that the MoIrOx interlayer suppresses localized electron accumulation at the interface, enabling stable operation with ultra-low catalyst loadings. While specific long-term degradation rates are not provided in the abstract, the corrosion-resistant nature of the coating is expected to prevent TiOx formation, thereby maintaining low interfacial resistance over extended operation. Uncoated Ti felts suffer from gradual passivation, leading to performance decay, whereas the coated PTL is designed to mitigate this issue.

How does the MoIrOx coating reduce reliance on precious metals, and what are the implications for cost reduction in PEMWE systems?

The MoIrOx coating uses a combination of molybdenum (a non-precious metal) and iridium (a precious metal) in a thin layer, reducing the overall iridium loading compared to conventional coatings that rely solely on noble metals. This minimizes precious metal reliance, lowering material costs. The improved performance (59.5% higher current density) also means that less catalyst material is needed to achieve the same hydrogen production rate, further reducing system costs. This is critical for the economic viability of large-scale green hydrogen production.

Related Chinese Research & Cross-Citations

Research Citation2026
Ammonium Vanadate Cathodes in Aqueous Zinc-Ion Batteries: Design Strategies and Research Progress

Ammonium Vanadate Cathodes in Aqueous Zinc-Ion Batteries: Design Strategies and Research Progress

Aqueous zinc-ion batteries (AZIBs) offer a compelling combination of high safety, environmental compatibility, and abundant zinc resources, positioning them as viable candidates for grid-scale energy storage. Their practical deployment, however, is constrained by cathode materials that suffer from structural degradation, sluggish Zn2+ diffusion, and inadequate electronic conductivity. Ammonium vanadates (AVOs) have emerged as high-performance cathodes owing to their layered or tunneled frameworks, which accommodate reversible Zn2+ (de)intercalation with diffusion coefficients superior to conventional vanadium oxides. This review systematically examines recent advances in AVO cathodes for AZIBs, correlating morphological variations—including nanowires, nanobelts, and microflowers—with electrochemical characteristics. The analysis establishes structure–performance relationships that govern capacity retention, rate capability, and cycling stability. Key optimization strategies are critically assessed: defect engineering to enhance electronic conductivity and active site density, interlayer spacing modulation via pre-intercalated cations or structural water to facilitate Zn2+ transport, and composite construction with conductive carbonaceous or polymeric matrices to mitigate dissolution and improve mechanical integrity. Despite these advances, challenges persist in achieving long-term cycling stability (>10,000 cycles) and high areal mass loading (>10 mg cm-2) required for commercial viability. The review concludes by outlining future research directions, including operando characterization of degradation mechanisms and scalable synthesis routes for AVO cathodes in practical AZIB configurations.

Examine Full Data & PDF
Research Citation2026
Microenvironment-responsive therapeutic platforms: Innovations for spinal cord injury repair

Microenvironment-responsive therapeutic platforms: Innovations for spinal cord injury repair

Spinal cord injury (SCI) remains a formidable clinical challenge due to the complex, dynamic lesion microenvironment that impedes axonal regeneration and functional recovery. This highlight examines a microenvironment-responsive therapeutic platform integrating microneedle delivery, ferroptosis modulation, and hydrogen therapy. The platform leverages the pathological hallmarks of SCI—oxidative stress, iron dyshomeostasis, and lipid peroxidation—to achieve spatiotemporally controlled cargo release. By combining microneedle arrays for minimally invasive intraparenchymal administration with hydrogen-releasing biomaterials, the system addresses the dual bottlenecks of poor drug penetration across the blood-spinal cord barrier and insufficient neutralization of reactive oxygen species. Ferroptosis inhibition is achieved through iron chelation and glutathione peroxidase 4 (GPX4) stabilization, while hydrogen gas scavenges hydroxyl radicals and peroxynitrite. This multimodal strategy attenuates secondary injury cascades, reduces glial scar formation, and promotes neural stem cell differentiation. The work is supported by the National Natural Science Foundation of China (82574518) and the Talent Cultivation Project of Paring Academicians with Young Talents in higher education institutions in Zhejiang. The authors declare no conflict of interest. This highlight underscores the translational potential of microenvironment-responsive platforms for SCI repair, emphasizing the need for rigorous preclinical validation and scalable manufacturing.

Examine Full Data & PDF
Research Citation2026
Dual-Site Adsorption over Phosphorus-Doped Copper Oxide for Efficient CO2 Electroreduction to Ethylene

Dual-Site Adsorption over Phosphorus-Doped Copper Oxide for Efficient CO2 Electroreduction to Ethylene

Electroreduction of CO2 to ethylene offers a promising route for renewable electricity storage, yet achieving high ethylene selectivity at industrial current densities remains challenging due to the large energy barrier for C–C coupling. Here, we report a “MOF-assisted in situ doping” strategy to introduce the oxophilic nonmetal phosphorus (P) into the copper oxide (CuO) lattice, constructing a localized Cu–P dual-site adsorption configuration for the key *OCCHO intermediate. The optimized catalyst delivers an impressive Faradaic efficiency of 64.6% for ethylene with a partial current density of 646 mA cm-2. Comprehensive structural characterizations demonstrate that P mainly occupies Cu sites, generating abundant lattice defects and oxygen vacancies. In situ synchrotron infrared spectroscopy and theoretical calculations reveal that P doping modulates the electronic structure of Cu, optimizes the binding energies of *CO and *CHO, and stabilizes *OCCHO via P–O/Cu–C dual-site adsorption, thereby significantly lowering the asymmetric C-C coupling energy barrier to 0.74 eV. This work highlights a dual-site microenvironment regulation strategy for CO2-to-ethylene electroreduction.

Examine Full Data & PDF
Research Citation2026
Hydrophilic Single-Atom Interface Unlocks Low-Potential CO Removal on Pt in PEMFCs

Hydrophilic Single-Atom Interface Unlocks Low-Potential CO Removal on Pt in PEMFCs

Proton exchange membrane fuel cells (PEMFCs) fed with reformate hydrogen suffer severe anode poisoning by trace CO, necessitating high CO electrooxidation potentials that degrade performance and durability. This work introduces a Pt@CrSA-N-C anode catalyst featuring a hydrophilic Cr single-atom interface that simultaneously weakens CO adsorption on Pt via electronic regulation and promotes water activation, thereby lowering the CO oxidation onset potential to approximately 0.13 V vs. RHE. The onset potential was determined by two independent methods: the first potential at which the background-corrected current exceeds 0 mA cm-2 during CO oxidation reaction tests in a three-electrode system, and the potential at which the forward scan current exceeds the N2 background current in CO-stripping voltammetry. The catalyst achieves a maximum power density under 100 ppm CO that surpasses reported advanced catalysts, as compiled in Table S5. Structural, spectroscopic, and electrochemical characterizations collectively establish a coherent rationale for the hydrophilic single-atom interface strategy. This approach addresses the longstanding trade-off between CO tolerance and Pt utilization, offering a viable route for low-potential CO removal in practical PEMFC anodes.

Examine Full Data & PDF
Research Citation2026
An Ionoelastomer-Based Bioinspired Wearable Electronics with Tele-Perception and Tactile Sensation for Machine Learning-Assisted Rehabilitation Management

An Ionoelastomer-Based Bioinspired Wearable Electronics with Tele-Perception and Tactile Sensation for Machine Learning-Assisted Rehabilitation Management

Comprehensive assessment of rehabilitation efficiency is essential for designing appropriate training programs for better musculoskeletal functional recovery. Existing contact-receptor-dependent rehabilitation assessment systems mostly focus on assessing the restoration of muscle function by evaluating grip strength or joint flexion angle; however, parameters reflecting neuromuscular synergistic function are always overlooked. Herein, we develop an ionoelastomer-based soft artificial electroreceptor (SAER) that integrates tele-perception and tactile sensation to track the rehabilitation process, collecting signals related to approaching speed and grip strength sequentially. The SAER uses polyurethane ionoelastomer incorporated with quasi-solid conductive salt as the electric field receptor, and is integrated on a rehabilitation-training ball after assembly to establish an untethered detection device; this enables the remote capture of hand approaching parameter within a 9 cm range, followed by the quantification of grip strength when contacting and grasping. Furthermore, a data-driven assessment system is established by integrating machine learning, which accurately classifies rehabilitation efficiency into six levels; it supports for rehabilitation evaluation and training programs adjustment. Overall, the SAER-based rehabilitation management system establishes a paradigm that synergistically evaluating parameters corresponding to neuromuscular functional restoration and holds strong potential for home-based active rehabilitation for minimizing dependence on frequent clinical supervision.

Examine Full Data & PDF
Research Citation2026
Microwave-Absorbing Materials with Strong Environmental Adaptability for Corrosion Protection, Anti-Icing, and Thermal Management

Microwave-Absorbing Materials with Strong Environmental Adaptability for Corrosion Protection, Anti-Icing, and Thermal Management

Microwave-absorbing materials (MAMs) deployed on naval vessels, aerospace vehicles, and critical electronic systems face coupled electromagnetic, marine salt-spray corrosion, and extreme-temperature loads that legacy single-function absorbers cannot withstand. This review consolidates progress on three environmentally adaptive MAM classes: corrosion-protective, anti-icing, and thermal-management absorbers. The electromagnetic loss and impedance-matching fundamentals are first established, then the synergistic mechanisms, design strategies, and characterization protocols for each class are examined against representative material systems and their measured performance. The analysis identifies a shared design logic—multiscale hierarchical architecture, interfacial polarization engineering, and multifunctional phase integration—while distinguishing the divergent protection mechanisms: barrier and passivation effects for corrosion, surface-energy and latent-heat regulation for anti-icing, and phonon–electron transport decoupling for thermal management. Persistent bottlenecks include the trade-off between impedance matching and protective-layer density, the absence of standardized coupled-field test protocols, and the scarcity of long-term salt-spray and thermal-cycling durability data. Future directions are delineated: intelligent self-adaptive absorbers, multiphysics-coupled simulation frameworks, and environmentally benign multifunctional integration. The review provides a theoretical and technical basis for the design, construction, and engineering scale-up of next-generation high-performance absorbers for aerospace, electronic, and marine equipment.

Examine Full Data & PDF